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Safety of use of oat lecithin as a food additive

机译:燕麦卵磷脂的使用安全性作为食品添加剂

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The EFSA Panel on Food Additives and Flavourings (FAF) provides a scientific opinion on the safety of oat lecithin for use as a new food additive in the proposed food category (FC05.1) ‘cocoa and chocolate products’. Oat lecithin is an oil, containing polar lipids (≥ 35% w/w) and non‐polar lipids (55–65% w/w),obtained by ethanol extraction and subsequent fractionation (water/ethanol) from oat suitable for food consumption. This lecithin does not meet the specification parameter for the authorised food additive lecithins (E 322) of ‘not less than 60% of substances insoluble in acetone’ which represents the polar lipid content (phospholipids and glycolipids). Oat lecithin is expected to undergo hydrolysis in the gastrointestinal tract and this hydrolysis resembles that of other edible vegetable oils. Oat lecithin did not induce gene mutations or structural chromosomal aberrations in the absence or presence of metabolic activation. No treatment‐related adverse effects were observed with oat lecithin in 28‐day studies in rats and dogs at the highest dose tested. The toxicological database for oat lecithin was limited. Considering the composition of oat lecithin (similar components in different ratio) and the fact that it undergoes the same biotransformation, resulting in similar metabolites as those from lecithins (E 322) re‐evaluated by the EFSA Panel on Food Additives and Nutrient Sources added to Food (EFSA ANS) in 2017, the Panel considered the possibility to use the read‐across approach from toxicological data on lecithins (E 322). Based on the toxicological data provided for oat lecithin along with read across from lecithins (E322) to oat lecithin no additional toxicological data were required. Therefore, the Panel considered that the previous conclusion for lecithins (E322) equally applies to oat lecithin to be used as food additive. Mean exposure ranged from < 0.01 mg/kg bw per day in infants to 7.1 mg/kg bw per day in children. The 95th percentile of exposure ranged from 0 mg/kg bw per day in infants to 22.5 mg/kg bw per day in children. The Panel concluded that there is no need for a numerical ADI and there is no safety concern for oat lecithin to be used as a food additive at the proposed use (FC 05.1) and use levels. The Panel recommended that the European Commission considers including specifications for oat lecithin as a new food additive.
机译:食品添加剂和调味料(FAF)的EFSA小组(FAF)为燕麦卵磷脂的安全提供了一种科学意见,以拟议的食品类别(FC05.1)'可可和巧克力产品'为新的食品添加剂。燕麦卵磷脂是一种油,含有极性脂质(≥35%w / w)和非极性脂质(55-65%w / w),通过乙醇萃取和随后的分馏(水/乙醇),适用于食品消耗。该卵磷脂不符合授权食品添加剂卵磷脂(E 322)的规范参数'不小于60%的物质不溶于丙酮的物质,这代表极性脂质含量(磷脂和糖脂)。燕麦卵磷脂预计将在胃肠道进行水解,这种水解类似于其他可食用植物油。燕麦卵磷脂在没有或存在代谢活化的情况下没有诱导基因突变或结构染色体畸变。在最高剂量的大鼠和狗的28天研究中,燕麦卵磷脂没有观察到治疗相关的不利影响。燕麦卵磷脂的毒理数据库有限。考虑燕麦卵磷脂的组成(不同比例的类似组分)以及其经历相同的生物转化的事实,导致类似于来自卵磷脂(E 322)的类似代谢物(e 322)通过EFSA面板对食品添加剂和营养来源进行再评估的食物(EFSA ANS)在2017年,小组认为可以使用读取方法从卵磷脂上的毒理学数据(E 322)。基于为燕麦卵磷脂提供的毒理学数据以及从卵磷脂(E322)的读数到燕麦卵磷脂,不需要额外的毒理学数据。因此,该专家组认为前一个对卵磷脂(E322)的结论同样适用于燕麦卵磷脂作为食品添加剂。平均暴露在婴儿每天<0.01mg / kg bw,每天每天儿童为7.1mg / kg bw。 95百分位的暴露在儿童中每天每天0毫克/千克/千克,每天22.5毫克/千克BW。该小组得出结论,无需数值ADI,燕麦卵磷脂没有安全担心以在所提出的用途(FC 05.1)和使用水平的食品添加剂中。小组建议欧洲委员会认为,包括燕麦卵磷脂的规格作为新的食品添加剂。

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