Turck Dominique, Castenmiller Jacqueline, De Henauw Stefaan, Hirsch-Ernst Karen Ildico, Kearney John, Maciuk Alexandre, Mangelsdorf Inge, McArdle Harry J, Naska Androniki, Pelaez Carmen, Pentieva Kristina, Siani Alfonso, Thies Frank, Tsabouri Sophia, Vinceti Marco, Cubadda Francesco, Engel Karl Heinz, Frenzel Thomas, Heinonen Marina, Marchelli Rosangela, Neuhäuser-Berthold Monika, Poulsen Morten, Schlatter Josef Rudolf, van Loveren Henk, Colombo Paolo, Knutsen Helle Katrine
EFSA J. 2020 May 14;18(5):e06097. doi: 10.2903/j.efsa.2020.6097. eCollection 2020 May.
Following a request from the European Commission, the EFSA Panel on Nutrition, Novel Foods and Food Allergens (NDA) was asked to deliver an opinion on 6'-Sialyllactose (6'-SL) sodium salt as a novel food (NF) pursuant to Regulation (EU) 2015/2283. The NF is mainly composed of the human-identical milk oligosaccharide (HiMO) 6'-SL but also contains D-lactose, sialic acid and a small fraction of other related oligosaccharides. The NF is produced by fermentation with a genetically modified strain of K-12 DH1. The information provided on the manufacturing process, composition and specifications of the NF does not raise safety concerns. The applicant intends to add the NF in a variety of foods, including infant and follow-on formula, foods for infants and toddlers, foods for special medical purposes and food supplements. The target population is the general population. The anticipated daily intake of 6'-SL from the NF at the maximum proposed use levels is unlikely to exceed the intake level of naturally occurring 6'-SL in breastfed infants on a body weight basis. The intake of 6'-SL in breastfed infants on a body weight basis is expected to be safe also for other population groups. The intake of other carbohydrate-type compounds structurally related to 6'-SL is also considered of no safety concern. Food supplements are not intended to be used if other foods with the added NF or breast milk are consumed on the same day. The Panel concludes that the NF is safe under the proposed conditions of use.
应欧盟委员会的要求,欧洲食品安全局营养、新型食品和食品过敏原小组(NDA)被要求根据欧盟法规(EU)2015/2283,就6'-唾液酸乳糖(6'-SL)钠盐作为新型食品(NF)发表意见。该新型食品主要由与人乳中相同的低聚糖(HiMO)6'-SL组成,但也含有D-乳糖、唾液酸和一小部分其他相关低聚糖。该新型食品是通过用基因改造的K-12 DH1菌株发酵生产的。关于该新型食品的生产工艺、成分和规格所提供的信息未引发安全问题。申请人打算将该新型食品添加到多种食品中,包括婴儿配方奶粉和后续配方奶粉、婴幼儿食品、特殊医学用途食品和食品补充剂。目标人群为普通人群。在建议的最大使用水平下,从该新型食品中摄入6'-SL的预期每日摄入量按体重计算不太可能超过母乳喂养婴儿中天然存在的6'-SL的摄入量水平。按体重计算,母乳喂养婴儿中6'-SL的摄入量对其他人群组预计也是安全的。与6'-SL结构相关的其他碳水化合物类化合物的摄入量也被认为不存在安全问题。如果同一天食用了添加了该新型食品的其他食品或母乳,则不打算使用食品补充剂。该小组得出结论,在建议的使用条件下,该新型食品是安全的。