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Research on esterified prodrugs of naproxen

机译:萘普生酯化前药研究

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Naproxen was a popular non-steroidal anti-inflammatory drug (NSAID), which might cause side effects. The subject hoped to reduce the side-effect of naproxen by the synthesis of its prodrugs and keep its therapeutic effect as an anti-inflammatory drug. Fifteen prodrugs of naproxen had been synthesized with the use of DCC as a dehydrater and DMAP as a catalyzer. The chemical stability of prodrugs had been investigated with acid-base titration. The anti-inflammatory effect of the prodrugs had been determined by the curing of engorgement in the ears of Mus musculus albus. The action of prodrugs in vivo was studied with HPLC. The paper also reported the preparation of the emulsion of prodrugs to help increase their bioavailability. The result indicated that naproxen-esterified prodrugs were stable against chemical hydrolysis, could remain or even enhance their effects and reduce by-effect.
机译:萘普生是一种受欢迎的非甾体抗炎药(NSAID),可能导致副作用。 主题希望通过合成其前药来减少萘普生的副作用,并将其治疗效果保持为抗炎药。 通过使用DCC作为脱氢和DMAP作为催化剂合成了十五个前药。 用酸碱滴定研究了前药的化学稳定性。 通过在Mus Musculus Albus的耳朵中的耳朵固化来确定前药的抗炎作用。 用HPLC研究了体内前药物的作用。 本文还报道了制备前药的乳液,有助于增加其生物利用度。 结果表明,萘芬酯化前药稳定对化学水解稳定,可以保留甚至增强它们的效果并减少效应。

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