A nonionic water-insoluble surfactant used as cosurfactant in oral lipid-based formulation SEDDS and SMEDDS. Cosurfactant and solubilizer in topical dosage forms.
Consists of propylene glycol mono- and di- esters of lauric (C12) acid, mainly composed of monoesters and a small fraction of diesters
Key characteristics
Product form
Liquid
Viscosity (mPa.s)
25 (20°C)
HLB
3
Main functionalities
Solubilizer for poorly-soluble APIs and bioavailability enhancer. Cosurfactant in LFCS Type II (SEDDS) and Type III (SMEDDS) formulations. Solubilizer and cosurfactant for microemulsion in topical formulation. Safety of use is inferred by precedence of use in approved pharmaceutical products.
Sensitive and sun-intolerant skin deserves effective and sensorial UV protection too! Formulated with Emulium® Illustro, this sunscreen is neither sticky nor greasy on the skin. It is easy to apply and gives the skin a sunshine glow thanks to Gatuline® Radiance.
Refresh and protect your skin with this sprayable suncare lotion. Thanks to Emulfree® CBG MB and its bi-gel technology, the formula is very fluid and refreshing during application and brings comfort without any greasy nor tacky afterfeel.
Perfectly adapted for beach or daily use, this suncare lotion SPF50 formulated with Emulium® Mellifera MB spreads easily and penetrates very quickly into the skin. It leaves a very light and dry feel, as if no product had been applied.
This very high protection SPF50 is the best ally for sun-sensitive skin, whether in the city or at the beach. Thanks to Emulium™ Dolcea MB, the texture is fluid, soft and comfortable and leaves a very smooth, non-greasy and non-sticky afterfeel.
This SPF30 sunscreen doesn’t look like it! Thanks to Emulium® Dolcea MB, the texture is soft and comfortable and leaves a very smooth, non-greasy and non-sticky afterfeel. It can be used for daily care routines or at the beach.
Some body areas are particularly prone to UV damage and deserve a foolproof sun protection: nose, cheekbones, scars, tattoos… This anhydrous sun stick is ideal due to its targeted application and its SPF50+. Once applied, it leaves a dry and powdery finish.
This natural sunscreen SPF30, composed exclusively of non-nano mineral filters, is perfect for protecting your skin from UV rays at the beach while limiting environmental damage! Unlike most natural sunscreens, its texture is soft, easy to spread, and leaves no sticky nor greasy film thanks to Emulium® Illustro. A mix of active ingredients brings energy and radiance to the skin.
This daily care is perfect to protect the skin from UV rays without worry. Its comfortable yet fluid texture penetrates quickly and leaves a soft film on the skin, while Solastemis™ protects the skin from the harmful effects of UVA and combats photo-aging.
\n
\n
Find out more about these formulas in our booklet HERE.
\n
\n
Other formulations are available on demand. Do not hesitate to contact your Gattefossé’s sales representative for more information about these new formulations or for any suncare development project to benefit from Gattefossé’s expertise.
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A glyceride with an intermediate melting point used as lubricant and flow aid in powder blends for capsule filling and as a coating agent for taste masking.
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Glyceryl distearate
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Glycerol distearate (type I)
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73071MW2KM
\n"},{"keys":"Preferred Substance Name (FDA)","value":"
GLYCERYL DISTEARATE
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Glyceryl palmitostearate
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Consists of esters of palmitic (C16) and stearic (C18) acids, the diester fraction being predominant
Coating agent for taste masking. Lubricant and flow aid for capsule filling with powders. Modified release matrix former for tablets. Safety of use is inferred by GRAS status and precedence of use in approved pharmaceutical products.
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Hot-melt coating with lipid excipients
\n
Jannin, V. and Cuppok, Y.
\n
International Journal of Pharmaceutics, 457[2], 480-487. 2013.
Modification of the drug release of ibuprofen by hot melt coating with mixes of Compritol® 888 ATO and non ionic surfactant
\n
Jannin V., Bérard V. and Andrés C.
\n
AAPS 2005
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Identify easily the excipients you need with a (multi) criteria search. Alternatively, search by pharmacopoeia name, FDA IID preferred substance name or UNII code using the keyword tool.
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for successful preclinical studies with Gattefossé excipients"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":9,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"","_yoast_wpseo_metadesc":""},"categories":[49],"tags":[],"acf":{"content_not_translated":true,"equivalent_fr":false,"equivalent_en":false,"component":"PageGenericContentPharma","title":"Guide for successful preclinical studies","introduction":"","":false,"content":"
Make better decisions earlier!
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We developed this guideline to help formulate molecules with poor solubility and oral bioavailability into more drug-like compounds. The approaches described provide effective strategies to obtain the target dose, sufficient to allow the characterization and optimization of the pharmacokinetic, efficacy and safety profile.
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Our aim is to help you work with our excipients to get the best results possibly reducing the risk of failure later on during development. Contact your local representative to get your copy of the guideline and technical support.
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What you will find in our guideline:
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Enabling strategies for efficacy, PK and safety evaluation
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During lead optimization the scientist in preclinical development aims to maximize solubility and exposure of the test compound in animal models.
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In this chapter we highlight the appropriateness of our single excipients to enhance the bioavailability of compounds. We further provide ready-to-use platform formulations that were reported efficient in vivo.
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Safety and tolerability information
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Understanding the excipient’s safety and tolerability profile in various species is crucial to prevent unexpected formulation-related effects.
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The compilation of our preclinical safety data helps you avoid long literature research and expensive evaluation of safe dosing volumes of Gattefosse excipients.How to correctly assess dosing volumes of excipient blends is also addressed in this chapter.
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Handling and dosing recommendations
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Appropriate excipient handling and proper dosing to animals prevent misinterpretation of study results.
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We herein underpin the need for some of our excipients to be handled with care and dosed under specific precautions. Considering these handling procedures and dosing recommendations provide the best practices to assure reliable outcomes.
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Excipient summary tables
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Functional excipients from Gattefosse are highly beneficial when used in enabled formulations for nonclinical evaluation and transfer to humans.
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Our excipients are thoroughly characterized and used in various medicines worldwide. Practical information is compiled at the end of this document enabling rapid retrieval of key information: physicochemical properties, regulatory status and precedence of use.
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Self-emulsifying drug delivery systems (SEDDS): In vivo-proof of concept for oral delivery of insulin glargine
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Victor Claus , Helen Spleis, Christoph Federer, Katrin Z ̈oller, Richard Wibel, Flavia Laffleur, Camille Dumont, Philippe Caisse, Andreas Bernkop-Schnürch
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International Journal of Pharmaceutics 639 (2023) 122964
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In this study, lipophilicity of insulin glargine (IG) was successfully increased via hydrophobic ion pairing (HIP) with sodium octadecyl sulfate to enable incorporation into self-emulsifying \n drug delivery systems (SEDDS). The SEDDS formulations F1 and F2 were administered to rats via oral gavage and resulted in a bioavailability of 0.55% and 0.44%, corresponding to a 7.7-fold and 6.2-fold increased bioavailability, respectively. Thus, incorporation of complexed insulin glargine into SEDDS formulations provides a promising approach to facilitate its oral absorption.
Successful oral delivery of poorly water-soluble drugs both depends on the intraluminal behavior of drugs and of appropriate advanced drug delivery systems
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Ben J. Boyd, Christel A.S. Bergström, Zahari Vinarov, Martin Kuentz, Joachim Brouwers, Patrick Augustijns, Martin Brandl, Andreas Bernkop-Schnürch, Neha Shrestha, Véronique Préat, Anette Müllertz, Annette Bauer-Brandl, Vincent Jannin
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European Journal of Pharmaceutical Sciences, Volume 137, 2019, 104967, \n ISSN 0928-0987, https://doi.org/10.1016/j.ejps.2019.104967.
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In this excellent review article issued from the UNGAP program (European Network on Understanding Gastro-intestinal Absorption-related Process) you will find relevant and up-to-date information on:
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Poorly water soluble drugs and the link between physico-chemical properties and solubility, lipophilicity and permeability
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Technologies to increase solubility and dissolution rate: salt formation, amorphous solid dispersions, lipid-based formulations
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How to avoid precipitation and create a concentration gradient to improve absorption
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Methods for modelling the performance such as Molecular Dynamics Simulations
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In vitro methods for solubility and dissolution assessments
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Methods to explore the absorption in the GI tract: GI concentration-time profile, in vitro digestion, in vitro models coupling dissolution and permeation, mucus diffusion
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Impact of molecularly dissolved drug versus apparently dissolved drug (ie in colloidal structure)
1 Initial identification and characterization of the active ingredient \n 1.1 Physico-chemical characteristics \n 1.2 Impact of physicochemical characteristics on absorption \n 1.3 Passive diffusion prediction tools \n 1.4 In silico prediction \n 2 Biopharmaceutical classifications
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III Formulation strategies
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1 prerequisites \n 2 techniques for increasing the dissolution rate \n 3 Solubility enhancement technologies \n 4 Improving the permeability, oral route
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IV Control, assessment, prediction of the bioavailability
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1 Physicochemical control methods for the manufacturing intermediates and finished products \n 2 Assessing an dpredicting the bioavailability of the formulations
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V Alternative strategy: changing the route of administration
Colloidal aspects of dispersion and digestion of self-dispersing lipid-based formulations for poorly water-soluble drugs
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Kapilkumar Vithani, Vincent Jannin, Colin W. Pouton, Ben J. Boyd
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In this review article, the authors explain the importance of the colloidal structures formed during dispersion and digestion of self emulsifying lipid-based formulations on drug solubilization and absorption.
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A review of the techniques used to characterize the colloidal structures is also carried out.
LIPID-BASED DELIVERY – Are Lipid-Based Drug Delivery Systems in Your Formulation Toolbox?
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Dr. Jason LePree Drug Development & Delivery, Issue: October 2017, Posted Date: 9/29/2017 This article reviews the causes of poor bioavailability for drugs. It provides an introduction to lipid-based drug delivery systems, and how the formulation approach can be used to overcome impediments to good bioavailability of therapeutic actives, including poor water solubility, low permeability, and degradation by stomach acid or enzymes in vivo.
Reaching milestones in lipid-based formulations: from effective prediction to successful development
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September 2015 This white paper describes the important milestones achieved in lipid based formulation (LBF) development for oral drug delivery. Collaborative research between academic and industrial partners has increased understanding of the functional properties of lipid excipients and the role they play in solubilizing poorly water soluble compounds. It has also led to the development of in vitro – in vivo predictive analytical tools. The key scientific articles describing these milestones are collected in this one White Paper, providing a single source of practical information for those interested in lipid formulation development.
This acticle describes the work undertaken in Gattefossé R&D labs (St Priest) to develop lipid formulations for low to medium lipophilicity API: piroxicam, nifedipine and curcurmin and evaluate the effect of in-vitro digestion on the solubilizing capacity of the formulations.
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Converting simple microemulsion into attractive foam for topical pain treatment. A case study with lidocaine base
Pharmaceutical foams are becoming more popular probably due to more topical medicines being switched to OTC and the need to innovate and differentiate ‘brands’ and an increasing awareness of the importance of formulating to deliver sensorial benefits and positive impact on patient experience and adherence. Gattefossé, as a leading provider of excipients for the pharmaceutical industry, manufactures solubilizers and texturizers for skin drug delivery. In this white paper we give formulation tips for propellant and propellant-free foams with guidelines on how to formulate and select excipients and case studies with model drugs.
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A 3D-Printed Polymer–Lipid-Hybrid Tablet towards the Development of Bespoke SMEDDS Formulations
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Bryce W. Barber, Camille Dumont, Philippe Caisse, George P. Simon, Ben J. Boyd
A Proof of Concept for 3D Printing of Solid Lipid-Based Formulations of Poorly Water-Soluble Drugs to Control Formulation Dispersion Kinetics
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Vithani K, Goyanes A, Jannin V, Basit AW, Gaisford S, Boyd BJ
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Pharm Res. 2019 May 16;36(7):102. \n doi: 10.1007/s11095-019-2639-y.
\n
In this study, the authors show that solid SMEDDS can be produced with a 3D printing process and solid and semi-solid lipid excipients. The proof of concept is established with cinnarizine and fenofibrate as model drugs.
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Anti-pollution (the skin is less reactive, durably soothed)
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Alphabet creams
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Skin perfectors
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Illuminating products
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Global antiaging lines
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Qualité et sécurité
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La qualité est pour nous un facteur-clé de progrès. Elle est partie intégrante de tout ce que nous entreprenons, depuis nos activités de R&D jusqu’à la commercialisation des produits.
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Nos politiques de qualité sont constamment mises à niveau afin de répondre aux attentes de nos clients et de les anticiper. Nous sommes régulièrement audités par nos principaux clients et nous nous efforçons d’améliorer de façon continue nos normes de qualité, validées par plusieurs certifications.
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Notre site industriel de Saint-Priest, en France, est certifié ISO 9001 depuis 1993.
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20 audits clients sont menés en moyenne chaque année sur notre site de Saint-Priest.
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Nos produits répondent aux standards exigés par divers référentiels tels qu’ECOCERT, COSMOS, National Organic Program, etc.
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Depuis 1990, Gattefossé est membre du programme Responsible Care, l’initiative mondiale de l’industrie chimique pour l’amélioration continue des performances dans les domaines de la santé, de la sécurité et de l’environnement.
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Bonnes pratiques de fabrication
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Nous appliquons strictement les bonnes pratiques de fabrication (BPF), que ce soit pour nos excipients pharmaceutiques ou nos ingrédients cosmétiques.
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En tant que membre actif de l’International Pharmaceutical Excipients Council (IPEC), nous avons mis notre système qualité en conformité avec le guide commun de l’IPEC et du PQG sur les bonnes pratiques de fabrication des excipients pharmaceutiques (« GMP Guide for Pharmaceutical Excipients »).
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Pour les ingrédients cosmétiques, notre système qualité respecte les bonnes pratiques de fabrication de l’EFfCI, fédération européenne dont nous sommes un membre actif.
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Sécurité
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Dans le cadre de notre politique de management, nous avons mis en place des mesures de sécurité strictes visant à prévenir les risques liés à nos activités – fabrication, chaîne d’approvisionnement, logistique et R&D – et nos installations – lignes de production, laboratoires d’applications et bâtiments administratifs.
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La formation de nos équipes fait l’objet d’une attention particulière de notre part et passe notamment par des campagnes de sensibilisation régulières. Nous définissons des indicateurs et mettons systématiquement en place des plans d’action pour assurer la sécurité de nos collaborateurs et l’innocuité de nos produits sur le long terme.
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Cet engagement en faveur de la qualité nous permet de partager des références communes avec nos clients en termes de systèmes et de normes industrielles et de les intégrer à nos propres procédures.
\n"},{"wysiwyg":"
Responsabilité sociale de l’entreprise
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Environnement
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Pour encourager l’innovation responsable, nos processus de production ont été modernisés avec pour objectif de dépenser moins d’énergie, de réduire nos déchets et de maximiser le recyclage.
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Depuis de nombreuses années, Gattefossé s’engage en faveur du développement durable, en réduisant sensiblement sa consommation énergétique tout en augmentant sa capacité de fabrication.
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Notre entreprise protège l’environnement en sélectionnant avec soin des matières premières d’origine naturelle pour ses processus de production. Ainsi, Gattefossé est membre depuis 2010 de l’organisation RSPOqui soutient les coopératives et les producteurs d’huile de palme responsables. En 2017, l’entreprise a obtenu la certification RSPO « Mass Balance » pour son site de fabrication en France. Gattefossé utilise également une huile de palme certifiée « Segregated » pour sa gamme d’ingrédients cosmétiques Lipocire™.
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Gattefossé offre la garantie que ses matières premières proviennent de sources fiables, identifiables et renouvelables, grâce à un traçage rigoureux de leurs origines et des méthodes de production. Nous établissons avec nos fournisseurs des relations pérennes et les considérons comme de véritables partenaires stratégiques.
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Développement humain
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Nous avons la conviction que la future croissance de notre entreprise dépend des talents qui la composent à travers le monde et qui œuvrent au quotidien pour faire de Gattefossé un acteur mondial. Le groupe est fier de sa forte culture d’entreprise, influencée par les personnalités de ses fondateurs et de ses dirigeants. Ils ont su faire évoluer la société tout en restant fidèles au code éthique établi dès sa création.
Gattefossé a établi des liens étroits avec la communauté scientifique internationale et partage ses connaissances par le biais de publications, de séminaires et de conférences. L’entreprise soutient des doctorants et gère des projets de recherche sous contrat avec divers groupes universitaires dans le monde.
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Lesjournées galéniques de Saint-Rémy de Provence
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Organisées sous l’égide de la Fondation Gattefossé, les Journées Galéniques de Saint-Rémy de Provencerassemblent chaque année la communauté scientifique internationale industrielle et académique autour d’un thème lié à la formulation des médicaments. Cet évènement vise à favoriser les échanges scientifiques en pharmacie galénique pour faire progresser les connaissances et les techniques dans ce domaine.
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En organisant ces rencontres, Gattefossé poursuit l’œuvre initiée dans les années 60 par Henri-Marcel Gattefossé,qui plaça l’entreprise sous le signe du dialogue avec les chercheurs du monde entier.
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Les conclusions des Journées Galéniques sont publiées sous forme d’un Bulletin Technique* mis à la disposition de tous les professionnels du secteur pharmaceutique.
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\n"}],"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false,"left_blocks":[{"visual":"https://www.gattefosse.com/wordpress/wp-content/uploads/2019/05/actionplan-2020-commitments.jpg","title":"Plan d’action RSE","description":"Nos engagements concrets de responsabilité au service de l’environnement et des hommes.","link":"https://www.gattefosse.com/fr/corporate-content/csr-action-plan-2"},{"visual":"https://www.gattefosse.com/wordpress/wp-content/uploads/2019/05/human-rights-vignette.jpg","title":"Engagement droit humain","description":"Nos engagements pour les droits humains, l'intégrité, la responsabilité et le respect de nos partenaires.","link":"https://www.gattefosse.com/fr/corporate-content/gattefosse-human-rights-commitments/"},{"visual":"https://www.gattefosse.com/wordpress/wp-content/uploads/2019/05/customer-oriented.jpg","title":"Notre Proximité client ","description":"Notre réseau mondial d’experts est à votre disposition.","link":"https://www.gattefosse.com/corporate-content/customer-oriented/"},{"visual":"https://www.gattefosse.com/wordpress/wp-content/uploads/2019/05/quality-security.jpg","title":"Notre démarche qualité et sécurité ","description":"La qualité et la sécurité sont pour nous des facteurs-clés de progrès.","link":"https://www.gattefosse.com/fr/corporate-content/quality-security-approach/"},{"visual":"https://www.gattefosse.com/wordpress/wp-content/uploads/2019/05/sharing-knowledge.jpg","title":"Partage des connaissances","description":"Gattefossé partage ses connaissances via des publications, séminaires et conférences.","link":"https://www.gattefosse.com/fr/corporate-content/knowledge-sharing/"},{"visual":"https://www.gattefosse.com/wordpress/wp-content/uploads/2019/05/gattefosse-foundation.jpg","title":"Fondation Gattefossé","description":"La Fondation agit pour promouvoir l’utilisation scientifique et clinique des huiles essentielles.","link":"https://www.gattefosse.com/fr/foundation/foundation-master"}],"events":[]},"_links":{"self":[{"href":"https://www.gattefosse.com/fr/wp-json/wp/v2/pages/15319"}],"collection":[{"href":"https://www.gattefosse.com/fr/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/fr/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/fr/wp-json/wp/v2/users/36"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/fr/wp-json/wp/v2/comments?post=15319"}],"version-history":[{"href":"https://www.gattefosse.com/fr/wp-json/wp/v2/pages/15319/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/fr/wp-json/wp/v2/media?parent=15319"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/fr/wp-json/wp/v2/categories?post=15319"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/fr/wp-json/wp/v2/tags?post=15319"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"applications":{"id":1340,"date":"2017-04-05T13:52:27","date_gmt":"2017-04-05T13:52:27","guid":{"rendered":"/?page_id=1340"},"modified":"2020-02-25T15:58:05","modified_gmt":"2020-02-25T13:58:05","slug":"applications","status":"publish","type":"page","link":"https://www.gattefosse.com/corporate-content/applications/","title":{"rendered":"Applications"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":36,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Technical support and applicative formulation | Gattefossé","_yoast_wpseo_metadesc":"Our 4 application laboratories worlwide provide the technical support you need to develop and improve your cosmetic care and drug formulas."},"categories":[48],"tags":[],"acf":{"component":"PageGenericContentCorporate","title":"Applications","content":"
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Gattefossé application laboratories are responsible for demonstrating the benefits our ingredients can offer to prototype formulations. They provide the technical support you need to develop your cosmetic care and drug formulas. Our experts use their detailed understanding of your sector to model and solve your formulation problems.
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Our formulators work in close collaboration with research and development to analyze the behavior of Gattefossé ingredients and excipients and demonstrate their benefits in formulations. We offer our customers efficient and innovative solutions that match global cosmetic and pharmaceutical trends and comply with applicable regulations.
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Four application laboratories inspiring innovation
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Gattefossé’s four application laboratories are located in France, China, India, and the United States. These strategic positions permit close, local relationships with our customers.
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The laboratories provide personalized service and technical support to help optimize the performance of your cosmetic and pharmaceutical products by using our ingredients. All four sites comply with the safety, hygiene, and quality standards required of our profession and are equipped with the same advanced technologies our customers use, thus guaranteeing manufacturing process reproducibility.
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Our pharmaceutical application laboratories
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The goals of our pharmaceutical application laboratories are:
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To create and share orientation supports,
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To provide customer assistance and formulation support,
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To offer technical trainings to our network and customers.
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Our formulators advocate the use of a variety of excipients and therefore address a range of dosage forms for different routes of administration:
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Oral administration—production of controlled-release oral dosage forms, enhancement of active ingredient bioavailability through self-emulsifying lipid formulations (SELFs), development of solid SELFs, etc.
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Topical administration—formulation of O/W and W/O emulsions, ointments, and anhydrous gels, and characterization of their sensorial properties
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Anal and vaginal administration—selection of the most appropriate suppository bases for an active ingredient and development and characterization of suppositories and pessaries
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Our cosmetic application laboratories
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Our cosmetic application laboratories apply their technical expertise to fulfill their missions:
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evaluation of our active and functional formulation ingredients
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qualification of new raw materials
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co-creation of innovative products in response to regulatory changes and new market trends, with the help of our R&D teams
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development of formulas specifically requested by our customers
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design of raw material formula kits
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Every day Gattefossé applies its full range of experience with dosage form design to offer customers original formulas—with textures matching current trends—for all applications: face, body, and hair care; makeup; \n ecofriendly products, sunscreens, and more.
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Sensory analysis, a unique expertise in textures
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Gattefossé knows skin care and beauty products stimulate all the senses, so we attach great importance to the sensorial evaluation of our products and formulas. We have been developing our expertise in sensorial analysis since 1996.
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As a leader in the field, we have established a panel of experts specialized in the characterization of textures—cosmetic products and topical pharmaceutical formulations in particular. They can accurately assess the physical and sensorial properties of any product and translate these impressions into objective data, regardless of whether they are evaluating our own formulas or other products on the market.
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Our sensory database has been constantly enriched over the course of twenty years and spans over 400 formulations to help us best respond to customer requests.
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Nature is a constant inspiration for cosmetics ingredients, but plants are not the only sources of natural actives. Mineral Matters™ liquid stone extracts apply special technology to extract important minerals from precious stones and make them bioavailable to the skin. The result is a unique line of substantiated stone actives that enhance and protect. Mala’Kîte™ is a protective copper complex extracted from malachite. A powerful free radical scavenger, it boosts cellular defenses offering protection against aging and detoxifying benefits. Mala’Kîte™ effectively protects both skin and hair against environmental stress. See the other actives in this Mineral Matters™ line:
Once used as an ore to produce copper, today malachite is more well known as a gemstone. This beautiful stone has a green color that does not fade over time or through exposure to light, ranging from a pastel blue-green all the way to a dark green verging on black.
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\n
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The stones used to create Mala’Kîte™ liquid stone extract are sourced in central Africa. Preservative free.
\n","img":{"id":3437,"alt":"friends relaxing in jacuzzi at health spa","title":"friends relaxing in jacuzzi at health spa","caption":"","description":"","mime_type":"image/jpeg","url":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/detox.jpg"},"video":""}],"claims":"
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Antioxidant
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Detoxifying
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Protects skin and hair from environmental stress
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Natural and stable colorant
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\n","applications":"
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Skin care—day and night products
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Anti-aging and antipollution lines
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Hair care—protective treatments
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Sun care—aftersun products
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Spa lines
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\n","actives":["protection"],"actives_secondary":["preservative_free","alcohol_free","bg_free"],"textures":"","textures_secondary":"","extract":false,"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/1703"}],"collection":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/users/36"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/comments?post=1703"}],"version-history":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/1703/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/media?parent=1703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/categories?post=1703"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/tags?post=1703"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"publications-on-topical-dosage-forms-with-improved-sensorial-properties":{"id":9032,"date":"2018-04-04T11:09:33","date_gmt":"2018-04-04T09:09:33","guid":{"rendered":"https://www.gattefosse.com/?page_id=9032"},"modified":"2021-01-21T11:54:39","modified_gmt":"2021-01-21T09:54:39","slug":"publications-on-topical-dosage-forms-with-improved-sensorial-properties","status":"publish","type":"page","link":"https://www.gattefosse.com/qualification-des-excipients/pharmaceuticals-special-content/publications-on-topical-dosage-forms-with-improved-sensorial-properties/","title":{"rendered":"Publications on topical dosage forms with improved sensorial properties"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":9,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Publications on topical dosage forms with improved sensorial properties | Gattefossé","_yoast_wpseo_metadesc":"Find out Gattefossé publications on topical dosage forms with improved sensorial properties."},"categories":[36],"tags":[],"acf":{"component":"PageSpecialContentPharma","title":"Publications on topical dosage forms with improved sensorial properties","introduction":"List of Gattefossé publications on topical dosage forms with improved sensorial properties.","":false,"content":[{"wysiwyg":"
Improving patient experience with sensorial topical dosage forms
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E Dauphin-Chanard, D Hoste and D Marchaud Poster – PBP 2018
\n"}],"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/qualification-des-excipients/wp-json/wp/v2/pages/9032"}],"collection":[{"href":"https://www.gattefosse.com/qualification-des-excipients/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/qualification-des-excipients/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/qualification-des-excipients/wp-json/wp/v2/users/9"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/qualification-des-excipients/wp-json/wp/v2/comments?post=9032"}],"version-history":[{"href":"https://www.gattefosse.com/qualification-des-excipients/wp-json/wp/v2/pages/9032/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/qualification-des-excipients/wp-json/wp/v2/media?parent=9032"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/qualification-des-excipients/wp-json/wp/v2/categories?post=9032"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/qualification-des-excipients/wp-json/wp/v2/tags?post=9032"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"microemulsion":{"id":2931,"date":"2017-04-25T09:41:32","date_gmt":"2017-04-25T09:41:32","guid":{"rendered":"https://www.gattefosse.com:443/?page_id=2931"},"modified":"2021-02-05T17:12:03","modified_gmt":"2021-02-05T15:12:03","slug":"microemulsion","status":"publish","type":"page","link":"https://www.gattefosse.com/pharmaceuticals-content/microemulsion/","title":{"rendered":"Microemulsion"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":9,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Exipients for microemulsion | Gattefossé","_yoast_wpseo_metadesc":"Understand how microemulsions are formed spontaneously by gentle mixing of oily vehicle, surfactant/cosurfactant and water."},"categories":[49],"tags":[],"acf":{"component":"PageGenericContentPharma","title":"Microemulsion","content":"
Microemulsions are thermodynamically stable systems formed spontaneously by gentle mixing of their components: oily vehicle, surfactant/cosurfactant, and water.
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A pseudoternary phase diagram determines the respective concentrations of the components yielding a microemulsion. Watch our video for more information on how to develop pseudoternary diagrams.
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Labrasol® is a liquid oil-in-water (O/W) surfactant (HLB=12) with excellent solubilizing capacity. It is often used in combination with a cosurfactant such as Plurol® Oleique CC 497 (HLB=3).
Our formulators have developed microemulsions for the preparation of pharmaceutical foams using propellant-free devices. Case studies with model drugs show that a foam can easily be produced with a microemulsion-based formulation.
\n","box_links":[],"useful_links":[{"text_link":"Access our video on pseudo ternary diagram","link":false,"external_link":"https://youtu.be/QWY41T3oR98"},{"text_link":"Excipients for solubilizing drugs","link":"https://www.gattefosse.com/pharmaceuticals-content/excipients-for-solubilizing-drugs/","external_link":""},{"text_link":"Excipients for topical drug delivery","link":"https://www.gattefosse.com/pharmaceuticals-range-of-products/range-of-products/","external_link":""},{"text_link":"Foams","link":"https://www.gattefosse.com/pharmaceuticals-content/pharmaceutical-foams/","external_link":""}],"":false,"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/2931"}],"collection":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/users/9"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/comments?post=2931"}],"version-history":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/2931/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/media?parent=2931"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/categories?post=2931"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/tags?post=2931"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"the-gattefosse-foundation-rewards-three-health-establishments":{"id":11031,"date":"2018-10-29T16:02:49","date_gmt":"2018-10-29T14:02:49","guid":{"rendered":"https://www.gattefosse.com/?page_id=11031"},"modified":"2019-05-03T14:27:10","modified_gmt":"2019-05-03T12:27:10","slug":"the-gattefosse-foundation-rewards-three-health-establishments","status":"publish","type":"page","link":"https://www.gattefosse.com/foundation-news/the-gattefosse-foundation-rewards-three-health-establishments/","title":{"rendered":"The Gattefossé Foundation rewards three Health establishments"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":36,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"The Gattefossé Foundation rewards three Health establishments","_yoast_wpseo_metadesc":"Discover the 3 establishments awarded by the Gattefossé foundation in recoginition of their non-therapeutic approach of care with aromatherapy."},"categories":[42],"tags":[],"acf":{"title":"The Gattefossé Foundation rewards three Health establishments","description":"The Gattefossé Foundation has awarded three establishments with a prize and two grants, following its call for applications 2018.","date":"10.29.2018","content":"
Doctor Anne Moro, paediatric plastic surgeon in La Réunion, receives the Gattefossé Foundation prize
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On October 16, 2018, the prize (10 000€) was awarded to Dr. Anne Moro’s team (University Hospital of La Réunion) at the Foundation’s headquarters in Lyon (France).
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Anne Moro has a degree in clinical aromatherapy from the University of Strasbourg. She coordonates the MAFACE expertise center in La Réunion for the treatment of facial malformations and cleft lip and palate. For the past 3 years, she has been using essential oils at the University Hospital of La Réunion to improve the healing of wounds and scars, prevent infections and calm the pain and stress of her patients. Anne Moro also contributes to a more general use of aromatherapy in the hospital: at the pharmacy, in the operating room and within the voluntary services. A PHRI* (hospital research nurse program) is underway for a research project that should begin in December 2018.
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\n With the association TSIKY RUN, she uses essential oils during humanitarian missions in Madagascar. The aim of the association is, on one hand, to support patients born with a cleft lip and palate (harelip) and to treat pre and post operative care with essential oils. On the other hand she trains Malagasy doctors in the use of essential oils, as a complementary care strategy or sometimes as a replacement to allopathic treatments. These missions are supported by the University Hospital of La Réunion, which grants leave to its employees who take part in humanitarian missions and lends surgical equipment as well.
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\n The Steering Committee on Aromatherapy has rewarded the innovative nature of the use of essential oils in pediatrics, particularly in repair surgery of the cleft lip and palate and in the operating room. Besides, the location of the project in a country that distills oils, the humanitarian nature of missions in Madagascar facilitating access to care for disadvantaged families and the quality of the protocols put in place were particularly emphasized.
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The Marin Hospital of Hendaye (AP HP) rewarded by the Foundation Grant
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On October 9, 2018, the Foundation Grant (5 000€) was awarded to the team of Marin Hospital of Hendaye (Hôpital Marin de Hendaye / Assistance Publique – Hôpitaux de Paris). Mr Andoni Alli, hospital pharmacist, is in charge of the aromatherapy approach. Trained at the Dijon DU, he initiated this approach in 2013.
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This rehabilitation and recuperative care facility uses aromatherapy as complementary medicine in the treatment of wounds, mycoses, gastrointestinal disorders, herpes, agitation, anxiety, insomnia, spasticity and pain in patients with heavy disabilities or rare neurological and endocrine diseases.
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The Steering Committee on Aromatherapy has rewarded the innovative nature of the use of oils in this type of establishment, the diversity of pathologies and areas of intervention, the internal dynamics initiated by the involvement of the pharmacist and the director of health, the training of a hundred people and the designation of aromatherapy referents in each department concerned, as well as the validation of protocols by the department of care and the doctors of the poles.
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The public health institution (EPS) Barthélémy Durand rewarded by the Foundation Grant
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On October 12, 2018, the Foundation Grant was awarded to the team of the Barthélemy Durand Public Health Institution (EPS) in Etampes (Essonne, France), which aromatherapy approach is carried by Mrs. Ioana Farcas, hospital pharmacist, trained in IUD Phyto-aroma of Paris V University.
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The Steering Committee on Aromatherapy has rewarded the innovative nature of the use of essential oils in the services of this reference institution in mental health since 2015, the supervision of the use of essential oils by a team of pharmacists, and the willingness to set up a scientific aromatherapy program with staff training and evaluation of the decline in chemical drug intake.
\n
The Committe also appreciated the engaging awareness and communication measures about aromatherapy and the inclusion of the development of the use of essential oils in the establishment project, within a global development of the non-medicated therapies.
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Solid lipid excipients: born to be extruded!
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White paper, November 2014
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Functional excipients are critical to the successful application of HME to resolve formulation challenges. Whilst polymers show potential in both controlled release and in improving the solubility and dissolution of poorly soluble compounds they are not ideal materials for extrusion. Lipid excipients are distinctly different to polymers and behave differently in HME. This article highlights two glyceride-esters: Compritol® 888 ATO and Precirol® ATO 5. They melt at relatively low temperatures and recrystallize quickly. They extrude well and can produce strand-like extrudates which can be down streamed into powders or granules.
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These glyceride-esters can be used as release retarding agents/dissolution modifiers for both insoluble and soluble drugs even for high drug loading. In combination with plastic polymers they also can act as plasticizer/processing aid enabling lower temperature process and continuous production.
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At Gattefossé we aim to share our knowledge to help formulators use lipid excipients to their best advantage.
Preparation of hot melt extruded supersaturating solid dispersions containing glyceryl behenate: effects of processability, supersaturation and rate of release
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Justin M. Keen, Justin R. Hughey, Ryan C. Bennett, Vincent Jannin and James W. McGinity AAPS 2011
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Bioanalytical Development for In Vivo Biomarkers and DMPK
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Physiochemical and Biophysical Stability Assessments across Therapeutic Modalities
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Computational Modeling to Aid Pharmaceutical Development- Solid State Chemistry
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Madagascan association AROVA receives a grant from Gattefossé Foundation"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":36,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Madagascan association AROVA gets a grant from Gattefossé Foundation","_yoast_wpseo_metadesc":"Gattefossé Foundation has awarded a grant to the AROVA association to fund the training of medical staff in the use of aromatherapy in Madagascar."},"categories":[42],"tags":[],"acf":{"title":"The Madagascan association AROVA receives a grant from Gattefossé Foundation","description":"Gattefossé Foundation has awarded a grant to the AROVA association to fund the training of medical staff in the use of aromatherapy in Madagascar.","date":"21.03.17","content":"
\n
\n
As part of its mission to promote the use of essential oils in healthcare establishments, the Gattefossé Foundation has created grants to reward and encourage the development of aromatherapy initiatives, in France and abroad.
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A 5000€ grant has just been awarded to the AROVA Association (Aromatherapists of the Vakinankaratra), which brings together doctors trained in aromatherapy and aims to teach the medical and paramedical staff of the island of Madagascar the use of essential oils. It then provides them with blends of oils for their daily practice in care centers. AROVA has trained nearly 80 professionals since 2013 and intends to train an additional 100 people thanks to this funding.
\n
This project has been selected by the Gattefossé Foundation because it stands at the heart of public health, social economy and sustainable development issues. Despite the fact that Madagascar produces over 30 different essential oils, the sector remains quite disorganised and all the oils produced are exported to foreign markets, benefiting neither the local populations nor the economy. Today, the essential oils used by the association are supplied at a wholesale price by a French NGO calledCoeur de forêt. While the General Directorate of the Ministry of Health of Madagascar has advocated for the development of phyto-aromatherapy, the Foundation intends with this grant to encourage the use of local essential oils.
\n
Read the press release
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Comparative evaluation of Compritol® HD5 ATO with Sodium Stearyl Fumarate and PEG 6000 as amphiphilic, hydrodispersible pharmaceutical lubricants
\n
Chhanda Kapadia and Ketkee Deshmukh
\n
J. Excipients and Food Chem. 8 (1) 2017 – 5
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In the present study the lubricant capacity of Compritol® HD5 ATO was compared with commonly used amphiphilic lubricants. The \n effect of the concentration and mixing time on flow properties, tablet ejection force, hardness, disintegration time and rate of dissolution of paracetamol tablets was evaluated. \n The physical properties of the lubricants such as crystallinity, wettability, thermal behaviour and surface area were also measured. \n Compritol® HD5 ATO was found to be an as effective a lubricant for a fast disintegrating paracetamol formulation containing microcrystalline cellulose, lactose and PVP prepared by wet granulation in comparison with sodium stearyl fumarate and PEG 6000.
Functional characterization of powders consisting of mixture of glyceryl behenate and a non-ionic surfactant applied by hot-melt coating: lubricant performance
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Jannin, V. Bérard, S. Chevrier, A. Malmazet, Y. Chavant, F. Demarne, C. Andrès
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Journal of Drug Delivery Science and Technology, Volume 23, Issue 2, 2013, Pages 181-185
Comparative study of the lubricant performance of Compritol®888 ATO either used by blending or by hot melt coating
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V Jannin, V Bérard, A N’Diaye, C Andrès, Y Pourcelot
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International Journal of Pharmaceutics. Volume 262, Issues 1–2, 27 August 2003, Pages 39–45
\n
In this study, the lubricant performance of Compritol 888 ATO is assessed in a classical blending process or by hot melt coating. The results suggest that the hot melt coating process induces an homogeneous repartition of the lubricant on the lactose surface, \n contrary to classical blending procedure. Thus, lubrication by hot melt coating seems to be a very efficient procedure. It could be used specifically for large surface area particulate systems producing a lot of friction.
Comparative study of the lubricant performance of Compritol® HD5 ATO and Compritol® 888 ATO: effect of polyethylene glycol behenate on lubricant capacity
\n
A. N’Diaye, V. Jannin, V. Bérard, C. Andrès, Y. Pourcelot
\n
International Journal of Pharmaceutics. Volume 254, Issue 2, 26 March 2003, Pages 263–269
\n
In this study the lubricant capacity of Compritol HD5 ATO is compared to Compritol 888 ATO. It shows that mixing lubricants with Lactopress present no structural differences and that they have equivalent compressibility and cohesiveness. This study concludes \n that Compritol HD5 ATO could be a very interesting excipient because it associates the glyceryl dibehenate lubricant capacity with the polyethylene glycol property of enhanced dissolution.
A nonionic water-insoluble surfactant used as cosurfactant in oral lipid-based formulation SEDDS and SMEDDS. Cosurfactant and solubilizer in topical dosage forms associated with skin penetration enhancement.
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Propylene glycol monolaurate (type I)
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Propylene glycol monolaurate (type I)
\n"},{"keys":"UNII Code (FDA)","value":"
40KT317HGP
\n"},{"keys":"Preferred Substance Name (FDA)","value":"
PROPYLENE GLYCOL LAURATES
\n"},{"keys":"Handbook of Pharmaceutical Excipients","value":"
Propylene glycol monolaurate
\n"},{"keys":"Chemical description","value":"
Consists of propylene glycol mono- and di- esters of lauric (C12) acid.
Solubilizer for poorly-soluble APIs and bioavailability enhancer. Cosurfactant in LFCS Type II (SEDDS) and Type III (SMEDDS) formulations. Solubilizer and cosurfactant for microemulsion in topical formulation. Safety of use is inferred by precedence of use in approved pharmaceutical products.
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Propylene glycol monolaurate (type II)
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\n
Product catalogue
\n
Find out quickly the excipient you are looking for! This updated version has been enriched with the precedence of use of our excipients.
\n"},{"wysiwyg":"
\n
Lipid excipients for oral drug delivery
\n
Interested in solubility and bioavailability enhancement? Sustained-release? Taste-masking? Lubricant?This brochure will help you choose the appropriate excipient!
\n"},{"wysiwyg":"
\n
Lipid excipients for topical drug delivery
\n
Emulsifiers, thickeners, solubilizers and penetration enhancers will have no secret for you after reading this brochure!
\n"},{"wysiwyg":"
\n
Lipid excipients for rectal drug delivery
\n
Discover our wide range of suppository bases and how Gattefossé expertise can speed up your development!
\n
\n"},{"wysiwyg":"
\n
Lipid excipients for cannabinoid drug products
\n
Find out about our solutions for cannabinoid drug products.
\n"},{"wysiwyg":"
\n
Pediatric medicines with lipid excipients
\n
Find out our solutions for oral, topical and rectal dosage forms suitable for pediatric patients.
\n
\n"},{"wysiwyg":"
Veterinary medicines with lipid excipients
\n
Find out our solutions for domestic and farm animals!
\n"},{"wysiwyg":"
Compritol® 888 ATO: a smart solution to sustain drug release
\n
Compritol® 888 ATO many advantages in sustained release are highlighted and its use in single or dual SR matrix is explained.
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Compritol® 888 ATO: the lubricant for challenging pharmaceutical tablets
\n
Inert, robust and efficient: 3 words that summarize the outstanding benefits of Compritol® 888 ATO
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Gelucire® 48/16 pellets. Solubility and oral bioavailability enhancement
\n
All you should know about this water soluble surfactant for successful lipid-based formulations
\n"},{"wysiwyg":"
Maisine® CC. A pharmaceutical oil for solubility and oral bioavailability enhancement
\n
All you should know about this functional oil for successful lipid-based formulations
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Find out quickly the excipient you are looking for! This updated version has been enriched with the precedence of use of our excipients.
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Want to formulate cannabinoids for oral, topical, transdermal or mucosal delivery? We deliver excipients for all routes of administration and dosage forms. Simply select the right one!
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Interested in solubility and bioavailability enhancement? Sustained-release? Taste-masking? Lubricant?This brochure will help you choose the appropriate excipient!
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Emulsifiers, thickeners, solubilizers and penetration enhancers will have no secret for you after reading this brochure!
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Discover our wide range of suppository bases and how Gattefossé expertise can speed up your development!
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Find out about our solutions for cannabinoid drug products.
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Find out our solutions for oral, topical and rectal dosage forms suitable for pediatric patients.
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Find out our solutions for domestic and farm animals!
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Learn more about the different capacities of lipid excipients on oral bioavailabilty.
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Compritol® 888 ATO many advantages in sustained release are highlighted and its use in single or dual SR matrix is explained.
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Inert, robust and efficient: 3 words that summarize the outstanding benefits of Compritol® 888 ATO as lubricant for pharmaceutical tablets
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We have a solution for all topical dosage forms, from traditional to innovative!
\n
Discover our full range of functional excipients to develop exciting topical dosage forms aiming at encouraging patient adherence to topical treatments.
A nonionic water-dispersible surfactant for lipid-based formulations to solubilize and increase oral bioavailability of poorly water-soluble APIs. Self-emulsifies in aqueous media forming a fine dispersion, i.e., microemulsion (SMEDDS).
An interactive brochure depicting comprehensive information on this new excipient in Gattefossé range of excipients for oral bioavailability enhancement
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All you should know about this functional oil for successful lipid-based formulations
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A concentrate of practical information for successful emulsion formulation
A safe solvent with high solubilizing and permeation enhancement capacity
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A gel formulation includes a gelling agent—carbomers, hydroxyethyl cellulose, and hydroxypropyl cellulose are the most widely used—and solubilizers. Depending on the excipients used, a gel can be transparent (most common), translucent, or opaque.
\n
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The challenge when developing a gel is to keep the drug in a solubilized state and to identify the right gelling agent. Thus the selection of appropriate solubilizer is very important and must be compatible with the gelling agent.
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Transcutol® P is compatible with all types of gelling agents and can be used at a very high concentration in the gel without altering its structure. Clear gels are obtained.
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Labrasol® is compatible with all types of gelling agents. Depending on the concentration, clear or opaque gels are obtained.
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Capryol® PGMC produces an opaque gel when used at <6% with hydroxypropyl cellulose.
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Transcutol® P is widely used as solubilizer in gels, creams and emulgels.
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A simple emulgel formulation with high level of Transcutol® P can be obtained.
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Glyceryl Mono and Dicaprylocaprate \n [NOTE – May also be labeled as USP Glyceryl Monocaprylocaprate (Type I) until May 1, 2025]
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Glycerol monocaprylocaprate (type I)
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GLYCERYL MONO AND DICAPRYLOCAPRATE
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Symbols of perfect beauty, Japanese women are renowned for the quality of their skin and consider in depth moisture as the secret to skin perfection.
\n
\n
All over the world, women are inspired by the Japanese ideal. The desire to obtain healthy and pure skin represents a new beauty paradigm where beauty is expressed without artifices and the skin must reflect its perfection naturally.
\n
\n
Guided by this new beauty philosophy, Gattefossé developed Gatuline® Renew. It kick-starts the cell renewal process and strengthens the barrier function. The skin is visibly more hydrated, softer and smoother both to the eyes and to the touch. Reflecting light better, the skin reveals all its natural beauty.
A natural extract of handpicked Japanese cedar buds, Gatuline® Renew is rich in energetic phytochemicals that stimulate epidermal renewal.
\n
\n
Native to Japan, the Japanese cedar (Cryptomeria japonica) has been transplanted to the Reunion Island. The plant thrives on the island, where Gattefossé sources the buds used in Gatuline® Renew.
\n
\n
\n
\n
A responsible sourcing: Japanese cedar buds are picked by hand. To ensure the longevity of the trees, only their lower branches are cut.
Boosts all essential steps of epidermis renewal and strengthens stratum corneum
\n
Improves the desquamation
\n
Restores a functional skin barrier
\n
Promotes proper water homeostasis
\n
Enhances skin surface aspect
\n
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Acts throughout the epidermis, from the basal layer to surface corneocytes
\n
Favors hydration from within
\n
Prevents dehydration
\n
Smoothes the skin, making it softer, more supple and comfortable
\n
Enhances global skin quality and appearance
\n
Adapted to sensitive skin (clinical test under dermatological control)
Solvent and powerful solubilizer. Cosolvent in surfactant oral formulations—LFCS Type III (SMEDDS) and Type IV (micellar solutions). Vehicle in nasal and ophthalmic formulations. Safety of use and low irritancy inferred by numerous toxicological studies and precedence of use in approved pharmaceutical products.
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Gelucire® 48/16: a safe wetting agent for tablet. A case study with fenofibrate
\n
E. Dauphin-Chanard ; JM. Girard ; C. Deleglise ; P. Caisse
In this study the authors developed a type IV lipid-based formulation to improve solubility and bioavailability of ticagrelor. The in vitro lipolysis test was shown to be a good tool to predict in vivo performance.
A solid dispersion of ticagrelor and Gelucire® 48/16 is prepared to increase drug solubility . The solid dispersion is converted into tablets. The formulated tablets showed improved dissolution rate compared to the market reference.
Novel Pegylated lipid excipients: Role in augmenting dissolution of a poorly soluble drug.
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AAPS 2016
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This poster describes the use of Gattefossé’s newest surfactant Gelucire® 48/16 (polyoxyl stearate type I USP-NF) and our hydrodispersible lubricant Compritol® HD5 ATO (behenoyl polyoxyl-8 glycerides USP-NF) in tablets of telmisartan, a BCS class II drug.
\n
Gattefossé excipients were combined with API in granulation processes and granules were compressed into tablets. Tablets of good quality and integrity were made and drug release was compared with a market reference product. Results showed improved drug dissolution in tablets made with Gelucire® 48/16 and Compritol® HD5 ATO.
This acticle describes the work undertaken in Gattefossé R&D labs (St Priest) to develop lipid formulations for low to medium lipophilicity API: piroxicam, nifedipine and curcurmin and evaluate the effect of in-vitro digestion on the solubilizing capacity of the formulations.
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Hot melt extrusion is a continuous solvent-free technology with precise process control. Lipid excipients are mainly used as matrix formers for modified release, or as solubilizers for solubility/bioavailability enhancement, alone or in combination with polymers.
\n
\n
\n
Advantages of lipid excipients in hot melt extrusion:
\n
\n
low melt viscosity, resulting in low torque
\n
low extrusion temperatures (30–75 °C)
\n
low melting point and instant solidification, thereby avoiding downstream cooling
In a collaborative study with the University of Austin, Gattefossé investigated hot melt extrusion using polyvinylpyrrolidone (PVP) as the polymer and Compritol® 888 ATO as the plasticizer and sustained-release agent. The study showed that Compritol® improves the processability of PVP dispersions, reducing extrusion torque and increasing yield.
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EnergiNius® protège les cellules de la peau de la lumière visible artificielle émise par les écrans, un stress environnemental additionnel induit par notre mode de vie moderne.
\n
Fortement renforcée, la peau est visiblement ravivée et les signes de fatigue disparaissent pour un teint plus lumineux et éclatant.
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Issu des racines de Ginseng Indien (Withania somnifera), EnergiNius® est certifié bio et obtenu grâce à la technologie innovante des NaDES. Sourcée en Oregon (USA), Withania somnifera est une plante emblématique de la médecine Ayurvédique et est utilisée en médecine traditionnelle depuis des siècles.
\n
\n
EnergiNius® est riche en acides aminés et withanolides ; l’action synergique de ces deux familles phytochimiques lui confère un haut niveau d’efficacité.
\n
\n
\n
\n
\n
Watch the video to get a comprehensive overview of EnergiNius®: \n
For the first time, the screen emitted artifical visible light (AVL) has been precisely characterized and Gattefossé has developed unique equipment accurately recreating the light emitted by screens.
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The major annual gathering of cosmetic industry professionals, in-cosmetics Global will be held in London on April 4th, 5th and 6th, 2017.
\n
Gattefossé will be present at booth H40.
\n
Over these three days, you will be able to meet our experts and discover our brand new thematic beauty concept called Show True Emotions. This concept gathers several solutions aiming at rejuvenate the skin and reduct the expression lines that may reveal misleading emotions.
\n
Our new active ingredient,Gatuline® Link n Lift, targeting the eye contour, will be launched during the show and has been shortlisted for the Innovation Zone Best Ingredient Award.
\n
The show will also give us the opportunity to present the new clinical substantiation study of Gatuline® Expression AF, which helps smooth the skin around the lips.
\n
In addition, 5 new formulations including these ingredients will be exhibited on our booth : the Gattefossé application laboratories have worked on five emotions reinvented with innovative textures.
\n
\n
Show True Emotions
\n
• 1 new active launched: Gatuline® Link n Lift \n• 1 new substantiated active: Gatuline® Expression AF \n• 5 new formulations: innovative textures to match emotions
\n
\n
To receive free admission to in-cosmetics London, remember topre-register.
\n
Gattefossé Booth H40 \nin-cosmetics London \n4 – 6 April 2017
\n
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Gels, crèmes, formes semi-solides : de leur développement à leur enregistrement.
\n
[Gels, creams, semi-solid forms: from their development to their registration]
\n
E. Beyssac, V. Boudy, E. Dauphin-Chanard, S. Delehouzé, L. Frances, B. Gos, C. Lacaze, V. Laffineur, A. Mestres, I. Ribeiro Dos Santos, X. Thomas and N. Zeng
\n
STP Pharma Pratiques – September October 2018 – 28(5) 181-250 – ISSN 1157-1497
\n
The SFSTP commission on topical dosage forms published an article reviewing all the steps for their development to registration.
\n
Interestingly this article is both in French and English languages.
II Tests and studies applicable in evaluation of semi-solid forms from development up to the phase of routine use \n
\n
2.1 Regulatory requirements \n 2.2 Relevant tests in development \n 2.2.1 Conventional characterization tests \n 2.2.2 Characterization tests specified to evaluate performance of the formulation \n 2.2.3 Additional characterization tests specified to evaluate performance of the formulation
\n
III QbD approach related to the formulation \n
\n
3.1 Different elements of the QbD \n 3.2 When to set up QbD ? \n 3.3 Definition of QTPP \n 3.4 CQAs toward evaluation of risks of process \n 3.5 Example of CMAs studied in case of a semi-solid formulation \n 3.6 Example of CPPs studied in case of a semi-solid formulation
A non-ionic pure surfactant for lipid-based formulation to solubilize and increase oral bioavailability of poorly soluble API. Forms micellar solution in aqueous media.
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Polyoxyl-32 stearate (type I) NF
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Macrogol-32 stearate (type I) EP
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33GX5WQC0M
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PEG-32 STEARATE
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Polyoxylethylene stearates
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Consists of PEG-32 (MW 1500) esters of palmitic (C16) and stearic (C18) acids
Solubilizer for low log P APIs and bioavailability enhancer. Single excipient formulation system: self-emulsifies in aqueous fluid into micellar solution—LFCS Type IV. Use in melt processes (granulation, extrusion), granulation, and compression. Wetting agent. Safety of use is inferred by precedence of use in approved pharmaceutical products.
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for Optimizing Texture and Sensorial Experience"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":9,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Excipients for optimizing texture of topical dosage forms | Gattefossé","_yoast_wpseo_metadesc":"Discover our range of excipients to improve texture and sensorial properties of topical dosage forms and positively impact patient experience."},"categories":[49],"tags":[],"acf":{"component":"PageGenericContentPharma","title":"Excipients for Optimizing Texture and Sensorial Experience","content":"
Improvement of topical dosage form texture and sensorial properties is an increasingly common formulation objective:
\n
\n
Improved texture and sensorial properties positively impact patient experience and adherence to treatment.
\n
A growing number of topical medicines switch over to OTC, where brand differentiation and patient choice comes into play.
\n
Innovation can be achieved by reformulating the dosage form with optimized texture and sensorial features.
\n
\n
Sensorial mapping evaluates product’ aspects during application and absorption. We have developed a database of prototype formulations with different textures and sensorial profiles. This helps our customers select formulations with excellent texture and sensorial properties. Dermacare is a collection of simple and effective prototypes of creams, emulgels, and lotions with optimized texture and sensorial properties. Our database also includes formulations for foams, sprays, microemulsions, and gels. Contact Gattefossé for our Dermacare guidelines.
\n
We know that ingredients or even formulation type—for example, cream versus emulgel—can directly affect sensorial properties. Sensorial panel experts at Gattefossé Application Laboratories can study these factors.
\n","box_links":[{"link":"https://www.gattefosse.com/pharmaceuticals-content/dermacare-textures-topical-dosage-forms-2/","title":"Dermacare","external_link":"","image":"https://www.gattefosse.com/wordpress/wp-content/uploads/2016/11/TOPIC-010-retouche-365-247-px.jpg"}],"useful_links":[],"":false,"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/3897"}],"collection":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/users/9"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/comments?post=3897"}],"version-history":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/3897/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/media?parent=3897"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/categories?post=3897"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/tags?post=3897"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"acticire-mb":{"id":1742,"date":"2017-04-29T14:45:24","date_gmt":"2017-04-29T14:45:24","guid":{"rendered":"/?page_id=1742"},"modified":"2019-05-03T15:39:00","modified_gmt":"2019-05-03T13:39:00","slug":"acticire-mb","status":"publish","type":"page","link":"https://www.gattefosse.com/personal-care-textures/acticire-mb/","title":{"rendered":"Acticire® MB"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":36,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Acticire® MB | Multifunctional active texture agent | Gattefossé","_yoast_wpseo_metadesc":"Acticire® MB acts as an emollient, bringing softness to the skin, and as an active, repairing, protecting, and moisturizing dry, damaged skin."},"categories":[14],"tags":[],"acf":{"component":"PageCosmeticProduct","product_codes":[{"code":"5843"}],"bandeau_image":{"id":13811,"alt":"","title":"young woman on field in summer","caption":"young woman on blooming sunflower field in summer","description":"","mime_type":"image/jpeg","url":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/Acticire.jpg","width":1144,"height":400,"sizes":{"thumbnail":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/Acticire-150x150.jpg","thumbnail-width":150,"thumbnail-height":150,"medium":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/Acticire-300x105.jpg","medium-width":300,"medium-height":105,"medium_large":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/Acticire-768x269.jpg","medium_large-width":474,"medium_large-height":166,"large":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/Acticire-1024x358.jpg","large-width":474,"large-height":166,"post-thumbnail":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/Acticire-672x372.jpg","post-thumbnail-width":672,"post-thumbnail-height":372,"twentyfourteen-full-width":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/Acticire-1038x400.jpg","twentyfourteen-full-width-width":1038,"twentyfourteen-full-width-height":400}},"image_product_finder":{"id":2313,"alt":"young woman on blooming sunflower field in summer","title":"Gattefossé Product Finder Acticire®","caption":"","description":"","mime_type":"image/jpeg","url":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/acticire-MB-1.jpg","width":244,"height":163,"sizes":{"thumbnail":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/acticire-MB-1-150x150.jpg","thumbnail-width":150,"thumbnail-height":150,"medium":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/acticire-MB-1.jpg","medium-width":244,"medium-height":163,"medium_large":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/acticire-MB-1.jpg","medium_large-width":244,"medium_large-height":163,"large":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/acticire-MB-1.jpg","large-width":244,"large-height":163,"post-thumbnail":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/acticire-MB-1.jpg","post-thumbnail-width":244,"post-thumbnail-height":163,"twentyfourteen-full-width":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/acticire-MB-1.jpg","twentyfourteen-full-width-width":244,"twentyfourteen-full-width-height":163}},"title":"Acticire® MB","tagline":"Active waxes","description_product_finder":"","introduction":"
Multifunctional ingredients that meet desired customer claim and ease the formulation process are becoming more and more in demand.
\n
The specific technology behing Acticire® MB makes it a distinct, multifunctional ingredient with several unique applications.
A 100% natural texturizing agent based on a complex of 3 functionalized waxes:
\n
\n
Jojoba wax
\n
Sunflower seed wax
\n
Mimosa wax
\n
\n
\n
\n
Jojoba wax is the only wax that is liquid at room temperature. This is due to its composition: unsaturated fatty alcohol esters combined with an unsaturated fatty acid.
\n
Sunflower seed wax is a hard wax made up of fully saturated monoesters that boasts excellent thermal stability
\n
Mimosa wax a coproduct of the perfumery industry, is not surprisingly rather sweet smelling. Softer than the other waxes, it melts at about 60 °C and has a more complex composition that includes long-chain esters, hydrocarbons, and a smaller amount of triterpenoid alcohols.
Acticire® MB is a multifunctional ingredient with several unique applications. This video illustrates how Acticire® MB can be used to introduce water based ingredients into anhydrous formulations.
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
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In this example, an hydrophilic dye is incorporated into the water phase to show how it is well dispersed in a lipstick with Acticire® MB.
These three waxes have been transesterified in the presence of vegetable polyglycerin, rendering them more compatible and stabler in emulsion, and confering new sensorial qualities and characteristics:
\n
\n
Physical properties midway between those of liquid and solid waxes
\n
Softness and spreadability upon application
\n
Comfortable skin feel that lasts throughout the day
\n
\n","img":{"id":3105,"alt":"Sensory analysis at Gattefossé","title":"Sensory Analysis","caption":"","description":"","mime_type":"image/jpeg","url":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/acticire.jpg"},"video":""},{"content":"
Acticire® MB brings three different and distinctive benefits to cosmetic formulations:
\n\n
Forms a soft, smooth film that protects from dehydration
\n
Improves the texture and application of both standard and natural formulations
\n
Makes it possible to include water or water-soluble actives in anhydrous systems while allowing them to remain stable
In emulsions, can be a substitute for some low HLB co-emulsifiers
\n
Can emulsify up to 15% of water in an oil phase, exhibits great heat stability, allows introduction of water or hydrosoluble actives to anhydrous formulations
\n
Reduces transepidermal water loss, moisturizes, and improves appearance of skin surface (in vivo tests)
\n
\n","img":{"id":2971,"alt":"facial cream for modern women","title":"balm","caption":"","description":"","mime_type":"image/jpeg","url":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/baume.jpg"},"video":""}],"claims":"
Sun care—formulations with high UV filter levels (improved skin feel)
\n
Makeup—foundations (emulsions or gels), lipsticks, mascaras
\n
\n","actives":"","actives_secondary":"","textures":["texturizing_specialties"],"textures_secondary":["natural","peg_free"],"extract":false,"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/1742"}],"collection":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/users/36"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/comments?post=1742"}],"version-history":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/1742/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/media?parent=1742"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/categories?post=1742"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/tags?post=1742"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"sensorial-analysis-pharmaceuticals":{"id":3654,"date":"2017-04-28T08:49:03","date_gmt":"2017-04-28T08:49:03","guid":{"rendered":"https://www.gattefosse.com:443/?page_id=3654"},"modified":"2017-09-11T15:41:52","modified_gmt":"2017-09-11T13:41:52","slug":"sensorial-analysis-pharmaceuticals","status":"publish","type":"page","link":"https://www.gattefosse.com/pharmaceuticals-special-content/sensorial-analysis-pharmaceuticals/","title":{"rendered":"Sensorial analysis"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":9,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"","_yoast_wpseo_metadesc":""},"categories":[36],"tags":[],"acf":{"component":"PageSpecialContentPharma","title":"Sensorial analysis","introduction":"Poor adherence to topical treatment is a serious problem with several contributing factors. Numerous studies have shown that poor texture and sensorial properties negatively impact patient experience and adherence to treatment. The good news is there is plenty of scope for innovation and improvement in topical dosage forms if the patient’s experience of texture and sensorial properties is taken into consideration during formulation development. \r\n \r\nSensory analysis is a scientific discipline that applies the principles of experimental design and statistical analysis to measure, analyze, and interpret the characteristics of a product as they are perceived by the senses. \r\n \r\nGattefossé has developed validated methods and established an in-house sensorial analysis panel. Using this approach, we can evaluate the sensorial properties of our prototype formulations to \r\n•\tevaluate the influence of new raw materials in formulation, \r\n•\tevaluate the main texture characteristics of our emulsifiers, \r\n•\tcompare prototypes with market references, \r\n•\tunderstand market preferences, \r\n•\tconstruct a broad texture database. \r\n","":false,"content":[{"wysiwyg":"
A trained panel and validated methods for reliable results
\n
\n
Our sensory panel brings together over a dozen trained staff members, both men and women. They test new formulations approximately twice a week. The assessments are carried out using specific protocols and standardized procedures, and the results are statistically analyzed.
\n
Tests cover vision and touch, and they evaluate the following criteria:
\n
\n\n
\n
Initial touch \n
\n
pick-up
\n
texture
\n
creaminess
\n
\n
\n
\n
\n
During application\n
\n
spreadability
\n
tackiness
\n
play time
\n
greasiness
\n
softness
\n
absorption
\n
\n
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After absorption\n
\n
residual film
\n
tackiness
\n
greasy after-feel
\n
soft after-feel
\n
shine
\n
\n
\n
\n\n
\n"},{"wysiwyg":"
The power of sensorial mapping
\n
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This sensorial map shows the results with cream formulations formulated with different Gattefossé pharmaceutical-grade emulsifiers. It enables direct and visual comparison and can help to select the emulsifier or appropriate prototype formulation.
\n
Click on the image to enlarge.
\n
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For more information on how to develop formulas for optimized texture and sensory properties, please see our topical formulation section.
\n
\n
\n
\n
\n"}]},"_links":{"self":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/3654"}],"collection":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/users/9"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/comments?post=3654"}],"version-history":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/3654/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/media?parent=3654"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/categories?post=3654"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/tags?post=3654"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"the-nades-technology-2":{"id":18608,"date":"2020-04-14T15:47:48","date_gmt":"2020-04-14T13:47:48","guid":{"rendered":"https://www.gattefosse.com/?page_id=18608"},"modified":"2021-05-19T22:19:29","modified_gmt":"2021-05-19T20:19:29","slug":"the-nades-technology-2","status":"publish","type":"page","link":"https://www.gattefosse.com/fr/personal-care-trend/the-nades-technology-2/","title":{"rendered":"Opening new horizons for natural cosmetics: The NaDES technology"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":28,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Using the NaDES technology for natural active ingredients","_yoast_wpseo_metadesc":"The NaDES technology is a new solution, adopted by Gattefossé, to create new, 100% natural, and highly functional active ingredients."},"categories":[56],"tags":[],"acf":{"component":"PageGenericContentCos","title":"The NaDES Technology","content":"
While requirements for sustainably driven product development have never been so real, the importance of natural actives as a key part of cosmetic formulations increases greatly.
\n
Consumer expects powerful efficacy from natural products. The challenge therefore is to find extraction methods that are both natural and effective in extracting the key active molecules from plants.
\n
When extracting active metabolites from botanicals, some molecules are more challenging than others. Despite perfect solubility in plant tissues, many of these molecules are poorly soluble in water or lipids, and even in the most efficient known solvents. Additionally, traditional solvents such as butylene glycol or alcohol are no longer acceptable to many consumers.
\n
Since 2012, Gattefossé scientists’ teams have been working on the design of a new generation of 100% natural solvents to create highly functional active ingredients: they are called Natural Deep Eutectic solvents or NaDES.
\n
\n
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A nature-inspired solution
\n
This new category of green solvents is directly inspired by botanicals and the way in which metabolites are solubilized inside the plant – through eutectic combinations of simple chemicals such as sugars, nitrogen compounds, and organic acids. \n Working with researchers from Leiden University, Gattefossé has developed and patented several natural eutectic solvents, perfectly adapted for the extraction of cosmetic active ingredients (1). This exciting class of solvents uses all-natural components such as sugars, polyols, amino acids.
\n
\n
But what does NaDES mean?
\n
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A NaDES can be defined as a eutectic mixture formed by a combination of natural compounds with specific molar ratio. It melts at a single, sharp unique temperature named the “eutectic point” (the lowest melting point for a specific composition) and is characterized by a supramolecular structure.
\n
This homogenous liquid is stable once the eutectic point is reached, making possible its use for extraction applications.
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NaDES by Gattefossé
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Through an ambitious research program, Gattefossé revealed many advantages linked to this extraction technology.
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Completely natural, NaDES combinations benefits from a perfect affinity with plants enabling to reach high extraction potential. The botanical extracts obtained unveil unique phytochemical signature, and performance that would be impossible to reach using conventional solvents. \n Gattefossé thus makes the most of this technology to rediscover well known plants in cosmetics (Calendula, Mallow, Rose, Horse Chesnut…), and opens therefore new fields of possibility. \n 2 applications patents have already been granted (2).
\n
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Bright perspectives
\n
\n From plants and solvents selection to industrialization stage, we master in house all the steps of the development and manufacturing process. \n Our research teams are committed to continue exploring the potential of NaDES. \n Our research perspectives are still wide, and the coming years will surely see the rise of new NaDES active ingredients. \n Natural, non-toxic and efficient at low temperatures, the NaDES technology is perfectly aligned with Gattefossé commitments to provide high-performance sustainable active ingredients.
\n\n
Want to know more about the NaDES technology? Do not hesitate to contact your local sales representative.
\n
\n (1) Patent FR3036618B1, GATTEFOSSE SAS, CAPRIN B, CHARTON V, DEMARNE F: Vegetable extracts for cosmetics, solvents and methods for obtaining same \n (2) Patent FR3053890B1, US10363212B2, GATTEFOSSE SAS, CHARTON V, CAPRIN B, BECHETOILE N: Aesculus Hippocastanum extract \n (2) Patent FR3067939A1, GATTEFOSSE SAS, BECHETOILE N, LOPIS-PRESLE S: Extract of Whitania Somnifera to fight against the harmful effects of visible light on skin
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Air pollutants disrupt the natural balance of the epidermis and lead to oxidation, cutaneous inflammation and irritation (up to sensitization). The hydrolipid film is altered and the barrier reduced. As a result, the skin becomes sensitive, with a dull complexion, greasy and dehydrated.
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Good microcirculation is crucial to help the skin fight pollution and improve the condition of sensitive skin: it induces a better oxygenation and nutrition, and thus a visible radiant skin.
\n
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From microcirculation to skin radiance
\n
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The efficacy of Gatuline® Radiance on skin microcirculation is the direct result of the extracellular release of nitric oxide (NO) from endothelial cells. By stimulating this physiological pathway, Gatuline® Radiance enables the relaxation of the microvessel walls, a phenomenon called vasodilation. Due to its stimulating effect on microcirculation, Gatuline® Radiance contributes to the nutrition of the support tissues of the skin. The face is revitalized and acquires a healthy glow, luminosity and a more even appearance.
\n
\n
Radiance in polluted conditions
\n
\n
A new clinical study has demonstrated that Gatuline® Radiance visibly enhanced skin brightness even under heavy pollution. Gatuline® Radiance was tested during 4 weeks, at 3% in an emulsion. The study took place in Wuhan, China (Air Quality Index was measured to confirm highly polluted environment). Results clearly show that Gatuline® Radiance induces a better oxygenation and nutrition, thus a visible radiant skin. The skin is soothed, its vitality is improved, with less visible pores.
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Efficacy confirmed by users
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Panelists have confirmed these results. They feel their skin reacts less to external aggressions.
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Discover or rediscover our wide range of botanicals. Oily or water-soluble, they bring a natural touch to any cosmetic formulation.
\n","use_level":"Depending on references","naturalite":"","inci":"31 references \r\nFor INCI, see Product TDS. \r\n","origin":"
We select the most appropriate manufacturing method and extraction medium for each plant. Gentle, prolonged maceration to help maintain the integrity of active plant components is followed by several filtration stages before final sterilization. Available references: Aloe, Arnica, Bearberry, Birch Tree, Calendula, Carrot, Common Nettle, Cornflower, Cucumber, Ginkgo Biloba, Ginseng, Grapefruit, Henna, Horse Chestnut, Horsetail, Hydrocotyl, Ivy, Lavender, Lemon, Lotus, Mallow, Matricaria, Oat, Quillai, Red Grapevine, Rose, Sage, Seaweed, Wild Pansy, Witch Hazel, Yeast.
Oily phase for topical formulations. Oily vehicle and solubilizer for solutions. Safety of use is inferred by substantial toxicological data and precedence of use in approved human and veterinary pharmaceutical products.
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Skin Penetration and Permeation Properties of Transcutol®—Neat or Diluted Mixtures
In this critical article, the authors have reviewed numerous studies in order to elucidate the mechanism of action of the highly purified diethylene glycol monoethyl ether TRANSCUTOL® on skin penetration and permeation.
A systematic approach to formulate and evaluate the stability of topical creams with high concentrations of Transcutol® HP
\n
Masumi Dave, M.S., Jason Le Pree, Ph.D., R.Ph. – Gattefossé USA
\n
AAPS PharmSci 360 – 2018
\n
In this study the authors developped stable anhydrous and hydrous creams containing 40% Transcutol® HP, using predictive techniques to select appropriate excipients.
Development of a daphnetin transdermal patch using chemical enhancer strategy: insights of the enhancement effect of Transcutol P and the assessment of pharmacodynamics.
\n
Shen M, Liu C, Wan X, Farah N, Fang L.
\n
Drug Dev Ind Pharm. 2018 Oct;44(10):1642-1649. doi: 10.1080/03639045.2018.1483391. Epub 2018 Jul 2.
\n
A patch for transdermal delivery of daphnetin was developped using Transcutol® P as permeation enhancer.
\n
The study showed:
\n
\n
10% Transcutol® P led to a significant increase in drug release from the patch.
\n
Patch exhibited analgesic and anti-inflammatory activity
Efficient skin delivery: no compromise with Transcutol®
\n
November 2015
\n
This white paper describes Transcutol®, the highest purified pharmaceutical grade of Diethylene Glyceryl monoEthylEther (DEGEE).
\n
Scientific publications asserting the safety of Transcutol® are listed to highlight the non-skin irritant property of Transcutol®. Moreover, solvent properties of Transcutol® are described and solubility data in different solvents are given to illustrate the remarkable solvent capacity of Transcutol®.
\n
This exceptional safety and solvent property make Transcutol® an ideal chemical penetration enhancer for topical formulations, where efficiency and non skin irritancy are key success factors. Examples of commercial uses of DEGEE are cited to illustrate the versatility of use of this excipient in many different topical dosage forms. Practical information is also given for the formulation of Transcutol® in many topical dosage forms.
\n"}],"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/4231"}],"collection":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/users/9"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/comments?post=4231"}],"version-history":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/4231/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/media?parent=4231"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/categories?post=4231"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/tags?post=4231"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"excipients-for-modified-release":{"id":3824,"date":"2017-05-02T06:27:29","date_gmt":"2017-05-02T06:27:29","guid":{"rendered":"https://www.gattefosse.com:443/?page_id=3824"},"modified":"2019-06-04T15:17:11","modified_gmt":"2019-06-04T13:17:11","slug":"excipients-for-modified-release","status":"publish","type":"page","link":"https://www.gattefosse.com/preformulation-guide/pharmaceuticals-content/excipients-for-modified-release/","title":{"rendered":"Excipients for Modified Release"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":9,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Excipients for modified release and sustained release | Gattefossé","_yoast_wpseo_metadesc":"Discover our range of modified-release agents to help you develop biopharmaceutically robust Sustained Release tablets."},"categories":[49],"tags":[],"acf":{"component":"PageGenericContentPharma","title":"Excipients for Modified Release","content":"
Modified- or sustained-release matrices are designed to release a drug slowly over an extended period of time. Formulations must be robust to ensure drug release over time and avoid dose-dumping. Lipid-based matrices are water-insoluble and do not swell or erode when in contact with aqueous media. When used as sustained-release agents, they form an inert matrix from which the drug diffuses slowly.
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Advantages of Gattefossé’s modified-release agents:
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• Drug release is a function of diffusion, which enables simple product design and offers both straightforward modulation of drug release and high reproducibility. • Tablets are biopharmaceutically robust as the lipid matrix is not sensitive to physiological variations (e.g., pH, digestive processes, alcohol level). • Agents are suitable for a wide range of processing techniques, including direct compression, granulation, melt coating, hot melt extrusion, and capsule molding.
finely atomized lipid excipient powder of well-defined, reproducible composition and particle size
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used at proportion of 10%–40%, depending on drug solubility and diluent properties
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suitable for direct compression, granulation, and hot processes (i.e., hot melt coating, granulation, and extrusion)
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crystalline material with narrow melting range (∼70 °C) and rapid recrystallization, ideal for hot melt processes
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GRAS status and precedence of use with many APIs (FDA IID)
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We can provide technical guidelines that offer useful tips on SR formulation development and numerous case studies with model drug molecules, e.g., bupropion HCl, levodopa, metformin HCl, metoprolol succinate, niacin, and theophylline.
finely atomized lipid excipient powder of well-defined, reproducible composition and particle size
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crystalline material with narrow melting range (∼55 °C) and rapid recrystallization, suitable for use in hot processes (i.e., hot melt coating, extrusion, and capsule molding)
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GRAS status and precedence of use with many APIs (FDA IID)
crystalline material with narrow melting range (∼60 °C) and rapid recrystallization, suitable for use in hot processes (i.e., hot melt coating, extrusion, and capsule molding)
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GRAS status and precedence of use with many APIs (FDA IID)
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\n","box_links":[{"link":false,"title":"Tech Chat SR matrix development","external_link":"https://youtu.be/yhEr3Av6gYI","image":"https://www.gattefosse.com/wordpress/wp-content/uploads/2019/03/tech-chat9-322x216.jpg"},{"link":false,"title":"Tech Chat Dual SR matrix","external_link":"https://youtu.be/vrwxwSzJjY4","image":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/05/tech-chat4-322x216.jpg"}],"useful_links":[{"text_link":"Access our publications","link":"https://www.gattefosse.com/preformulation-guide/pharmaceuticals-special-content/publications-sustained-release/","external_link":""},{"text_link":"Dual SR matrix","link":"https://www.gattefosse.com/preformulation-guide/pharmaceuticals-content/dual-sr-matrix/","external_link":""}],"":false,"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/preformulation-guide/wp-json/wp/v2/pages/3824"}],"collection":[{"href":"https://www.gattefosse.com/preformulation-guide/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/preformulation-guide/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/preformulation-guide/wp-json/wp/v2/users/9"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/preformulation-guide/wp-json/wp/v2/comments?post=3824"}],"version-history":[{"href":"https://www.gattefosse.com/preformulation-guide/wp-json/wp/v2/pages/3824/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/preformulation-guide/wp-json/wp/v2/media?parent=3824"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/preformulation-guide/wp-json/wp/v2/categories?post=3824"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/preformulation-guide/wp-json/wp/v2/tags?post=3824"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"excipients-for-api-taste-masking-and-protection":{"id":3835,"date":"2017-05-02T07:23:13","date_gmt":"2017-05-02T07:23:13","guid":{"rendered":"https://www.gattefosse.com:443/?page_id=3835"},"modified":"2019-05-13T17:55:46","modified_gmt":"2019-05-13T15:55:46","slug":"excipients-for-api-taste-masking-and-protection","status":"publish","type":"page","link":"https://www.gattefosse.com/laboratory-assistance/pharmaceuticals-content/excipients-for-api-taste-masking-and-protection/","title":{"rendered":"Excipients for API Taste Masking and Protection"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":9,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Excipients for API Taste Masking and Protection | Gattefossé","_yoast_wpseo_metadesc":"Discover our range of excipients for taste-masking and API protection, suitable for coating, extrusion, granulation or capsule molding processes."},"categories":[49],"tags":[],"acf":{"component":"PageGenericContentPharma","title":"Excipients for API Taste Masking and Protection","content":"
Some APIs present poor organoleptic properties; therefore, taste or odor need to be masked. Others are sensitive to water, oxidation, or temperature and need to be protected to maintain stability. Certain lipid excipients are used in melt processes to effectively protect the API from degradation or mask taste and odor.
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Advantages of Gattefossé’s taste-masking and API protection agents:
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• thermoplastic behavior conducive to processes used (high shear coating, hot melt coating, granulation, extrusion, and capsule molding) • solvent-free process • chemically inert—highly compatible with other excipients in the formulation • plastic deformation for high resistance to compaction • lipid coating that does not impact bioavailability
lipid excipient with intermediate melting point (43 °C)
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ideal for capsule molding process
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\n","box_links":[{"link":false,"title":"Tech chat","external_link":"https://youtu.be/G3M8EE7fkhw","image":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/05/tech-chat5-322x216.jpg"}],"useful_links":[{"text_link":"Access our publications","link":"https://www.gattefosse.com/laboratory-assistance/pharmaceuticals-special-content/publications-on-taste-masking/","external_link":""},{"text_link":"High shear coating","link":"https://www.gattefosse.com/laboratory-assistance/pharmaceuticals-content/high-shear-coating-2/","external_link":""},{"text_link":"Hot melt coating","link":"https://www.gattefosse.com/laboratory-assistance/pharmaceuticals-content/hot-melt-coating/","external_link":""}],"":false,"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/laboratory-assistance/wp-json/wp/v2/pages/3835"}],"collection":[{"href":"https://www.gattefosse.com/laboratory-assistance/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/laboratory-assistance/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/laboratory-assistance/wp-json/wp/v2/users/9"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/laboratory-assistance/wp-json/wp/v2/comments?post=3835"}],"version-history":[{"href":"https://www.gattefosse.com/laboratory-assistance/wp-json/wp/v2/pages/3835/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/laboratory-assistance/wp-json/wp/v2/media?parent=3835"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/laboratory-assistance/wp-json/wp/v2/categories?post=3835"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/laboratory-assistance/wp-json/wp/v2/tags?post=3835"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"50-years-of-bulletins-techniques":{"id":5073,"date":"2017-06-01T13:57:22","date_gmt":"2017-06-01T11:57:22","guid":{"rendered":"https://www.gattefosse.com:443/?page_id=5073"},"modified":"2019-05-28T16:06:43","modified_gmt":"2019-05-28T14:06:43","slug":"50-years-of-bulletins-techniques","status":"publish","type":"page","link":"https://www.gattefosse.com/pharmaceuticals-content/50-years-of-bulletins-techniques/","title":{"rendered":"More than 50 years of Bulletins Techniques"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":36,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"An open library of the Journées Galéniques | Bulletins Techniques","_yoast_wpseo_metadesc":"Gattefossé gathered 50 years of scientific exchange and pharmaceutical knowledge in its Bulletins Techniques. Now available for download!"},"categories":[49],"tags":[],"acf":{"component":"PageGenericContentPharma","title":"More than 50 years of Bulletins Techniques","content":"
In 1966, Gattefossé pioneered the first event to exchange on galenical formulations with the institution of the Journées Galéniques of Saint Remy de Provence. Throughout the years numerous subjects have been addressed by internationally recognized researchers, academic and industrial, always sharing their latest findings for the benefit of the whole pharmaceutical community.
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Each year the proceedings of the meetings have been published in a Bulletin Technique, progressively building a rich collection. In a long tradition of sharing knowledge and for the 50th anniversary of Les Journées Galéniques, the Gattefossé Foundation is pleased to make the entire collection now available.
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We invite you to open the doors of this unique and eclectic library to benefit from this knowledge of pharmaceutical science, formulation and drug delivery.
Published as an open access article in International Journal of Pharmaceutics 558 (2019) 128-142 \n
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In pharmaceutical technology, lipids and polymers are considered pillar excipients for the fabrication of most dosage forms, irrespective of the administration route. They play various roles ranging from support vehicles to release rate modifiers, stabilizers, solubilizers, permeation enhancers and transfection agents. Focusing on selected applications, which were discussed at the Biennial Scientific Meeting of the Gattefossé Foundation 2018, this manuscript recapitulates the fundamental roles of these two important classes of excipients, either employed alone or in combination, and provides insight on their functional properties in various types of drug formulations. Emphasis is placed on oral formulations for the administration of active pharmaceutical ingredients with low aqueous solubilities or poor permeation properties. Additionally, this review article covers the use of lipids and polymers in the design of colloidal injectable delivery systems, and as substrates in additive manufacturing technologies for the production of tailor-made dosage forms.
The 49th Journées Galéniques gathered together leading academics and industrial scientists from around the world to provide a contemporary and updated understanding of the challenges and opportunities in drug development for molecules which are outside the traditional ‘rule-of-5’ drug space.
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In this 108th Edition of the Bulletin Technique you will find the abstracts and information about the presenters. However the majority of full articles have been published in the Advanced Drug Delivery Reviews entitled ‘Understanding the challenges of beyond the rule of 5 compounds: Volume 101 June 1, 2016.
This year’s edition is essential reading for anyone working in the delivery of therapeutic molecules across thin or thick mucosal barriers. It contains insight and foresight from leading experts in drug delivery science from around the world.
The 44th annual Conference of the Journées Galéniques (June 2010) was devoted to aromatherapy, coinciding with the 130th anniversary of the Gattefossé company and a tribute to René-Maurice Gattefossé, a pioneer of aromatherapy as we know it. This special conference focused on the potential of aromatherapy as a complementary therapy as a means of achieving improved health equilibrium.
Description of the latest technologies available to produce nanoparticles and illustration of their potential in specific drug delivery across mucosalmembranes.
Understanding the pharmacokinetics of the drug molecules, assessing their potential using latest cell culture methods and other biopharmaceutical tools
Since antiquity, women have been wearing makeup to transform their appearance. From the kohl of ancient Egypt to the powdered chalk of old Greece to the greasy blushes of the Victorian era, while beauty ideals have changed remarkably with the years, makeup has been an integral part in the lives of women throughout history.
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Even in recent years, we’ve seen a marked shift in beauty ideals from bold, powerful makeup to the more subtle and natural look that is preferred by women today. To understand the shift in attitudes towards complexion makeup, Gattefossé conducted a global survey of over 1200 women in Korea, France, and the US in which we asked them about their makeup habits and perceptions.
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Foundation Perceptions
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Overall, the women felt that foundation makes them feel beautiful, allows them to hide flaws, and can be comfortable to wear. However, especially in South Korea, they also believe that it can contain ingredients that are bad for the skin, and can cause pimples.
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In France and the US, women have difficulty finding the right shade when purchasing foundations, which has led to the movement for more inclusive shades and customizable, personalized products that is currently emerging.
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When asked about natural complexion makeup, we saw that consumers in all regions believe that natural products are better for them, better for the environment, and a good alternative to conventional makeup, but that interest in natural makeup was still low due to perceptions of poor performance, expense, and lack of availability.
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Emulium® Illustro – Pigment Empowered
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Emulium® Illustro has been designed as a solution to the natural makeup dilemma. This high-performance, vegan and natural W/O emulsifier was specifically developed to work with pigments to deliver the benefits customers expect from natural complexion makeup.
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Emulium® Illustro is the first emulsifier developed as a direct collaboration between the Gattefossé R&D and application laboratories. At each step of the development process, the application lab worked with the ingredient to ensure that the end result is high-performance, easy to formulate, and brings a unique sensory imprint to makeup formulations.
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The resulting ingredient is designed to work well with pigments, film formers, pearls, emollients, UV filters, and more. It can create textures that range from ultra-fluid serums to sticks, it is globally approved, and it brings unique sensoriality not only to makeup but also to sun care and skin care formulations.
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Clinically Tested
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Two clinical studies have been conducted on Emulium® Illustro. The first substantiates the “non-comedogenic” claim for the product. In this study, 20 female volunteers with oily skin, all regular users of silicone foundations, used a foundation containing Emulium® Illustro once a day for 27 days. At the end of the study, a dermatologist found no statistically significant increase in retentional and inflammatory signs, validating the claim “non-comedogenic” for Emulium® Illustro.
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In the second study, 34 female volunteers, all regular users of silicone foundations, replaced their normal foundation with an Emulium® Illustro foundation for 27 days. Foundation performance and skin quality were evaluated. At the end of the study, the women were satisfied with the performance of the foundation, and interestingly, they saw in improvement in overall skin quality.
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The impact of natural
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Lastly, the women were asked at the end of the study if they would like to continue using the foundation beyond the end of the study. Without knowing the formula composition, 74% of women said they would like to continue using the foundation. When they were then informed of the natural, PEG-free, silicone-free composition however, this number increased to an astounding 91% of panelists who were willing to abandon their traditional silicone foundation for the product tested. This interest really highlights the interest of the market in high-performing natural makeup formulations.
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It’s a winner!
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The industry has recognized both the need for better natural solutions for complexion makeup and the innovation and quality of Emulium® Illustro by awarding this ingredient the Gold prize for the 2019 In-Cosmetics Global Innovation Zone Best Functional Ingredient Award.
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Stay tuned
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If you’re interested in the results of our global consumer perception study, stay tuned here over the next 3 months as we release the details about the ways consumer think about complexion makeup region by region.
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1951-1959: The rising power of pharmaceutical clients
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In the 1950s, Gattefossé decided to focus on industrial pharmaceutical clients. Pierre Chapus had been employed as a sales rep in 1946 to help Louis Schmuck, and he also took responsibility for prospecting in the pharmaceutical sector. He offered laboratories new cream formulations – those tested at the hospital by Gattefossé some ten years before. He had some “expressions of interest”, but quite unexpectedly, it was not the creams that made him successful, but suppository base material.
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It is worth examining this story more closely. In 1953, the Société Industrielle des Oléagineux (SIO) based in Arras in the North of France, asked Pierre Chapus to bring Gattefossé’s hydrogenated palm oil to market as it was a good substitute for cocoa butter in the manufacture of lipstick. While prospecting, Pierre Chapus had noticed that cocoa butter was often used as an excipient for suppositories and he replied to the SIO, saying that he would agree to have the product tested by clients in cosmetics, but that he would also like to make suppositories. To do this, the SIO had to carry out new tests on interesterified palm oil with precise diglyceride and triglyceride concentrations and different fusion points. Émile Mahler led the physicochemical study of suppository “prototypes” and Jacques Batteur, an industrial pharmacist working at Clin-Comar (Pfizer), was in charge of pharmaceutical testing. Once the product had been tested at a hospital in Paris to confirm the correct levels of physiological tolerance, Gattefossé registered the product in 1954 under the brand name Suppocire®, signing an exclusivity agreement with the SIO. The SIO was responsible for manufacturing while Gattefossé was in charge of control methods, specifications, pharmaceutical formulations, application trials and bringing products to market. Suppocire® became highly successful, both commercially and within the industry, and made Gattefossé the largest supplier of suppository base material in France.
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The interesterification of oils carried out by the SIO when manufacturing Suppocire® inspired Émile Mahler to study the related chemical process in more detail. He successfully transformed a type of vegetable oil into a hydrophilic substance, and that was how Labrafil® came about. A related trademark application was filed in 1954, followed by a patent application in 1956. Labrafil® would soon generate a lot of enthusiasm from pharmaceutical clients as they made active ingredients soluble in medication, notably antibiotics. And the improvement in bioavailability offered by these new excipients was soon proven thanks to studies carried out by Gattefossé in partnership with researchers at the National Veterinary School in Lyon. This innovation was highly significant in the pharmaceutical world and gave the business a very important scientific edge, pointing the company more firmly towards the study of products and processes that would improve the therapeutic effectiveness of medicines.
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Throughout the 1950s, there was a significant increase in Gattefossé products aimed at the pharmaceutical industry, thanks to new products developed by Émile, with Suppocire® and Labrafil® leading the way. The products were created with the support of Jacques Batteur, who agreed to Labrafil® testing in his laboratory.
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Despite all that, the company did not neglect the cosmetics market and also developed “placental extracts”: new products aimed at Gattefossé’s cosmetic client base. A Russian ophthalmologist uncovered the restorative properties of the extracts at the start of the 1930s and those qualities were studied further by doctors at the Antiquaille hospital in Lyon. One of those doctors was Jean Cotte, a pharmacist and biologist at the Lyon hospitals, a friend of Marcel. Cotte suggested carrying out studies of placental extracts supplied by the Mérieux research institute, also in Lyon. Jean Cotte then developed specific control techniques while Gattefossé worked with academics at the National Veterinary School to test the metabolic activity of the extracts. The extracts were then successfully launched by Gattefossé under the brand name Phylderm®, and used at Vichy, followed by L’Oréal and Pier Augé.
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At that particular time, Gattefossé’s visible commercial success was limited to France and the company’s research accomplishments had not yet extended beyond the country’s borders. While Pierre Chapus had recruited trusted sales representatives in the US, Spain, Italy and Belgium, export volumes were still quite weak. However, despite the company struggling to boost international sales and make a name for itself overseas, Gattefossé had still established itself as a national industry leader, a key player in the French sector. In 1955, true to the wishes of René-Maurice who believed in supporting the profession and uniting the medical and academic worlds, the business introduced the “Journées de l’Aromatique” (conferences on aromatics) in partnership with Établissements Vibert, inventors of Pétrole Hahn, a popular hair product. In 1956, Gattefossé helped create the European Centre for Dermocosmetology. The center, managed by Jean Cotte, was instrumental in raising awareness of formulation in both the academic and pharmaceutical worlds. On the picture: Jean Cotte (on the left), Mario Paulet (at the center) who was a friend of René-Maurice and Henri-Marcel Gattefossé (on the right).
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1960-1975: Commercial success and scientific partnerships:
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In 1961, the Société Française de Produits Aromatiques (SFPA) became Gattefossé Société Anonyme (an incorporated company). This new name recognized the fact that the business was reducing its perfumery activity and instead focusing on pharmacy; the majority of innovations emerging from Émile’s lipid chemistry lab were aimed at the pharmaceutical industry. The small business now comprised around thirty employees and Suppocire® made up the majority of sales with 300 tons of the product being manufactured each year. Thanks to these sales, in 1963 Gattefossé was in a position to purchase a vast plot of land in Saint-Priest, an industrial area to the east of Lyon. A new factory was built there, and the business moved into its new premises in 1966.
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During the 1960s, Gattefossé SA was managed by Marcel and his brother-in-law, Émile, who were soon assisted by newcomers to the business. At that time, the company offered internal expertise in chemistry but had no specific knowledge of pharmacy as that area was still relatively new. In 1960, Marcel decided to fill this gap by recruiting Bernard Guillot, a pharmacist who would drive forward “industrial galenics” at Gattefossé. Guillot set up an applications laboratory with the help of another newcomer, André Lombard, who went on to be an incredible commercial ambassador for the business because he enjoyed close relationships with development services in all the French pharmaceutical laboratories. Marcel put a lot of trust in the two young executives who gave talks – often together – at a number of universities in France and overseas. Around the same time, an important piece of work was being conducted internally on technical and control documentation. Gattefossé prepared technical and analytical datasheets to show clients that the company fully complied with the quality standards introduced by industry regulators. And thanks to Jean Cotte and Bernard Guillot, Suppocire® and Labrafil® were even listed in Pharmacopée Française (Codex).
\n
\n
Technology evolved and Gattefossé’s catalog continued to expand with Tefose®, Gelucire®, Plurol®, Labrafac™ and Labrasol® all adding to the list of company products. The business also extended its range of Suppocire® and Labrafil® following internal laboratory tests and external client testing. Émile Mahler created Lipocire™ (the cosmetic equivalent of Suppocire®) with the help of Lucien Waginaire, a recently appointed chemist who would go on to play a decisive role in the company over the years to come. The Lipocire range was used in the development of lipstick formulations. Meanwhile, André Lombard and Bernard Guillot were developing excipients for “dry forms”, creating Precirol® and Compritol®, which were all tested in pharmaceutical labs. By doing so, they highlighted the fact that these products provided a slow-release delivery system. And from this point on, the concept of “sustained release medication” would keep a number of people busy at Gattefossé.
\n
\n
The company was still marketing and selling its “biological products” (placental extracts) developed at the start of the 1950s and supplied by the Mérieux institute. And in the 1960s, Gattefossé started to take an interest in bovine collagen. The Centre Technique du Cuir (CTC; Technical Center for Leather) in Lyon was conducting research on protein derived from cow skin: collagen. The work caught Marcel Gattefossé’s attention and he asked CTC researchers to develop solutions for beauty products. It took a number of years, but the first of these solutions was finally launched in 1976 under the brand name Pancogene®. Gattefossé was also keen to develop biological products derived from plants by extracting active ingredients suitable for cosmetic and dermo-pharmaceutical preparations. And in the 1960s, Gattefossé launched the Vegetol® range (on the initiative of Bernard Guillot), firmly establishing the company in this new market (on the picture: an advertisement for Vegetol® in 1975). \n
\n
\n
As new products were developed and existing ranges expanded, Gattefossé built a close relationship with the academic world. The business contributed to university seminars, with practical work taking place in the company laboratories. This opened up the academic world to Gattefossé, allowing the company to blossom beyond its four walls. In 1966, Marcel, Bernard Guillot and academics Dolique and Etter, jointly created the “Journées Galéniques de Saint-Rémy de Provence” conference series. Every summer, colleagues, industry partners and academics would meet to discuss matters of interest to the profession. These “journées” led to long-term collaborations that would help the business progress and prepare the way for future projects. Creating such partnerships was an approach that had been embraced by previous generations, when René-Maurice worked with medics and pharmacists, for instance. An annual publication called the Bulletin Technique (a strictly “in-house” spin-off of La Parfumerie Moderne) continued the discussions that were generated at the journées. This led to unique scientific relationships that strengthened the company’s reputation within the profession.
\n
\n
1975 was a turning point in the history of the business. After twenty-five years of growth, Gattefossé entered a period of decline. The oil crisis affected all industrialized countries and Gattefossé was not spared. Marcel, at the age of 65, made an announcement to the board of directors saying he wished to bring in additional help and take a step back from the operational management of the business.
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Discover Dermacare and learn how our pharmaceutical grade emulsifiers can be used to create an exciting range of topical dosage forms with excellent texture and sensorial properties that will delight patients.
An incredible texture for this balm, well-adapted for massage.
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The thickness is brought by a subtle combination of Compritol® 888 Pellets, Geleol™ Mono and Diglecerides NF and hydrogenated castor oil.
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Traditionally, youth has been the driving message behind fashion and beauty advertising. The overwhelming message in advertising and media has been that youth is the holy grail. However, today the message is changing, to better reflect the reality of aging and beauty of life.
\n
\n
Aging Gracefully
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\n
According to recent articles, the way you perceive aging can actually influence how you age. “Positive and negative attitudes can affect your health behaviorally, psychologically, and even biologically. Being ‘pro-aging’, or satisfied with your own aging, can make you adopt healthier behaviors, feel in control of how you age, and even heighten your immune system.”1
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Pro-Aging in Beauty
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We are beginning to see this shift towards pro-aging make its way into beauty and cosmetics. Baby boomers, as they age, are realizing that aging can’t be fought forever and are instead embracing the changes that come with time. And cosmetics companies are moving with the mindset of their customers.
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Pro-aging doesn’t mean a rejection of cosmetics, but rather a more targeted selection towards products designed to enhance the appearance at any age, instead of hiding and fighting every symptom of aging. The philosophy behind pro-aging is to remove all “anti” claims and replace them with more positive imagery. “Pro-age products are more about nourishing and moisturizing the skin, enhancing features rather than trying to fill them in or mask them.”2
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Pro-Aging Solutions from Gattefossé
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Gattefossé offers ingredients that meet the demands of the pro-aging trend.
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Gatuline® Renew specifically acts on the problem of skin texture, smoothing, hydrating and softening the skin.
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Gatuline® Radiance enhances micro-circulation for a healthy, glowing complexion at any age.
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Gatuline® Spot-Light effectively works on age spots and complexion for a brighter, more homogeneous complexion.
Discover REVEAL, a range of skin care products formulated by the Gattefossé’s laboratories:
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\n
Download the formula sheets in the “Related documents” box in the right column.
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Skin Rejuvenation Elixir
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Daily Revitalizer
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Powdery Blur Reinvented
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Night Regenerator
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Reviving Body Cocoon
\n
\n
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\n
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Gattefossé has developed Emulium® Kappa MB to answer formulators’ need for a multifunctional PEG-free emulsifier of natural origin that yields stable emulsions; offers the added value of greater activity; and creates a unique sensorial identity.
\n
Oil-in-water emulsions based on Emulium® Kappa MB are very glossy and have a rich and luxurious feel. They are easy to apply, have a long play time, create a sensation of comfort, are softly textured (comparable to silicone elastomers), and exert a remarkable, lasting cushion effect—for baby-soft, replumed skin.
\n","img":{"id":2971,"alt":"facial cream for modern women","title":"balm","caption":"","description":"","mime_type":"image/jpeg","url":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/baume.jpg"},"video":""},{"content":"
Properties
\n
\n
allows the creation of voluptuous O/W cream
\n
possesses sensorial qualities similar to those of silicone elastomers
\n
truly active textures and natural moisturizing efficacy of hydrophilized wax complex and SSL (formation of a protective lipid film preventing transepidermal water loss; instrumental test)
Skin care—day or night creams, naturally moisturizing
\n
Anti-aging creams, “green” lines
\n
Supple creams, thick creams
\n
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The skin automatically responds to attacks with inflammation, a controlled reaction that is part of a natural defense and repair process. In today’s environment, the skin is constantly under assault by pollution and the environment. These conditions can trigger the inflammatory reaction in an uncontrollable manner with harsh effects. It’s no wonder that 62% of women say they have sensitive skin. Sensitive skin is an uncomfortable condition associated with redness, itching, flaking, and stinging. Skin gets drier with age; so, as dryness and sensitivity are often linked, the discomfort only worsens over time. Gatuline® Derma Sensitive is a natural active designed to comfort and protect sensitive skin. This oily extract of caper buds helps reduce clinical signs of inflammation and soothe sensitive skin.
\n","use_level":"2%","naturalite":"ECOCERT/COSMOS approved \r\nNSF compliant","inci":"Octyldodecyl Myristate (and) \r\nCapparis Spinosa Fruit Extract","origin":"
Gatuline® Derma Sensitive applies gemmotherapy, an approach that turns to the highly energetic substances contained in the embryonic plant tissues of buds and seeds. It is extracted from the buds of caper flowers, sourced in the Mediterranean region. This all-natural; non-GMO; preservative-, pesticide-, and allergen-free active is approved for use in natural formulations certified by Ecocert. Preservative free.
In vitro and in vivo tests prove Gatuline® Derma Sensitive
\n
\n
significantly improves condition of sensitive skin by all dermatologic criteria,
\n
soothes skin of study subjects,
\n
significant reduces pro-inflammatory mediators,
\n
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\n
Reduces secretion of pro-inflammatory mediators
\n
Diminishes clinical signs of inflammation
\n
Improves comfort of sensitive and hyperreactive skin
\n
\n","applications":"
\n
Hypersensitive and reactive skin—repairing products
\n
Daily protection—fragile skin, baby lines, sun care products
\n
Makeup and anhydrous products
\n
\n","actives":["soothing"],"actives_secondary":["natural","preservative_free","alcohol_free","bg_free"],"textures":"","textures_secondary":"","extract":false,"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/1709"}],"collection":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/users/36"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/comments?post=1709"}],"version-history":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/1709/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/media?parent=1709"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/categories?post=1709"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/tags?post=1709"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"inauguration-north-america-center-of-excellence":{"id":2495,"date":"2017-04-21T10:13:04","date_gmt":"2017-04-21T10:13:04","guid":{"rendered":"https://www.gattefosse.com:443/?page_id=2495"},"modified":"2017-10-25T16:31:09","modified_gmt":"2017-10-25T14:31:09","slug":"inauguration-north-america-center-of-excellence","status":"publish","type":"page","link":"https://www.gattefosse.com/corporate-news/inauguration-north-america-center-of-excellence/","title":{"rendered":"Gattefossé inaugurates its North America Center of Excellence"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":36,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Gattefossé inaugurates its North America Center of Excellence","_yoast_wpseo_metadesc":"Gattefossé is glad to announce the opening of a state-of-the-art application laboratory in the facilities of our affiliate Gattefossé Corp. in Paramus, NJ."},"categories":[41],"tags":[],"acf":{"title":"Gattefossé inaugurates its North America Center of Excellence","description":"We are glad to announce the opening of a state-of-the-art application laboratory in the facilities of our affiliate Gattefossé Corporation in Paramus, NJ.","date":"21.04.17","content":"\n
The North American region is a leading market for pharmaceuticals and personal care with important local production, consumption and a major influence on global trends. Within this favorable context, Gattefossé North America has enjoyed continuous growth in its business activity since its creation in 1982.
\n
To expand its presence in the region, the Gattefossé Group has decided to establish its fourth Technical Center of Excellence in Paramus, New Jersey. Mr. Jacques Moyrand, Gattefossé Group Chairman, Mr. Olivier Midler, Gattefossé Group CEO and Mr. Eric Brun, President and CEO of Gattefossé USA and Canada, will inaugurate the North America Technical Center of Excellence on Wednesday, April 26th 2017. This center brings together pharmaceutical and personal care application laboratories in a 5,300 ft² (492 m²) space with state-of-the-art equipments.
\n
The technical team will offer an essential interface with both pharmaceutical and personal care customers throughout North America by providing formulation troubleshooting, inspiration and technical support.
\n
For pharmaceuticals, high priority will be given to oral bioavailability enhancement and modified release applications. For personal care, the laboratory will develop specific formulas to answer local needs and to capture local trends.“The latest sign of our investment in this strategic market is the creation of the Gattefossé North America Technical Center of Excellence. These state-of-the-art application laboratories located in Paramus, New Jersey, will ensure our customers responsive service adapted to their market”.
\n
Eric Brun, President and CEO of Gattefossé USA and Canada
\n
\n
About Gattefossé North America
\n
\n\n
The USA and Canadian affiliates of Gattefossé (created respectively in 1982 and 1997) were established to provide local service and support to the.pharmaceutical and personal care industries in North America. Since its creation, Gattefossé North America has enjoyed continuous growth, expanding its presence as a provider of innovative solutions involving performance ingredients.
\n
Under the leadership of Eric Brun, Ph. D, a specialized team of professionals, including marketing, customer service, supply chain, quality, and technical support, is fully committed to servicing customers from the corporate offices in Paramus, NJ, Toronto, ON and Montreal, QC. Local service is also provided by long-term partners in the US Midwest and West Coast, as well as Mexico.
\n
Today, Gattefossé has 34 employees and 3 offices in North America as well as 3 warehouses in Edison (NJ), La Mirada (CA) and Toronto (Canada).
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\n
What You Should Know About Lipid-Based Formulations: \nOral Delivery of Peptides
\n
July 16, 2017 \n9:00-10:00 a.m. \nConvention Center, Room E
\n
\n
Oral administration of peptides is challenged by a number of physiological barriers including presystemic degradation by proteases, deactivation by reduced glutathione, and poor intestinal membrane permeability. Lipid formulations, notably self-emulsifying drug delivery systems (SEDDS), can successfully overcome these challenges.
\n
In an interesting series of recently published works, model peptides leuprorelin, insulin and desmopressin were formulated in SEDDS following hydrophobic ion-pairing of the peptides. The newly designed formulations facilitated payloads of >10% for peptide drugs, provided 100% protection against proteases, and reduced glutathione, and improved their intestinal permeability.
\n
This session shares the intricacies and the promising results of the aforesaid work.
\n
Speakers:
\n
Vincent Jannin HDR (Dir. R&D Projects) \nJasmine Musakhanian, M.Sc. Scientific and Marketing Dir
\n
For all registered attendees, this event is complimentary. Gattefossé will also be exhibiting at Booth 404 in the main hall.
\n","link_all_news":"https://www.gattefosse.com/corporate-news-social/news-social/","component":"PageNewsPharma","thumbnail":{"id":5342,"alt":"CRS Annual Meeting 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Expression AF"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":36,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Gatuline® Expression AF | Smoothing anti-wrinkle active | Gattefossé","_yoast_wpseo_metadesc":"Gatuline® Expression AF is a fast-acting ingredient that redefines both the eye and lip contours in record time and prevents expression lines."},"categories":[6],"tags":[],"acf":{"component":"PageCosmeticProduct","product_codes":[{"code":"5891"}],"bandeau_image":{"id":13758,"alt":"","title":"Gatuline 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showing perfect toothy selfie","title":"Gattefossé Gatuline Expression 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Expression AF","tagline":"Immediate smoothing","description_product_finder":"","introduction":"
Expression lines (i.e., fine lines) are the result of thousands of daily involuntary microcontractions of the facial muscles. They become more visible and deeper as we age and are a real concern for people who want to maintain a youthful appearance. Gatuline® Expression effectively prevents the appearance of expression lines and visibly smooths the skin surface. This fast-acting ingredient redefines both the eye and lip contours in record time.
\n","use_level":"2-5%","naturalite":"ECOCERT/COSMOS approved","inci":"Propanediol (and) Water (and) \r\n Acmella Oleracea Extract","origin":"
Natural, safe, preservative-free extract of a non-GMO plant grown in a protected environment. Acmella oleracea is a plant with small yellow flowers commonly used as a spice and anesthetic agent in Madagascar, from which it is sourced. In fact, its unique numbing effect led to its popularity in cocktails and the nickname “buzz buttons.” This anesthetic effect is also what drew the attention of Gattefossé researchers. Other grade available: Gatuline® Expression (INCI : Alcohol (and) Water (and) Acmella Oleracea Extract)
In vitro and in vivo tests prove Gatuline® Expression AF
\n
\n
exerts a powerful, reversible myorelaxant effect; visibly smooths crow’s-feet after just one day of treatment;
\n
clearly reduces vertical wrinkles (i.e., bar code wrinkles and bitterness folds);
\n
redefines lip contour, making it sharper, finer, and more intense;
\n
continues to act on wrinkles over the long term.
\n
\n","img":{"id":3286,"alt":"lip contour is redesigned","title":"Gatuline expression AF","caption":"","description":"","mime_type":"image/png","url":"https://www.gattefosse.com/wordpress/wp-content/uploads/2017/04/expression.png"},"video":""}],"claims":"
\n
Exerts myorelaxant effect
\n
Yields instantly visible results
\n
Provides natural alternative to injections
\n
Erases expression lines
\n
Reduces bar code wrinkles and bitterness folds
\n
Smooths and redesigns the lip contour
\n
Recurves Cupid’s bow
\n
\n","applications":"
\n
Anti-aging products
\n
Anti wrinkle care
\n
Eye and lip contour treatments
\n
\n","actives":["wrinkles"],"actives_secondary":["natural","preservative_free","alcohol_free","bg_free"],"textures":"","textures_secondary":"","extract":false,"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/pharma/wp-json/wp/v2/pages/1635"}],"collection":[{"href":"https://www.gattefosse.com/pharma/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/pharma/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/pharma/wp-json/wp/v2/users/36"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/pharma/wp-json/wp/v2/comments?post=1635"}],"version-history":[{"href":"https://www.gattefosse.com/pharma/wp-json/wp/v2/pages/1635/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/pharma/wp-json/wp/v2/media?parent=1635"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/pharma/wp-json/wp/v2/categories?post=1635"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/pharma/wp-json/wp/v2/tags?post=1635"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"clean-beauty":{"id":10080,"date":"2018-07-22T20:17:49","date_gmt":"2018-07-22T18:17:49","guid":{"rendered":"https://www.gattefosse.com/?page_id=10080"},"modified":"2019-05-03T11:11:55","modified_gmt":"2019-05-03T09:11:55","slug":"clean-beauty","status":"publish","type":"page","link":"https://www.gattefosse.com/personal-care-trend/clean-beauty/","title":{"rendered":"The New No-Nos"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":36,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"","_yoast_wpseo_metadesc":""},"categories":[56],"tags":[],"acf":{"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false,"component":"PageGenericContentCos","title":"The New No-Nos","content":"
A look at Clean Beauty
\n
The typical beauty consumer applies 150 different ingredients to his or her face each and every day (Figaro, 2017). In today’s environment of increasing transparency and accountability, consumers want to know the risks they incur when they apply products to their face or body.
\n
Where “green” or “natural” used to be the key buzzwords, today we see more and more products moving to “clean beauty” where naturality is good, but safety is paramount.
\n
\n
\n
Clean Beauty Defined
\n
Still a recent concept in beauty, “clean” is an idea that originally began in the food industry and moved into personal care with the introduction of slow beauty, which goes beyond natural and focuses on conscious consumption. Not to be confused with “natural” or “organic”, the term “clean” refers to products formulated without so-called harmful ingredients such as parabens, phthalates, or even retinol.
\n
Consume smarter, respect the environment, monitor what we use: many people today pay more attention to their well-being, but also to their impact on the planet, than ever before. Consumers are already well tuned to transparency, environmental and safety concerns when talking about food, sport, or wellness, and their increased awareness is rubbing off on their cosmetic consumption. In other words, today’s consumer wants to take back the reigns of their beauty routine and put common sense and understanding into it.
\n
\n
#cleanbeauty \n The hashtags #eatclean or #healthyeating are already widely used on Instagram, but #cleanbeauty isn’t far behind – with 813,000 posts as of July 2018.
\n
\n
\n
A Trend with a Future
\n
A growing segment of consumers are looking for natural beauty products – natural ingredients, claims, and labels continue to grow in prevalence and popularity. But clean goes is a similar but different direction. With a positioning that sits between ethics and safety, the target for this claim is huge, even universal – since all consumers of cosmetics want and expect safe products.
\n
And major retailers like Sephora are jumping on board. Sephora has recently launched “clean at Sephora” which identifies certain products as being “they beauty you want, minus the ingredients you don’t”. Brands that are granted the “clean at Sephora” seal must be free from SLS, SLES, parabens, formaldehydes, phthalates, mineral oil, retinyl palmitate, oxybenzone, and more. They must also contain less than 1% of synthetic fragrances. It’s the no-no list taken to the next level.
\n
\n
Saavy Consumers turn to their Phones
\n
For all but the most knowledgeable consumers, the INCI listing remains largely indecipherable. To assist consumers in their purchasing decisions, many apps have emerged promising to decode the composition of all kinds of products from home cleansers to skin care.
\n
By scanning a product’s bar code, the consumer can have an immediate assessment of the supposed danger or safety of the product and a run-down of the controversial ingredients or allergens it contains.
\n
\n
\n\n
\n
\n
Apps like ThinkDirty allow consumers \n to analyze ingredients and make clean \n purchasing decisions.
\n
\n\n
\n
\n
Just as Shazam lets us recognize the title of any song we hear, in one click these apps let us know if a product is good for our skin and health.
\n
It’s important to note that these apps are controversial due to the sometimes questionable scores they provide, but it’s equally important to realize that many consumers are relying on this information for clarity in what they consider a murky situation.
\n
\n
EWG
\n
The Environmental Working Group (EWG) is a non-profit organization that strives to “protect human health and the environment”. As part of these efforts, the group has created a ranking system for cosmetic products and ingredients, designed to reflect potential health hazards. The ranking system goes from 1-10 with a rating of 1-2 considered as low hazard (green).
\n
The EWG ranking has rapidly gained interest in certain markets, particularly in Asia, where the claim “EWG Green” has become increasingly important. Additionally, many companies in other markets, such as the US, are also turning to EWG as a basis for the creation of clean products and formulations.
\n
\n
\n
Creating Clean Beauty
\n
Gattefossé ingredients are well positioned to meet both the natural and clean beauty movements. Many of our textures and actives are both natural and EWG green, meeting the needs of both markets.
\n
\n
For a complete list of our natural and EWG Green ingredients, click here.
\n
\n
\n
\n","box_links":[{"title":"5 Things to Know About Natural Formulating","image":"https://www.gattefosse.com/wordpress/wp-content/uploads/2018/07/5natural-right-box.jpg","link":"https://www.gattefosse.com/personal-care-trend/5-things-natural-formulating/","external_link":"","description":""}],"useful_links":[{"text_link":"Clean at Sephora (www.sephora.com)","link":false,"external_link":"https://www.sephora.com/clean-beauty-products"},{"text_link":"EWG Skin Deep (www.ewg.org)","link":false,"external_link":"https://www.ewg.org/skindeep/"},{"text_link":"Think Dirty (www.thinkdirtyapp.com)","link":false,"external_link":"https://www.thinkdirtyapp.com/"}],"":false,"main_img_article":{"id":13970,"alt":"","title":"the-new-no-nos","caption":"","description":"","mime_type":"image/jpeg","url":"https://www.gattefosse.com/wordpress/wp-content/uploads/2018/01/the-new-no-nos.jpg","width":1536,"height":510,"sizes":{"thumbnail":"https://www.gattefosse.com/wordpress/wp-content/uploads/2018/01/the-new-no-nos-150x150.jpg","thumbnail-width":150,"thumbnail-height":150,"medium":"https://www.gattefosse.com/wordpress/wp-content/uploads/2018/01/the-new-no-nos-300x100.jpg","medium-width":300,"medium-height":100,"medium_large":"https://www.gattefosse.com/wordpress/wp-content/uploads/2018/01/the-new-no-nos-768x255.jpg","medium_large-width":474,"medium_large-height":157,"large":"https://www.gattefosse.com/wordpress/wp-content/uploads/2018/01/the-new-no-nos-1024x340.jpg","large-width":474,"large-height":157,"post-thumbnail":"https://www.gattefosse.com/wordpress/wp-content/uploads/2018/01/the-new-no-nos-672x372.jpg","post-thumbnail-width":672,"post-thumbnail-height":372,"twentyfourteen-full-width":"https://www.gattefosse.com/wordpress/wp-content/uploads/2018/01/the-new-no-nos-1038x510.jpg","twentyfourteen-full-width-width":1038,"twentyfourteen-full-width-height":510}},"description":"","view_all":"personal-care/trends-education-inspiration/","filter_categories":["inspiration-trends"]},"_links":{"self":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/10080"}],"collection":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/users/36"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/comments?post=10080"}],"version-history":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/10080/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/media?parent=10080"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/categories?post=10080"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/tags?post=10080"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"taylor-dispersion-analysis":{"id":16268,"date":"2019-07-30T14:19:43","date_gmt":"2019-07-30T12:19:43","guid":{"rendered":"https://www.gattefosse.com/?page_id=16268"},"modified":"2019-07-30T14:43:16","modified_gmt":"2019-07-30T12:43:16","slug":"taylor-dispersion-analysis","status":"publish","type":"page","link":"https://www.gattefosse.com/pharmaceuticals-special-content/taylor-dispersion-analysis/","title":{"rendered":"Taylor Dispersion Analysis"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":9,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"","_yoast_wpseo_metadesc":"Taylor Dispersion Analysis enables to determine the size of colloidal structures, including Gelucire 44/14, Labrasol ALF and during their digestion"},"categories":[36],"tags":[],"acf":{"component":"PageSpecialContentPharma","title":"Taylor Dispersion Analysis","introduction":"This work was carried out in collaboration with the University of Montpellier (France) and led to four publications. TDA enables to determine the size of the micelles and has been used to characterize our self-emulsifyinig excipients Gelucire® 44/14 (Chamieh et al. 2015) and Labrasol® ALF (Chamieh et al. 2016). It has also been used to follow the evolution of micelles during lipolysis (Chamieh et al. 2018) and the release of peptides from SEDDS (Chamieh et al. 2019). \r\n","":false,"content":[{"wysiwyg":"
Principle
\n
In this technique a microcapillary is used (75 µm section, 75 to 130 cm length) into which a laminar flow of buffer is applied. The sample (solute) is injected in this flow and spreads out axially due to the combined action of convection (red arrow) and radial (blue arrows) diffusion.
\n
Detection of the equilibrium concentration profile (Taylorgram) allows to calculate the absolute molecular diffusion coefficient and hence the hydrodynamic radius of the solute molecules.
\n
\n
\n\n
\n
\n
\n
\n"},{"wysiwyg":"
Application to Gelucire® 44/14 (Chamieh et al. 2015)
\n
Taylorgrams were obtained for a range of Gelucire® 44/14 concentrations (1 to 70 g/L) and the molecular diffusion coefficient (D) and the hydrodynamic radius (Rh) were calculated.
\n
The results are not impacted by temperature as the radius obtained at 25 and 37°C are identical using TDA, which is not the case with DLS. The difference in the radius obtained by both techniques is explained by the presence of small quantities of large aggregates which give higher radius values using DLS, but not with TDA.
\n
Gelucire® 44/14 microdroplet radius increases from 1 to 5.5 nm with increasing concentration from 1 to 70 g/L using TDA.
\n
\n"},{"wysiwyg":"
Application to Labrasol® ALF (Chamieh et al. 2016)
\n
Since Labrasol® ALF forms coacervates below 20 g/L at 25°C and below 40 g/L at 37°C, TDA is coupled with fluorescent detection to avoid the noise associated with the coacervates.
\n
Labrasol® AFL microdroplet radius decreases from 90 to 6 nm with increasing concentration from 1 to 70 g/L.
\n
\n"},{"wysiwyg":"
Application to the evolution of micelle size during lipolysis (Chamieh et al. 2018)
\n
The lipolysis test was applied to solutions of Gelucire® 44/14 and Labrasol® ALF. Samples were taken over time and analysed using TDA coupled with fluorescence detection.
\n
During Gelucire® 44/14 lipolysis there is a plateau for about 30-40 min, then the hydrodynamic radius of Gelucire® 44/14 micelles increases with a sigmoidal shape from about 5 nm to about 25 nm.
\n
During Labrasol® ALF lipolysis, the size of the micelles decreases from about 12 nm to reach a plateau at about 3.5 nm after 20 minutes.
\n
Although both excipients behave very differently upon lipolysis, micelles could still be detected up to 120 minutes of digestion.
\n"},{"wysiwyg":"
Application to determine the proportion of peptide in the micelle (Chamieh et al. 2019)
\n
The aim of this study is to quantify the free fraction of peptides in ion pair SEDDS formulations using TDA and leuprorelin and desmopressin as model peptides. The influence of the ionic strength on peptide release is also evaluated.
\n
In the case of leuprorelin the radius decreases exponentially from about 11.9 nm to 2.8 nm at 150 mM ionic strength, suggesting the release of a large amount of peptide.
\n
In the case of desmopressin, the radius decreases from about 4.1 nm to 0.7 nm at 150 mM ionic strength, showing a total release of the peptide.
\n
The proportion of free peptide as a function of ionic strength could be deduced.
\n
Desmopressin appears to be totally released from the SEDDS at physiological saline conditions (150 mM), whereas leuprorelin is released at 80%.
\n"}],"content_not_translated":false,"equivalent_fr":false,"equivalent_en":false},"_links":{"self":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/16268"}],"collection":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages"}],"about":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/types/page"}],"author":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/users/9"}],"replies":[{"embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/comments?post=16268"}],"version-history":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/pages/16268/revisions"}],"wp:attachment":[{"href":"https://www.gattefosse.com/wp-json/wp/v2/media?parent=16268"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/categories?post=16268"},{"taxonomy":"post_tag","embeddable":true,"href":"https://www.gattefosse.com/wp-json/wp/v2/tags?post=16268"}],"curies":[{"name":"wp","href":"https://api.w.org/{rel}","templated":true}]}},"excipients-for-suppositories-and-pessaries":{"id":3900,"date":"2017-05-04T07:51:21","date_gmt":"2017-05-04T07:51:21","guid":{"rendered":"https://www.gattefosse.com:443/?page_id=3900"},"modified":"2021-04-07T10:36:14","modified_gmt":"2021-04-07T08:36:14","slug":"excipients-for-suppositories-and-pessaries","status":"publish","type":"page","link":"https://www.gattefosse.com/fr/pharmaceuticals-content/excipients-for-suppositories-and-pessaries/","title":{"rendered":"Excipients for Suppositories and Pessaries"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":9,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_yoast_wpseo_title":"Excipients for suppositories and pessaries | Gattefossé","_yoast_wpseo_metadesc":"Discover our wide range of hard fat bases for suppositories and pessaries and select the most appropriate base for your active ingredient."},"categories":[49],"tags":[],"acf":{"component":"PageGenericContentPharma","title":"Excipients for Suppositories and Pessaries","content":"
Suppocire® and Ovucire™ are our well-established brands of semi-synthetic hard fat bases comprising fatty acid esters. Their physicochemical properties have been optimized to provide excellent drug delivery for both solid and liquid active pharmaceutical ingredients (APIs), across the range of water solubility.
\n
\n
\n
Advantages of Suppocire® and Ovucire™
\n
\n
proven safety and mucosal tolerance
\n
excellent drug dispersion and physicochemical stability
\n
narrow melting range for high performance in vivo
\n
solidification behavior adapted for a wide range of manufacturing equipment
\n
\n
Range of bases for suppositories
\n
We offer a wide range of bases for suppositories and pessaries. Here you will find a selection of the most versatile grades. Our bases and formulation expertise enable you to:
\n
\n
simplify existing formulations by reducing the number of excipients;
\n
optimize the manufacturing process and reduce quality issues;
\n
obtain excellent product quality attributes including drug dissolution, i.e., efficacy.
\n
\n
Versatile bases
\n
These multipurpose vehicles span a range of melting points and hydroxyl values and are suitable for a wide spectrum of APIs. They are ideal for straightforward formulations using manual, semi-automated, or fully automated equipment.
Low melting point; long-chain glycerides enable production of hard suppository units
\n
\n\n
\n
Bases for challenging APIs
\n
Some APIs are more difficult to formulate due to properties such as hydrophilicity, sensitivity to oxidation, or high drug load. They require special bases like the following:
With additive to enhance API dispersion and wettability
\n
\n\n
\n
\n
With over 50 years of industrial experience, we have developed our products to address manufacturing and formulation challenges. Our know-how can genuinely speed up drug development time by helping you with\n
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selection of the appropriate Suppocire® and Ovucire™ base by considering API characteristics and the manufacturing process;
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rapid product development benefiting from our database of validated formulations;
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laboratory-scale formulation development, troubleshooting, scale-up, and manufacturing advice.
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Contact Gattefossé to obtain reference formulations with APIs such as acetaminophen, clotrimazole, diclofenac sodium, econazole nitrate, hydrocortisone acetate, ketoprofen, lidocaine hydrochloride, mesalamine, metronidazole, miconazole nitrate, nystatin, papaverine, phloroglucinol, piroxicam, probiotics, procaine, progesterone, and ruscogenin in association with trimebutine.
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