Self-assembled nanoparticles from hyaluronic acid-paclitaxel prodrugs for direct cytosolic delivery and enhanced antitumor activity

被引:42
|
作者
Xu, Chaoran [1 ]
He, Wei [1 ]
Lv, Yaqi [1 ]
Qin, Chao [1 ]
Shen, Lingjia [2 ]
Yin, Lifang [1 ]
机构
[1] China Pharmaceut Univ, Sch Pharm, Dept Pharmaceut, Nanjing 210009, Jiangsu, Peoples R China
[2] Natl Engn & Res Ctr Target Drugs, Lianyungang 222047, Peoples R China
基金
中国国家自然科学基金;
关键词
Self-assembly; Nanoparticles; Prodrug; Paclitaxel; Cytosolic delivery; Internalization pathway; Antitumor activity; DRUG-DELIVERY; IN-VIVO; POLYMERIC MICELLES; CANCER-CELLS; THERAPY; TAXOL; NANOCARRIERS; NANOCAPSULES; DOXORUBICIN; STRATEGIES;
D O I
10.1016/j.ijpharm.2015.07.069
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A prodrug-based nanosystem obtained by formulating prodrug and nanotechnology into a system is one of the most promising strategies to enhance drug delivery for disease treatment. Herein, we report a new nanosystem based on HA-PTX conjugates (HA-PTX Ns), which penetrated across cell membranes into cytosol, thus enhancing paclitaxel (PTX) delivery. HA-PTX Ns were successfully obtained based on HA-PTX, and their average particle size was approximately 200 nm. Importantly, unlike other prodrug-based nanosystems, HA-PTX Ns obtained cellular entry without entrapment within the lysosomal-endosomal system by using pathways including clathrin-mediated endocytosis, microtubule-associated internalization, macropinocytosis and cholesterol-dependence. Due to significant accumulation in tumors, HA-PTX Ns had more than a 4-fold decrease in tumor volume on day 14 in contrast with PTX alone. In conclusion, HA-PTX Ns could enter cells, bypass the lysosomal-endosomal system and improve PTX delivery. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:172 / 181
页数:10
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