A comprehensive quantitative LC-MS/MS method for rapid gelatin source identification in food products: Comparison with PCR.

Jeongeun Kwon, Dasom Shin, Geon Woo Park, Gunyoung Lee, Eunju Lee, Hui-Seung Kang
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Abstract

Authentication of gelatin sources are required for cultural beliefs and food integrity. This paper describes a sensitive and rapid detection of gelatin sources using liquid chromatography-tandem mass spectrometry (LC-MS/MS) method. The specific peptide markers were adopted to accurately identify bovine and porcine gelatin in pharmaceutical capsules and jellies. Multiple reaction monitoring (MRM) was employed to identify and quantify over five specific peptide markers, each characterized by its unique precursor and product ion transitions. The developed method was validated at three concentration levels in gelatin-containing products to assess its accuracy and precision. The recovery (accuracy) of the proposed method was between 80 % and 107 %, and relative standard deviation (precision) was in the range of 5.16-9.97 %. Linearity was obtained ≥ 0.99 (R2). To ensure the accuracy of ingredient labeling, the LC-MS/MS results were compared with those obtained from PCR assays. The LC-MS/MS method demonstrated exceptional sensitivity, reliably detecting gelatin adulteration at concentrations as low as 0.01 %. The developed LC-MS/MS method provides a rapid and accurate results for authenticating gelatin sources in various food products within 4 hours.

食品中明胶来源快速鉴定的LC-MS/MS综合定量方法:与PCR的比较。
明胶来源的认证是文化信仰和食品完整性所必需的。本文介绍了液相色谱-串联质谱(LC-MS/MS)快速、灵敏地检测明胶来源的方法。采用特异性肽标记对药用胶囊和凝胶中的牛明胶和猪明胶进行了准确的鉴别。多重反应监测(MRM)被用来鉴定和量化超过五种特定的肽标记,每个标记都有其独特的前体和产物离子转变。在含明胶产品的三种浓度水平下对所建立的方法进行了验证,以评估其准确性和精密度。方法的回收率(准确度)在80% ~ 107%之间,相对标准偏差(精密度)在5.16 ~ 9.97%之间。线性关系≥0.99 (R2)。为了确保成分标记的准确性,将LC-MS/MS结果与PCR分析结果进行比较。LC-MS/MS方法具有很高的灵敏度,可以可靠地检测到低至0.01%浓度的明胶掺假。所建立的LC-MS/MS方法可在4小时内快速准确地鉴定各种食品中的明胶来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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