Impact of hydrogenation on physicochemical and biomedical properties of pH-sensitive PMAA-b-HTPB-b-PMAA triblock copolymer drug carriers

被引:2
|
作者
Xu, Feng [1 ]
Xu, Jing-Wen [1 ]
Luo, Yan-Ling [1 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Key Lab Macromol Sci Shaanxi Prov, Xian 710062, Peoples R China
关键词
Amphiphilic block copolymers; hydrogenation; core-shell structure; micellar behavior; PTX release; SELECTIVE HYDROGENATION; CROSS-LINKING; MICELLES; BLOCK; DELIVERY; BEHAVIOR; SYSTEM;
D O I
10.1177/0885328216633891
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
pH-Sensitive poly(methacrylic acid)-block-hydroxyl-terminated polybutadiene-block-poly(methacrylic acid) (PMAA-b-HTPB-b-PMAA) was synthesized and then hydrogenated in this work. The chain structure, phase behavior and thermal properties were characterized by H-1 NMR, FTIR, XRD, DSC, TGA, etc., and the physicochemical and biomedical properties were investigated via fluorescence spectroscopy, TEM, DLS, loading and release of drug and MTT, and so on. The experimental results indicated that the hydrogenation led to the change in the chain aggregate structure of hydrophobic HTPB blocks and the formation of more stable spherical core-shell micelle aggregates, and the critical micelle concentration decreased from 41.8mgL(-1) before hydrogenation to 4.4mgL(-1) after hydrogenation. The hydrogenated block copolymer micelle aggregates exhibited pH-triggered response, and could entrap twice as much hydrophobic drug as the unhydrided counterparts and the encapsulation efficiency was significantly improved, which makes them fine to meet the requirements for drug carriers. Therefore, the hydrogenated PMAA-b-HTPB-b-PMAA copolymer micelles as drug target release carriers can be well used in the field of prevention and treatment of cancers.
引用
收藏
页码:1473 / 1484
页数:12
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