Younes Maged, Aquilina Gabriele, Castle Laurence, Engel Karl-Heinz, Fowler Paul, Frutos Fernandez Maria Jose, Fürst Peter, Gürtler Rainer, Husøy Trine, Mennes Wim, Moldeus Peter, Oskarsson Agneta, Shah Romina, Waalkens-Berendsen Ine, Wölfle Detlef, Aggett Peter, Cupisti Adamasco, Fortes Cristina, Kuhnle Gunter, Lillegaard Inger Therese, Scotter Michael, Giarola Alessandra, Rincon Ana, Tard Alexandra, Gundert-Remy Ursula
EFSA J. 2019 Jun 12;17(6):e05674. doi: 10.2903/j.efsa.2019.5674. eCollection 2019 Jun.
The Panel on Food Additives and Flavourings added to Food (FAF) provided a scientific opinion re-evaluating the safety of phosphates (E 338-341, E 343, E 450-452) as food additives. The Panel considered that adequate exposure and toxicity data were available. Phosphates are authorised food additives in the EU in accordance with Annex II and III to Regulation (EC) No 1333/2008. Exposure to phosphates from the whole diet was estimated using mainly analytical data. The values ranged from 251 mg P/person per day in infants to 1,625 mg P/person per day for adults, and the high exposure (95th percentile) from 331 mg P/person per day in infants to 2,728 mg P/person per day for adults. Phosphate is essential for all living organisms, is absorbed at 80-90% as free orthophosphate excreted via the kidney. The Panel considered phosphates to be of low acute oral toxicity and there is no concern with respect to genotoxicity and carcinogenicity. No effects were reported in developmental toxicity studies. The Panel derived a group acceptable daily intake (ADI) for phosphates expressed as phosphorus of 40 mg/kg body weight (bw) per day and concluded that this ADI is protective for the human population. The Panel noted that in the estimated exposure scenario based on analytical data exposure estimates exceeded the proposed ADI for infants, toddlers and other children at the mean level, and for infants, toddlers, children and adolescents at the 95th percentile. The Panel also noted that phosphates exposure by food supplements exceeds the proposed ADI. The Panel concluded that the available data did not give rise to safety concerns in infants below 16 weeks of age consuming formula and food for medical purposes.
食品中添加的食品添加剂和香料小组(FAF)提供了一份科学意见,重新评估了作为食品添加剂的磷酸盐(E 338 - 341、E 343、E 450 - 452)的安全性。该小组认为有足够的暴露量和毒性数据。根据欧盟法规(EC)No 1333/2008的附件II和III,磷酸盐是欧盟批准使用的食品添加剂。主要利用分析数据估算了通过整个饮食摄入的磷酸盐量。数值范围从婴儿每天每人251毫克磷到成年人每天每人1625毫克磷,高暴露量(第95百分位数)从婴儿每天每人331毫克磷到成年人每天每人2728毫克磷。磷酸盐对所有生物体都是必需的,以游离正磷酸盐形式被吸收的比例为80 - 90%,通过肾脏排泄。该小组认为磷酸盐的急性经口毒性较低,并且不存在遗传毒性和致癌性方面的担忧。发育毒性研究中未报告有影响。该小组得出了以磷表示的磷酸盐的群体每日允许摄入量(ADI)为每天每千克体重40毫克,并得出结论认为该ADI对人群具有保护作用。该小组指出,在基于分析数据的估计暴露情况下,平均水平下婴儿、学步儿童和其他儿童以及第95百分位数下婴儿、学步儿童、儿童和青少年的暴露估计值超过了提议的ADI。该小组还指出,通过食品补充剂摄入的磷酸盐超过了提议的ADI。该小组得出结论,现有数据并未引起16周龄以下食用配方奶粉和医用食品的婴儿存在安全问题。