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用于保护一氧化氮诱导的细胞毒性的基于石墨烯/环糊精纳米平台的光触发碳释放

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

作者信息

Hu Zhen, Zhang Dayu, Yu Long, Huang Yudong

机构信息

School of Chemistry and Chemical Engineering, MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, Harbin Institute of Technology, Harbin 150001, China.

出版信息

J Mater Chem B. 2018 Jan 21;6(3):518-526. doi: 10.1039/c7tb02624b. Epub 2018 Jan 8.

DOI:10.1039/c7tb02624b
PMID:32254531
Abstract

An ultraviolet (UV) light-triggered nanocarbon hybrid is developed for controlled C release with excellent nitric oxide (NO) quenching ability. This nanocarrier, consisting of reduced graphene oxide (rGO) and β-cyclodextrin (β-CD), is capable of hosting azobenzene functionalized C (Azo-C) synthesized by diazo chemistry. The hybridization of rGO, β-CD and Azo-C enhances cellular uptake and limits the aggregation of C, 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 molecules exhibit photo-controlled release from rGO/β-CD in living cells. In vitro studies show that rGO/β-CD/C 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 μg mL). This represents an excellent NO quenching efficiency, better than other reports of the graphene/C 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.

摘要

开发了一种紫外线(UV)触发的纳米碳杂化物,用于可控的碳释放,并具有出色的一氧化氮(NO)淬灭能力。这种纳米载体由还原氧化石墨烯(rGO)和β-环糊精(β-CD)组成,能够容纳通过重氮化学合成的偶氮苯功能化碳(Azo-C)。rGO、β-CD和Azo-C的杂化增强了细胞摄取并限制了碳的聚集,并对NO诱导的细胞毒性显示出增强的保护作用。更有趣的是,偶氮基团在紫外线照射下可以在反式和顺式异构体之间可逆切换,从而使Azo-C分子在活细胞中表现出从rGO/β-CD的光控释放。体外研究表明,经紫外线照射处理的rGO/β-CD/C具有更高的NO清除效率,在低负载水平(50μg mL)下,这进一步将细胞活力从32.6%显著提高到88.4%。这代表了出色的NO淬灭效率,优于石墨烯/C纳米杂化物的其他报道,并表明这种材料可以成为对抗氧化损伤的有效纳米平台。由于主客体化学和重氮化学具有通用性和广泛适用性,值得注意的是,本策略也可应用于制备其他光响应纳米杂化物,这在生命科学和材料科学中应具有重要价值。

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