Delivery of Doxorubicin from Hyaluronic Acid-Modified Glutathione-Responsive Ferrocene Micelles for Combination Cancer Therapy

被引:28
|
作者
Mao, Hong-Lin [1 ,2 ]
Qian, Feng [1 ,2 ]
Li, Shun [1 ,2 ]
Shen, Jia-Wei [1 ,2 ]
Ye, Cheng-Kun [1 ,2 ]
Hua, Lei [1 ,2 ]
Zhang, Long-Zhen [3 ,4 ]
Wu, Dong-Mei [5 ]
Lu, Jun [5 ]
Yu, Ru-Tong [1 ,2 ]
Liu, Hong-Mei [1 ,2 ]
机构
[1] Xuzhou Med Univ, Inst Nervous Syst Dis, Xuzhou 221002, Jiangsu, Peoples R China
[2] Xuzhou Med Univ, Brain Hosp, Affiliated Hosp, Xuzhou 221002, Jiangsu, Peoples R China
[3] Xuzhou Med Univ, Affiliated Hosp, Dept Radiat Oncol, Xuzhou 221002, Jiangsu, Peoples R China
[4] Xuzhou Med Univ, Canc Inst, Xuzhou 221002, Jiangsu, Peoples R China
[5] Jiangsu Normal Univ, Key Lab Biotechnol Med Plants Jiangsu Prov, Sch Life Sci, Xuzhou 221116, Jiangsu, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
combination cancer therapy; GSH-responsive; prodrug micelle; DOX delivery; DRUG-DELIVERY; IN-VITRO; NANOPARTICLE; SYSTEM; RESISTANCE; LIPOSOME; PROSTATE; CELLS; SIRNA; DNA;
D O I
10.1021/acs.molpharmaceut.8b00862
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
A combination of different chemotherapy approaches can obtain the best response for many cancers. However, the greatest challenge is the development of a nanoparticle formulation that can encapsulate different chemotherapeutic agents to achieve the proper synergetic chemotherapy for the tumor. Here, amphiphilic ferrocenium-tetradecyl (Fe-C-14) was constructed to form cationic micelles in an aqueous solution via self-assembly. Then, it was coated by hyaluronic acid (HA) through electrostatic interactions to generate HA Fe-C-14 micelles. The HA Fe-C-14 micelles were used to deliver doxorubicin (DOX), and it showed that the DOX could be released rapidly under a high-GSH tumor environment. The HA Fe-C-14/DOX micelles were able to accumulate efficiently in tumor and showed significant anticancer effect both in vitro and in vivo. These results suggest that HA-Fe-C-14/DOX micelles are a useful drug delivery system that enhances synergic antitumor treatment effects.
引用
收藏
页码:987 / 994
页数:8
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