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[Synthesis and bioactivies of salicylic acid-g-chitosan derivatives]. | LitMetric

AI Article Synopsis

  • The study focuses on the development of derivatives from salicylic acid and chitosan and analyzes their combined anti-inflammatory and analgesic effects using various mouse models.
  • Results show that these new derivatives have stronger anti-inflammatory properties compared to salicylic acid, chitosan, and dexamethasone cream, as well as presenting milder effects on stomach mucous membranes than aspirin.
  • Although the immediate pain-relief effects of the derivatives are not as strong as aspirin, their longer-lasting analgesic effects are comparable, indicating a potential for beneficial combined health applications.

Article Abstract

To prepare the derivatives of salicylic acid-g-chitosan and study their synergistic and complementary actions, the synergism of anti-inflammatory action of the derivatives was investigated with the experiments of xylene-induces mice ear edema, the analgesic activities by the tartaric emetic-induced mice twist test and the hot-plate test, and the complementary effects between salicylic acid and chitosan through morphological changes of stomach mucous membrane of rat, separately. The anti-inflammatory activities of salicylic acid-g-chitosan derivatives for anti-inflammatory activities were more potent than that of salicylic acid and chitosan and dexamethasone cream in external use, and more potent than that of aspirin orally. However, immediate analgesic activity of the derivatives was lower than that of aspirin and persistent activity was similar as that of aspirin. And the stomach mucous membrane morphology change of the derivatives was much milder than that of aspirin. The salicylic acid grafted chitosan derivatives showed synergistic and complementary effect on the anti-inflammatory and analgesic activities and so on.

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