首页> 外文期刊>Combinatorial chemistry & high throughput screening >Simultaneous Electrochemical Evaluation of Ascorbic Acid, Epinephrine and Uric Acid at Disposable Pencil Graphite Electrode: Highly Sensitive Determination in Pharmaceuticals and Biological Liquids by Differential Pulse Voltammetry
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Simultaneous Electrochemical Evaluation of Ascorbic Acid, Epinephrine and Uric Acid at Disposable Pencil Graphite Electrode: Highly Sensitive Determination in Pharmaceuticals and Biological Liquids by Differential Pulse Voltammetry

机译:一次性铅笔石墨电极同时电化学评价抗坏血酸,肾上腺素和尿酸:差分脉冲伏安法的药物和生物液体高度敏感测定

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Aim and Objective: As is known, AA, EP and UA can also coexist in biological fluids.Therefore, the determination of the levels of these compounds in biological fluids is extremelyimportant both for the diagnosis and treatment of the related diseases. In the presence of manyinterfering substances in biological fluids such as blood and urine samples, it is very important thatthese compounds can be selectively analyzed.Materials and Methods: All electrochemical experiments were performed using an AutolabPGSTAT 128N potentiostat. Before beginning the electrochemical measurements, the PGE wasactivated. The electrochemical pretreatment of PG was exercised by anodically +1.40 V for 60 s.Then, measurements were performed with CV (-0.4 V to 1.2 V) and DPV (-0.2 V to 0.7 V) for singleand simultaneous voltammetric behaviour of AA, EP, and UA in the electrochemical method.Results: The anodic peak potentials of AA and UA were observed at about +0.32 V and +0.62 V,respectively. On the other hand, for EP, while anodic peak potential was observed at about +0.53 V,in the reverse scan, cathodic peak potentials were observed at about +0.41 V and +0.007 V. Thereduction peak observed at +0.3 V with the oxidation peak observed at +0.53 V are the reversiblepeaks. In the method developed for the electrochemical simultaneous determination of AA, EP andUA using PGE with DPV technique in BR buffer solution (pH 4.0), the anodic peak potentials aresufficiently separated from each other.Conclusion: A voltammetric method was developed for the simultaneous determination of AA, EPand UA with PGE for the first time. Here, the most important thing is that the simultaneousdetermination of AA, EP and UA was successfully achieved with that targeted voltammetric methodwhich was sensitive, low-cost, practical and well-repeated; and that these were proven to beselectively applicable in pharmaceutical products and biological liquids.
机译:目的和目标:众所周知,AA,EP和UA也可以在生物流体中共存。因此,在生物流体中的这些化合物的水平对于相关疾病的诊断和治疗而言,这些化合物的水平非常重要。在存在的生物液中的许多液体和尿液中的物质存在下,可以选择性地分析这些化合物是非常重要的。材料和方法:所有电化学实验都是使用Autolabpgstat 128N potentiostoStat进行的。在开始电化学测量之前,PGE呈现。 PG的电化学预处理通过阳极+1.40V来锻炼60秒。然后,用CV(-0.4V至1.2V)和DPV(-0.2V至0.7V)进行测量,用于AA,EP的单次同时伏安行为和uA在电化学方法中。结果:分别观察到AA和UA的阳极峰值电位分别在约+ 0.32V和+ 0.62 V.另一方面,对于EP,在约+0.53V观察到阳极峰值电位,在反向扫描中,在约+0.41V和+ 0.007 V和+ 0.007V的+0.007 V.Theration峰随氧化时观察到阴极峰电位。在+0.53 V观察到的峰是可逆的斑块。在为使用PGE在BR缓冲溶液(pH4.0)中使用PGE的电化学同时测定AA的电化学同时测定的方法中,阳极峰电位彼此不充分地分离。结论:开发了伏安法用于同时测定AA,第一次PGE的EPAND UA。在这里,最重要的是,通过敏感,低成本,实用且重复的靶向伏安法成功地实现了AA,EP和UA的同时确定的AA,EP和UA;并且这些这些被证明可以在药品产品和生物液体中不可思议。

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