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一种用于牛和猪血浆中类固醇测定的 LC-MS/MS 方法的内部验证和因子效应分析。

In-house validation and factorial effect analysis of a LC-MS/MS method for the determination of steroids in bovine and porcine blood plasma.

机构信息

Federal Office of Consumer Protection and Food Safety, Unit 501, Berlin, Germany.

出版信息

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2013;30(6):1027-36. doi: 10.1080/19440049.2013.779751. Epub 2013 May 8.

Abstract

Anabolic steroids are banned from use in food-producing animals in the European Union (Council Directive 96/22/EC). To control the zero-tolerance concept, an LC-MS/MS method for the screening and confirmation of most of the relevant natural and synthetic estrogenic and androgenic steroids in bovine and porcine blood plasma was developed and validated. The method permits confirmation and quantification of all analytes above a concentration of 0.65 µg L(-1). The validation was carried out according to Commission Decision 2002/657/EC, Chapter 3.1.3 "Alternative Validation", by applying a matrix-comprehensive in-house validation concept. Decision limit CCα, detection capability CCβ, recovery, repeatability, within-laboratory reproducibility and the uncertainty of measurement were calculated. Furthermore, a factorial effect analysis was carried out to identify factors that have a significant influence on the method. Factors considered to be relevant for the method in routine analysis (e.g., operator, storage duration of the extracts before measurement and different cartridge lots) were systematically varied on two levels.

摘要

在欧盟,合成代谢类固醇被禁止用于生产食用动物(理事会指令 96/22/EC)。为了控制零容忍概念,开发并验证了一种用于牛和猪血浆中大多数相关天然和合成雌激素和雄激素类固醇的 LC-MS/MS 筛选和确证方法。该方法允许对浓度高于 0.65µg L(-1) 的所有分析物进行确证和定量。验证按照委员会决定 2002/657/EC,第 3.1.3 章“替代验证”,采用基质综合内部验证概念进行。计算了决策限 CCα、检测能力 CCβ、回收率、重复性、实验室内部再现性和测量不确定度。此外,还进行了析因效应分析,以确定对方法有显著影响的因素。在常规分析中被认为与方法相关的因素(例如,操作人员、测量前提取物的储存时间和不同的试剂盒批次)在两个水平上系统地变化。

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