新型聚二水合比斯(1,10-菲罗啉)氯化铜修饰玻碳电极方波伏安法测定阿司匹林片剂样品

Asnakech Mebrie , Meareg Amare , Adane Kassa , Yonas Beyene Yohannes , Alemu Tesfaye , Atakilt Abebe , Tihitina Asmelash
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引用次数: 3

摘要

在本研究中,报道了动态电位法制备的聚(二萘比斯(1,10-菲罗啉)氯化铜修饰玻碳电极(poly(A2P2CuC)/GCE)用于阿司匹林片剂样品的检测。Fe(CN)6]3-/4-在修饰电极上的EIS和CV分析表明,电活性聚合物材料对电极表面进行了修饰,提高了电极的有效表面积和电荷转移电阻。在poly(A2P2CuC/GCE上,阿司匹林在相反的扫描方向上有一个没有还原峰的氧化峰,随着扫描速率的峰电位位移增强,表明ASA在电极上的电化学氧化是不可逆的。峰值电流与扫描速率平方根关系的R2(0.9983)优于扫描速率的R2(0.9612),表明阿司匹林在poly(A2P2CuC)/GCE上的氧化主要受扩散质量输运控制。在优化的PBS pH(5.5)和方波参数下,poly(A2P2CuC)/GCE氧化峰电流响应与阿司匹林浓度在1 ~ 200 μM范围内呈线性关系,RSD < 3.7% (n = 3),检测限为0.039 μM,定量限为0.13 μM。在50-200%的尿酸、抗坏血酸和葡萄糖作为潜在干扰物的情况下,干扰回收率在97.2-103.4%范围内,验证了所建立的方法测定片剂样品中阿司匹林含量的适用性。用本方法对所研究的片剂样品中阿司匹林的含量进行检测,其含量为其标称值的99.4 ~ 101.5%,RSD < 2.6%,表明该方法可用于控制片剂样品中阿司匹林的含量。本方法比以往报道的片剂样品中阿司匹林的测定方法表现出更好的性能,使其成为一个很好的候选方法。
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Novel poly(diaquabis(1,10-phenanthroline)copper(II)chloride) modified glassy carbon electrode for square wave voltammetric determination of aspirin in tablet samples

In this study, potentiodynamically fabricated poly (diaquabis(1,10-phenanthroline) copper(II)chloride) modified glassy carbon electrode (poly(A2P2CuC)/GCE) is reported for detection of aspirin in tablet samples. EIS and CV analysis of Fe(CN)6]3-/4- at the modified electrode revealed surface modification by an electroactive polymer material that improved electrode effective surface area and charge transfer resistance. An oxidative peak without a reductive peak in the reverse scan direction for aspirin at poly(A2P2CuC/GCE augmented by peak potential shift with scan rate showed the irreversibility of the electrochemical oxidation of ASA at the electrode. A better R2 (0.9983) for dependence of peak current on square root of scan rate than R2 (0.9612) on scan rate indicated that oxidation of aspirin at poly(A2P2CuC)/GCE was predominantly diffusion mass transport controlled. Under optimized PBS pH (5.5), and square wave parameters, oxidative peak current response of poly(A2P2CuC)/GCE showed linear dependence on the concentration of aspirin in the range 1–200 ​μM with associated %RSD under 3.7% (n ​= ​3), limit of detection 0.039 ​μM, and limit of quantification and 0.13 ​μM. Spike recovery result in the range 96.5–100.5% with %RSD under 1.9% (n ​= ​3), and interference recovery in the range 97.2–103.4% in the presence of 50–200% of uric acid, ascorbic acid, and glucose as potential interferents validated the applicability of the developed method for determination of aspirin content in tablet samples. Detection of aspirin in the studied tablet samples in an amount 99.4–101.5% of their nominal values with %RSD under 2.6% using the present method showed the applicability of the method to control the aspirin content in tablet samples. The present method showed better performance over the previously reported methods for determination of aspirin in tablet samples making it an excellent candidate.

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