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Rapid Evaluation of Spermidine from 12 Bean Cultivars by Direct Real-Time Mass Spectrometry Analysis

机译:直接实时质谱分析法快速评估12个豆类品种中的亚精胺

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摘要

The routine spermidine (SPD) detection method is time-consuming and laborious due to the lengthy chromatographic separation and/or tedious sample derivatization pretreatment. In this study, direct analysis in real-time ionization mode coupled with mass spectrometry (DART-MS) was developed to rapidly determine the SPD content of 12 bean cultivars. The results were compared in detail with those of the classical UHPLC-ESI-QTOF method. After conducting a series of optimizations, a simple sample extraction procedure employing 80% aqueous methanol, was followed by determination of sample extracts directly without any chromatographic separation or prior derivatization. The validated method showed excellent performance with low limits of detection (LOD of 0.025 mg·kg−1) and good recovery rates (102.79–148.44%). The investigation highlighted that the DART-MS method (~1.3 min per three samples) could be used as a high-throughput alternative to the classic UHPLC-ESI-QTOF method (~15 min per three samples).
机译:由于漫长的色谱分离和/或繁琐的样品衍生化预处理,常规的亚精胺(SPD)检测方法既费时又费力。在这项研究中,开发了在实时电离模式下直接分析结合质谱(DART-MS)来快速确定12个豆类品种中SPD含量的方法。将结果与经典UHPLC-ESI-QTOF方法进行了详细比较。进行一系列优化后,使用80%甲醇水溶液进行简单的样品提取,然后直接测定样品提取物,而无需进行色谱分离或事先衍生化。经验证的方法具有良好的性能,检测限低(LOD为0.025 mg·kg −1 ),回收率良好(102.79–148.44%)。研究强调,DART-MS方法(每三个样品约1.3分钟)可以用作传统UHPLC-ESI-QTOF方法(每三个样品约15分钟)的高通量替代方法。

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