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载有药物的 HPMA 共聚物,具有受控制的肿瘤特异性药物释放。

HPMA Copolymer-Drug Conjugates with Controlled Tumor-Specific Drug Release.

机构信息

Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovský Sq. 2, 162 06 Prague 6, Czech Republic.

出版信息

Macromol Biosci. 2018 Jan;18(1). doi: 10.1002/mabi.201700209. Epub 2017 Aug 14.

Abstract

Over the past few decades, numerous polymer drug carrier systems are designed and synthesized, and their properties are evaluated. Many of these systems are based on water-soluble polymer carriers of low-molecular-weight drugs and compounds, e.g., cytostatic agents, anti-inflammatory drugs, or multidrug resistance inhibitors, all covalently bound to a carrier by a biodegradable spacer that enables controlled release of the active molecule to achieve the desired pharmacological effect. Among others, the synthetic polymer carriers based on N-(2-hydroxypropyl) methacrylamide (HPMA) copolymers are some of the most promising carriers for this purpose. This review focuses on advances in the development of HPMA copolymer carriers and their conjugates with anticancer drugs, with triggered drug activation in tumor tissue and especially in tumor cells. Specifically, this review highlights the improvements in polymer drug carrier design with respect to the structure of a spacer to influence controlled drug release and activation, and its impact on the drug pharmacokinetics, enhanced tumor uptake, cellular trafficking, and in vivo antitumor activity.

摘要

在过去的几十年中,设计并合成了许多聚合物药物载体系统,并对其性能进行了评估。其中许多系统基于水溶性聚合物载体的低分子量药物和化合物,例如细胞抑制剂、抗炎药或多药耐药抑制剂,它们都通过可生物降解的间隔物共价结合到载体上,从而实现活性分子的控制释放,以达到所需的药理效果。在其他方面,基于 N-(2-羟丙基)甲基丙烯酰胺(HPMA)共聚物的合成聚合物载体是最有前途的载体之一。本文综述了 HPMA 共聚物载体及其与抗癌药物的偶联物的发展进展,特别是在肿瘤组织中,尤其是在肿瘤细胞中引发药物激活的进展。具体而言,本文强调了通过改变间隔物的结构来改进聚合物药物载体设计,以影响控制药物释放和激活的方式,及其对药物药代动力学、增强肿瘤摄取、细胞转运和体内抗肿瘤活性的影响。

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