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Low-Level Quantitation of Formaldehyde in Drug Substance by HPLC-UV

机译:HPLC-UV低含量定量测定药物中甲醛的含量

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摘要

Formaldehyde has been highlighted as potential genotoxic impurity (GTI). Trace-level quantification of GTIs in drug substances requires sensitive, precise and accurate analytical methodologies for their estimation in drug substances and control. Analysis and estimation of formaldehyde is very challenging due to its properties namely volatility, high polarity, low molecular weight and over and above the absence of chromophore. This article presents a validated HPLC-UV method which is sensitive to quantification of formaldehyde in active pharmaceutical ingredient. As formaldehyde does not possess chromophore, the developed HPLC method involves derivatization with 2,4-dinitrophenylhydrazine. Using this method, the detection and quantitation limits achieved are 0.5 and 1.5 ppm, respectively. The calibration curve of formaldehyde was linear over the concentration range of 1.5-20 ppm. The method was found to be sensitive, precise and accurate and the proposed method has been successfully applied to estimate formaldehyde content in scale-up batches of bulk drug.
机译:甲醛已被强调为潜在的遗传毒性杂质(GTI)。痕量级的定量GTIs在原料药中的估计需要灵敏,准确和准确的分析方法,以便对其进行原料药和对照品的估算。由于甲醛具有挥发性,高极性,低分子量以及不存在生色团的特性,因此对甲醛的分析和估计非常具有挑战性。本文介绍了一种经过验证的HPLC-UV方法,该方法对活性药物成分中的甲醛定量敏感。由于甲醛不具有发色团,因此开发的HPLC方法涉及用2,4-二硝基苯肼衍生化。使用这种方法,检测限和定量限分别为0.5和1.5 ppm。甲醛的校准曲线在1.5-20 ppm的浓度范围内是线性的。结果表明该方法灵敏,准确,准确,已成功地应用于估计批量药品中甲醛含量。

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