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Determination of the Antiretroviral Drug Acyclovir in Diluted Alkaline Electrolyte by Adsorptive Stripping Voltammetry at the Mercury Film Electrode

机译:汞膜电极吸附溶出伏安法测定稀释碱性电解质中抗逆转录病毒药物阿昔洛韦。

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摘要

This paper describes a stripping method for the determination of acyclovir at the submicromolar concentration level. This method is based on controlled adsorptive accumulation of acyclovir at thin-film mercury electrode, followed by a linear cyclic scan voltammetry measurement of the surface species. Optimal experimental conditions include a NaOH solution of 2.0 × 10−3 mol L−1 (supporting electrolyte), an accumulation potential of −0.40 V, and a scan rate of 100 mV s−1. The response of acyclovir is linear over the concentration range 0.02 to 0.12 ppm. For an accumulation time of 4 minutes, the detection limit was found to be 0.42 ppb (1.0 × 10−9 mol L−1). More convenient methods to measure the acyclovir in presence of the didanosine, efavirenz, nevirapine, nelfinavir, lamivudine, and zidovudine were also investigated. The utility of this method is demonstrated by the presence of acyclovir together with Adenosine triphosphate (ATP) or DNA.
机译:本文描述了一种在亚微摩尔浓度水平上测定无环鸟苷的溶出方法。该方法基于无环鸟苷在薄膜汞电极上的受控吸附积累,然后进行表面物种的线性循环扫描伏安法测量。最佳实验条件包括2.0×10 −3 mol L -1 (支持电解质)的NaOH溶液,-0.40 V的累积电势和100的扫描速率mV s -1 。在0.02至0.12 ppm的浓度范围内,阿昔洛韦的响应呈线性关系。对于4分钟的累积时间,发现检出限为0.42 ppb(1.0×10 -9 mol L -1 )。还研究了在去羟肌苷,依非韦伦,奈韦拉平,奈非那韦,拉米夫定和齐多夫定存在下测定阿昔洛韦的更方便方法。阿昔洛韦与三磷酸腺苷(ATP)或DNA的存在证明了该方法的实用性。

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