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歐盟評(píng)估布枯油作為所有動(dòng)物飼料添加劑的安全性和有效性

來(lái)源:食品伙伴網(wǎng) 時(shí)間: 2022-03-10


202238日,,據(jù)歐盟食品安全局(EFSA)消息,,應(yīng)歐盟委員會(huì)要求,,歐盟動(dòng)物飼料添加劑和產(chǎn)品(FEEDAP)研究小組就布枯油 (buchu leaf oil)作為所有動(dòng)物飼料添加劑的安全性和有效性發(fā)表科學(xué)意見(jiàn),。

經(jīng)過(guò)評(píng)估,專家小組認(rèn)為在建議的使用條件下該添加劑對(duì)目標(biāo)物種和環(huán)境是安全的。由于其在飼料中的功能與在食品中的功能基本相同,,因此認(rèn)為沒(méi)有必要進(jìn)一步證明其功效,。

部分原文報(bào)道如下:

 

Following a request from the European Commission, the EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety and efficacy of an essential oil from the leaves of Agathosma betulina (P.J. Bergius) Pillans (buchu leaf oil), when used as a sensory additive (flavouring) in feed and water for drinking for all animal species. The FEEDAP Panel concluded that the essential oil under assessment is safe up to the maximum proposed use levels in complete feed of 0.1 mg/kg for chickens for fattening, 0.15 mg/kg for laying hens, turkeys for fattening and rabbits, 0.20 mg/kg for piglets, 0.25 mg/kg for pigs for fattening, 0.30 mg/kg for sows and dairy cows, 0.45 mg/kg for cattle for fattening, sheep, goats and horses, 0.5 for veal calves (milk replacer), fish, ornamental fish and dogs. For cats, the calculated maximum safe level in feed is 0.2 mg/kg complete feed. The FEEDAP Panel considered that the use in water for drinking is safe provided that the total daily intake of the additive does not exceed the daily amount that is considered safe when consumed via feed. No concerns for consumer safety were identified following the use of the additive up to the highest safe levels in feed. The essential oil under assessment should be considered as irritant to skin and eyes, and as a skin and respiratory sensitiser. The use of the additive in animal feed under the proposed conditions was not expected to pose a risk for the environment. Buchu leaf oil was recognised to flavour food. Since its function in feed would be essentially the same as that in food, no further demonstration of efficacy was considered necessary.