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Reconsideration of the temporary ADI and refined exposure assessment for Sunset Yellow FCF (E 110)

机译:重新考虑临时ADI和日落黄FCF的精细暴露评估(E 110)

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The Panel on Food Additives and Nutrient Sources added to Food (ANS Panel) has previously provided a scientific opinion re‐evaluating the safety of Sunset Yellow FCF (E 110) as a food additive in the EU and establishing a temporary acceptable daily intake (ADI) of 1 mg/kg bw/day (EFSA ANS Panel, 2009). Following a request by the European Commission, the ANS Panel was asked to assess newly submitted data from a study conducted as a result of the recommendations contained in the 2009 opinion. In addition, EFSA was requested to carry out the refined exposure assessment of Sunset Yellow FCF. The new information assessed comprised an evaluation of the 28‐day study report, the data considered by the Joint FAO/WHO Expert Committee on Food Additives (JECFA) in its latest evaluation from 2011, and any additional toxicological information that had become available since the completion of the previous evaluation by the ANS Panel. The ANS Panel has considered that the newly submitted data from the 28‐day study and the overall available toxicological database on Sunset Yellow FCF provides a basis to revise the established temporary ADI and concluded that, based on the NOAEL of 375 mg/kg bw/day from the long‐term feeding study in rats and an uncertainty factor of 100, a new ADI for Sunset Yellow FCF of 4 mg/kg bw/day can be established, in agreement with the latest evaluation by JECFA. Exposure estimates for Sunset Yellow FCF based both on the currently authorised MPLs and reported use levels provided are well below the new ADI of 4 mg/kg bw/day for all population groups. Overall, the Panel concluded that, using data provided by the food industry and Member States, the reported uses and use levels of Sunset Yellow FCF (E 110) would not be of safety concern.
机译:食品中添加的食品添加剂和营养来源专家小组(ANS Panel)先前已经提供了一项科学意见,重新评估了日落黄FCF(E 110)作为欧盟食品添加剂的安全性,并确定了暂时可接受的每日摄入量(ADI ),每天1 mg / kg bw(EFSA ANS Panel,2009)。应欧洲委员会的要求,要求ANS小组评估根据2009年意见中的建议进行的一项研究中新提交的数据。此外,欧洲食品安全局被要求对日落黄FCF进行精确的暴露评估。评估的新信息包括对28天研究报告的评估,粮农组织/世卫组织食品添加剂联合专家委员会(JECFA)在2011年以来的最新评估中考虑的数据以及自2007年以来可获得的任何其他毒理学信息。由ANS小组完成之前的评估。 ANS小组认为,来自28天研究的新提交数据以及日落黄FCF的全部现有毒理学数据库为修订已建立的临时ADI提供了基础,并得出结论,基于375 mg / kg bw /在大鼠长期喂养研究的第二天,不确定因素为100,可以与JECFA的最新评估相一致,建立一个新的ADI,用于日落黄FCF的4 mg / kg bw /天。根据当前授权的MPL和所提供的报告使用量,对日落黄FCF的暴露估算值远低于所有人群的新ADI每日4 mg / kg bw /天。总体而言,评估小组得出结论,使用食品工业和成员国提供的数据,日落黄色FCF(E 110)的报告用途和使用水平不会引起安全问题。

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    《EFSA Journal》 |2014年第7期|共39页
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