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抗体靶向的聚合物结合药物。

Antibody-targeted polymer-bound drugs.

作者信息

Ríhová B

机构信息

Department of Immunology and Gnotobiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic.

出版信息

Folia Microbiol (Praha). 1995;40(4):367-84. doi: 10.1007/BF02814745.

Abstract

Drug targeting is an attractive new approach to killing cancer cells while leaving normal tissue unharmed. Recently we have developed a new generation of antibody-targeted immunosuppressive (cyclosporin A) and cytostatic (daunomycin, doxorubicin) drugs and photosensitizers (chlorin e6) effective in vitro and in vivo. The drugs and the targeting antibody (polyclonal and monoclonal) are conjugated to the oligopeptidic side chains of a water-soluble synthetic carrier, copolymer of N-(2-hydroxypropyl)methacrylamide. The composition of the side chains ensures the stability of the linkage between the drug and the polymeric carrier in the bloodstream and its intralysosomal degradability which is a prerequisite for the pharmacological activity of the preparation. Antibody-targeted polymer bound drugs show considerably decreased hepatotoxicity, cardiotoxicity, myelotoxicity and nephrotoxicity. Two adriamycin-HPMA copolymers are in Phase I/II clinical trials in United Kingdom.

摘要

药物靶向是一种极具吸引力的新方法,可在不损害正常组织的情况下杀死癌细胞。最近,我们开发了新一代抗体靶向的免疫抑制剂(环孢素A)、细胞生长抑制剂(柔红霉素、阿霉素)和光敏剂(氯e6),它们在体外和体内均有效。这些药物和靶向抗体(多克隆和单克隆)与水溶性合成载体N-(2-羟丙基)甲基丙烯酰胺共聚物的寡肽侧链偶联。侧链的组成确保了药物与聚合物载体之间的连接在血流中的稳定性及其溶酶体内的可降解性,这是该制剂药理活性的前提条件。抗体靶向聚合物结合药物的肝毒性、心脏毒性、骨髓毒性和肾毒性显著降低。两种阿霉素-HPMA共聚物正在英国进行I/II期临床试验。

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