Zwitterionic pH-responsive hyaluronic acid polymer micelles for delivery of doxorubicin

被引:40
作者
Gao, Qin-Qin [1 ,2 ]
Zhang, Chuan-Min [1 ,2 ]
Zhang, En-Xia [3 ]
Chen, Hui-Ying [2 ]
Zhen, Yu-Hong [3 ]
Zhang, Shu-Biao [2 ]
Zhang, Shu-Fen [1 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Dalian Minzu Univ, Key Lab Biotechnol & Bioresources Utilizat, Minist Educ, Dalian 116600, Peoples R China
[3] Dalian Med Univ, Coll Pharm, Dalian 116044, Peoples R China
基金
中国国家自然科学基金;
关键词
Zwitterionic polymers; Drug delivery; Biocompatibility; pH-responsiveness; ANTICANCER DRUG; COPOLYMER MICELLES; SYSTEMIC TOXICITY; IN-VITRO; NANOPARTICLES; REDOX; ADSORPTION; RELEASE; PROTEIN; CHARGE;
D O I
10.1016/j.colsurfb.2019.03.007
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
As zwitterionic polymers show great promise in drug delivery, hyaluronic acid (HA) was deacetylated and grafted with dodecylamine to prepare a pH-sensitive zwitterionic polymer dHAD used as a carrier for antitumor drugs. The polymer was negatively charged at pH 7.4 and became positive at pH 6.2. In vitro delivery of DOX against MCF-7 cells showed that the blank micelle dHAD had low cytotoxicity and the dHAD-DOX micelles could greatly prohibit the growth of the MCF-7 cells. In addition, the dHAD-DOX micelles had higher cellular uptake, indicating that the micelles were rapidly internalized into the cells via CD44 receptor-mediated endocytosis. The in vivo delivery of DOX to tumor-bearing mice confirmed that the dHAD-DOX micelles greatly inhibited the tumor growth and significantly reduced systemic toxicity of DOX. These results demonstrated that biocompatible pH-responsive zwitterionic dHAD micelles are promising carriers for the delivery of DOX.
引用
收藏
页码:412 / 420
页数:9
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