LOGO

EU assessed safety of Glucosyl Hesperidin as novel food

Snipaste_2024-08-14_13-54-29.jpg


August 8, 2024 - According to the European Food Safety Authority (EFSA), the EU Nutrition, Novel Foods and Food Allergens (NDA) Study Group issued a scientific opinion on the safety of glucosyl hesperidin as a novel food.

 

After evaluation, the panel concluded that glucosyl hesperidin is safe as a novel food under the proposed conditions of use. Part of the original report follows:

 

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 glucosyl hesperidin (GH) as a novel food (NF) pursuant to Regulation (EU) 2015/2283. The NF, which is produced from hesperidin and dextrin by enzymatic reactions, is a powder consisting mainly of monoglucosyl hesperidin (MGH) and unreacted hesperidin (flavonoid), which account in total for up to 92.8% (on dry basis) of the product. The applicant proposed to use the NF in specific drinks and food supplements leading to a maximum intake of up to 364 mg per day for adults. The target population is the general population, except for food supplements for which the proposed target population is children from 1 year onwards and adults. Taking into consideration the composition of the NF and the proposed uses, the consumption of the NF is not nutritionally disadvantageous. There are no concerns regarding genotoxicity of the NF. based on a 90-day oral toxicity study conducted with the NF, the Panel considers the NOAEL at the mid-dose group, i.e. ~ 1000 mg/kg body weight (bw) per day. By applying an uncertainty factor of 200, the resulting intake providing sufficient margin of exposure for humans would be 5 mg/kg bw per day. The available human intervention studies did not report clinically relevant changes in haematological or clinical chemistry parameters following the administration of GH/MGH at supplemental doses of up to 3 g/day for 12 weeks. Overall, the Panel considers that the margin of exposure (~ 200) between the intake of the NF at the proposed uses and use levels and the NOAEL from the 90-day study is sufficient. The Panel concludes that the NF, glucosyl hesperidin, is safe for the target population at the proposed uses and use levels.


TABLE 4. Specifications of the NF.

1723614705166442.png

TABLE 5. Food categories and maximum use levels intended by the applicant.

1723614755851257.png

Learn more: https://efsa.onlinelibrary.wiley.com/doi/10.2903/j.efsa.2024.8911


Need help or have a question?

Send mail