Glutathione responsive cubic gel particles cyclodextrin metal-organic frameworks for intracellular drug delivery

被引:50
|
作者
Xue, Qian [1 ]
Ye, Chao [1 ]
Zhang, Mengmeng [1 ]
Hu, Xiongwei [1 ]
Cai, Ting [1 ,2 ]
机构
[1] China Pharmaceut Univ, Sch Pharm, Dept Pharmaceut, Nanjing 210009, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Jiangsu Key Lab Drug Screening, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Cyclodextrin based metal-organic; framework; Cubic gel particle; Cross linking; Glutathione sensitive; Intracellular drug release; NANOPARTICLES; PRINCIPLES;
D O I
10.1016/j.jcis.2019.04.096
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
Novel cubic gel particles (ssCGP) with Glutathione (GSH) triggered drug release features were prepared by crosslinking the cyclodextrin based metal-organic frameworks (CD-MOFs) templets with a newly synthesized biodegradable disulfide bond-bearing linker and removing of the potassium ion in sequence. The morphology and size of ssCGP were investigated by field emission scanning electron microscope (FESEM) and dynamic light scattering. Energy dispersive x-ray spectroscopy (EDX), fourier transform infrared spectroscopy (FT-IR), powder x-ray diffraction (PXRD) and Brunauer-Emmett-Teller (BET) were employed to characterize the structure of ssCGP. ssCGP have regular hexahedron shape with edge length about 200-400 nm. Excellent ability of drug adsorption was achieved by using doxorubicin (DOX) as a model drug. The GSH triggered drug release of ssCGP was observed both in GSH contained solutions and intracellular environments. ssCGP have been demonstrated as a biocompatible porous nanocarrier, particular for intracellular drug delivery. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:39 / 46
页数:8
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