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食用竹炭粉的安全性评估:90天亚慢性经口毒性和致突变性研究。

Safety assessment of dietary bamboo charcoal powder: a 90-day subchronic oral toxicity and mutagenicity studies.

作者信息

Zhenchao Jia, Yuting Zhong, Jiuming Yan, Yedan Lu, Yang Song, Jinyao Chen, Lishi Zhang

机构信息

West China School of Public Health, Sichuan University, No. 16, third section, South Renmin Road, Chengdu, Sichuan 610041, China.

West China School of Public Health, Sichuan University, No. 16, third section, South Renmin Road, Chengdu, Sichuan 610041, China; Food Safety Monitoring and Risk Assessment Key Laboratory of Sichuan Province, China.

出版信息

Food Chem Toxicol. 2015 Jan;75:50-7. doi: 10.1016/j.fct.2014.11.002. Epub 2014 Nov 13.

Abstract

Vegetable carbon has been used as food additive in EU (E153) and China for many years; however, no experimental data have been available on its dietary safety. This study was designed to evaluate the subchronic toxicity and genotoxicity of bamboo charcoal powder (BCP). In the study of subchronic oral toxicity, BCP was administered orally at doses of 2.81, 5.62, and 11.24 g/kg BW for 90 days to SD rats. Additional satellite groups from the control group and high dose group were observed for a 28-day recovery period. At the end of the treatment and recovery periods, animals were sacrificed, and their organs were weighed and blood samples were collected. The toxicological endpoints observed included clinical signs, food consumption, body and organ weights, hematological and biochemical parameters, macroscopic and microscopic examinations. The results showed no significant differences between the BCP treated groups and control group. The genotoxicity of BCP was assessed with the Salmonella typhimurium mutagenicity assay (Ames test) and a combination of comet assay and mammalian erythrocyte micronucleus protocol. The results did not reveal any genotoxicity of BCP. Based on our study, the no-observed-adverse-effect level (NOAEL) for BCP is 11.24 g/kg BW/day.

摘要

多年来,植物炭黑在欧盟(E153)和中国一直被用作食品添加剂;然而,尚无关于其饮食安全性的实验数据。本研究旨在评估竹炭粉(BCP)的亚慢性毒性和遗传毒性。在亚慢性经口毒性研究中,将BCP以2.81、5.62和11.24 g/kg体重的剂量经口给予SD大鼠90天。从对照组和高剂量组中选取额外的卫星组,观察28天的恢复期。在治疗期和恢复期结束时,处死动物,称量其器官重量并采集血样。观察的毒理学终点包括临床症状、食物消耗、体重和器官重量、血液学和生化参数、大体和显微镜检查。结果显示,BCP处理组与对照组之间无显著差异。采用鼠伤寒沙门氏菌致突变试验(Ames试验)以及彗星试验和哺乳动物红细胞微核试验组合评估BCP的遗传毒性。结果未显示BCP有任何遗传毒性。基于我们的研究,BCP的未观察到有害作用水平(NOAEL)为11.24 g/kg体重/天。

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