Multifunctional Fe3O4@SiO2-CDs magnetic fluorescent nanoparticles as effective carrier of gambogic acid for inhibiting VX2 tumor cells

被引:18
作者
Guan, Yuxia [1 ]
Yang, Yuxiang [1 ,2 ]
Wang, Xinxin [1 ]
Yuan, Hongming [3 ]
Yang, Yuxing [4 ]
Li, Na [1 ]
Ni, Chaoying [2 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China
[2] Univ Delaware, Dept Mat Sci & Engn, Newark, DE 19716 USA
[3] Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
[4] Changzhou Tumor Hosp, Changzhou 213000, Peoples R China
基金
中国国家自然科学基金;
关键词
Magnetic nanoparticles; Fluorescent carbon quantum dots; Magnetic targeting; Tumor therapy; Drug sustained release;
D O I
10.1016/j.molliq.2020.114783
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This paper reports a dual-functional platform that can be used for synergistic therapy, including drug release and magnetic targeting. The platformis realized through an amide reaction between high-fluorescence carbon quantumdots (CD) prepared bymicrowave method and amino-functional Fe3O4@SiO2 with high saturation magnetic strength and a core-shell structure to obtain multifunctional magnetic fluorescent nanocomposite particles Fe3O4@SiO2-CDs. The structure, drug release behavior, cytotoxicity, fluorescence and distribution in vivo of Fe3O4@SiO2-CDs nanoparticleswere studied. The results showthat the Fe3O4@SiO2-CDs with a dynamic diameter of about 155.0 nm and a magnetic saturation intensity of 31.2 emu/g has a higher loading of gambogic acid (GA), and is more conducive to drug release in an environment of pH= 5.7. In addition, Fe3O4@SiO2-CDs has low cytotoxicity and can enter VX2 cells. However, GA-loaded Fe3O4@SiO2-CDs has an inhibitory effect on VX2 cells, and the cell survival rate is less than 20% at a concentration of 100 mu g/mL. Magnetic targeting experiments show that bifunctional magnetic nanoparticles have an outstanding magnetic targeting effect on tumors. (C) 2020 Elsevier B.V. All rights reserved.
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页数:11
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