首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Adsorptive anodic stripping differential pulse voltammetric determination of CellCept at Fe3O4 nanoparticles decorated multi-walled carbon nanotubes modified glassy carbon electrode
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Adsorptive anodic stripping differential pulse voltammetric determination of CellCept at Fe3O4 nanoparticles decorated multi-walled carbon nanotubes modified glassy carbon electrode

机译:吸附阳极剥离差分脉冲伏安法测定Fe3O4纳米粒子的Celcept装饰多壁碳纳米管改性玻碳电极

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摘要

A simple and sensitive method based on adsorptive anodic stripping differential pulse voltammetry (AASDPV) for the determination of cellcept, using a magnetic Fe3O4 nanoparticles and functionalized (carboxylated) multi-walled carbon nanotubes modified glassy carbon electrode (f-MWCNs/Fe3O4/GCE) was developed. In phosphate buffer solution (pH = 5), the voltammogram of cellcept exhibited tow anodic peaks and the well-defined peak at about 0.611 V vs SCE was used for its monitoring. The modified electrode was characterized by different methods such as electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM) and cyclic voltammetry (CV). The experimental parameters, such as pH, deposition potential and time, as well as scan rate were optimized. Under the optimized conditions, I-p (mu A) was proportional to the cellcept concentration in the range of 0.05 -200 mu M (R-2 = 0.9989) with a detection limit of 9.0 nM and limit of quantification of 30.2 nM. The recovery was >98%. The practical analytical utilities of the modified electrode were demonstrated by the determination of cellcept in human urine and blood serum samples. Modified electrode showed an adequate sensitivity and stability for evaluated samples. (C) 2016 Elsevier Inc. All rights reserved.
机译:一种简单敏感的基于吸附阳极剥离差分脉冲伏安法(AASDPV)用于测定Celcept,使用磁Fe3O4纳米颗粒和官能化(羧化)多壁碳纳米管改性玻碳电极(F-MWCNS / Fe3O4 / GCE)已开发。在磷酸盐缓冲溶液(pH = 5)中,表现出触发阳极峰值的伏安图,并且在约0.611V Vs SCE下的明确定义的峰被用于其监测。改性电极的特征在于不同的方法,例如电化学阻抗谱(EIS),扫描电子显微镜(SEM)和循环伏安法(CV)。优化实验参数,例如pH,沉积电位和时间以及扫描速率。在优化条件下,I-P(MU A)与0.05-200μm(R-2 = 0.9989)的静脉浓度成比例,检测限为9.0nm和30.2nm的量化限制。回收率为98%。通过测定人类尿液和血清样品的纤维型,证明了改性电极的实际分析实用性。改性电极显示出评估样品的充分敏感性和稳定性。 (c)2016年Elsevier Inc.保留所有权利。

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