Academy of Scientific and Innovative Research (AcSIR), CSIR - Central Electrochemical Research Institute (CECRI) Campus, Karaikudi-630 003, India; Electrodics and Electrocatalysis Division, CSIR - Central Electrochemical Research Institute, Karaikudi-630 003, Tamilnadu, India.
Academy of Scientific and Innovative Research (AcSIR), CSIR - Central Electrochemical Research Institute (CECRI) Campus, Karaikudi-630 003, India; Electrodics and Electrocatalysis Division, CSIR - Central Electrochemical Research Institute, Karaikudi-630 003, Tamilnadu, India.
Colloids Surf B Biointerfaces. 2018 Oct 1;170:109-114. doi: 10.1016/j.colsurfb.2018.05.066. Epub 2018 May 30.
In this work, we report a methodology for the quantification of Homocysteine (HcySH) at neutral pH (pH-7.0) using Au nanoparticles incorporated reduced graphene oxide (AuNP/rGO/GCE) modified glassy carbon electrode. The modified electrode was characterized using SEM and XRD techniques. The electrode exhibited a typical behavior against the standard redox probe [Fe(CN)] and resulted in 0.06 V peak to peak potential value. The modified electrode exhibited electrocatalytic activity towards electrochemical biosensing of HcySH, which is established using voltammetric studies. HcySH oxidation peak potential is observed at 0.12 V on AuNP/rGO/GCE which is 0.7 V cathodic than bare glassy carbon electrode (0.82 V). The large peak potential shift observed is reasoned as the interaction of SH group of HcySH with the gold nanoparticles and the electrocatalytic property of reduced graphene oxide that enhances the electrochemical detection at reduced overpotential. Further, successive addition of HcySH showed a linear increment in the sensitivity within the concentration range of 2-14 mM. From an amperometric protocol, the limit of detection is found as 6.9 μM with a sensitivity of 14.8 nA/μM. From a set of cyclic voltammetric measurements, it is observed that the electrode produces a linear signal on the concentration of HcySH in the presence of hydrogen peroxide. Thus it can be concluded that the matrix can detect HcySH even in the presence of hydrogen peroxide.
在这项工作中,我们报告了一种在中性 pH(pH-7.0)下定量测定同型半胱氨酸(HcySH)的方法,该方法使用了金纳米粒子掺入还原氧化石墨烯(AuNP/rGO/GCE)修饰的玻碳电极。修饰后的电极采用 SEM 和 XRD 技术进行了表征。该电极对标准氧化还原探针 [Fe(CN)]63-表现出典型的行为,导致峰到峰电位值为 0.06V。修饰后的电极对 HcySH 的电化学生物传感表现出电催化活性,这是通过伏安研究建立的。在 AuNP/rGO/GCE 上观察到 HcySH 氧化峰电位为 0.12V,比裸玻碳电极(0.82V)的阴极化电位低 0.7V。观察到的大峰电位偏移归因于 HcySH 的 SH 基团与金纳米粒子的相互作用,以及还原氧化石墨烯的电催化性质,这增强了在低过电势下的电化学检测。此外,连续加入 HcySH 显示出在 2-14mM 浓度范围内灵敏度的线性增加。从安培协议中,检测限被发现为 6.9μM,灵敏度为 14.8nA/μM。从一组循环伏安测量中可以看出,在存在过氧化氢的情况下,电极在 HcySH 的浓度上产生线性信号。因此可以得出结论,即使存在过氧化氢,该基质也可以检测 HcySH。