详细信息

Construction of Core-Cross-Linked Polymer Micelles with High Biocompatibility and Stability for pH/Reduction Controllable Drug Delivery  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Construction of Core-Cross-Linked Polymer Micelles with High Biocompatibility and Stability for pH/Reduction Controllable Drug Delivery

作者:Liu, Yehong[1,2];Chen, Miaoxin[1,2];Li, Gaoyang[1,2];Xu, Shouhong[1,2];Liu, Honglai[1,2]

机构:[1]East China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China

年份:2023

卷号:39

期号:36

起止页码:12671

外文期刊名:LANGMUIR

收录:;EI(收录号:20233814758996);WOS:【SCI-EXPANDED(收录号:WOS:001064980100001)】;

基金:This work was supported by the National Natural Science Foundation of China (no. 22078087).

语种:英文

外文关键词:Biocompatibility - Controlled drug delivery - Crosslinking - Micelles - Synthesis (chemical) - Targeted drug delivery

摘要:Polymer micelles have been studied extensively in drug delivery systems (DDS), and their stability is well known to directly affect drug delivery. In this article, a series of amphiphilic copolymers LA-PDPAn-PVPm were synthesized to prepare core-cross-linked nanoparticles (CNP) applied to controllable and targeted anticancer drug delivery. The copolymers could self-assemble in aqueous solution and form homogeneous spherical micelles with particle sizes of between 100 and 150 nm. A comparison between un-cross-linked UCNP and CNP showed that the cross-linking of LA could significantly improve the stability and responsive ability of the nanoparticles. From the in vitro-simulated drug release experiments, CNP was found to have great drug blocking ability under normal physiological conditions and could achieve rapid and efficient drug release under acidic/reducing conditions. In addition, cell experiments showed that CNP had superior biocompatibility and could target tumor cells for drug release. In conclusion, a drug carrier based on copolymer LA-PDPA-PVP realized effective controlled drug release due to the cross-linking of LA. The results will provide guidance for the design strategy of polymer micelles for drug carriers.

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