“…Due to these properties, trans -resveratrol is quickly metabolized, therefore skin application may be an alternative to oral administration [10,11,12]. Various formulation strategies, including the use of liposomes, solid dispersions, cyclodextrin complexes, solid lipid nanoparticles, emulsions, polymeric micelles, polymeric nanoparticles, and nanocrystals, have been evaluated to attempt to overcome current limitations of trans -resveratrol [13,14,15,16,17,18,19,20,21]. In particular, a pharmacokinetic study of twelve healthy volunteers given an oral administration of a capsule formulation of resveratrol via solubilization with micelles consisting of polysorbate 80, polysorbate 20, and medium chain triacylglycerol yielded increases in the area under the plasma concentration versus time curve ( AUC ) and maximum plasma concentration ( C max ) of resveratrol of 5.0-fold and 10.6-fold, respectively, compared to volunteers ingesting a resveratrol powder [19].…”