A glyceride with a high melting point used as a modified release agent or lubricant in tablets. Can also be used in lipid coating technologies and as lipid carrier for nanoparticles.
Consists of mono-, di- and triesters of behenic acid (C22), the diester fraction being predominant.
Key characteristics
Product form
Powder
Melting range (°C)
65 – 77
HLB
2
Main functionalities
Modified release matrix former for tablet. Lubricant for tablet—independent of mixing time and speed. Lipid carrier former for solid lipid nanoparticle (SLN) and nanostructured lipid carrier (NLC). Coating agent for taste masking and protection of sensitive APIs. Listed in the European STEP database for excipients in pediatric medicines. Safety of use is inferred by GRAS status and 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
\n
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.
\n
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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
\n
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)
\n"},{"keys":"EP Name","value":"
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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PROPYLENE GLYCOL LAURATES
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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.
\n"},{"wysiwyg":"
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
\n"},{"wysiwyg":"
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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