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, Frenzel Thomas, Heinonen Marina, Marchelli Rosangela, Neuhauser-Berthold Monika, Poulsen Morten, Prieto Maradona Miguel, Schlatter Josef Rudolf, van Loveren Henk, Roldán-Torres Ruth, Knutsen Helle Katrine
EFSA J. 2021 Apr 8;19(4):e06516. doi: 10.2903/j.efsa.2021.6516. eCollection 2021 Apr.
Following a request from the European Commission, the EFSA Panel on Nutrition, Novel Foods and Food Allergens (NDA) was asked to deliver a scientific opinion on vitamin D mushroom powder as a novel food (NF) pursuant to Regulation (EU) 2015/2283. The NF is an ingredient produced from mushroom powder that has been exposed to ultraviolet (UV) irradiation to induce the conversion of provitamin D (ergosterol) to vitamin D (ergocalciferol). The NF contains concentrations of vitamin D provided by vitamin D in the ranges of 580-595 μg/g. 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 and beverages, including food for special medical purposes and food supplements. The target population is the general population except for food supplements and Foods for Special Medical Purposes (FSMPs), for which the target population is individuals above 1 year of age. The Panel concludes that the NF, used as an ingredient, is safe for the general population at the proposed condition of use in foods and beverages and that the NF used as a food supplement, is safe for individuals above 1 year.
应欧盟委员会要求,欧洲食品安全局(EFSA)营养、新型食品及食品过敏原专家小组(NDA)被要求根据欧盟法规(EU)2015/2283就维生素D蘑菇粉作为新型食品(NF)发表科学意见。该新型食品是一种由蘑菇粉制成的成分,经过紫外线(UV)照射,促使维生素原D(麦角固醇)转化为维生素D(麦角钙化醇)。该新型食品中维生素D的含量为580 - 595μg/g。所提供的关于该新型食品生产工艺、成分和规格的信息不存在安全问题。申请人打算将该新型食品添加到多种食品和饮料中,包括特殊医学用途食品和食品补充剂。除食品补充剂和特殊医学用途食品(FSMPs)外,目标人群为普通人群,对于食品补充剂和FSMPs,目标人群为1岁以上个体。专家小组得出结论,在食品和饮料中按提议的使用条件用作成分时,该新型食品对普通人群是安全的,用作食品补充剂时,对1岁以上个体是安全的。