Simultaneous and Quantitative Determination of Pyrrolizidine and Tropane Alkaloids in Food by LC-MS/MS, First Action 2025.02.

IF 1.7
Thomas Bessaire, Claudia Mujahid, Pascal Mottier, Ke Du, Andrew Savage, Xun Fu, Leland Hunter, Charmaine Teo, Wai-Chinn Chan
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Abstract

Background: Pyrrolizidine alkaloids (PAs) are natural toxins produced by > 6,000 flowering plant species. Some PAs are hepatotoxic and genotoxic carcinogens. Reported cases of direct poisoning in humans have already been documented, but the highest risk of human exposure occurs through the consumption of crops contaminated with PA-producing weeds. The European Commission Regulation EU 2023/915 set maximum levels (MLs) for the sum of 35 PAs in tea, herbal teas, herbs, and spice seeds at levels ranging from 75 to 1000 µg/kg (dry matter basis).

Objective: The study describes the performance characteristics of a quantitative liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the determination of the 35 PAs mentioned in AOAC INTERNATIONAL Standard Method Performance Requirements (SMPRs®) 2023.002 in tea, herbal infusions, herbs, seed spices, cereals, and honey. The analyte scope also comprised of nine additional PAs along with two tropane alkaloids (TAs, namely atropine and scopolamine) for which MLs are also set in plant-based products in European Union (EU 2023/915).

Method: The protocol involves an extraction of toxins from food using aqueous sulfuric acid followed by solid-phase extraction purification. After elution and evaporation to dryness, the residue is reconstituted in water-methanol solution prior to LC-MS/MS analysis. Alkaline mobile phases are used to favor the separation of isomers. Identification of the analytes is conducted according to the confirmation criteria defined in EU 2023/2783 and SANTE 11312/2021v2 documents. Quantification is performed by isotopic dilution using four isotopically labelled PAs and two isotopically labelled TAs as internal standards.

Results: Method validation workload was shared by three different laboratories on representative matrices from the following commodities: dried herbs, dried tea, dried herbal infusions, seed spices, cereals, and honey. The 35 target analytes specifically listed in the AOAC SMPR 2023.002 have been successfully validated (recovery 70-120%, repeatability < 20%, intermediate reproducibility < 20%), allowing LOQs down to 1 µg/kg.

Conclusions: The performances of the method are in agreement with criteria defined in AOAC SMPR 2023.002.

Highlights: The Expert Review Panel for Pyrrolizidine Alkaloids approved the present method as AOAC Official First Action 2025.02.

LC-MS/MS同时定量测定食品中吡咯利西啶和Tropane生物碱,第1期,2015.02。
背景:吡咯lizidine alkaloids (PAs)是由近6000种开花植物产生的天然毒素。一些PAs是肝毒性和基因毒性致癌物。人类直接中毒的报告病例已有记录,但人类接触的最高风险发生在食用被产生pa的杂草污染的作物。欧盟委员会法规EU 2023/915规定了茶叶、草药茶、草药和香料种子中35个PAs的最大含量(ml),含量范围为75至1000µg/kg(干物质基础)。目的:建立定量液相色谱-串联质谱(LC-MS/MS)测定AOAC国际标准方法性能要求(SMPRs®)2023.002中茶叶、草药冲剂、草药、种子香料、谷物和蜂蜜中35种PAs的方法。分析物范围还包括9个额外的pa以及两种tropane生物碱(TAs,即阿托品和东莨菪碱),其ml也在欧盟(EU 2023/915)的植物性产品中设置。方法:采用硫酸水溶液提取食品中的毒素,然后进行固相萃取纯化。洗脱和蒸发至干燥后,残留物在水-甲醇溶液中重构,然后进行LC-MS/MS分析。碱性流动相有利于同分异构体的分离。根据EU 2023/2783和SANTE 11312/2021v2文件中定义的确认标准进行分析物的鉴定。定量是通过同位素稀释进行的,使用四个同位素标记的PAs和两个同位素标记的TAs作为内标。结果:方法验证的工作量由三个不同的实验室分担,其代表性基质来自以下商品:干草药、干茶、干草药冲剂、种子香料、谷物和蜂蜜。AOAC SMPR 2023.002中专门列出的35种目标分析物已成功验证(回收率70-120%,重复性< 20%,中间重现性< 20%),loq低至1 μ g/kg。结论:该方法性能符合AOAC SMPR 2023.002标准。重点:吡咯lizidine生物碱专家评审小组批准本方法为AOAC官方第一次行动2025.02。
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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