聚合物囊泡
纳米载体
化学
阿霉素
紫杉醇
药物输送
细胞毒性
生物物理学
细胞凋亡
丙烯酸
共聚物
生物化学
两亲性
化疗
有机化学
聚合物
体外
医学
外科
生物
作者
Zacharoula Iatridi,Athina Angelopoulou,Efstathia Voulgari,Konstantinos Avgoustakis,Constantinos Tsitsilianis
出处
期刊:ACS omega
[American Chemical Society]
日期:2018-09-25
卷期号:3 (9): 11896-11908
被引量:10
标识
DOI:10.1021/acsomega.8b01437
摘要
We report the fabrication of polymersomes, using as building blocks star-graft quarterpolymers, composed of hydrophobic polystyrene and pH-sensitive poly(2-vinylpyridine)-b-poly(acrylic acid) (P2VP-b-PAA) arms, emanated from a common nodule, enriched by thermosensitive poly(N-isopropylacrylamide) grafts covalently bonded on the PAA block-arms. These multicompartmental polymersomes were evaluated as nanocarriers for the encapsulation and controlled co-delivery of doxorubicin (hydrophilic) and paclitaxel (hydrophobic) chemotherapeutic agents. The polymersomes can load these drugs in different compartments and can efficiently be internalized in the human lung adenocarcinoma epithelial cells, delivering their cargo and inducing high cell apoptosis. The release kinetics of both anticancer agents was controlled differently by the environmental conditions (pH and temperature). Enhanced release was observed at the acidic pH 6.0 and under physiological temperature (37 °C). At the same total drug level, co-delivery of these drugs with the polymersomes caused enhanced cytotoxicity and induced significantly higher cell apoptosis in the cancer cell line compared to the polymersomes loaded with either of the two drugs.
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