Cisplatin and doxorubicin high-loaded nanodrug based on biocompatible thioether- and ethane-bridged hollow mesoporous organosilica nanoparticles

被引:31
|
作者
Zhang, Junjie [1 ,2 ]
Weng, Lixing [1 ,2 ,3 ]
Su, Xiaodan [1 ,2 ]
Lu, Guangming [4 ,5 ]
Liu, Wenfei [4 ]
Tang, Yuxia [4 ]
Zhang, Yunlei [4 ]
Wen, Jun [6 ]
Teng, Zhaogang [1 ,2 ,4 ,5 ]
Wang, Lianhui [1 ,2 ]
机构
[1] Nanjing Univ Posts & Telecommun, Key Lab Organ Elect & Informat Displays, Nanjing 210046, Jiangsu, Peoples R China
[2] Nanjing Univ Posts & Telecommun, Inst Adv Mat, Nanjing 210046, Jiangsu, Peoples R China
[3] Nanjing Univ Posts & Telecommun, Coll Geog & Biol Informat, Nanjing 210046, Jiangsu, Peoples R China
[4] Nanjing Univ, Clin Sch, Med Coll, Dept Med Imaging,Jinling Hosp, Nanjing 210002, Jiangsu, Peoples R China
[5] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
[6] Xuzhou Med Univ, Sch Med Imaging, Xuzhou 221004, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Nanodrug; High-loading capacity; Mesoporous; Organosilica; SILICA NANOPARTICLES; TOPOLOGICAL TRANSFORMATION; BIOMEDICAL APPLICATIONS; FACILE SYNTHESIS; DELIVERY; THERAPY; SPHERES; HYBRIDIZATION; FRAMEWORKS; PLATFORMS;
D O I
10.1016/j.jcis.2017.10.116
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
Herein, a mesoporous organosilica nanoparticle (MON) based nanodrug highly loaded with cisplatin (CDDP) and doxorubicin (DOX) (denoted as MONs/CDDP/DOX) has been successfully prepared for the first time. The MONs are characterized with core-contained double hollow shells, thioether and ethane groups separately incorporated frameworks, uniform diameter (420 nm), large surface area (592 m(2)/g), and ordered pore size (2.5 nm). The safety evaluation of the MONs based on cell viability, haemolytic activity, histological change, and serum biochemical index demonstrates that they have excellent biological compatibility. The efficient uptake of the MONs by human breast cancer MCF-7 cells is further confirmed via confocal laser scanning imaging and flow cytometry. Importantly, the contents of CDDP and DOX in the MONs/CDDP/DOX nanodrug are as high as 120 mg/g and 85 mg/g, respectively. Therefore, the MONs/CDDP/DOX shows a significant improved killing effect against human breast cancer MCF-7 cells compared with sole DOX or CDDP loaded MONs, demonstating the promise of the nanodrug for cancer treatment. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:214 / 221
页数:8
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