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采用 LC-MS-MS 法同时测定谷物和食品中的六种主要麦角生物碱及其差向异构体。

Simultaneous determination of six major ergot alkaloids and their epimers in cereals and foodstuffs by LC-MS-MS.

机构信息

Christian Doppler Laboratory for Mycotoxin Research, Department for Agrobiotechnology (IFA Tulln), University of Natural Resources and Applied Life Sciences Vienna, Konrad Lorenz Strasse 20, 3430, Tulln, Austria.

出版信息

Anal Bioanal Chem. 2008 May;391(2):563-76. doi: 10.1007/s00216-008-2036-6. Epub 2008 Apr 16.

Abstract

This paper describes a new and rapid method for accurate quantification of the six ergot alkaloids, ergometrine, ergotamine, ergosine, ergocristine, ergocryptine, and ergocornine, by liquid chromatography-tandem mass spectrometry (LC-MS-MS). The six ergot alkaloids studied have been defined by the European Food Safety Authority (EFSA) as among the most common and physiologically active ones. In addition, the method enables the quantification of the corresponding six epimers (ergo-inines) of these ergot alkaloids. This is of considerable importance in terms of the differences in toxicity of the isomeric forms. The method involves extraction under alkaline conditions using a mixture of acetonitrile and ammonium carbonate buffer followed by a rapid clean-up using dispersive solid-phase extraction with PSA (primary secondary amine) and a short chromatographic LC-run (21 min) with subsequent MS-MS detection. The method was developed and validated using ten different cereal and food samples. The major strength of the new method compared with previously published techniques is the simplicity of the clean-up procedure and the short analysis time. The limits of quantification were 0.17 to 2.78 μg kg(-1) depending on the analyte and matrix. Recovery values for the 12 ergot alkaloids spiked into ten different matrices at levels of 5, 50, and 100 μg kg(-1) were between 69 and 105% for 85 of 90 recovery measurements made over six days. Measurement uncertainty values were highly satisfactory. At a concentration level of 5 μg kg(-1) the expanded measurement uncertainty ranged from ±0.56 to ±1.49 μg kg(-1), at a concentration level of 100 μg kg(-1) the expanded measurement uncertainty ranged from ±8.9 to ±20 μg kg(-1). Both LOQs and measurement uncertainties were dependent on the analyte but almost independent of the matrix. The method performance was satisfactory when tested in a mini-intercomparison study between three laboratories from three different countries.

摘要

本文描述了一种新的快速方法,用于通过液相色谱-串联质谱(LC-MS-MS)准确定量六种麦角生物碱,即麦角胺、麦角新碱、麦角胺、麦角柯宁、麦角隐亭和麦角柯宁。欧洲食品安全局(EFSA)已将这六种麦角生物碱定义为最常见和生理活性最强的生物碱之一。此外,该方法还能够定量测定这些麦角生物碱的相应六种差向异构体(麦角辛)。这在异构形式毒性差异方面具有重要意义。该方法涉及在碱性条件下使用乙腈和碳酸铵缓冲液混合物进行提取,然后使用 PSA(伯仲胺)进行快速分散固相萃取和短色谱 LC 运行(21 分钟),随后进行 MS-MS 检测。该方法是使用十种不同的谷物和食品样品开发和验证的。与以前发表的技术相比,新方法的主要优势在于净化程序的简单性和分析时间的缩短。根据分析物和基质的不同,定量限为 0.17 至 2.78μgkg(-1)。在十种不同基质中添加 5、50 和 100μgkg(-1)水平的 12 种麦角生物碱的回收率值在 69%至 105%之间,在六天内进行了 90 次回收率测量中的 85 次。测量不确定度值非常令人满意。在 5μgkg(-1)浓度水平下,扩展测量不确定度范围为±0.56 至±1.49μgkg(-1),在 100μgkg(-1)浓度水平下,扩展测量不确定度范围为±8.9 至±20μgkg(-1)。LOQ 和测量不确定度都取决于分析物,但几乎与基质无关。在三个不同国家的三个实验室之间进行的小型相互比较研究中,该方法的性能令人满意。

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