Conjugation of methotrexate onto dedoped Fe3O4/PPy nanospheres to produce magnetic targeting drug with controlled drug release and targeting specificity for HeLa cells

被引:16
|
作者
Jiang, Haihui [1 ]
Zhao, Lichun [1 ]
Gai, Ligang [1 ]
Wang, Yang [1 ]
Hou, Yunhua [3 ]
Liu, Hong [2 ]
机构
[1] Qilu Univ Technol, Sch Chem & Pharmaceut Engn, Jinan 250353, Peoples R China
[2] Shandong Univ, Key Lab Crystal Mat, Jinan 250100, Peoples R China
[3] Qilu Univ Technol, Sch Food & Bioengn, Shandong Prov Key Lab Microbial Engn, Jinan 250353, Peoples R China
基金
中国国家自然科学基金;
关键词
Dedoped Fe3O4/PPy nanospheres; Methotrexate; Fluorescent Fe3O4/PPy/MTX; Hela cells; NANOPARTICLES; POLYPYRROLE; NANOCOMPOSITE; PARTICLES; FUNCTIONALIZATION; POLYMER; DESIGN;
D O I
10.1016/j.synthmet.2015.06.006
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Magnetic composite nanospheres carrying amino groups have attracted much interest due to their potential applications in the fields of catalysis, sensor, water purification, enzyme immobilization, DNA extraction, and drug delivery. In this paper, dedoped Fe3O4/polypyrrole (PPy) nanospheres with core-shell structure, high magnetization, superparamagnetism, and size meeting the demand of biorelated applications in vivo have been achieved by an in situ polymerization approach. The amount of the surface amino groups of Fe3O4/PPy is greatly enhanced by dedoping treatment due to liberation of the amino groups ever sheltered by the dopants, a situation that is responsible for facile conjugation of fluorescein and methotrexate (MIX) onto the magnetic composite through the EDC/NHS coupling chemistry to produce the desirable fluorescent Fe3O4/PPy/MTX targeting drug with a high MTX loading of ca. 109 mu g mg(-1). The as-obtained magnetic targeting drug exhibits controlled drug release, enhanced intracellular drug retention, and specific targeting ability to HeLa cells, presenting a promising candidate for treatment of cancer cells overexpressing folate receptors. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:18 / 25
页数:8
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