A leather-based in vitro model for determining the effect of cosmetics on skin microbes

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A leather-based in vitro model for determining the effect of cosmetics on skin microbes
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A leather-based in vitro model for determining the effect of cosmetics on skin microbes Cosmetics Skin Microbiome microbiology prebiotics formulation MDPIOpenAccess hsrheinwaal

By Dr. Priyom Bose, Ph.D.Aug 28 2022Reviewed by Benedette Cuffari, M.Sc. Human skin harbors a wide range of microorganisms, including fungi, bacteria, and viruses. In fact, recent estimates indicate that over 1011 microbial cells could be present on skin surfaces.

Background Numerous prebiotic supplements have been used in cosmetics to promote the growth of beneficial bacteria, such as coagulase-negative Staphylococci, while suppressing Cutibacterium growth. About the study Seven ubiquitous Gram-positive skin bacteria were selected to analyze how they were affected by the tested prebiotic actives. The actives used in this study included plant-based glycerol, diglycerol, glyceryl caprylate, and multifunctional ingredient.

Study findings The possibility of microbial growth or growth inhibition was studied using liquid culture media that contained prebiotic actives at different concentrations. The culture media with a greater optical density at a given time indicated the promotion of bacterial growth. Similarly, cultures with lower ODs indicated bacterial growth inhibition.

Dissimilarity in microbial growth promotion and inhibitory effects might be observed between in vivo and in vitro experiments using similar microbial strains and active ingredients. This is because the complexities of the interaction between bacteria and skin cells cannot be analyzed in a cell-culture-based model.

Although general sera-containing actives exhibited a similar pattern in bacterial colonization, some minor changes and exceptions were observed. As compared to the colonization pattern of serum alone, the addition of actives led to minor alterations, including less pronounced inhibition of S. aureus and a higher rate of C. jeikeium inhibition.

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