‘Mutual Prodrug’ and approach to increase the effectiveness of Non-Steroidal Anti-inflammatory Drugs

Manish S. Junagade, A. Goyal
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Abstract

A clinically useful drug may have limitations in practice because of undesirable side effects, poor solubility, and poor bioavailability, short duration of action, first-pass effect, poor absorption & adverse effects. There are increased efforts in research to increase the therapeutic efficacy of drugs by eliminating or minimizing the undesirable properties of drug molecules. Some of the problems can be solved using a formulation development approach but in some cases, chemical modification in the molecule is necessary to correct the pharmacokinetic parameters. One of the approaches to convert the existing molecule to a more efficient molecule is prodrug design. Mutual Prodrug is the molecule in which an active drug molecule is attached to a carrier molecule having pharmacological activity. So a mutual prodrug consists of two pharmacologically active molecules connected by a bio labile linkage. Both molecules in this act as a pro moiety of each other. The design of mutual prodrug is very fruitful in the area of research & has given successful results in increasing the clinical & therapeutic effectiveness of the drugs. The present article takes a review of various applications of mutual prodrugs & development in this field in the last few decades.
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“相互前药”和提高非甾体抗炎药有效性的方法
临床有用的药物在实践中可能由于不良副作用、溶解度差、生物利用度差、作用时间短、首过效应、吸收不良和不良反应而受到限制。通过消除或最小化药物分子的不良性质来提高药物的治疗效果的研究越来越多。有些问题可以通过配方开发方法解决,但在某些情况下,需要对分子进行化学修饰以纠正药代动力学参数。将现有分子转化为更有效分子的方法之一是前药设计。互前药是一种分子,其中活性药物分子附着在具有药理活性的载体分子上。因此,相互前药由两个具有药理活性的分子组成,它们由一个生物活性链连接。这两种分子都是彼此的亲体。相互前药的设计在研究领域取得了丰硕的成果,在提高药物的临床疗效和治疗效果方面取得了成功的成果。本文综述了近几十年来相互前药的各种应用及其在该领域的研究进展。
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