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76 NATURALS


20 18 16 14 12 10 8 6 4 2 0


Control +32% +22% +25%


25 20 15 10 5 0


0.5% 1% 2.5%


Figure 8: Evaluation of the anti-microbial effect of the skincare active on human keratinocytes, study of the antimicrobial peptide HBD-2


to stimulate the production of these important peptides. The skincare active was found to enhance the expression of antimicrobial peptides LL-37, beta-defensin 2, and psoriasin. These peptides are crucial for the skin’s innate immune response and contribute to its ability to combat harmful microorganisms. At concentrations of 0.5%, 1% and 2.5%,


the skincare active increased the expression of Beta-defensine2 (HBD-2) by 22%, 26% and 32% respectively. At concentrations of 0.5%, 1% and 2.5%, the skincare active increased the expression of peptide LL-37 by 19%, 24% and 31% respectively. At concentrations of 0.5%, 1% and 2.5%,


the skincare active increases the expression of psoriasin 19%, 28% and 36%. These findings highlight the protective


effect of the skincare active, as it enhances the expression of antimicrobial peptides that strengthen the skin’s defence mechanisms against potential pathogens. This information is valuable for understanding how the skincare active supports overall skin health and maintains a balanced microbial environment.


Soothing and immuno-modulating effect The anti-inflammatory potential of the skincare active has been evaluated on reconstituted


200 180 160 140 120 100 80 60 40 20 0


Negative control


+68% -20% -26% -30% Control +31% +19% +24%


3.5 3


+19%


2.5 2


1.5 1


0.5 0


0.5% 1% 2.5%


Figure 9: Evaluation of the anti-microbial effect of the skincare active on human keratinocytes, study of the antimicrobial peptide LL-37


epidermis using the CellSystems model. Keratinocytes, which play a crucial role in the immune response, not only produce antimicrobial peptides but also pro- inflammatory cytokines such as IL1 (alpha and beta), IL8, IL6, and TNF-alpha. When using the skincare active at 0.5%, the


results showed a decrease in TNF-alpha levels of 17% and IL1-alpha levels of 20%. When using the skincare active at 1%, the results showed a significant decrease in TNF-alpha levels of 21% and IL1-alpha levels of 26%. When using the skincare active at 1.5%, the


results showed a significant decrease in TNF- alpha levels of 24% and IL1-alpha levels of 30%. These pro-inflammatory cytokines are


associated with skin inflammation, and their reduction indicates the potential of the skincare active to calm and soothe irritated skin, making it suitable for sensitive skin types.


Conclusion This skincare active from Naolys represents a significant breakthrough in skincare, harnessing the power of the skin microbiome to enhance radiance and soothe the skin. Its multi-faceted action on the skin’s defence mechanisms reinforces the cutaneous barrier, promotes cellular renewal, rebalances the microbial environment, and enhances the expression of


200 180 160 140 120 100 80 60 40 20 0


Passive control (UVB)


(0.5%) + UVB


+ UVB (1%)


(2.5%) + UVB


Figure 11: Evaluation of the anti-microbial effect of the skincare active on human keratinocytes, study of the antimicrobial peptide Psoriasin


PERSONAL CARE October 2023


Negative control


Control 0.5% 1% 2.5%


Figure 10: Evaluation of the anti-microbial effect of the skincare active on human keratinocytes, study of the antimicrobial peptide Psoriasin


antimicrobial peptides. These scientifically validated effects are


supported by in vitro and clinical studies, providing a solid foundation for the efficacy and benefits of Serene Skin Sage. By combining the wisdom of nature with


advanced biotechnology, Naolys continues to drive innovation in the skincare industry, offering consumers an attractive and effective solution for their skincare needs. Experience the transformative power of nature and cutting- edge biotechnology with Serene Skin Sage – a skincare active that represents a harmonious fusion of science and botanical wonders.


References 1. Baricevic D, Sosa S, Della Loggia R, Tubaro A, Simonovska B, Krasna A, Zupancic A. (2001). Topical anti-inflammatory activity of Salvia officinalis L. leaves: the relevance of ursolic acid. Journal of Ethnopharmacology. 75(2-3), 125-132


2. Misra BB, Dey S, Prajapati V, Singh S, Yadav N, Gupta, AK. Phytochemical and pharmacological potential of Salvia officinalis L. Journal of Pharmacy and Pharmacology. 2016; 68(2), 137-161


3. Barnes J, Anderson LA. Herbal medicines: A guide for healthcare professionals. 2012. Pharmaceutical Press


+55% -17% -21% -24%


+36% +28%


PC


Passive control (UVB)


(0.5%) + UVB


+ UVB


(1%)


(2.5%) + UVB


Figure 12: Study of the anti-inflammatory potential on reconstituted epidermis using the CellSystems model, expression of the pro-inflammatory cytokine TNF-alpha


www.personalcaremagazine.com


IL1-a (pg/ml)


HBD-2(ng/ml)


LL-37 (ng/ml)


IL1-a (pg/ml)


Psoriasin (ng/ml)


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