n -溴代琥珀酰亚胺脱色法间接光度法测定对乙酰氨基酚

Theia’a N. Al-Sabha, Zahraa Jameel Al-Gubouri
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引用次数: 2

摘要

本文描述了一种简单、精确、灵敏的间接分光光度法测定纯品对乙酰氨基酚和水介质中制剂的含量。该方法是在碱性介质中用过量的n -溴代琥珀酰亚胺(NBS)氧化对乙酰氨基酚(Paracetamol),剩余的氧化剂将紫色的Eriochrome black-T (EBT)漂白为无色,在室温下516 nm测得。校正曲线在0.5 ~ 9 μg mL 1范围内呈线性,摩尔吸光度为3.7×10 L.mol.cm。检测限为0.068 μgmL,定量限为0.229 μgmL。准确度(平均回收率%)为98.57,精密度(RSD)≤1.5。没有观察到药物制剂中存在的赋形剂的干扰效应。该方法已成功地应用于对乙酰氨基酚商业制剂(针剂、糖浆和片剂)的测定,并与使用不同试剂的其他分光光度法进行了比较。提出了对乙酰氨基酚与EBT氧化的反应机理。
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Indirect Spectrophotometric Determination of Paracetamol Via Decolorization of Eriochrom Black-T With N-Bromosuccinimide
A simple, precise and sensitive indirect spectrophotometric method is described for the assay of Paracetamol in its pure form and pharmaceutical formulations in the aqueous medium. The method is based on the oxidation of the Paracetamol with an excess of N-Bromosuccinimide (NBS) in alkaline medium and the residual oxidizing agent bleaches the purple-colored Eriochrome black-T (EBT) to colorless species which is measured at 516 nm at room temperature. Calibration graph is linear over 0.5-9 μg mL 1 and molar absorptivity is 3.7×10 L.mol.cm. The detection and quantification limits were 0.068 and 0.229 μgmL respectively. The accuracy (Average recovery %) is 98.57, and Precision (RSD) is ≤ 1.5. No interference effect has been observed from the excipients that exist in drug formulations. The method has been applied successfully in the determination of the Paracetamol in its commercial formulations (injection, syrup, and tablet), and compared favorably with other spectrophotometric methods used different reagents. The reaction mechanism for the oxidation of Paracetamol and EBT was postulated.
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