Controlled release of drug from folate-decorated and graphene mediated drug delivery system: Synthesis, loading efficiency, and drug release response

被引:346
作者
Depan, D. [1 ]
Shah, J. [2 ]
Misra, R. D. K. [1 ]
机构
[1] Univ Louisiana Lafayette, Biomat & Biomed Engn Res Lab, Ctr Struct & Funct Mat, Lafayette, LA 70504 USA
[2] Global Nanotech, Bombay 400062, Maharashtra, India
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2011年 / 31卷 / 07期
关键词
Chitosan; Graphene oxide; Folic acid; Doxorubicin; Controlled drug release; WALLED CARBON NANOTUBES; TARGETED DELIVERY; CHITOSAN; NANOPARTICLES; OXIDE; CARRIER; NANOSPHERES; DOXORUBICIN; POLYMER; ACIDS;
D O I
10.1016/j.msec.2011.04.010
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
A novel folate-decorated and graphene mediated drug delivery system was prepared that involves uniquely combining graphene oxide (GO) with anticancer drug for controlled drug release. The nanocarrier system was synthesized by attaching doxorubicin (DOX) to graphene oxide via strong pi-pi stacking interaction, followed by encapsulation of graphene oxide with folic acid conjugated chitosan. The pi-pi stacking interaction, simplified as a non-covalent type of functionalization, enables high drug loading and subsequent controlled release of the drug. The encapsulated graphene oxide enhanced the stability of the nanocarrier system in aqueous medium because of the hydrophilicity and cationic nature of chitosan. The loading and release of DOX indicated strong pH dependence and imply hydrogen-bonding interaction between graphene oxide and DOX. The proposed strategy is advantageous in terms of targeted drug delivery and has high potential to address the current challenges in drug delivery. Thus, the prepared nanohybrid system offers a novel formulation that combines the unique properties of a biodegradable material, chitosan, and graphene oxide for biomedical applications. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1305 / 1312
页数:8
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