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首页> 外文期刊>Sensors and Actuators >Electroanalytical Determination Of Sulfadiazine And Sulfamethoxazole In Pharmaceuticals Using A Boron-doped Diamond Electrode
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Electroanalytical Determination Of Sulfadiazine And Sulfamethoxazole In Pharmaceuticals Using A Boron-doped Diamond Electrode

机译:掺硼金刚石电极电分析测定药物中的磺胺嘧啶和磺胺甲恶唑

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Two sulfonamides, namely sulfadiazine and sulfamethoxazole, were independently quantified in pharmaceutical products by square-wave voltammetry (SWV) using a boron-doped diamond (BDD) electrode. The electroanalytical determination of sulfadiazine was carried out in ethanol + 0.5 mol L~(-1) H_2SO_4 50/50 (v/v) and of sulfamethoxazole in ethanol + pH 6.0 phosphate buffer 50/50 (v/v) solutions. Both analytes showed one well-resolved irreversible oxidation peak at around +1.1 V, which served as the analytical response. Calibration curves were obtained in the concentration ranges of 8.01 × 10~(-6) to 1.19 × 10~(-4) mol L~(-1) (r = 0.9995) for sulfadiazine and 6.10 × 10~(-6) to 6.01 × 10~(-5) mol L~(-1) (r = 0.9995) for sulfamethoxazole, with respective detection limits of 2.19 × 10~(-6) and 1.15 × 10~(-6) mol L~(-1). For both sulfonamides, recovery values were in the range of 95-104% for all samples, indicating no matrix interference effects on the analytical results. The accuracy of the electroanalytical methodology reported herein was compared to the standard HPLC method, and the values for the relative error between the proposed and standard methods were -4.31% for sulfadiazine and -0.79% for sulfamethoxazole. The data suggest a potential and interesting alternative method for the electroanalytical determination of sulfa drugs in Pharmaceuticals and other products.
机译:两种磺酰胺,即磺胺嘧啶和磺胺甲恶唑,是通过使用掺硼金刚石(BDD)电极的方波伏安法(SWV)在药物产品中独立定量的。在乙醇+ 0.5 mol L〜(-1)H_2SO_4 50/50(v / v)和磺胺甲恶唑在乙醇+ pH 6.0磷酸盐缓冲液50/50(v / v)溶液中进行电分析测定。两种分析物在+1.1 V左右均显示出一个良好解析的不可逆氧化峰,可作为分析响应。对于磺胺嘧啶,在8.01×10〜(-6)到1.19×10〜(-4)mol L〜(-1)(r = 0.9995)的浓度范围内,以及在6.10×10〜(-6)的浓度范围内,得到的校准曲线。磺胺甲恶唑6.01×10〜(-5)mol L〜(-1)(r = 0.9995),检出限分别为2.19×10〜(-6)和1.15×10〜(-6)mol L〜(- 1)。对于两种磺酰胺,所有样品的回收率均在95-104%的范围内,表明对分析结果无基质干扰影响。将本文报告的电分析方法的准确性与标准HPLC方法进行了比较,拟议的方法与标准方法之间的相对误差值对于磺胺嘧啶为-4.31%,对于磺胺甲恶唑为-0.79%。数据表明,电分析测定药品和其他产品中的磺胺类药物是一种潜在且有趣的替代方法。

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