Abstract

Sunscreens have been shown to be extremely effective in preventing DNA lesions due to ultraviolet (UV) radiation. Indeed, recent studies indicate that the number of UV-induced lesions decreased up to 95% depending on sunfilter combination and sun protection factor (SPF). Thus, sunblockers protect the skin from the harmful effects of UV, but they do not provide 100% protection. As a result, sunscreens are now being developed with antioxidants to provide additional protection against oxidative stress-mediated cell damage especially reactive oxygen species (ROS). We investigated the bioavailability, release and antioxidative properties of a sunscreen formulation (emulsion) containing two antioxidants, oxothiazolidine (OTZ) and delta-tocopheryl glucoside (DTG) using reconstructed human epidermis (RHE) model. OTZ reacts directly with ROS to form taurine; while DTG is metabolized into α-tocopherol to achieve antioxidative activities. Their penetration and metabolism 0.5-24 h were measured after solar-simulated irradiation as well as their antioxidative responses on RHE models. Oxidative stress markers included malondialdehyde (MDA), superoxide dismutase (SOD) and catalase activities. The two antioxidants had different penetration profiles: OTZ was rapidly and extensively absorbed whereas DTG was slowly absorbed. The yield of protection increased over time, with maximal protection 2 h post-irradiation. DTG slowly penetrated in the RHE and was present in the epidermis at all post-irradiation timepoints, thus allowing a slow but constant supply of α-tocopherol over at least 24 h. By contrast, the OTZ antioxidative protection was immediate but short-lived due to its rapid penetration. These results indicate a complementary sunlight protective action of OTZ and DTG; with immediate bioavailability of OTZ, and a prolonged skin delivery of α-tocopherol from the slower bioavailability and metabolism of DTG.

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