共 50 条
Redox-sensitive micelles based on retinoic acid modified chitosan conjugate for intracellular drug delivery and smart drug release in cancer therapy
被引:38
|作者:
Luo, Tingting
[1
]
Han, Jingtian
[1
]
Zhao, Feng
[1
]
Pan, Xiaohong
[1
]
Tian, Baocheng
[1
]
Ding, Xiujuan
[1
]
Zhang, Jing
[1
]
机构:
[1] Binzhou Med Univ, Sch Pharm, 346 Guanhai Rd, Yantai 264003, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Paclitaxel;
Redox-sensitive;
Retinoic acid;
Polymeric micelles;
Chitosan;
LOW-DENSITY-LIPOPROTEIN;
CO-DELIVERY;
MIXED MICELLES;
POLYMERIC NANOPARTICLES;
TARGETED DELIVERY;
TUMOR-CELLS;
IN-VITRO;
PACLITAXEL;
REDUCTION;
PH;
D O I:
10.1016/j.carbpol.2019.03.064
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Novel chitosan-cystamine-retinoic acid conjugate (CS-SS-RA) was synthesized and could self-assemble into redox-sensitive micelles in aqueous environment with low critical micelle concentration value. CS-SS-RA micelles were characterized with spherical shape, desirable particle size, negative zeta potential, high paclitaxel (PTX) loading and encapsulation efficiency and redox-sensitivity. Hemolysis and cytotoxicity studies proved the safety of CS-SS-RA micelles for intravenous administration. Cytotoxicity study against HepG2 cells and the growth inhibition study on three-dimensional multicellular tumor spheroids (MCTSs) revealed that PTX-loaded CS-SS-RA micelles exhibited higher antitumor activity than free PTX. The in vitro cellular uptake profiles of FITC-labeled CS-SS-RA micelles evaluated via confocal laser scanning microscopy and flow cytometry indicated that CS-SS-RA micelles could enhance cellular uptake efficiency of PTX, and their internalization by HepG2 cells were mediated by clathrin-mediated endocytosis and macropinocytosis. These results demonstrated that CS-SS-RA micelles could be developed as a promising platform for intracellular delivery of hydrophobic antitumor agents.
引用
收藏
页码:8 / 19
页数:12
相关论文