Turck Dominique, Bohn Torsten, Cámara Montaña, Castenmiller Jacqueline, De Henauw Stefaan, Jos Ángeles, Maciuk Alexandre, Mangelsdorf Inge, McArdle Harry J, McNulty Breige, Naska Androniki, Pentieva Kristina, Siani Alfonso, Thies Frank, Aguilera-Gómez Margarita, Cubadda Francesco, Frenzel Thomas, Heinonen Marina, Neuhäuser-Berthold Monika, Knutsen Helle Katrine, Poulsen Morten, Maradona Miguel Prieto, Schlatter Josef Rudolf, Siskos Alexandros, van Loveren Henk, Roldán-Torres Ruth, Gelbmann Wolfgang, Hirsch-Ernst Karen Ildico
EFSA J. 2025 May 14;23(5):e9373. doi: 10.2903/j.efsa.2025.9373. eCollection 2025 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 yellow tomato extract used as a novel food (NF) pursuant to Regulation (EU) 2283/2015. The NF which is the subject of the application is a carotenoid-rich extract from the yellow tomato containing predominantly phytoene plus phytofluene (PE/PF) at up to 10% of the NF, as well as a lesser amount of zeta-carotene (≤ 5%), beta-carotene (≤ 0.5%) and lycopene (≤ 0.4%). The NF is produced from the tomato pulp using supercritical CO extraction. The applicant proposes to use the NF in food supplements (FS) for adults only at a maximum daily dose of 100 mg. The intake of lycopene from such FS would correspond to 0.4 mg/day which corresponds to 5.7 μg/kg body weight and day for an adult weighing 70 kg. This is approximately 1.1% of the acceptable daily intake (ADI) for lycopene established by EFSA (i.e. 0.5 mg/kg body weight), which does not raise safety concerns. According to the exposure assessment performed by EFSA, which included all population age groups, the highest mean and highest P95 intakes/kg bw estimates for PE/PF from the background diet of infants and toddlers are higher than the combined exposure of adults from the background diet and the NF under its proposed use and use levels in food supplements. Noting that the main sources for PE/PF are commonly and regularly consumed also by the youngest age groups and that PE/PF exposure from the background diet does not raise safety concern, the Panel considers that the NF is nutritionally not disadvantageous at the proposed intake of the NF of up to 100 mg/day used in FS in adults. The Panel concludes that the NF, yellow tomato extract, is safe under the proposed conditions of use.
应欧盟委员会的要求,欧洲食品安全局(EFSA)营养、新型食品及食品过敏原专家委员会(NDA)被要求根据(欧盟)第2283/2015号法规,就用作新型食品(NF)的黄色番茄提取物发表意见。申请所涉及的新型食品是一种富含类胡萝卜素的黄色番茄提取物,主要含有八氢番茄红素和六氢番茄红素(PE/PF),含量高达新型食品的10%,还含有少量的ζ-胡萝卜素(≤5%)、β-胡萝卜素(≤0.5%)和番茄红素(≤0.4%)。该新型食品采用超临界CO萃取法从番茄果肉中提取。申请人提议仅在成人食品补充剂(FS)中使用该新型食品,最大日剂量为100毫克。从这种食品补充剂中摄入的番茄红素相当于0.4毫克/天,对于体重70千克的成年人来说,相当于5.7微克/千克体重/天。这约为欧洲食品安全局确定的番茄红素每日可接受摄入量(ADI)的1.1%(即0.5毫克/千克体重),不存在安全问题。根据欧洲食品安全局进行的暴露评估,其中包括所有年龄组的人群,婴幼儿背景饮食中PE/PF的最高平均摄入量和最高P95摄入量/千克体重估计值高于成年人在背景饮食和按提议的使用和使用水平在食品补充剂中使用该新型食品时的综合暴露量。鉴于最年幼年龄组通常也经常食用PE/PF的主要来源,且背景饮食中PE/PF的暴露不存在安全问题,专家委员会认为,就成人食品补充剂中提议的高达100毫克/天的新型食品摄入量而言,该新型食品在营养方面并无不利之处。专家委员会得出结论,在所提议的使用条件下,新型食品黄色番茄提取物是安全的。