首页> 外文OA文献 >EFSA CEF Panel (EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids), 2016 Scientific Opinion on Flavouring Group Evaluation 75, Revision 1 (FGE.75Rev1): Consideration of tetrahydrofuran derivatives evaluated by JECFA (63rd meeting) structurally related to tetrahydrofuran derivatives evaluated by EFSA in FGE.33 (2008)
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EFSA CEF Panel (EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids), 2016 Scientific Opinion on Flavouring Group Evaluation 75, Revision 1 (FGE.75Rev1): Consideration of tetrahydrofuran derivatives evaluated by JECFA (63rd meeting) structurally related to tetrahydrofuran derivatives evaluated by EFSA in FGE.33 (2008)

机译:EFsa CEF专家组(EFsa食品接触材料,酶,调味剂和加工助剂专家组),2016年调味品组评估科学意见75,修订版1(FGE.75Rev1):JECFa(第63次会议)评估的四氢呋喃衍生物的结构与EFsa在FGE.33(2008)中评估的四氢呋喃衍生物

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摘要

The Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF) of the EFSA was requested to consider evaluations of flavouring substances assessed since 2000 by the Joint FAO/WHO Expert Committee on Food Additives (the 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 10 tetrahydrofuran derivatives and one furanone derivative evaluated by the JECFA at the 63rd meeting in 2004. This revision is made due to additional toxicity data have become available for anhydrolinalool oxide (5) [FL-no: 13.097]. 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. The JECFA concluded all the 11 tetrahydrofuran derivatives at step A3. The Panel agrees with the application of the Procedure as performed by the JECFA for 10 of the 11 substances. For the remaining substance [FL-no: 13.097] the Panel did not find that it could be metabolised to innocuous products and should accordingly be evaluated via the B-side of the Procedure scheme. A no observed adverse effect level (NOAEL) of 52 mg/kg body weight was derived from a 90-day study in rats and compared with an exposure estimate of 0.9 µg/ capita / per day for anhydrolinalool oxide a margin of safety of 3.5 × 106 was calculated. Accordingly, the Panel agrees with the JECFA conclusion ‘No safety concern at estimated level of intake as flavouring substances’ based on the maximised survey-derived daily intake (MSDI) approach. The specifications for the materials of commerce have also been considered and for all 11 substances, the information is adequate.
机译:要求欧洲食品安全局的食品接触材料,酶,调味剂和加工助剂小组(CEF)考虑对2000年以来粮农组织/世界卫生组织食品添加剂联合专家委员会(JECFA)评估的调味物质的评估,并决定是否根据委员会法规(EC)1565/2000的规定,有必要进行进一步评估。目前的考虑涉及JECFA在2004年第63次会议上评估的一组10种四氢呋喃衍生物和一种呋喃酮衍生物。之所以进行此修订是因为可获得有关脱水芳樟醇氧化物(5)的更多毒性数据[FL-no:13.097] 。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的信息。 JECFA在步骤A3中得出所有11种四氢呋喃衍生物。专家组同意JECFA对11种物质中的10种实施该程序。对于其余物质[FL-no:13.097],小组未发现其可以代谢为无害产品,因此应通过程序方案的B面进行评估。在90天的大鼠研究中未观察到52 mg / kg体重的不良反应水平(NOAEL),并将其与脱水萘二酚氧化物的暴露估计值为0.9 µg /人均/天相比,安全系数为3.5×计算得出106。因此,专家组同意JECFA的结论“根据调查得出的每日最大摄入量(MSDI)最大化方法得出的食用香料的估计摄入量没有安全问题”。还考虑了商业材料的规范,对于所有11种物质,信息都是足够的。

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