DOX delivery based on chitosan-capped graphene oxide-mesoporous silica nanohybride as pH-responsive nanocarriers

被引:23
作者
Khoee, Sepideh [1 ,2 ]
Bafkary, Reza [1 ,2 ]
Fayyazi, Faeze [1 ,2 ]
机构
[1] Univ Tehran, Sch Sci, Dept Chem, Polymer Lab, Tehran, Iran
[2] Univ Tehran, Sch Sci, Dept Chem, Polymer Lab, Tehran, Iran
关键词
pH-responsive drug delivery system; Chitosan; Doxorubicin; Graphene oxide; Mesoporous silica; Nanohybrid composites; TARGETED DRUG-DELIVERY; CARBON NANODOTS; NANOPARTICLES; RELEASE; SYSTEM; GRAPHITE; BEHAVIOR; THERAPY;
D O I
10.1007/s10971-016-4213-y
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
pH-responsive chitosan-coated graphene oxide-mesoporous silica nanoparticles (GMSN-Cs) was synthesized as a core-shell nanosheets to be used as DOX delivery system. First of all, an inorganic nanohybrid (GMSN) was prepared and subsequently, chitosan was attached to the mesoporous silica part through firm covalent bonds to form a reliable vector for DOX delivery. The chemico-physical properties of the nanosheets were specified, and DOX-loading efficiency and drug releasing was characterized in different pHs. At lower pH, the cumulative release of DOX-loaded GMSN-Cs was more than physiological pH. The in vitro hemolysis and in vivo biochemical analysis results demonstrate negligible toxicity of GMSN-Cs in mice at a high dosage of nanosheets and a disposal time (up to 10 days). DOX can be loaded efficiently on GMSN-Cs, and the resulting DOX-GMSN-Cs represents meaningful cytotoxicity in different pHs and concentrations for MCF-7 cells. The results and observations confirmed that the drug release of DOX-loaded GMSN-Cs can be controlled by physiological stimulant to reduce the side effects.
引用
收藏
页码:493 / 504
页数:12
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