Light-triggered C60 release from a graphene/cyclodextrin nanoplatform for the protection of cytotoxicity induced by nitric oxide

被引:44
作者
Hu, Zhen [1 ]
Zhang, Dayu [1 ]
Yu, Long [1 ]
Huang, Yudong [1 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, Harbin 150001, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
POST-POLYMERIZATION MODIFICATION; RAT PHEOCHROMOCYTOMA CELLS; GRAPHENE OXIDE; FUNCTIONALIZATION; HYBRID; CYCLODEXTRIN; FABRICATION; NANOHYBRID; DIARYLCARBENE; OPPORTUNITIES;
D O I
10.1039/c7tb02624b
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
An ultraviolet (UV) light-triggered nanocarbon hybrid is developed for controlled C-60 release with excellent nitric oxide (NO) quenching ability. This nanocarrier, consisting of reduced graphene oxide (rGO) and beta-cyclodextrin (beta-CD), is capable of hosting azobenzene functionalized C-60 (Azo-C-60) synthesized by diazo chemistry. The hybridization of rGO, beta-CD and Azo-C-60 enhances cellular uptake and limits the aggregation of C-60, and shows enhanced protective effects on NO-induced cytotoxicity. More interestingly, azo groups can reversibly switch between trans-and cis-isomers upon UV irradiation, so that the Azo-C-60 molecules exhibit photo-controlled release from rGO/beta-CD in living cells. In vitro studies show that rGO/b-CD/C-60 treated with UV irradiation causes higher NO scavenging efficacy, which further significantly increases the cell viability from 32.6% to 88.4% at low loading levels (50 mg mL(-1)). This represents an excellent NO quenching efficiency, better than other reports of the graphene/C-60 nanohybrids, and indicates that this material can be an effective nanoplatform to combat oxidative damage. As the host-guest chemistry and diazo chemistry are versatile and universally applicable, it is worth noting that the present strategy can also be applied in preparing other photo-responsive nanohybrids, which should be valuable for use in life science and materials science.
引用
收藏
页码:518 / 526
页数:9
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