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Safety of hot water extract of fruits and peduncles of Hovenia dulcis as a novel food pursuant to Regulation 1(EU) 2015/2283

机译:Heovenia Dulcis水果和花梗的热水提取物的安全性是根据规则1(欧盟)2015/2283的新型食物

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摘要

Following a request from the European Commission, the Panel on Nutrition, Novel Foods and Food Allergens ( ) was asked to deliver an opinion on the safety of ‘ fruit extract’ as a novel food ( ) for its use in food supplements. The concerns a hot water extract of sliced and dried fruits and peduncles of Thun. The production process is described in sufficient detail but contains contradictory information regarding the mixing with another ingredient of the . The is comprised of mostly carbohydrates (about 90%), about 2% proteins, 5% moisture, less than 1% fat and about 2% ash. In addition, the contains small amounts of flavonoids such as dihydromyricetin, myricetin and quercetin. The Panel notes limitations of the data provided from the batch testing regarding proximate analyses and plant secondary metabolites. Given these limitations, the Panel considers that the data provided by the applicant do not demonstrate that different batches produced with the described production process meet the proposed specifications. The target population is the general adult population excluding pregnant and lactating women and people with a chronic disease, such as liver malfunction. Limited information was provided on a history of consumption of fruits and on an extract approved in South Korea. A number of toxicological studies were performed. However, the study reports did not allow to verify that the test item was representative of the . The same applied to a human study provided by the applicant. The Panel concludes that the safety of the has not been established.
机译:遵循欧盟委员会的请求后,营养小组,新型食品和食品过敏原()被要求向其在食品补充剂中使用“水果提取物”作为一种新型食品的意见。涉及切片和干果的热水提取物和Thun的小组。生产过程以足够的细节描述,但含有关于与另一种成分混合的矛盾信息。该碳水化合物(约90%),约2%蛋白质,水分为5%,小于1%脂肪和约2%灰分。此外,含有少量的黄酮类化合物,如Diydromyricetin,Myricetin和槲皮素。小组注意到分批测试提供的数据的限制,关于近分析和植物次生代谢物。鉴于这些限制,小组认为,申请人提供的数据没有证明用描述的生产过程产生的不同批次符合所提出的规格。目标人口是不包括怀孕和哺乳期妇女和患有慢性疾病的人的一般成年人口,例如肝脏故障。提供了有限的信息,并提供了果实消费史以及韩国批准的提取物。进行了许多毒理学研究。但是,研究报告不允许验证测试项目是否代表。这同样适用于由申请人提供的人类研究。小组得出结论,尚未建立的安全。

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