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Scientific Opinion on the revised exposure assessment of steviol glycosides (E 960) for the proposed uses as a food additive

机译:关于对拟用作食品添加剂的甜菊醇糖苷的修订暴露评估(E 960)的科学意见

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Following a request from the European Commission, the European Food Safety Authority (EFSA) carried out an exposure assessment of steviol glycosides (E 960) from its use as a food additive, taking into account the proposed extension of uses. In 2010, the EFSA Panel on Food Additives and Nutrient Sources added to Food (ANS) adopted a scientific opinion on the safety of steviol glycosides (E 960) and established an Acceptable Daily Intake (ADI) of 4 mg/kg body weight (bw) per day. Conservative estimates of exposure, both in adults and children, suggested that it is likely that the ADI would be exceeded at the maximum proposed use level. In 2011, EFSA carried out a revised exposure assessment for steviol glycosides based on revised proposed uses and concluded that high level dietary exposure in children may still exceed the ADI. The current refined exposure estimates are based on the currently authorised uses, the proposed extension, and the EFSA Comprehensive Food Consumption Database. The mean dietary exposure to steviol glycosides ranges from 0.1 mg/kg bw/day in adults and the elderly, to 2.4 mg/kg bw/day in toddlers. Estimates at the 95~(th) percentile of exposure range from 0.3 to 4.3 mg/kg bw/day in the elderly and toddlers, respectively. The Panel concluded that dietary exposure to steviol glycosides is considerably lower than that in the previous exposure assessment. Overall, the revised exposure estimates for all age groups remain below the ADI, except for toddlers at the upper range of the high level (95~(th) percentile) estimates, in one country. Moreover, the Panel noted that table top sweeteners may represent an important source of exposure and therefore a MPL with a numerical value, rather than quantum satis , would be preferable, to allow for a more precise estimation of the potential maximum level of exposure from table top sweeteners.
机译:应欧洲委员会的要求,欧洲食品安全局(EFSA)考虑到拟议的用途扩展,对甜菊糖苷作为食品添加剂的使用进行了暴露评估(E 960)。 2010年,欧洲食品安全局(EFSA)向食品中添加的食品添加剂和营养来源专家小组(ANS)通过了关于甜菊糖苷安全性的科学意见(E 960),并确定了4 mg / kg体重(bw)的每日可接受摄入量(ADI) ) 每天。保守估计成人和儿童的接触量均表明,在最大建议使用量下可能会超过ADI。在2011年,欧洲食品安全局(EFSA)根据修订后的拟议用途对甜菊糖苷进行了修订后的暴露评估,并得出结论,儿童的高饮食摄入量仍可能超过每日允许摄入量(ADI)。当前的精确暴露估算基于当前的授权用途,拟议的扩展范围和EFSA综合食品消费数据库。饮食中甜菊糖苷的平均饮食暴露量从成人和老年人的0.1 mg / kg bw /天到幼儿的2.4 mg / kg bw /天。估计老年人和幼儿的第95%暴露量分别为0.3至4.3 mg / kg bw /天。专家小组的结论是,饮食中对甜菊糖苷的饮食摄入量大大低于先前的接触评估。总体而言,一个国家所有年龄组的修订暴露估计值均低于ADI,但高水平估计值(95%)的幼儿除外。此外,小组指出,台式甜味剂可能是暴露的重要来源,因此,最好使用具有数字值而不是令人满意的量子点的MPL,以便更精确地估算其潜在最大含量。桌面甜味剂的暴露。

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