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通过水相原子转移自由基聚合制备具有可控形态的铜纳米药物。

Copper Nanodrugs with Controlled Morphologies through Aqueous Atom Transfer Radical Polymerization.

机构信息

MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310058, China.

Department of Surgical Oncology, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China.

出版信息

Biomacromolecules. 2024 Jul 8;25(7):4545-4556. doi: 10.1021/acs.biomac.4c00552. Epub 2024 Jun 20.

Abstract

Copper (Cu) nanodrugs can be facilely prepared through atom transfer radical polymerization (ATRP) in an aqueous medium. However, it is difficult to control the morphology of Cu nanodrugs and thereby optimize their anticancer activity. In this work, aqueous ATRP was combined with polymerization-induced self-assembly (PISA) to prepare Cu nanodrugs with various morphologies. We mapped the relationship between polymerization condition and product morphology in which each morphology shows a wide preparation window. Decreasing the reaction temperature and feeding more Cu catalysts can improve the mobility of chains, facilitating the morphology evolution from sphere to other high-order morphologies. The resultant Cu nanodrugs with high monomer conversion and high Cu loading efficiency could be easily taken by cancer cells, showing excellent anticancer efficacy in vitro. This work proposed a potential strategy to prepare Cu nanodrugs with a specific morphology in batches, providing the method to optimize the anticancer efficacy through morphology control.

摘要

铜(Cu)纳米药物可以通过原子转移自由基聚合(ATRP)在水介质中轻松制备。然而,很难控制 Cu 纳米药物的形态,从而优化其抗癌活性。在这项工作中,水相 ATRP 与聚合诱导自组装(PISA)相结合,制备出具有各种形态的 Cu 纳米药物。我们绘制了聚合条件与产物形态之间的关系,其中每种形态都有一个较宽的制备窗口。降低反应温度和加入更多的 Cu 催化剂可以提高链的迁移率,促进形态从球体向其他高阶形态演变。所得的 Cu 纳米药物具有高单体转化率和高 Cu 负载效率,很容易被癌细胞摄取,在体外表现出优异的抗癌效果。这项工作提出了一种批量制备特定形态 Cu 纳米药物的潜在策略,为通过形态控制优化抗癌效果提供了方法。

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