Dual stimuli-responsive nanoplatform based on core-shell structured graphene oxide/mesoporous silica@alginate

被引:25
|
作者
Li, Shangji [1 ]
Cao, Cheng [2 ]
Gao, Jun [3 ]
Li, Kelin [1 ]
Kang, Jing [1 ]
Wu, Datong [1 ]
Kong, Yong [1 ]
机构
[1] Changzhou Univ, Jiangsu Key Lab Adv Mat & Technol, Sch Petrochem Engn, Changzhou 213164, Peoples R China
[2] Nanjing Med Univ, Dept Orthoped, Affiliated Suzhou Sci & Technol Town Hosp, Suzhou 215153, Peoples R China
[3] Changzhou Municipal Hosp Tradit Chinese Med, Dept Orthoped, Changzhou 213003, Peoples R China
关键词
Graphene oxide; Mesoporous silica; Alginate; Core-shell structure; Chemo-photothermal therapy;
D O I
10.1016/j.ijbiomac.2021.02.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A dual stimuli-responsive nanoplatform was rationally designed for controlled drug delivery. The nanosheets of graphene oxide (GO) were first modified with aminated mesoporous silica (NH2-mSiO(2)), and then methotrexate (MTX) was loaded into the mesopores of mSiO(2). Alginate (Alg) acted as the "gatekeeper" was then anchored to the MTX-loaded GO/NH2-mSiO(2) by amidation reaction, achieving the encapsulation of MIX in the core-shell structured GO/mSiO(2)@Alg. Due to the high pH sensitivity of amide bond and the excellent photothermal conversion ability of GO, the constructed nanoplatform could be used for pH and near-infrared (NIR) controlled delivery of MTX. The results of cell viability test demonstrate the high inhibitory rate of the dual stimuli-responsive nanoplatform toward hepatoma (HepG2) cells. (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页码:209 / 216
页数:8
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