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Pharmacological Evaluation and Preliminary Pharmacokinetics Studies of a New Diclofenac Prodrug without Gastric Ulceration Effect

机译:一种新型无胃溃疡双氯芬酸前药的药理评价和初步药代动力学研究

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摘要

Long-term nonsteroidal anti-inflammatory drugs (NSAIDs) therapy has been associated with several adverse effects such as gastric ulceration and cardiovascular events. Among the molecular modifications strategies, the prodrug approach is a useful tool to discover new safe NSAIDs. The 1-(2,6-dichlorophenyl)indolin-2-one is a diclofenac prodrug which demonstrated relevant anti-inflammatory properties without gastro ulceration effect. In addition, the prodrug decreases PGE(2) levels, COX-2 expression and cellular influx into peritoneal cavity induced by carrageenan treatment. Preliminary pharmacokinetic studies have shown in vivo bioconversion of prodrug to diclofenac. This prodrug is a new nonulcerogenic NSAID useful to treat inflammatory events by long-term therapy.
机译:长期非甾体类抗炎药(NSAIDs)治疗已与多种不良反应(例如胃溃疡和心血管事件)相关。在分子修饰策略中,前药方法是发现新的安全NSAID的有用工具。 1-(2,6-二氯苯基)吲哚啉-2-酮是一种双氯芬酸前药,其显示出相关的抗炎特性,而没有胃溃疡作用。此外,前药降低了角叉菜胶处理引起的PGE(2)水平,COX-2表达和细胞向腹腔的流入。初步的药代动力学研究表明前药在体内生物转化为双氯芬酸。该前药是一种新的非致溃疡性非甾体抗炎药,可用于通过长期疗法治疗炎症事件。

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