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药物-聚合物偶联物:改善化疗的潜力。

Drug-polymer conjugates: potential for improved chemotherapy.

作者信息

Duncan R

机构信息

Department of Biological Scineces, University of Keele, Staffordshire, UK.

出版信息

Anticancer Drugs. 1992 Jun;3(3):175-210. doi: 10.1097/00001813-199206000-00001.

Abstract

Use of polymeric drug delivery systems is rapidly becoming an established approach for improvement of cancer chemotherapy. Zoladex, a poly lactide-co-glycolide subcutaneous implant that delivers a luteinizing hormone releasing hormone analog over 28 days, is now the treatment of choice for prostate cancer, and a polyanhydride matrix containing BCNU is currently in phase III evaluation for treatment of glioma multiforme. Soluble polymers were first proposed as targetable drug carriers in the mid-1970s, and although the first conjugates are still at an early stage of development some, e.g. SMANCS (styrene maleic acid-neocarzinostatin) and monomethoxypolyethyleneglycolasparaginase, are now undergoing clinical evaluation and show considerable promise. Polymeric drug delivery systems are usually designed to produce an improved pharmacokinetic profile of an antitumor agent (controlled release) and in addition soluble carriers can achieve either first-order (organ specific) or second-order (tumor specific) drug targeting by virtue of the fact that they are usually administered intravenously and should theoretically access primary and secondary disease. Soluble polymeric carriers have the potential to improve the activity of conventional antitumor agents, peptide and protein drugs, and have recently been used in constructs for delivery of oligonucleotides. With increased awareness that the successful design of a polymeric drug delivery systems can only be achieved with prior consideration of the pathology and stage of the disease, tumor accessibility, biochemistry and cell biology of the target site, choice of appropriate therapeutic agent(s) and understanding of their fundamental mode of action, we have seen the emergence of a number of exciting and potentially more selective antitumor therapies based on polymer technologies. Here, the basic principles for design of soluble polymeric drug delivery systems are explained and illustrated using examples drawn from our studies on the development of N-(2-hydroxypropyl)methacrylamide copolymer conjugates for use in cancer chemotherapy. Those soluble polymeric carriers that are undergoing clinical evaluation are briefly reviewed.

摘要

使用聚合物药物递送系统正迅速成为一种公认的改善癌症化疗的方法。诺雷德是一种聚丙交酯-乙交酯皮下植入剂,可在28天内递送促黄体生成素释放激素类似物,现已成为前列腺癌的首选治疗方法,而含有卡莫司汀的聚酸酐基质目前正处于治疗多形性胶质母细胞瘤的III期评估阶段。可溶性聚合物在20世纪70年代中期首次被提议作为可靶向药物载体,尽管首批偶联物仍处于早期开发阶段,但一些产品,如SMANCS(苯乙烯马来酸-新制癌菌素)和单甲氧基聚乙二醇天冬酰胺酶,目前正在进行临床评估,并显示出相当大的前景。聚合物药物递送系统通常旨在产生抗肿瘤药物改善的药代动力学特征(控释),此外,可溶性载体可以实现一级(器官特异性)或二级(肿瘤特异性)药物靶向,因为它们通常通过静脉给药,理论上应该能够到达原发性和继发性疾病部位。可溶性聚合物载体有潜力提高传统抗肿瘤药物、肽和蛋白质药物的活性,并且最近已用于递送寡核苷酸的构建体中。随着人们越来越意识到,只有在事先考虑疾病的病理和阶段、肿瘤的可及性、靶部位的生物化学和细胞生物学、选择合适的治疗药物以及了解其基本作用模式的情况下,才能成功设计聚合物药物递送系统,我们已经看到出现了一些基于聚合物技术的令人兴奋且可能更具选择性的抗肿瘤疗法。在此,将使用我们在开发用于癌症化疗的N-(2-羟丙基)甲基丙烯酰胺共聚物偶联物的研究中的例子,解释和说明可溶性聚合物药物递送系统设计的基本原理。对那些正在进行临床评估的可溶性聚合物载体进行简要综述。

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