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具有共轭和封装药物的红光响应金属聚合物纳米载体用于多药耐药肿瘤的光疗

Red-Light-Responsive Metallopolymer Nanocarriers with Conjugated and Encapsulated Drugs for Phototherapy Against Multidrug-Resistant Tumors.

作者信息

Chen Mingjia, Gong Ningqiang, Sun Wen, Han Jianxiong, Liu Yuanli, Zhang Shouwen, Zheng Aiping, Butt Hans-Jürgen, Liang Xing-Jie, Wu Si

机构信息

Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.

CAS Center for Excellence in Nanoscience and CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology, Chinese Academy of Sciences, Beijing, 100190, China.

出版信息

Small. 2022 Jul;18(27):e2201672. doi: 10.1002/smll.202201672. Epub 2022 Jun 3.

Abstract

It is challenging to treat multidrug-resistant tumors because such tumors are resistant to a broad spectrum of structurally and functionally unrelated drugs. Herein, treatment of multidrug-resistant tumors using red-light-responsive metallopolymer nanocarriers that are conjugated with the anticancer drug chlorambucil (CHL) and encapsulated with the anticancer drug doxorubicin (DOX) is reported. An amphiphilic metallopolymer PolyRuCHL that contains a poly(ethylene glycol) (PEG) block and a red-light-responsive ruthenium (Ru)-containing block is synthesized. Chlorambucil is covalently conjugated to the Ru moieties of PolyRuCHL. Encapsulation of DOX into PolyRuCHL in an aqueous solution results in DOX@PolyRuCHL micelles. The DOX@PolyRuCHL micelles are efficiently taken up by the multidrug-resistant breast cancer cell line MCF-7R and which carries DOX into the cells. Free DOX, without the nanocarriers, is not taken up by MCF-7R or pumped out of MCF-7R via P-glycoproteins. Red light irradiation of DOX@PolyRuCHL micelles triggers the release of chlorambucil-conjugated Ru moieties and DOX. Both act synergistically to inhibit the growth of multidrug-resistant cancer cells. Furthermore, the inhibition of the growth of multidrug-resistant tumors in a mouse model using DOX@PolyRuCHL micelles is demonstrated. The design of red-light-responsive metallopolymer nanocarriers with both conjugated and encapsulated drugs opens up an avenue for photoactivated chemotherapy against multidrug-resistant tumors.

摘要

治疗耐多药肿瘤具有挑战性,因为此类肿瘤对多种结构和功能上无关的药物具有抗性。本文报道了使用与抗癌药物苯丁酸氮芥(CHL)共轭并包裹抗癌药物阿霉素(DOX)的红光响应金属聚合物纳米载体治疗耐多药肿瘤。合成了一种两亲性金属聚合物聚钌 - 苯丁酸氮芥(PolyRuCHL),其包含聚乙二醇(PEG)嵌段和红光响应性含钌(Ru)嵌段。苯丁酸氮芥共价连接到PolyRuCHL的Ru部分。在水溶液中将阿霉素包裹到PolyRuCHL中形成阿霉素@聚钌 - 苯丁酸氮芥(DOX@PolyRuCHL)胶束。DOX@PolyRuCHL胶束被耐多药乳腺癌细胞系MCF - 7R有效摄取,并将阿霉素带入细胞。没有纳米载体的游离阿霉素不会被MCF - 7R摄取,也不会通过P - 糖蛋白从MCF - 7R中泵出。对DOX@PolyRuCHL胶束进行红光照射会触发共轭的苯丁酸氮芥 - Ru部分和阿霉素的释放。两者协同作用抑制耐多药癌细胞的生长。此外,还证明了使用DOX@PolyRuCHL胶束在小鼠模型中抑制耐多药肿瘤的生长。具有共轭和包裹药物的红光响应金属聚合物纳米载体的设计为针对耐多药肿瘤的光活化化疗开辟了一条途径。

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