01. Studying skin’s cellular tolerability
when cosmetics are administered
02. Analysis of an active agent’s penetration
03. Evidence of an anti-aging mechanism
04. Evaluation of a soothing product designed for over-reactive skin
05. Evaluation of solar protection
06. Evaluation of a depigmenting or pro pigmenting effect
07. Evaluation of anti-inflammatory effect
08. Objectification of elastin synthesis
09. Objectification of glycosaminoglycans synthesis
10. Evaluation of cellular desquamation
11. Study of cellular re-growth on an experimental model following superficial burns:
12. Anti-radical effect on an experimental model highlighting oxidative stress:
13. Evaluation of an anti-pollution effect (environmental or tobacco):
14. Evaluation of an anti-cellulite response:
I. Evaluation of cosmetic and dermatologic products carried out on human skin kept in a life-like state
- Evaluation de la cohésion du stratum cornéum :
- Evaluation of stratum corneum cohesiveness
- Establishment of semi-quantitative scores
- Comparative study with the desquamation obtained by a standardized product of reference (glycolic acid 10%)
- Histological analysis (hemalun-eosine)
- Immunohistochemical analysis of a marker of differentiation with the aide of an anti-involucrine antibody
- Evaluation of the final differentiation of the stratum corneum
Immunohistochemical analysis of a marker of differentiation with the aide of an anti-involucrine antibody
Immunohistochemical analysis
Immunohistochemical analysis of a marker of differentiation with the aide of an anti-involucrine antibody
Analysis of exfoliation of the skin
Desquamated skin
- Experimental model of epithelial alteration by burns after the application of agarose gel heated to 85°C
- Study of cellular rehabilitation :
Normal skin
Skin altered by burns
- Quantification of the number of altered cells by histological analysis, of cytoplasmic clarification, picnotic nucleus
Vasodilatation analysis:
- Morphometric measure of the capillairies` diameter (µm2)
- Measure of percentage of dilated vessels - Dosage of pro-inflammatory cytokines (IL1a, IL 8)
- Experimental model of cellular alteration due to oxidative stress : UVA-UVB radiation or application of xanthine oxydase/hypoxantine or hydroperoxides to generate free radicals
Anti-radical effect
Experimental model of cellular alteration due to oxidative stress
- dosage of nitrites (NO2 en µM)
- dosage of residual carbonyls to the epidermis (test ELISA) (results recorded in DO or in µM of carbonyl)
- Evaluation of collagen cross-linking (dosage of hydroxyproline in µg/mg of proteins after denaturingby a collagenase)
- Analysis of cellular viability (viability of mitochondrial deshydrogenases) by an exclusion test MTT(mitochondrial tetrazolium test)
- Immunohistochemistry analysis of the natural destructive enzymes of oxygenized free-radicals (semi-quantitative scores) :catalase and superoxide dismutase with manganese
- Experimental model of pollution through superficial administration of hypochlorous soda, carbon particles, lead acetate
- Model of excessive exposure to tobacco amidst a smoking location (dose equivalent to 2 packs /day)
Model of excessive exposure to tobacco
Evaluation of an anti-pollution effect (environmental or tobacco).
- Dosage of carbonyl residue on epidermis (test ELISA) (results recorded in DO or in µM de carbonyl)
- Evaluation of collagen cross-linking (dosage of hydroxyproline after denaturing by a collagenase)
- Model serves of whole human skin, complete with hypoderm
Evaluation of an anti-cellulite response
- Dosage of AMPc, reflection of the activation of the triglyceride lipase (test EIA, noted in pmoles /ml according to the quantity of proteins)
- Dosage of glycerol freed by the adipose tissues (nmoles /g of lipids)
Update : december 2010
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