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建立并验证了一种用于分析苹果和苹果汁中棒曲霉素的液相色谱-串联质谱方法。

Development and validation of a liquid chromatographic tandem mass spectrometric method for the analysis of patulin in apple and apple juice.

机构信息

National Reference Laboratory, ICAR-National Research Centre for Grapes, P.O. Manjri Farm, Pune, 412 307, India.

Institute for Global Food Security, School of Biological Sciences, Queen's University, Belfast, UK.

出版信息

Mycotoxin Res. 2021 May;37(2):119-127. doi: 10.1007/s12550-021-00422-2. Epub 2021 Feb 22.

DOI:10.1007/s12550-021-00422-2
PMID:33619699
Abstract

This study reports a robust and sensitive method for rapid testing of patulin in apple and apple juice. The method involved extraction of homogenised samples (10 g) with ethyl acetate (10 mL) and clean up by dispersive-solid phase extraction using primary secondary amine (25 mg/mL). Prior to the LC-MS/MS analysis, the cleaned extract was reconstituted in methanol/water (2:8). The optimised LC-MS condition provided a symmetric peak of patulin within a short LC-runtime of 5 min. The recoveries at the limit of quantification (0.005 mg/kg) and higher levels were satisfactory (> 80%), with the precision-RSD (< 11%). In an inter-laboratory comparison study involving 13 accredited laboratories, the reproducibility-RSD and HorRat values ranged between 4.80 and 6.08% and between 0.18 and 0.23 respectively, indicating a satisfactory method-precision. The z-scores of the participating laboratories were within ± 2. When the method was applied to incurred samples, the contamination range was 0.008-0.225 mg/kg and 0.018-0.034 mg/kg for apple and juice respectively, demonstrating a satisfactory performance in terms of precision. Based on the solvent standard, matrix-matched standard and standard-addition approaches, the calibration graphs provided similar quantitative performances. Because of its reliability, robustness and time-effectiveness, the method can be recommended for regulatory testing purposes.

摘要

本研究报告了一种快速检测苹果和苹果汁中棒曲霉素的灵敏、稳健方法。该方法包括用乙酸乙酯(10 mL)提取均质样品(10 g),并用正相分散固相萃取(PSA)(25 mg/mL)净化。在进行 LC-MS/MS 分析之前,将净化后的提取物在甲醇/水(2:8)中复溶。优化后的 LC-MS 条件使棒曲霉素在 5 分钟的短 LC 运行时间内达到对称峰。在定量限(0.005 mg/kg)和更高水平的回收率令人满意(>80%),精密度-RSD(<11%)。在涉及 13 个认可实验室的实验室间比较研究中,重现性-RSD 和 HorRat 值分别在 4.80%至 6.08%和 0.18%至 0.23%之间,表明方法具有良好的精密度。参与实验室的 z 值在±2 以内。当该方法应用于实际样品时,苹果和果汁的污染范围分别为 0.008-0.225 mg/kg 和 0.018-0.034 mg/kg,表明该方法具有良好的精密度。基于溶剂标准、基质匹配标准和标准添加方法,校准曲线具有相似的定量性能。由于其可靠性、稳健性和时效性,该方法可推荐用于监管测试目的。

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Food Chem Toxicol. 2019 Jul;129:249-256. doi: 10.1016/j.fct.2019.04.048. Epub 2019 Apr 28.
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