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用于多西紫杉醇靶向递送至乳腺癌的聚(D,L-丙交酯-co-乙交酯)/透明质酸嵌段共聚物的可生物降解自组装纳米粒子。

Biodegradable self-assembled nanoparticles of poly (D,L-lactide-co-glycolide)/hyaluronic acid block copolymers for target delivery of docetaxel to breast cancer.

机构信息

Department of Pharmaceutical Science, School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai 200433, China.

出版信息

Biomaterials. 2014 Jan;35(1):550-66. doi: 10.1016/j.biomaterials.2013.09.089. Epub 2013 Oct 15.

Abstract

To develop biodegradable docetaxel-loaded self-assembled nanoparticles of poly (D,L-lactide-co-glycolide)/hyaluronic acid block copolymers were successfully synthesized. These copolymers could form nanoparticles with small size (<200 nm), an acceptable CMC (~7.9 mg/L), typical core/shell structure and superior stability in one week. DTX-loaded PLGA(502H)-b-HA(5.6k) nanoparticles (DTX/SANPs) showed a biphasic release pattern within 120 h, and exhibited enhanced cytotoxicity toward CD44-overexpressing MDA-MB-231 cells. Cellular uptake study indicated that PLGA(502H)-b-HA(5.6k) nanoparticles (SANPs) were taken up in MDA-MB-231 cells by CD44-mediated endocytosis. Pharmacokinetics study revealed DTX/SANPs could prolong the circulation of DTX in the blood. In vivo studies demonstrated that SANPs exhibited enhanced tumor targeting and antitumor activity with lower systemic toxicity. In conclusion, DTX/SANPs have great potential for targeted chemotherapy for CD44-overexpressing breast cancer.

摘要

成功合成了可生物降解的载多西紫杉醇自组装纳米粒的聚(D,L-丙交酯-共-乙交酯)/透明质酸嵌段共聚物。这些共聚物可以在一周内形成具有小尺寸(<200nm)、可接受的 CMC(~7.9mg/L)、典型的核/壳结构和优异稳定性的纳米粒。载多西紫杉醇的 PLGA(502H)-b-HA(5.6k)纳米粒(DTX/SANPs)在 120h 内表现出两相释放模式,并对 CD44 过表达的 MDA-MB-231 细胞表现出增强的细胞毒性。细胞摄取研究表明,PLGA(502H)-b-HA(5.6k)纳米粒(SANPs)通过 CD44 介导的内吞作用被 MDA-MB-231 细胞摄取。药代动力学研究表明,DTX/SANPs 可以延长 DTX 在血液中的循环时间。体内研究表明,SANPs 表现出增强的肿瘤靶向和抗肿瘤活性,同时降低了全身毒性。总之,DTX/SANPs 具有针对 CD44 过表达乳腺癌的靶向化疗的巨大潜力。

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