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聚合物前药

Polymeric prodrugs.

作者信息

Azori M

机构信息

Department of Macromolecular Chemistry, Hungarian Academy of Sciences, Budapest.

出版信息

Crit Rev Ther Drug Carrier Syst. 1987;4(1):39-65.

PMID:3315236
Abstract

Polymeric prodrugs can be defined as latent pharmaceutical agents which must undergo chemical or enzymatic transformation to the active or parent drug in the organism after administration. Polymeric prodrugs may also be considered special types of drug delivery systems where the drug release is realized by cleavage of a chemical bond. The concept of polymeric prodrugs finds application in the design of novel agents when pharmacokinetical modification of a parent drug is necessary, or when the aim is to achieve selective action at a target site, utilizing enzymatic activation specific for that site. The types of polymeric prodrugs synthetized in the last decade are reviewed regarding the chemical structure of the carrier backbone and the drug linkages applied. Relationship between the chemical structure, physicochemical characteristics of polymeric prodrugs, and their physiological behavior is discussed, with special regard to the bioavailability, body distribution, and rate of elimination of the carrier from the living organism. In vitro and in vivo experimental data concerning drug activation processes, as well as potential clinical applications of polymeric prodrugs, are surveyed.

摘要

聚合物前药可定义为潜在的药物制剂,给药后必须在生物体内经过化学或酶促转化成为活性药物或原药。聚合物前药也可被视为特殊类型的药物递送系统,其中药物释放是通过化学键的断裂来实现的。当需要对原药进行药代动力学修饰,或者旨在利用对特定靶点具有特异性的酶促激活作用在靶位点实现选择性作用时,聚合物前药的概念可应用于新型药物的设计。本文综述了过去十年合成的聚合物前药的类型,涉及载体主链的化学结构和所应用的药物连接方式。讨论了聚合物前药的化学结构、物理化学特性与其生理行为之间的关系,特别关注其生物利用度、体内分布以及载体从生物体中的消除速率。还调查了有关药物激活过程的体外和体内实验数据,以及聚合物前药的潜在临床应用。

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