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首页> 外文期刊>Electrochimica Acta >Electrochemical preparation of over-oxidized polypyrrole/multi-walled carbon nanotube composite on glassy carbon electrode and its application in epinephrine determination
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Electrochemical preparation of over-oxidized polypyrrole/multi-walled carbon nanotube composite on glassy carbon electrode and its application in epinephrine determination

机译:玻碳电极上过氧化的聚吡咯/多壁碳纳米管复合材料的电化学制备及其在肾上腺素的测定中的应用

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A composite film constructed of surfactant doped over-oxidized polypyrrole and multi-walled carbon nanotube was prepared on the surface of glassy carbon electrode by the electro-polymerization method. Surface characterization of the modified electrode was performed by scanning electron microscopy, cyclic voltammetry and electrochemical impedance spectrometry. The investigations have been proved that the over-oxidation of the modifier film resulted in a porous thin layer that improves the interlayer diffusion mechanism for the electroactive species. On the other hand, the negative charge density on the surface of the electrode excludes the negative analytes (e.g. ascorbate and Fe(CN)_6~(3-/4-)) and attracts the positive ones (e.g. dopamine and epinephrine). A remarkable enhancement in the microscopic area of the electrode resulted in a considerable increase of the peak current of epinephrine (EN) oxidation (~35 times). Differential pulse voltammetry has been applied as a very sensitive analytical method for the determination of sub-micromolar amounts of EN. Two linear ranges have been obtained for the EN concentration within the ranges of 0.1-8.0 and 10-100 μM. The voltammetric detection limit of the modified electrode for EN (based on 3σ) was 40nM. On the other hand, this sensor has an excellent selectivity and sensitivity for the EN determination in the presence of clinical interferences (e.g. uric acid, ascorbic acid, and the human serum contents). The recovery for the EN determination in pharmaceutical injections was obtained as 96.4% with a RSD of 4.8%, based on 5 replicate determinations. These excellent properties make the prepared sensor suitable for the analysis of the trace amounts of EN in pharmaceutical and clinical preparations.
机译:采用电聚合法在玻璃碳电极表面制备了由表面活性剂掺杂的过氧化聚吡咯和多壁碳纳米管构成的复合膜。修饰电极的表面表征通过扫描电子显微镜,循环伏安法和电化学阻抗谱法进行。研究已经证明,改性剂膜的过度氧化产生了多孔的薄层,其改善了电活性物质的层间扩散机理。另一方面,电极表面上的负电荷密度排除了负分析物(例如抗坏血酸盐和Fe(CN)_6〜(3- / 4-))并吸引了正分析物(例如多巴胺和肾上腺素)。电极微观区域的显着增强导致肾上腺素(EN)氧化的峰值电流显着增加(约35倍)。差分脉冲伏安法已被用作测定亚微摩尔量EN的非常灵敏的分析方法。 EN浓度已在0.1-8.0和10-100μM范围内获得两个线性范围。修饰电极对EN的伏安检测极限(基于3σ)为40nM。另一方面,在存在临床干扰(例如尿酸,抗坏血酸和人体血清含量)的情况下,此传感器对于EN测定具有极好的选择性和灵敏度。基于5次重复测定,药物注射剂中EN的回收率为96.4%,RSD为4.8%。这些优异的性能使所制备的传感器适用于分析药物和临床制剂中的痕量EN。

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