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Simple Fabrication of Glutathione-Responsive PEGylated Micellar Nanocarriers for Dual Drugs Delivery
被引:9
|作者:
Zhao, Shuling
[1
]
Wang, Dongdong
[1
]
Zhang, Kelin
[1
]
Zhang, Haixia
[1
]
机构:
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
基金:
美国国家科学基金会;
关键词:
Drug delivery;
dual drugs;
glutathione;
morphology;
PEGylated nanoparticles;
MACROMOLECULAR THERAPEUTICS;
POLYMER THERAPEUTICS;
CANCER-CHEMOTHERAPY;
RELEASE;
NANOPARTICLES;
THERAPY;
PRODRUG;
LIPOSOMES;
SYSTEMS;
SMANCS;
D O I:
10.1080/00914037.2015.1030649
中图分类号:
TB3 [工程材料学];
R318.08 [生物材料学];
学科分类号:
0805 ;
080501 ;
080502 ;
摘要:
The authors report a feasible simple method to fabricate two kinds of micellar nanocarriers (MPEG-SS-CPT/DOX) with polyethylene glycol (PEG) based on the self-assembly of glutathione (GSH)-responsive amphiphilic PEGylated polymers (MPEG-SS-CPT) in free doxorubicin (DOX) solution, which could carry two anticancer drugs of camptothecin (CPT) and DOX toward cancer cells together. In in vitro release studies, the micelles of MPEG-SS-CPT/DOX could undergo the triggered disassembly to release CPT and DOX under GSH stimulus much faster than without GSH. Furthermore, the MPEG-SS-CPT nanocarriers could release CPT with no change of its original structure after degradation. From the experiments of loading and release of drugs, the cell viability assay, cellular uptake, and flow cytometry studies, it was found that the fibrous micelles modified by PEG with a molecular weight of 350 had greater potential in the field of drug delivery than the other with a molecular weight of 1900. [GRAPHICS] .
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页码:792 / 799
页数:8
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