Suppr超能文献

液相色谱-串联质谱法检测和定量选择的食物过敏原:2017.17 年第一行动。

Detection and Quantitation of Selected Food Allergens by Liquid Chromatography with Tandem Mass Spectrometry: First Action 2017.17.

机构信息

AB SCIEX (Distribution), 10 Biopolis Rd, Chromos, Singapore.

SCIEX, 500 Old Connecticut Path, Framingham, MA.

出版信息

J AOAC Int. 2020 Apr 1;103(2):570-583. doi: 10.5740/jaoacint.19-0112.

Abstract

BACKGROUND

In response to a need for accurate and reliable methods for food allergen regulatory compliance, a method for the detection and quantitation of whole egg, whole milk, peanut, and hazelnut in eight food matrices was developed and evaluated in a single-laboratory validation. The matrices include cookies, cookie dough, bread, breakfast cereal, salad dressing, ice cream, and red wine.

OBJECTIVE

The method was compared with Standard Method Performance Requirements (SMPR) 2016.002 established by the AOAC Stakeholder Panel on Strategic Food Analytical Methods.

METHODS

The method involves tryptic digestion of allergen proteins in food matrices incurred or spiked with allergen standards [reference materials (RMs), Standard RMs (SRMs), or in-house prepared standard] and uses labeled peptide internal standards. LC-tandem MS analysis of the signature tryptic peptides of the four allergens is performed using multiple reaction monitoring.

RESULTS

For 10 allergen/matrix combinations, the method demonstrated adequate sensitivity with a minimum quantitation limit of 3 mg/kg for whole egg and 10 mg/kg for milk, peanut, and hazelnut allergens. Repeatability precision across 3 days of analyses was <17% with analytical range of 10-1000 mg/kg. Recovery from incurred and spiked matrix-matched standards varied from 60 to 118%.

CONCLUSIONS

The method met the minimum performance requirements of SMPR 2016.002 for whole egg in cookies, bread, cookie dough, and salad dressing; whole milk in cookies and red wine; peanut in breakfast cereal; and hazelnut in cookies.

HIGHLIGHTS

The ERP determined that the data presented met the SMPR and accordingly recommended the method to be granted First Action status. In September 2017, the Official Methods Board approved the method as First Action.

摘要

背景

为了满足食品过敏原法规遵从性的准确可靠方法的需求,开发并评估了一种在单一实验室验证中检测和定量八种食品基质中的全蛋、全脂牛奶、花生和榛子的方法。这些基质包括饼干、饼干面团、面包、早餐麦片、沙拉酱、冰淇淋和红酒。

目的

该方法与 AOAC 利益相关者战略食品分析方法小组制定的标准方法性能要求(SMPR)2016.002 进行了比较。

方法

该方法涉及在含有过敏原标准[参考物质(RMs)、标准参考物质(SRMs)或内部制备标准]或掺入过敏原标准的过敏原蛋白质在食品基质中的胰蛋白酶消化,并使用标记的肽内标。使用多重反应监测对四种过敏原的特征性胰蛋白酶肽进行 LC-串联 MS 分析。

结果

对于 10 种过敏原/基质组合,该方法表现出足够的灵敏度,全蛋的最低定量限为 3mg/kg,牛奶、花生和榛子过敏原的最低定量限为 10mg/kg。在 3 天的分析中,重复性精度<17%,分析范围为 10-1000mg/kg。从掺入和掺入基质匹配标准的回收率在 60%到 118%之间变化。

结论

该方法满足 SMPR 2016.002 中对饼干、面包、饼干面团和沙拉酱中的全蛋;饼干和红酒中的全脂牛奶;早餐麦片中的花生;以及饼干中的榛子的最低性能要求。

亮点

ERP 确定所呈现的数据符合 SMPR,并因此建议该方法获得第一行动地位。2017 年 9 月,官方方法委员会批准该方法为第一行动。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验