Facile synthesis of a hyperbranched polymer prodrug as unimolecular micelles for overcoming multidrug resistance

被引:7
|
作者
Li, Jie [1 ]
Liu, Peng [1 ]
机构
[1] Lanzhou Univ, State Key Lab Appl Organ Chem, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
关键词
TARGETED DRUG-DELIVERY; BLOCK-COPOLYMERS; RELEASE; THERAPY;
D O I
10.1039/d1py01670a
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Unimolecular micelles have attracted more interest as drug delivery systems (DDSs) owing to their superior stability. Here, a hyperbranched polymer prodrug (HBPP) was designed with a high drug content of 57.6% as unimolecular micelles for enhanced intracellular drug delivery via self-condensing vinyl polymerization (SCVP) of the pH-responsive doxorubicin-based prodrug monomer MH-DOX and polyethylene glycol methacrylate (PEGMA) with p-chloromethylstyrene (CMS) as an inimer. It could easily form unimolecular micelles with a hydrodynamic diameter of about 130 nm. Enhanced intracellular pH-triggered drug release was achieved owing to the unique structure, with a cumulative release of 91.8% within 58.5 h due to an auto-acceleration effect but with a minimal premature drug leakage of 3.9%. The enhanced intracellular drug delivery performance endowed the proposed unimolecular micelles with good inhibition of tumor growth on DOX-resistant MCF-7 (MCF-7/ADR) cells, showing promising potential for overcoming multidrug resistance.
引用
收藏
页码:1369 / 1375
页数:7
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