Ursolic acid liposomes with chitosan modification: Promising antitumor drug delivery and efficacy

被引:89
|
作者
Wang, Meili [1 ]
Zhao, Tingting [1 ]
Liu, Yanping [1 ]
Wang, Qianqian [1 ]
Xing, Shanshan [1 ]
Li, Lei [1 ]
Wang, Longgang [1 ]
Liu, Lanxiang [2 ]
Gao, Dawei [1 ]
机构
[1] Yanshan Univ, Applying Chem Key Lab Hebei Prov, 438 Hebei St, Qinhuangdao 066004, Peoples R China
[2] First Hosp Qinhuangdao, 258 Cultural Rd, Qinhuangdao 066000, Peoples R China
关键词
Chitosan; Ursolic acid; Liposomes; pH-responsive release; Antitumor; IN-VITRO RELEASE; COATED LIPOSOMES; CANCER-THERAPY; GOLD NANORODS; DOXORUBICIN; CELLS; NANOPARTICLES; STABILITY; CHEMOTHERAPY; TEMPERATURE;
D O I
10.1016/j.msec.2016.11.014
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
There are tremendous challenges on antitumor and its therapeutic drugs, and preparation of highly efficient nano-vehicles represents one of the novel topics in antitumor pharmaceutical field. Herein, the novel chitosan-coated ursolic acid (UA) liposome (CS-UA-L) was efficiently prepared with highly tumor targeting, drug controlled release and low side-effect. The CS-UA-L was uniformly spherical particles with diameter of similar to 130 nm, and the size was more easily trapped into the tumor tissues. Chitosan modification can make liposomes carrying positive charges, which were inclined to combine with the negative charges on,the surface of tumor cells, and then the CS-UA-L could release UA rapidly at pH 5.0 comparing with pH 7.4. Meanwhile, the CS-UA-L exhibited obvious anti-proliferative effect (76.46%) on HeLa cells and significantly antitumor activity (61.26%) in mice bearing U14 cervical cancer. The tumor tissues of CS-UA-L treated mice had enhanced cell apoptosis, extensive necrosis and low cell proliferation activity. These results demonstrated that the multifunctional CS-UA-L allowed a precision treatment for localized tumor, and reducing the total drug dose and side-effect, which hold a great promise in new safe and effective tumor therapy. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1231 / 1240
页数:10
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