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      Improvement of quercetin protective effect against oxidative stress skin damages by incorporation in nanovesicles

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          Abstract

          Quercetin was incorporated in glycerosomes, new phospholipid-glycerol vesicles, and their protective effect against oxidative stress skin damages was extensively evaluated. In particular, the concentration-dependent effect of glycerol (from 10 to 50%) on vesicle suitability as cutaneous carriers of quercetin was carefully assessed. All vesicles were unilamellar and small in size (∼80-110 nm), as confirmed by cryo-TEM observation, with a drug incorporation efficiency ranging between 81 and 91%. SAXS studies, performed to investigate the bilayer arrangement, indicated a strong, dose-dependent interaction of glycerol with the polar portions of the phospholipid molecules, while quercetin did not significantly change the bilayer packing. In vitro studies on newborn pig skin underlined the concentration-dependent ability of glycerosomes to promote quercetin accumulation in the different layers, also confirmed by confocal microscopic observation of skin treated with fluorescent vesicles. Quercetin incorporated into liposomal and glycerosomal nanoformulations showed a strong ability to scavenge free radicals (DPPH test) and protect human keratinocytes in vitro against hydrogen peroxide damage. Moreover, quercetin-loaded vesicles were avidly taken up by keratinocytes in vitro. Overall, results indicate 40 and 50% glycerosomes as promising nanosystems for the improvement of cutaneous quercetin delivery and keratinocyte protection against oxidative stress damage.

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          Author and article information

          Journal
          Colloids and Surfaces B: Biointerfaces
          Colloids and Surfaces B: Biointerfaces
          Elsevier BV
          09277765
          November 2014
          November 2014
          : 123
          : 566-574
          Article
          10.1016/j.colsurfb.2014.09.059
          25444664
          9a8e9e06-f462-43d9-ad0b-a0e60db209d7
          © 2014

          https://www.elsevier.com/tdm/userlicense/1.0/

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