Dybdahl Marianne, Selesko David Benjamin, Mikkelsen Ulla Ramer
SAXOCON A/S, Bredevej 2D, 2830, Virum, Denmark.
Arla Foods Ingredients Group P/S, Soenderhoej 10, 8260, Viby J, Denmark.
Toxicol Rep. 2021 Mar 19;8:617-626. doi: 10.1016/j.toxrep.2021.03.012. eCollection 2021.
The safety of Lacprodan® BLG, a whey-based protein, was evaluated with respect to genotoxicity and sub-chronic toxicity according to regulatory requirements. Lacprodan® BLG did not show any mutagenic potential in a bacterial reverse mutation assay or any clastogenic or aneugenic potential in an micronucleus assay performed in human lymphocytes. In a sub-chronic toxicity study, groups of 10 male and 10 female Wistar rats received the test item orally by gavage for 90 days at dose levels of 100, 300 and 1000 mg/kg bw/day. A control group, also including 10 male and 10 female rats, received sterile water, as vehicle. No treatment-related clinical observations or toxicological effects on body or organ weights, food consumption, ophthalmic effects, hematology, clinical chemistry, fertility, urinalysis, or pathology were identified. Therefore, the no-observed-adverse-effect level (NOAEL) for Lacprodan® BLG in the 90-day toxicity study was established as 1000 mg/kg bw/day, corresponding to the highest dose level administered.
根据监管要求,对基于乳清的蛋白质Lacprodan® BLG的遗传毒性和亚慢性毒性进行了安全性评估。在细菌回复突变试验中,Lacprodan® BLG未显示出任何致突变潜力;在人淋巴细胞微核试验中,也未显示出任何染色体断裂或非整倍体诱导潜力。在一项亚慢性毒性研究中,每组10只雄性和10只雌性Wistar大鼠以100、300和1000 mg/kg体重/天的剂量水平经口灌胃给予受试物90天。一个同样包括10只雄性和10只雌性大鼠的对照组接受无菌水作为赋形剂。未发现与处理相关的临床观察结果,也未发现对体重、器官重量、食物消耗、眼科效应、血液学、临床化学、生育力、尿液分析或病理学的毒理学影响。因此,在90天毒性研究中,Lacprodan® BLG的未观察到不良反应水平(NOAEL)确定为1000 mg/kg体重/天,相当于所给予的最高剂量水平。