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Re‐evaluation of carrageenan (E?407) and processed Eucheuma seaweed (E?407a) as food additives

机译:重新评估角叉菜胶(E?407)和加工的Eucheuma海藻(E?407a)作为食品添加剂

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The present opinion deals with the re‐evaluation of the safety of food‐grade carrageenan (E 407) and processes Eucheuma seaweed (E 407a) used as food additives. Because of the structural similarities, the Panel concluded that processed Eucheuma seaweed can be included in the evaluation of food‐grade carrageenan. Poligeenan (average molecular weight 10–20 kDa) has not been authorised as a food additive and is not used in any food applications. In its evaluation of carrageenan (E 407) and processed Eucheuma seaweed (E 407a), the Panel noted that the ADME database was sufficient to conclude that carrageenan was not absorbed intact; in a subchronic toxicity study performed with carrageenan almost complying with the EU specification for E 407 in rats, the no‐observed‐adverse‐effect level (NOAEL) was 3,400–3,900 mg/kg body weight (bw) per day, the highest dose tested; no adverse effects have been detected in chronic toxicity studies with carrageenan in rats up to 7,500 mg/kg bw per day, the highest dose tested; there was no concern with respect to the carcinogenicity of carrageenan; carrageenan and processed Eucheuma seaweed did not raise a concern with respect to genotoxicity; the NOAEL of sodium and calcium carrageenan for prenatal developmental dietary toxicity studies were the highest dose tested; the safety of processed Eucheuma seaweed was sufficiently covered by the toxicological evaluation of carrageenan; data were adequate for a refined exposure assessment for 41 out of 79 food categories. However, the Panel noted uncertainties as regards the chemistry, the exposure assessment and biological and toxicological data. Overall, taking into account the lack of adequate data to address these uncertainties, the Panel concluded that the existing group acceptable daily intake (ADI) for carrageenan (E 407) and processed Eucheuma seaweed (E 407a) of 75 mg/kg bw per day should be considered temporary, while the database should be improved within 5 years after publication of this opinion.
机译:本意见涉及对食品级角叉菜胶(E 407)的安全性进行重新评估,并加工用作食品添加剂的Eucheuma海藻(E 407a)。由于结构上的相似性,专家小组得出结论,加工后的Eucheuma海藻可纳入食品级角叉菜胶的评估中。 Poligeenan(平均分子量10–20 kDa)未获批准作为食品添加剂,也未在任何食品应用中使用。在评估角叉菜胶(E 407)和加工后的Eucheuma海藻(E 407a)时,小组指出,ADME数据库足以得出角叉菜胶未被完整吸收的结论。在对角叉菜胶进行的几乎符合大鼠E 407欧盟规范的亚慢性毒性研究中,未观察到的不良作用水平(NOAEL)为每天3,400-3,900 mg / kg体重(bw),最高剂量经过测试每天以最高剂量7,500 mg / kg bw服用角叉菜胶的大鼠进行的慢性毒性研究中未发现不良反应;不用担心角叉菜胶的致癌性;角叉菜胶和加工的Eucheuma海藻并未引起遗传毒性方面的关注;产前发育饮食毒性研究中钠和角叉菜胶的NOAEL是测试的最高剂量;角叉菜胶的毒理学评估已充分涵盖了加工的Eucheuma海藻的安全性;数据足以对79种食品中的41种进行精确的暴露评估。但是,小组注意到在化学,接触评估以及生物学和毒理学数据方面的不确定性。总体而言,考虑到缺乏足够的数据来解决这些不确定性,小组得出结论,现有的组每天可接受的角叉菜胶(E 407)和加工的Eucheuma海藻(E 407a)的每日摄入量为75 mg / kg bw应该被视为临时的,而数据库应在发表此意见后的5年内进行完善。

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