Multilayer nanoparticles with a magnetite core and a polycation inner shell as pH-responsive carriers for drug delivery

被引:62
作者
Guo, Miao [1 ,2 ]
Yan, Yu [1 ,2 ]
Liu, Xiaozhou [1 ,2 ]
Yan, Husheng [1 ,2 ]
Liu, Keliang [3 ]
Zhang, Hongkai [4 ,5 ]
Cao, Youjia [4 ,5 ]
机构
[1] Nankai Univ, Key Lab Funct Polymer Mat, Minist Educ, Tianjin 300071, Peoples R China
[2] Nankai Univ, Inst Polymer Chem, Tianjin 300071, Peoples R China
[3] Beijing Inst Pharmacol & Toxicol, Beijing 100850, Peoples R China
[4] Nankai Univ, Coll Life Sci, Tianjin 300071, Peoples R China
[5] Nankai Univ, Minist Educ, Key Lab Bioact Mat, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
POLYMERIC MICELLES; CANCER-THERAPY; CONTROLLED-RELEASE; BLOCK-COPOLYMERS; EXTRACELLULAR PH; NANOCARRIERS; ACRYLATE; DESIGN;
D O I
10.1039/b9nr00244h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanocarriers with multilayer core-shell architecture were prepared by coating a superparamagnetic Fe3O4 core with a triblock copolymer. The first block of the copolymer formed the biocompatible outermost shell of the nanocarrier. The second block that contains amino groups and hydrophobic moiety formed the inner shell. The third block bound tightly onto the Fe3O4 core. Chlorambucil ( an anticancer agent) and indomethacin (an anti-inflammation agent), each containing a carboxyl group and a hydrophobic moiety, were loaded into the amino-group-containing inner shell by a combination of ionic and hydrophobic interactions. The release rate of the loaded drugs was slow at pH 7.4, mimicking the blood environment, whereas the release rate increased significantly at acidic pH, mimicking the intracellular conditions in the endosome/lysosome. This can be attributed to the disruption of the ionic bond caused by protonation of the carboxylate anion of the drugs and the swelling of the inner shell caused by protonation of the amino groups.
引用
收藏
页码:434 / 441
页数:8
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