Additional Supporting Information may be found online in the supporting information tab for this article:Data S1 Supplementary Material, Methods and References.Figure S1 Erdr1 is significantly decreased in psoriatic lesional skin. Figure S2 Expression of Erdr1 increases after treatment using cyclosporin A (CsA) in psoriasis-like skin inflammation mouse model. Figure S3 Recombinant Erdr1 exerts anti-inflammatory properties in a psoriasis-like skin inflammation mouse model.
BackgroundFacial wrinkles are one of the major features of ageing. Traditionally, hyaluronic acid (HA) is used as a potent antiwrinkle compound. HyaCare â Filler CL (Evonik Industries AG, Essen, Germany) is a new anti-ageing ingredient with a cross-linked polysaccharide made from fermentation-derived HA, contributing to the reduction in facial fine lines and wrinkles as well as increasing skin elasticity and hydration (1). Recently, the same purposes were made for caffeine. Extracts from two species of coffee directly combat UV damage improving strength, resilience and elasticity of facial skin (2). Coffea arabica seed oil significantly improves collagen and elastin production, while Coffea robusta has a high concentration of chlorogenic acid (which reduces redness) and caffeine (2). A new tendency in cosmetic formulations is the use of ingredients obtained from food by-products discarded as waste, answering to sustainability concerns (3-7). Coffee silverskin (CS) is a coffee roasting by-product with no commercial value. According to the International Coffee Organization (ICO), in 2014, the world coffee production has been around 141 620 million bags of 60 kg, which means that about 3 823 740 kg of these wastes were produced. Recent studies reveal its antioxidant potential, caffeine content and low cytotoxicity (6). Rodrigues et al. evaluated the CS skin and ocular irritation potential, using reconstructed human epidermis, EpiSkin TM (SkinEthics Laboratories, Lyon, France), and human corneal epithelial model, SkinEthics TM HCE (SkinEthics Laboratories, Lyon, France), respectively (7). Results demonstrated that CS is not irritant and the in vivo assay revealed that extract can be regarded as safe for topical application (7).
Questions addressed and experimental design
ResultsFranz diffusion cells were used and pig ear skin selected as model barrier, to evaluate the caffeine permeation. Results are presented in Fig. 1. After 8 h, a very small amount of caffeine crossed the skin, respectively, about 20% of the extract content. The extract improves skin hydration after 48 h of a patch test when compared to the negative control used (P < 0.05) (Table S1). Probably, this effect is due to the well-detailed extract composition (6,7). For keratinocyte (HaCaT) and fibroblast (HFF-1), no cytotoxicity was observed for the different concentrations tested (1, 5 and 10 mg/ml), which means that these formulations are potentially safe (Table S2).
In vivo evaluationStandardized clinical photographs were taken at baseline and at 28 days using a Visioface â (Cou...