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通过ROP-RAFT联合策略制备的抗菌超支化聚合物-松萝酸复合物

Antimicrobial Hyperbranched Polymer-Usnic Acid Complexes through a Combined ROP-RAFT Strategy.

作者信息

Rauschenbach Moritz, Lawrenson Stefan B, Taresco Vincenzo, Pearce Amanda K, O'Reilly Rachel K

机构信息

M. Rauschenbach, Dr. S. B. Lawrenson, Dr. A. K. Pearce, Prof. R. K. O'Reilly, School of Chemistry, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.

Dr. V. Taresco, School of Chemistry, The University of Nottingham, University Park, Nottingham, NG7 2RD, UK.

出版信息

Macromol Rapid Commun. 2020 Sep;41(18):e2000190. doi: 10.1002/marc.202000190. Epub 2020 May 13.

DOI:10.1002/marc.202000190
PMID:32400917
Abstract

Polymer-drug conjugates have received considerable attention over the last decades due to their potential for improving the clinical outcomes for a range of diseases. It is of importance to develop methods for their preparation that have simple synthesis and purification requirements but maintain high therapeutic efficacy and utilize macromolecules that can be cleared via natural excretory pathways upon breakdown. Herein, the combination of ring-opening polymerization (ROP) and reversible addition-fragmentation chain-transfer (RAFT) polymerization is described for the straightforward synthesis of amphiphilic, stimuli-responsive, biodegradable, and highly functionalizable hyperbranched polymers. These unimolecular nanoparticles demonstrate a versatile platform for the synthesis of polymer-drug conjugates owing to the inclusion of a Boc-protected polycarbonate moiety in either a block or random copolymer formation. A proof-of-concept study on the complexation of the poorly water-soluble antimicrobial drug usnic acid results in polymer-drug complexes with powerful antimicrobial properties against gram-positive bacteria. Therefore, this work highlights the potential of amphiphilic and biodegradable hyperbranched polymers for antimicrobial applications.

摘要

在过去几十年中,聚合物 - 药物偶联物因其有改善一系列疾病临床疗效的潜力而受到广泛关注。开发其制备方法很重要,这些方法要有简单的合成和纯化要求,同时保持高治疗效果,并使用在分解后可通过天然排泄途径清除的大分子。在此,描述了开环聚合(ROP)和可逆加成 - 断裂链转移(RAFT)聚合的结合,用于直接合成两亲性、刺激响应性、可生物降解且高度可功能化的超支化聚合物。由于在嵌段或无规共聚物形成中包含Boc保护的聚碳酸酯部分,这些单分子纳米颗粒展示了一个用于合成聚合物 - 药物偶联物的通用平台。一项关于难溶性抗菌药物松萝酸络合的概念验证研究产生了对革兰氏阳性细菌具有强大抗菌特性的聚合物 - 药物复合物。因此,这项工作突出了两亲性和可生物降解超支化聚合物在抗菌应用中的潜力。

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