PH and redox dual-responsive polymeric micelles with charge conversion for paclitaxel delivery

被引:5
作者
Li, Bo [1 ]
Pang, Shigang [1 ]
Li, Xinxin [1 ]
Li, Yanhai [1 ]
机构
[1] Binzhou Peoples Hosp, Binzhou, Peoples R China
关键词
dual-responsive; charge conversion; proton sponge effect; paclitaxel; TARGETED DRUG-DELIVERY; INTRACELLULAR DELIVERY; POLYGLUTAMIC ACID; PRODRUG MICELLES; CANCER; DOXORUBICIN; NANOPARTICLES; CHEMOTHERAPY; STABILITY; RELEASE;
D O I
10.1080/09205063.2020.1793708
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Here we demonstrate a type of pH and redox dual-responsive micelles, which were self-assembled in aqueous solution by an amphiphilic polymer, methoxypoly(ethylene glycol)-cystamine-poly(L-glutamic acid)-imidazole (mPEG-SS-PGA-IM). Considering tumor cells or tissues exhibiting low pH values and high glutathione (GSH) concentration, mPEG-SS-PGA-IM micelles possessed the charge conversion at pH of tumor tissues, which can facilitate cellular uptake of tumor cells. Furthermore, mPEG-SS-PGA-IM micelles can escape from endo/lysosomes based on the proton sponge effect, following degraded by higher concentration of GSH in cytoplasm. CLSM images of HCT116 cells indicated that mPEG-SS-PGA-IM micelles can escape from endo/lysosomes and enter cytoplasm. MTT assay showed that (paclitaxel) PTX-loaded mPEG-SS-PGA-IM micelles had higher cytotoxicity against HCT116 cells compared with PTX-loaded mPEG-PBLG and mPEG-SS-PBLG micelles. These results indicated that these mPEG-SS-PGA-IM micelles, as novel and effective pH- and redox-responsive nanocarriers, have great potential to both improve drug targeting efficiency while also enhancing the antitumor efficacy of PTX.
引用
收藏
页码:2078 / 2093
页数:16
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