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Scientific Opinion on Flavouring Group Evaluation 35, Revision 1 (FGE.35Rev1): Three quinine salts from the Priority list from chemical group 30

机译:关于调味组评估35的科学意见,修订版1(FGE.35Rev1):来自化学组30的优先列表中的三种奎宁盐

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The Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids of the European Food Safety Authority was requested to evaluate three flavouring substances in the Flavouring Group Evaluation 35, Revision 1, using the Procedure in Commission Regulation (EC) No 1565/2000. The present revision includes new specification data on quinine sulphate [FL‐no: 14.152] and quinine monohydrochloride dihydrate [FL‐no: 14.155], new intake data on all three candidate substances and toxicological and genotoxicity data on quinine hydrochloride [FL‐no: 14.011] and quinine monohydrochloride dihydrate [FL‐no: 14.155], as well as two structurally related quinine salts (quinine dihydrochloride and deoxyquinine). A search in open literature has been made and the relevant data are presented. This evaluation concerns only the use of these quinine salts in beverages, where they are legally permitted. Because of the availability of well conducted human studies at much higher quinine exposures than those occurring when quinine is used as flavouring substance and which were considered in this FGE.35Rev1, the Panel considered the use of the Procedure for these substances inappropriate. However, based on human data available on quinine, the Panel concluded that the quinine salts are not expected to be of safety concern at their estimated level of intake as flavouring substances, provided that hypersensitivity reactions are avoided by the legally required labelling of quinine‐containing beverages. The Panel noted that a very high intake (e.g. more than 1 litre) of non‐alcoholic beverages containing quinine or its salts at the maximum permitted level could result in adverse health effects in humans. Besides the safety assessment of these three flavouring substances, the specifications for the materials of commerce have also been considered. Adequate specifications, including complete purity criteria and identity, have been provided for all three candidate substances.
机译:要求欧洲食品安全局食品接触材料,酶,调味剂和加工助剂小组使用委员会法规(EC)第1565/2000号中的程序,对调味剂组评估35,修订1中的三种调味剂进行评估。本修订版包括有关硫酸奎宁[FL-no:14.152]和奎宁一水合二水合奎宁[FL-no:14.155]的新规格数据,有关所有三种候选物质的新摄入量数据以及关于盐酸奎宁的毒理和遗传毒性数据[FL-no: 14.011]和奎宁一盐酸盐二水合物[FL-no:14.155],以及两种结构相关的奎宁盐(奎宁二盐酸盐和脱氧奎宁)。在公开文献中进行了搜索,并提供了相关数据。此评估仅涉及在法律允许的范围内在饮料中使用这些奎宁盐。由于可以进行良好的人体研究,而奎宁暴露量远高于使用奎宁作为调味剂时发生的暴露,并且在本FGE.35Rev1中被考虑,因此专家小组认为对这些物质使用该程序是不合适的。但是,根据有关奎宁的现有人类数据,专家小组得出结论,假设通过法律要求的含奎宁标签来避免超敏反应,预计奎宁盐作为调味品的估计摄入量不会引起安全问题。饮料。专家小组指出,摄入含有最大允许水平的奎宁或其盐的非酒精饮料(例如,超过1升)非常高,可能对人类健康产生不利影响。除了对这三种调味剂的安全性评估之外,还考虑了商业材料的规格。已经为所有三种候选物质提供了足够的规格,包括完整的纯度标准和特性。

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    《EFSA Journal》 |2015年第9期|共37页
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