首页> 外文OA文献 >Voltammetric Determination of Acetaminophen in the Presence of Codeine and Ascorbic Acid at Layer-by-Layer MWCNT/Hydroquinone Sulfonic Acid-Overoxidized Polypyrrole Modified Glassy Carbon Electrode
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Voltammetric Determination of Acetaminophen in the Presence of Codeine and Ascorbic Acid at Layer-by-Layer MWCNT/Hydroquinone Sulfonic Acid-Overoxidized Polypyrrole Modified Glassy Carbon Electrode

机译:在逐层MWCNT /氢醌磺酸过氧化聚吡咯改性玻碳电极中,致致胆酸存在乙酰氨基酚的伏安测定乙酰氨基酚

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摘要

A very sensitive electrochemical sensor constructed of a glassy carbon electrode modified with a layer-by-layer MWCNT/doped-overoxidized polypyrrole (oppy/MWCNT /GCE) was used for the determination of acetaminophen (AC) in the presence of codeine and ascorbic acid (AA). In comparison to the bare glassy carbon electrode, a considerable shift in the peak potential together with an increase in the peak current was observed for AC on the surface of oppy/MWCNT/GCE, which can be related to the enlarged microscopic surface area of the electrode. The effect of the experimental conditions on the electrode response, such as types of counter ion, pyrrole and counter ion concentration, potential and number of cycles in the polymerization procedure, amount of MWCNT, and the pH, were investigated. Under the optimized conditions, the calibration curve was obtained over two concentration ranges of 2 × 10−7–6 × 10−6 M and 4 × 10−5–1 × 10−4 M of AC with a linear correlation coefficient (R2) of 0.9959 and 0.9947, respectively. The estimated detection limit (3σ) for AC was obtained as 5 × 10−8 M. The developed method was successfully applied to analyze the pharmaceutical preparations of AC, and a recovery of 95% with a relative standard deviation of 0.98% was obtained for AC.
机译:由用乙基MWCNT /掺杂过氧化的聚吡咯(OPPENT / MWCNT / GCE)改性的玻璃化碳电极构成的非常敏感的电化学传感器用于测定可待因和抗坏血酸存在下的乙酰氨基酚(AC) (AA)。与裸露的玻璃状碳电极相比,在OPPENT / MWCNT / GCE的表面上观察到峰值电位的相当大的升降峰值,该AC在ACP的表面上观察到,这可以与升高的显微镜表面积有关电极。研究了实验条件对电极响应的影响,例如反离子,吡咯和反离子浓度,聚合过程中的潜力和循环次数,MWCNT的量和pH值。在优化条件下,校准曲线在具有线性相关系数(R2)的两个浓度范围内的2×10-7-6×10-6米和4×10-5-1×10-4m中获得分别为0.9959和0.9947。获得AC的估计检测限(3σ)为5×10-8M。成功地应用开发方法以分析Ac的药物制剂,并获得95%的回收率,相对标准偏差为0.98% AC。

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