4.5 Article

Anti-inflammatory and Antioxidant Activity of Nanoencapsulated Curcuminoids Extracted from Curcuma longa L. in a Model of Cutaneous Inflammation

期刊

INFLAMMATION
卷 44, 期 2, 页码 604-616

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10753-020-01360-4

关键词

curcuminoids; inflammation; oxidative stress; photoacoustic spectroscopy; ear edema

资金

  1. CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico)
  2. FA (Fundacao Araucaria-PR), Brazil

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The study found that nanoencapsulated curcuminoid preparations and free curcuminoids had similar anti-inflammatory effects in topical treatment, while oral administration of nanoencapsulated curcuminoid preparations had a higher anti-inflammatory effect than free curcuminoids. Additionally, nanoencapsulated curcuminoid preparations showed better bioavailability compared to free curcuminoids.
The present study evaluated the anti-inflammatory effect of nanoencapsulated curcuminoid preparations of poly(vinyl pyrrolidone) (Nano-cur) and free curcuminoids (Cur) in an experimental model of croton oil-induced cutaneous inflammation. Male Swiss mice, weighing 25-30 g, received oral treatment by gavage 1 h before CO application or topical treatment immediately after CO application (200 mu g diluted in 70% acetone) with a single dose of Cur and Nano-cur. After 6 h, the animals were anesthetized and euthanized. The ears were sectioned into disks (6.0 mm diameter) and used to determine edema, myeloperoxidase (MPO) activity, and oxidative stress. Photoacoustic spectroscopy (PAS) was used to evaluate the percutaneous penetration of Cur and Nano-cur. Topical treatment with both preparations had a similar inhibitory effect on the development of edema, MPO activity, and the oxidative response. The PAS technique showed that the percutaneous permeation of both topically applied preparations was similar. Oral Nano-cur administration exerted a higher anti-inflammatory effect than Cur. Topical Cur and Nano-cur application at the same dose similarly inhibited the inflammatory and oxidative responses. Oral Nano-cur administration inhibited such responses at doses that were eight times lower than Cur, suggesting the better bioavailability of Nano-cur compared with Cur.

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