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Scientific Opinion on Flavouring Group Evaluation 57, Revision 1 (FGE.57Rev1): consideration of isopulegone and three flavouring substances evaluated by JECFA (55th?meeting)

机译:关于调味剂组评估的科学意见57,修订版1(FGE.57Rev1):考虑异戊烯酮和JECFA评估的三种调味剂(第五十五次会议)

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The EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids was requested to consider evaluations of flavouring substances assessed since 2000 by the Joint FAO/WHO Expert Committee on Food Additives (JECFA), and to decide whether further evaluation is necessary, as laid down in Commission Regulation (EC) No 1565/2000. The present consideration concerns a group of four flavouring substances consisting of isopulegone and three other substances evaluated by JECFA at the 55th meeting. This revision is made due to additional toxicity data available for (1R,2S,5R)‐isopulegol [FL‐no: 02.067]. The substances were evaluated through a stepwise approach that integrates information on structure–activity relationships, intake from current uses, toxicological threshold of concern, and available data on metabolism and toxicity. p‐Mentha‐1,4(8)‐dien‐3‐one [FL‐no: 07.127] is no longer supported by the flavour industry and was not evaluated. In agreement with JECFA, the Panel evaluated the candidate substances in this Flavouring Group Evaluation (FGE) via the B‐side of the Procedure. Based on a no observed adverse effect level (NOAEL) from a 90‐day oral toxicity study on [FL‐no: 02.067], adequate margins of safety for the three candidate substances could be calculated. Therefore, the Panel agrees with the JECFA conclusion, ‘No safety concern at estimated levels of intake as flavouring substances’ based on the maximised survey‐derived daily intake (MSDI) approach. Besides the safety assessment of these flavouring substances, the specifications for the materials of commerce have also been considered and found adequate. For the three substances evaluated in this FGE, use levels have become available and the modified theoretical added maximum daily intakes (mTAMDIs) were estimated. For [FL‐no: 02.067 and 07.067], the mTAMDI exceeds the toxicological threshold of concern for their structural classes and need more refined exposure assessment to finalise the evaluation.
机译:欧洲食品安全局食品接触材料,酶,调味剂和加工助剂小组被要求考虑对粮农组织/世卫组织食品添加剂联合专家委员会(JECFA)自2000年以来评估的调味剂进行评估,并决定是否有必要进一步评估,因为根据委员会法规(EC)1565/2000的规定。目前的考虑涉及由JECFA在第五十五次会议上评估的一组四种调味物质,其中包括异普勒酮和其他三种物质。进行本修订的原因是可用于(1R,2S,5R)-异胡薄荷醇的其他毒性数据[FL-no:02.067]。通过逐步方法对这些物质进行了评估,该方法综合了结构-活性关系,当前使用量,所关注的毒理学阈值以及有关代谢和毒性的可用数据。 p‐Mentha‐1,4(8)‐dien‐3‐one [FL‐no:07.127]不再受香料行业支持,也未进行评估。与JECFA达成一致,小组通过程序的B面对本调味组评估(FGE)中的候选物质进行了评估。根据对[FL-no:02.067]进行的90天口服毒性研究的未观察到的不良反应水平(NOAEL),可以计算出三种候选物质的足够的安全限度。因此,小组同意JECFA的结论,即“基于调查得出的每日最大摄入量(MSDI)最大化方法”,“在估计摄入的调味料中没有安全隐患”。除了对这些调味物质的安全性进行评估之外,还考虑了商业材料的规格,并认为这些规格是适当的。对于在该FGE中评估的三种物质,已达到使用水平,并估算了改良的理论增加的最大每日摄入量(mTAMDI)。对于[FL-no:02.067和07.067],mTAMDI超出了其结构分类所关注的毒理学阈值,需要更精细的暴露评估才能最终确定评估。

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