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Safety in use of glucosylated steviol glycosides as a food additive in different food categories

机译:在不同食品类别中使用糖基甜菊醇糖苷作为食品添加剂的安全性

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The EFSA Panel on Food Additives and Nutrient Sources added to Food (ANS) provides a scientific opinion on the safety of glucosylated steviol glycosides proposed for use as a new food additive in different food categories. According to the applicant, glucosylated steviol glycosides preparations consist of not less than 95% (on anhydrous basis) total steviol glycosides, made up of glucosylated steviol glycosides of different molecular weights as well as any remaining steviol glycosides. The applicant proposed that glucosylated steviol glycosides and parent steviol glycosides undergo a common metabolic process in pathway following ingestion and suggested that data from steviol glycosides can be used for read‐across to glucosylated steviol glycosides. The limited evidence provided in the application dossier did not demonstrate the complete hydrolysis of the glucosylated steviol glycosides. No toxicological studies on glucosylated steviol glycoside preparations under evaluation have been provided for its assessment. The Panel concluded that the submitted data are insufficient to assess the safety of the glucosylated steviol glycoside preparations to be used as a new food additive.
机译:食品中添加的EFSA食品添加剂和营养来源专家组(ANS)对提议用作不同食品类别的新型食品添加剂的糖基甜菊醇糖苷的安全性提供了科学见解。申请人认为,葡糖基化甜菊糖苷制剂包括不少于95%(以无水为基础)的总甜菊糖苷,由不同分子量的葡糖基化甜菊糖苷以及任何剩余的甜菊糖苷组成。申请人提出,糖基甜菊醇糖苷和母体甜菊糖苷在摄入后会经历一个共同的代谢过程,并建议将甜菊糖苷的数据用于对糖基甜菊糖苷的重新读取。本申请档案中提供的有限证据并未证明糖基化甜菊糖苷的完全水解。评估中未提供对糖基甜菊醇糖苷制剂的毒理研究。专家小组得出结论,所提交的数据不足以评估用作新食品添加剂的糖基甜菊醇糖苷制剂的安全性。

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