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欧洲生物分析论坛建议:加速器质谱法定量分析的科学验证

European Bioanalysis Forum recommendation: scientific validation of quantification by accelerator mass spectrometry.

作者信息

Higton David, Young Graeme, Timmerman Philip, Abbott Richard, Knutsson Magnus, Svensson Leif D

机构信息

AstraZeneca, Alderley Park, UK.

出版信息

Bioanalysis. 2012 Nov;4(22):2669-79. doi: 10.4155/bio.12.242.

DOI:10.4155/bio.12.242
PMID:23210650
Abstract

Accelerator mass spectrometry (AMS) is being used more widely to provide PK data for early decision making or to generate absolute bioavailability data in later phases of development. Presently, there is no clear consensus on the level of the scientific validation required for these assays. The European Bioanalysis Forum (EBF) has conducted two surveys with its members and presented the results at its 4th Open Symposium. With AMS being used for discrete scientific assessment, method establishment of AMS assays should focus on science rather than trying to fit the assay parameters into validation criteria used for Regulated Bioanalysis guidance, and an amount of freedom of execution and interpretation is needed. Hence, the EBF focuses their recommendation on introducing terminology around scientific qualification or validation to be used in relation to AMS. Guidance is given on which parameters should be investigated when a qualified method is required. The recommendations of the EBF for scientific validation are described herein. The scientific validation of AMS assays will be different to that applied for LC-MS/MS assays, and an example is that accuracy and precision limits, as used for ligand-binding assays, would be more appropriate.

摘要

加速器质谱法(AMS)正被更广泛地用于提供药代动力学(PK)数据以支持早期决策,或在研发后期生成绝对生物利用度数据。目前,对于这些分析方法所需的科学验证水平尚无明确共识。欧洲生物分析论坛(EBF)对其成员进行了两项调查,并在其第四届公开研讨会上公布了结果。鉴于AMS用于离散的科学评估,AMS分析方法的建立应侧重于科学性,而非试图将分析参数套用到法规生物分析指南所使用的验证标准中,并且需要一定的执行和解释自由度。因此,EBF将其建议重点放在引入与AMS相关的科学鉴定或验证的术语上。针对需要合格方法时应研究哪些参数给出了指导意见。本文描述了EBF关于科学验证的建议。AMS分析方法的科学验证将不同于液相色谱-串联质谱(LC-MS/MS)分析方法,例如,用于配体结合分析的准确度和精密度限度会更合适。

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