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用于抗癌药物递送的聚合物-药物缀合物

Polymer-Drug Conjugates for Anticancer Drug Delivery.

作者信息

Wadhwa Saurabh, Mumper Russell J

机构信息

Regeneron Pharmaceuticals, Tarrytown, New York.

Division of Molecular Pharmaceutics, UNC Eshelman School of Pharmacy, Center for Nanotechnology in Drug Delivery, and UNC Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.

出版信息

Crit Rev Ther Drug Carrier Syst. 2015;32(3):215-45. doi: 10.1615/critrevtherdrugcarriersyst.2015010174.

Abstract

Polymer-drug conjugates (PDCs) are drug delivery systems where one or more drug(s) are covalently attached to the functional groups of the polymer directly or through a spacer. Several anticancer drugs that have been used to synthesize PDCs are currently under clinical trials. PDCs have shown enhanced tumor accumulation, increased therapeutic index, and prolonged circulation, accompanied by a sustained release of the bound drug. Distinct cell uptake mechanisms make PDCs less sensitive to efflux pumps associated with the development of multi-drug resistance. However, the effectiveness of PDCs as a delivery system primarily depends on the drug, polymer, type of linkage, and presence of targeting groups. Due to the availability of different functional groups and spacers, it is possible to control drug release as well as multi-functionalize PDCs, thereby increasing their versatility as drug carriers. Furthermore, active tumor uptake may be achieved by using the concept of drug targeting. However, functionalization alters the in vivo behavior of the polymer, signifying the evaluation of safety and effectiveness of PDCs. Several PDCs are currently being tested in different phases of clinical trials. This review focuses on critical aspects in the design of PDCs when used in cancer drug delivery.

摘要

聚合物-药物偶联物(PDCs)是一种药物递送系统,其中一种或多种药物直接或通过间隔基共价连接到聚合物的官能团上。目前,几种已用于合成PDCs的抗癌药物正在进行临床试验。PDCs已显示出增强的肿瘤蓄积、提高的治疗指数和延长的循环时间,同时结合的药物能持续释放。不同的细胞摄取机制使PDCs对与多药耐药性发展相关的外排泵不太敏感。然而,PDCs作为一种递送系统的有效性主要取决于药物、聚合物、连接类型和靶向基团的存在。由于存在不同的官能团和间隔基,因此可以控制药物释放并使PDCs多功能化,从而增加其作为药物载体的通用性。此外,通过药物靶向的概念可以实现肿瘤的主动摄取。然而,功能化会改变聚合物的体内行为,这意味着需要评估PDCs的安全性和有效性。目前有几种PDCs正在不同阶段的临床试验中进行测试。本综述重点关注PDCs用于癌症药物递送时设计中的关键方面。

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