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當(dāng)前位置: 首頁 » 食品資訊 » 外訊導(dǎo)讀 » 歐盟評估枳椇果、梗熱水提取物作為新型食品的安全性

歐盟評估枳椇果、梗熱水提取物作為新型食品的安全性

放大字體  縮小字體 時間:2020-08-31 09:47 來源:食品伙伴網(wǎng) 作者: 澤夕   
核心提示:2020年8月28日,據(jù)歐盟食品安全局(EFSA)消息,歐盟營養(yǎng)、新型食品和食物過敏原(NDA)研究小組就枳椇果、梗熱水提取物(hot water extract of fruits and peduncles of Hovenia dulcis)作為新型食品的安全性發(fā)表科學(xué)意見。
   食品伙伴網(wǎng)訊  2020年8月28日,據(jù)歐盟食品安全局EFSA)消息,歐盟營養(yǎng)、新型食品和食物過敏原(NDA)研究小組就枳椇果、梗熱水提取物(hot water extract of fruits and peduncles of Hovenia dulcis)作為新型食品的安全性發(fā)表科學(xué)意見。
 
  經(jīng)過評估,專家小組得出結(jié)論,枳椇果、梗熱水提取物作為新型食品的安全性尚未確定。部分原文報道如下:
 
  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 the safety of ‘Hovenia dulcis fruit extract’ as a novel food (NF) for its use in food supplements. The NF concerns a hot water extract of sliced and dried fruits and peduncles of Hovenia dulcis Thun. The production process is described in sufficient detail but contains contradictory information regarding the mixing with another ingredient of the NF. The NF is comprised of mostly carbohydrates (about 90%), about 2% proteins, 5% moisture, less than 1% fat and about 2% ash. In addition, the NF 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 Hovenia dulcis 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 NF. The same applied to a human study provided by the applicant. The Panel concludes that the safety of the NF has not been established.
 
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日期:2020-08-31
 
 
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