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Square Wave and Square Wave Adsorptive Stripping Voltammetric Comparison of the Anti-Inflammatory Drugs Piroxicam and Tenoxicam

机译:消炎药吡罗昔康和替诺昔康的方波和方波吸附溶出伏安法比较

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摘要

Two nonsteroid anti-inflammatory drugs, Piroxicam and Tenoxicam, are shown to be strongly adsorbed on mercury electrodes. Using this phenomenon to accumulate these compounds at the static mercury-drop electrode prior to square-wave voltammetric measurement, sub-nanomole sensitivities are readily achieved. A preconcentration potential of -0.6 V vs. Ag/AgCl/KCl(s) was used for both drugs. The adsorptive stripping response was evaluated with respect to accumulation time and potential, analyte concentration, and electrolyte nature and concentration. Ascorbic acid up to 1×10-4 M has no effect on the Piroxicam peak, but results in enhanced response for the Tenoxicam adsorptive stripping peak. Studies were performed at pH 4.0 and 2.0 for the two drugs; at these values two and four electrons are transferred, respectively. The detection limit was 7×10-10 M for Piroxicam and 1×10-10 M for Tenoxicam, the latter being even more sensitive (5×10-11 M) in the presence of ascorbic acid. Applicability of square wave voltammetry to urine samples was demonstrated. The detection limit is 5×10-8 M and 5×10-9 M (in presence of 1×10-5 M ascorbic acid) for Piroxicam and Tenoxicam, respectively, in urine samples diluted ten-fold with the supporting electrolyte. © 1990, The Japan Society for Analytical Chemistry. All rights reserved.
机译:两种非甾体类抗炎药,吡罗昔康和替诺昔康,显示出强烈吸附在汞电极上。使用这种现象在方波伏安法测量之前将这些化合物积聚在静态汞滴电极上,可以轻松实现亚纳摩尔灵敏度。两种药物的预浓缩电位相对于Ag / AgCl / KCl均为-0.6V。针对累积时间和电势,分析物浓度以及电解质的性质和浓度评估了吸附剥离反应。高达1×10-4 M的抗坏血酸对吡罗昔康峰没有影响,但导致对Tenoxicam吸附剥离峰的响应增强。对这两种药物在pH 4.0和2.0下进行了研究。在这些值下,两个和四个电子分别转移。吡罗昔康的检出限为7×10-10 M,替诺昔康的检出限为1×10-10 M,后者在抗坏血酸的存在下甚至更敏感(5×10-11 M)。证明了方波伏安法对尿液样品的适用性。在用辅助电解质稀释十倍的尿液样本中,吡罗昔康和替诺昔康的检出限分别为5×10-8 M和5×10-9 M(在1×10-5 M抗坏血酸存在下)。 ©1990,日本分析化学学会。版权所有。

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