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Polymeric nanocapsules as a technological alternative to reduce the toxicity caused by meloxicam in mice. | LitMetric

Polymeric nanocapsules as a technological alternative to reduce the toxicity caused by meloxicam in mice.

Regul Toxicol Pharmacol

Grupo de Pesquisa em Neurobiotecnologia, Universidade Federal de Pelotas, Capão do Leão, CEP: 96010-900, RS, Brazil. Electronic address:

Published: November 2016

AI Article Synopsis

  • - The study investigated whether meloxicam in nanocapsules can reduce stomach and liver damage compared to free meloxicam in mice.
  • - Mice were treated with either blank nanocapsules, meloxicam in nanocapsules, or free meloxicam, and various biochemical markers were analyzed, showing no significant difference between the groups.
  • - Results indicated that meloxicam in nanocapsules reduced ulcerogenic potential and histological damage, suggesting polymeric nanocapsules may be a better option for decreasing meloxicam toxicity.

Article Abstract

This study determined whether meloxicam in nanocapsules modifies stomach and liver damage caused by free meloxicam in mice. Male Swiss mice were treated with blank nanocapsules or meloxicam in nanocapsules or free meloxicam (10 mg/kg, intragastrically, daily for five days). On the seventh day, blood was collected to determine biochemical markers (glutamic oxaloacetic transaminase, glutamic pyruvic transaminase, total bilirubin, unconjugated bilirubin, albumin and alkaline phosphatase). Stomachs and livers were removed for histological analysis. There was no significant difference in the biochemical markers in the plasma of mice. Meloxicam in nanocapsules did not have an ulcerogenic potential in the stomach or cause lipid peroxidation in the stomach and liver. Free meloxicam increased the ulcerogenic potential in the stomach and lipid peroxidation in the stomach and liver. Meloxicam in nanocapsules caused less histological changes than free meloxicam. In conclusion, polymeric nanocapsules can represent a technological alternative to reduce the toxicity caused by meloxicam.

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Source
http://dx.doi.org/10.1016/j.yrtph.2016.09.023DOI Listing

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