Enhanced delivery of artesunate by stimuli-responsive polymeric micelles for lung tumor therapy

胶束 纳米载体 共聚物 化学 分散性 材料科学 药物输送 氧化还原 生物物理学 高分子化学 化学工程 纳米技术 有机化学 聚合物 水溶液 生物 工程类
作者
Miaomiao Long,Jiamin Xu,Wenjie Fang,Jing Mao,Jie Zhang,Shenhuan Liu,Lipeng Qiu
出处
期刊:Journal of Drug Delivery Science and Technology [Elsevier]
卷期号:66: 102812-102812 被引量:8
标识
DOI:10.1016/j.jddst.2021.102812
摘要

Artesunate (ART) as a traditional chinese medicine has been reported to have a good antitumor effect on some cancers. However, the poor hydrophilicity and instability in the intestine limit its bioavailability and further application. Herein, this work reported a redox-sensitive micelle system encapsulating ART to enhance the therapeutic effect on lung tumor. Specifically, K5 capsular polysaccharide-SS-d-α-tocopheryl succinate (K5-SS-TOS, KSST) copolymers can self-assemble to form micelles and effectively load ART into the hydrophobic core. Simultaneously, redox-insensitive K5 capsular polysaccharide-d-α-tocopheryl succinate (K5-TOS, KT) copolymers were synthesized as control. ART-loaded micelles (ART/KSST) with a spherical particle size had good polydispersity. The drug loading content and entrapment efficiency of the ART/KSST were (13.5 ± 0.92) % and (81.09 ± 2.61) %, respectively. Moreover, ART/KSST can release ART quickly in the presence of glutathione, showing a good redox release behavior. In addition, the ART loaded micelles had negligible toxicity to normal cells. However, ART/KSST which can be uptaken through energy-dependent pathways by A549 cells showed higher cytotoxicity than ART/KT. The results suggested that disulfide bond can be ruptured in the tumor cells, resulting in disintegration of the micelle structure and fast release of ART to achieve better therapeutic effect. Therefore, the redox-sensitive KSST copolymers as potential nanocarriers can deliver ART effectively to improve the therapeutic effect of lung tumors.
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