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更新:在为动物源性食品中存在的非允许使用的药理活性物质确定行动参考点(RPA)时应考虑的方法学原则和科学方法。

Update: methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non-allowed pharmacologically active substances present in food of animal origin.

作者信息

Knutsen Helle Katrine, Alexander Jan, Barregård Lars, Bignami Margherita, Brüschweiler Beat, Ceccatelli Sandra, Cottrill Bruce, Dinovi Michael, Edler Lutz, Grasl-Kraupp Bettina, Hogstrand Christer, Nebbia Carlo Stefano, Oswald Isabelle P, Petersen Annette, Rose Martin, Roudot Alain-Claude, Schwerdtle Tanja, Vollmer Günter, Vleminckx Christiane, Wallace Heather, Filipič Metka, Fürst Peter, O'Keeffe Michael, Penninks André, Van Leeuwen Rolaf, Baert Katleen, Hoogenboom Laurentius Ron

出版信息

EFSA J. 2018 Jul 24;16(7):e05332. doi: 10.2903/j.efsa.2018.5332. eCollection 2018 Jul.

Abstract

EFSA was asked by the European Commission to update the Scientific Opinion on methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non-allowed pharmacologically active substances in food of animal origin. This guidance document presents a simple and pragmatic approach which takes into account both analytical and toxicological considerations. The RPA shall be based on the reasonably achievable lowest residue concentration that can unequivocally be determined by official control laboratories, i.e. the reasonably achievable lowest decision limit (CCα). The aim is to check whether this concentration is low enough to adequately protect the consumers of food commodities that contain that substance. The proposed step-wise approach applies toxicological screening values (TSVs), based on genotoxic potential, pharmacological activity, as well as other effects of the substance. The highest dietary exposure corresponding to the reasonably achievable lowest CCα for the substance has to be estimated and compared with the TSV. Where equal to or lower than the TSV, the reasonably achievable lowest CCα can be accepted as the RPA. If higher, the sensitivity of the analytical method needs to be improved. In the case where no further analytical improvements are feasible within a short to medium time frame, a substance-specific risk assessment should be considered. This also applies when the potential adverse effects do not allow use of the decision tree, as for high potency carcinogens, inorganic substances or compounds with allergenic effects or causing blood dyscrasias. The CONTAM Panel concluded that RPAs should be food matrix independent. RPAs cannot be applied to non-edible matrices, which are also monitored for non-allowed pharmacologically active substances.

摘要

应欧盟委员会要求,欧洲食品安全局(EFSA)更新了关于在确定动物源性食品中禁用的药理活性物质行动参考点(RPA)时应考虑的方法学原则和科学方法的科学意见。本指导文件提出了一种简单实用的方法,兼顾了分析和毒理学方面的考虑因素。RPA应基于官方控制实验室能够明确测定的合理可及最低残留浓度,即合理可及最低决策限(CCα)。目的是检查该浓度是否足够低,以充分保护含有该物质的食品商品消费者。拟议的逐步方法应用基于遗传毒性潜力、药理活性以及该物质的其他效应的毒理学筛选值(TSV)。必须估算与该物质合理可及最低CCα相对应的最高膳食暴露量,并与TSV进行比较。若等于或低于TSV,则合理可及最低CCα可被接受为RPA。若高于TSV,则需要提高分析方法的灵敏度。在短至中期内无法进一步改进分析方法的情况下,应考虑进行特定物质的风险评估。对于高效致癌物、无机物质或具有致敏作用或导致血液系统疾病的化合物等潜在不良反应不允许使用决策树的情况,这一点同样适用。CONTAM专家组得出结论,RPA应与食品基质无关。RPA不适用于非食用基质,对非食用基质也会监测禁用的药理活性物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29fb/7009670/265d66d205ff/EFS2-16-e05332-g001.jpg

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