2017
DOI: 10.2174/1389200218666170222145908
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Antioxidant Nanoplatforms for Dermal Delivery: Melatonin

Abstract: The use of nanoplatforms for the dermal melatonin delivery as antioxidant agent could improve the efficacy of conventional melatonin administration due to the preservation of the drug from premature oxidation and the enhancement of drug permeation through the skin providing greater exposure times.

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Cited by 13 publications
(11 citation statements)
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“…However, apart from their antioxidant properties, the mechanisms of actions through which assayed vitamins exert the healing action are confusing and controversial [59][60][61]. On the other hand, antiapoptotic and p53-inhibitory processes seem to be involved in the healing mechanism of MLT [62].…”
Section: Discussionmentioning
confidence: 99%
“…However, apart from their antioxidant properties, the mechanisms of actions through which assayed vitamins exert the healing action are confusing and controversial [59][60][61]. On the other hand, antiapoptotic and p53-inhibitory processes seem to be involved in the healing mechanism of MLT [62].…”
Section: Discussionmentioning
confidence: 99%
“…Orally ingested melatonin is rapidly metabolized in the liver by CYP450 into 6-hydroxymelatonin while sublingual (transmucosal) melatonin administration can bypass liver metabolism. Transdermal application of melatonin appears to be optimal for local application due to slow absorption, deposition in the skin, lack of identifiable site effects, and availability of different formulations (Flo et al, 2016, 2017; Milan et al, 2017; Romic et al, 2016; Scheuer et al, 2016b; Zetner et al, 2016). Because there is a cutaneous melatonin metabolism with metabolites sharing similar activities as melatonin (Slominski et al, 2017b), the effects summarized in the central column may also be secondary to the action of its metabolites.…”
Section: Figurementioning
confidence: 99%
“…Poly(D,L-lactide-co-glycolide) (PLGA) polymers have been used for the preparation of nanoparticles and microparticles loaded with melatonin [35,36]. Both of them are prepared by the emulsion-diffusion-evaporation method and the addition of 0.2% (w/v) melatonin in the aqueous phase.…”
Section: Polymeric Nanoparticles and Polymer-based Drug Delivery Nanomentioning
confidence: 99%
“…Both of them are prepared by the emulsion-diffusion-evaporation method and the addition of 0.2% (w/v) melatonin in the aqueous phase. The size of nanoparticles was about 200 nm and the entrapment efficiency around 14%, while the size of microparticles was about 3.5 micrometers and the encapsulation efficiency 27% [35,36]. The toxicity and the effectiveness of the prepared systems are also evaluated using cell lines.…”
Section: Polymeric Nanoparticles and Polymer-based Drug Delivery Nanomentioning
confidence: 99%