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Experimental and theoretical studies of electrochemical oxidation of nicotinamide adenine dinucleotide at the modified SWCNT and graphene oxide

机译:在改性的SWCNT和石墨烯氧化物在改性SWCNT和石墨烯二核苷酸电化学氧化的实验与理论研究

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In recent years, nicotinamide adenine dinucleotide (NADH) and its oxidized form (NAD(+)) have withdrawn a substantial attention since they possess a significant place in both biosensor and biofuel cell studies. However, the transformation of NADH to NAD(+) brings about the surface passivation and fouling at the most of corresponding conductive materials; consequently, significant decrease takes place in the current. In order to overcome these drawbacks, we have performed the surface functionalization of single-walled carbon nanotube (SWCNT) and graphene oxide (GO) immobilized onto glassy carbon surface with dihydroxybenzene (di-HB) using solid-phase synthesis methodology. The di-HB-modified SWCNT and GO were found to exhibit great catalytic activity as they reduce required overpotential of electrochemical oxidation of NADH and lead to enhancement in the peak current, compared with unmodified carbon electrodes. Molecular docking simulation technique was also carried out to enlighten attained experimental findings in detail, and we have found that increase in the binding affinity of NAD(+) to functionalized carbon surfaces with di-HB is related to formation of hydrogen bonding interactions Furthermore, our experimental and theoretical outputs were also found to be quite consistent in terms of reactivity of modified surfaces to NADH oxidation.
机译:近年来,烟酰胺腺嘌呤二核苷酸(NADH)及其氧化形式(NAD(+))已经取出了大量关注,因为它们在生物传感器和生物燃料细胞研究中具有重要的位置。然而,NADH对NAD(+)的转化带来了大多数相应导电材料的表面钝化和污垢;因此,在电流中发生显着减少。为了克服这些缺点,我们使用固相合成方法对二羟基苯(DI-HB)固定在玻璃碳表面上的单壁碳纳米管(SWCNT)和石墨烯(GO)的表面官能化。发现DI-HB改性的SWCNT和去具有很大的催化活性,因为它们减少了NADH电化学氧化所需的过电位并与未经修改的碳电极相比,峰值电流的提高。还进行了分子对接模拟技术以详细阐述了对实验结果的启发性,并且我们发现NAD(+)与DI-Hb的官能化碳表面的结合亲和力的增加与氢键相互作用的形成有关,我们在NADH氧化的改性表面的反应性方面,还发现实验和理论输出是非常一致的。

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