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Quantitative determination method for trace amount of penicillin contaminants in commercially available drug product by HPLC coupled with tandem mass spectrometry

机译:高效液相色谱-串联质谱法定量测定市售药品中微量青霉素类污染物

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摘要

A quantitative determination method for trace amount of penicillin contaminants in an active pharmaceutical ingredient (API) has been developed. Selective extraction of penicillin contaminants from the matrix containing API and specific separation among penicillin contaminants were achieved through an on-line column switching technique with gradient elution, followed by tandem mass spectrometric determination. Validation was conducted on the developed method in terms of specificity, linearity, accuracy, precision, and detection limit, and appeared reasonable. The detection limit was estimated as 0.03 ng/ml or lower of the concentration of penicillin contaminants in the preparation, corresponding to 4 parts par billion (ppb) against the API. This fulfilled the regulatory requirement by the authorities.
机译:已经开发了一种定量测定活性药物成分(API)中青霉素污染物的定量方法。通过使用梯度洗脱的在线柱切换技术,然后通过串联质谱测定,从含有API的基质中选择性提取青霉素污染物,并在青霉素污染物之间进行特定分离。在特异性,线性,准确度,精密度和检测限方面对开发的方法进行了验证,结果是合理的。检出限估计为制剂中青霉素污染物浓度的0.03 ng / ml或更低,对应于API的4十亿分之一(ppb)。这满足了主管部门的监管要求。

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