Beitollahi Hadi, Ardakani Mohammad Mazloum, Ganjipour Bahram, Naeimi Hossein
Department of Chemistry, Faculty of Science, Yazd University, Yazd 89195-741, Iran.
Biosens Bioelectron. 2008 Nov 15;24(3):362-8. doi: 10.1016/j.bios.2008.04.009. Epub 2008 Apr 18.
The electro-oxidation of epinephrine (EP), uric acid (UA), folic acid (FA), and their mixture has been studied by modified carbon nanotube paste electrode of 2,2'-[1,2-ethanediylbis(nitriloethylidyne)]-bis-hydroquinone using cyclic voltammetry, chronoamperometry and differential pulse voltammetry. This modified electrode exhibited potent and persistent electron mediating behavior followed by well-separated oxidation peaks towards EP, UA and FA with activation overpotential. For the ternary mixture containing EP, UA and FA the three compounds can be well separated from each other at the scan rate of 20 mV s(-1). The obtained catalytic peak current, was linearly dependent on the EP, UA and FA concentrations in the range of 0.7-1200 microM, 25-750 microM and 15-800 microM and the detection limits for EP, UA and FA were 0.216+/-0.004, 8.8+/-0.2 and 11.0+/-0.3 microM, respectively. The diffusion coefficient (D), and the kinetic parameters such as electron transfer coefficient, (alpha) and heterogeneous rate constant, (k') for EP were also determined using electrochemical approaches. The modified electrode showed good sensitivity, selectivity and stability, and was employed for the determination of EP, UA and FA in the real samples.
采用循环伏安法、计时电流法和差分脉冲伏安法,研究了2,2'-[1,2-乙二基双(次氮基乙叉基)]-双对苯二酚修饰的碳纳米管糊电极对肾上腺素(EP)、尿酸(UA)、叶酸(FA)及其混合物的电氧化作用。该修饰电极表现出强大而持久的电子介导行为,随后对EP、UA和FA呈现出分离良好的氧化峰,并具有活化过电位。对于含有EP、UA和FA的三元混合物,在扫描速率为20 mV s(-1)时,这三种化合物能够很好地彼此分离。所获得的催化峰电流与EP、UA和FA的浓度在0.7 - 1200 microM、25 - 750 microM和15 - 800 microM范围内呈线性关系,EP、UA和FA的检测限分别为0.216±0.004、8.8±0.2和11.0±0.3 microM。还采用电化学方法测定了EP的扩散系数(D)以及电子转移系数(α)和异相速率常数(k')等动力学参数。该修饰电极具有良好的灵敏度、选择性和稳定性,并用于实际样品中EP、UA和FA的测定。