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1.
Skin Pharmacol Physiol ; 22(6): 299-304, 2009.
Article in English | MEDLINE | ID: mdl-19786823

ABSTRACT

Green tea (Camellia sinensis) and Ginkgo biloba extracts in cosmetic formulations have been suggested to protect the skin against UV-induced damage and skin ageing. Thus, it is very important to assess the human skin penetration of their major flavonoids to verify if they penetrate and remain in the skin to exert their proposed effects. The aim of this study was to evaluate the human skin penetration of epigallocatechin-3-gallate (EGCG) and quercetin from green tea and G. biloba extracts vehiculated in cosmetic formulations. This study was conducted with fresh dermatomed human Caucasian skin from abdominal surgery mounted on static Franz diffusion cells. Skin samples were mounted between two diffusion half-cells and 10 mg/cm(2) of formulations supplemented with 6% of green tea or G. biloba extract were applied on the skin surface. The receptor fluid was removed after 6 and 24 h and analyzed by high-performance liquid chromatography for the quantification of the flavonoids. The stratum corneum was removed by tape stripping and immersed in methanol and the epidermis was mechanically separated from the dermis and triturated in methanol to extract EGCG and quercetin. The results showed that the flavonoids under study penetrated into the skin, without reaching the receptor fluid. The majority of EGCG was quantified in the stratum corneum (0.87 microg/cm(2)), which was statistically higher than the EGCG concentrations found in viable epidermis (0.54 microg/cm(2)) and in the dermis (0.38 microg/cm(2)). The majority of quercetin was quantified in the viable epidermis (0.23 microg/cm(2)), which was statistically higher than the EGCG concentration found in the stratum corneum layer (0.17 microg/cm(2)). Finally, it can be concluded that EGCG and quercetin from green tea and G. biloba extracts vehiculated in cosmetic formulations presented good skin penetration and retention, which can favor their skin effects.


Subject(s)
Antioxidants/pharmacokinetics , Catechin/analogs & derivatives , Quercetin/pharmacokinetics , Skin Absorption , Administration, Cutaneous , Antioxidants/isolation & purification , Camellia sinensis/chemistry , Catechin/isolation & purification , Catechin/pharmacokinetics , Chromatography, High Pressure Liquid , Cosmetics/chemistry , Cosmetics/pharmacokinetics , Diffusion Chambers, Culture , Ginkgo biloba/chemistry , Humans , In Vitro Techniques , Permeability , Plant Extracts/pharmacokinetics , Quercetin/isolation & purification , Time Factors
3.
Int J Cosmet Sci ; 27(6): 301-8, 2005 Dec.
Article in English | MEDLINE | ID: mdl-18492167

ABSTRACT

Lipowheat is an entirely biodegradable 100% natural active ingredient, extracted from non-transgenic wheat. Thanks to its very interesting properties, it can integrate the composition of most cosmetic and pharmaceutical products. The aim of this work was first to realize a large range of stable simple or multiple emulsions, in order to determine and evaluate the ability of a new glucolipidic surfactant Lipowheat to form and stabilize emulsions. The rheological properties of these emulsions were tested during a 30-day storage period at three different storage conditions (cold, room temperature and at 40 degrees C). In addition to dynamic and static rheological tests, droplet size distribution of the cream was also determined. Furthermore, a stable simple emulsion was selected to realize percutaneous absorption and evaluate the properties of Lipowheat.

4.
Ann Dermatol Venereol ; 129(1 Pt 2): 131-6, 2002 Jan.
Article in French | MEDLINE | ID: mdl-11976540

ABSTRACT

In the stratum corneum, the water binds to the intracellular hygroscopic and hydrosoluble substances called "natural moisturizing factors" or NMF. These "natural moisturizing factors" contained in the corneocytes are formed during epidermal differentiation and may represent up to 10 p. cent of the corneocyte mass. They are principally amino acids, carboxylic pyrrolidone acid, lactic acid, urea, glucose and mineral ions. Keratinization plays an important part in the formation of NMF that exhibit strong osmotic potential attracting the water molecules. The binding of water to NMF is the static aspect of cutaneous hydration. The second, dynamic, aspect is related to the selective permeability of the stratum corneum and to its lipid barrier properties, the permeability of which depends on the integrity and nature of the inter-corneocyte lipids and their lamellar organization between the cells. In these conditions, hydration cosmetics rely on two concepts that can be isolated or associated: the supply of hydrophilic substances to the stratum corneum, capable of attracting and retaining water (moisturizer) or capable of restoring the barrier in order to restore normal water loss or of protecting it against aggression (occlusive).


Subject(s)
Body Water/metabolism , Dehydration/drug therapy , Dermatologic Agents/therapeutic use , Epidermis/physiology , Skin Care/methods , Skin Diseases/drug therapy , Cell Membrane Permeability , Cosmetics , Dehydration/physiopathology , Emollients/administration & dosage , Epidermis/chemistry , Humans , Hydrotherapy/methods , Keratinocytes/physiology , Membrane Lipids/physiology , Skin Diseases/physiopathology , Surface-Active Agents/administration & dosage
5.
J Colloid Interface Sci ; 218(1): 335-337, 1999 Oct 01.
Article in English | MEDLINE | ID: mdl-10489309

ABSTRACT

The present work attempted to apply the theoretical framework described by Taylor to different multiple emulsions under shear. The results were in relatively good agreement with the theory. The correlation between the fragmentation and release studies was well proved. Moreover, these studies showed that mechanisms taking place during the breakup were complex and did not always lead to a total release of the entrapped electrolyte. Some phenomena such as a partial leakage of the internal aqueous compartment or the expulsion of aqueous microglobules covered by a residual lipophilic film were able to restrict the release. Copyright 1999 Academic Press.

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