https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=pubmed&id=30216760&retmode=xml&tool=Litmetric&email=readroberts32@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09 302167602018101920181019
1873-26821882018NovJournal of photochemistry and photobiology. B, BiologyJ Photochem Photobiol BProtective effect of Thai silk extracts on drug-induced phototoxicity in human epidermal A431 cells and a reconstructed human epidermis model.505950-5910.1016/j.jphotobiol.2018.08.022S1011-1344(17)31274-5Bombyx mori silk extracts, derived from the cocoon degumming process of draw and dye silk in the textile industry, are mainly composed of sericin protein. To add value to the Thai silk extracts, and hence the silk industry, a simple enrichment process was recently developed and the enriched silk extracts were then applied in nano-cosmeceutical products and nano-delivery systems. In this study, the protective effect of Thai silk extracts from three different strains of Bombyx mori on the drug-induced phototoxicity was evaluated in vitro using chlorpromazine (CPZ), a commonly used antipsychotic drug, as a representative phototoxic drug. The human epidermal A431 cell line and reconstructed human epidermis (RhE) model were used as the in vitro skin model. The silk extracts significantly improved the viability of A431 cells after CPZ exposure and ultraviolet A (UVA) irradiation, as shown by the significantly increased CPZ and UVA IC50 values and the decreased proportion of apoptotic cells. The protective effect of these silk extracts against the CPZ-induced UVA-phototoxicity in A431 cells was associated with the attenuation of intracellular oxidative stress via an increased intracellular glutathione level. Likewise, the silk extracts exhibited a protective effect on the CPZ-induced UVA-phototoxicity in the RhE model, in terms of an improved tissue viability and attenuation of the released inflammatory cytokine, interleukin-1α. These findings support the potential usefulness of silk extracts in novel applications, especially in the protection of drug-induced phototoxicity.Copyright © 2018 Elsevier B.V. All rights reserved.RosenaApiwanANano Safety and Risk Assessment Laboratory, National Nanotechnology Center, National Science and Technology Development Agency, Thailand Science Park, Pathum Thani, Thailand.KoobkokkruadThongchaiTNano-Cosmeceuticals Laboratory, National Nanotechnology Center, National Science and Technology Development Agency, Thailand Science Park, Pathum Thani, Thailand.EaknaiWaleewanWNano-Cosmeceuticals Laboratory, National Nanotechnology Center, National Science and Technology Development Agency, Thailand Science Park, Pathum Thani, Thailand.BunwatcharaphansakunPhichapornPNano-Cosmeceuticals Laboratory, National Nanotechnology Center, National Science and Technology Development Agency, Thailand Science Park, Pathum Thani, Thailand.ManiratanachoteRawiwanRNano Safety and Risk Assessment Laboratory, National Nanotechnology Center, National Science and Technology Development Agency, Thailand Science Park, Pathum Thani, Thailand.AueviriyavitSasitornSNano Safety and Risk Assessment Laboratory, National Nanotechnology Center, National Science and Technology Development Agency, Thailand Science Park, Pathum Thani, Thailand. Electronic address: sasitorn@nanotec.or.th.engJournal Article20180901
SwitzerlandJ Photochem Photobiol B88049661011-13440Cytokines0Protective Agents0Reactive Oxygen Species0SilkGAN16C9B8OGlutathioneU42B7VYA4PChlorpromazineIMAnimalsBombyxmetabolismCell LineCell Survivaldrug effectsradiation effectsChlorpromazinepharmacologyCytokinesmetabolismEpidermisdrug effectspathologyradiation effectsGlutathioneHumansProtective AgentschemistrypharmacologyReactive Oxygen SpeciesmetabolismSilkchemistrymetabolismSkin, ArtificialThailandUltraviolet RaysChlorpromazineDrug-induced phototoxicityRhE modelSericinSilk extract
20171011201882420188262018915602018102060201891560ppublish3021676010.1016/j.jphotobiol.2018.08.022S1011-1344(17)31274-5