Van Egmond H P
Laboratory for Residue Analysis, National Institute of Public Health and Environmental Protection, Bilthoven, The Netherlands.
Food Addit Contam. 1993 Jan-Feb;10(1):29-36. doi: 10.1080/02652039309374127.
Currently, more than 50 countries have enacted or proposed regulations for mycotoxins in food and feed. There are various factors that may influence the establishment of tolerances for certain mycotoxins, such as the availability of toxicological data, the availability of data on dietary exposure, the distribution of mycotoxins over commodities, legislation of other countries with which trade contacts exist, and the availability of methods of analysis. In practice, only few countries have formally presented the rationale for the need to regulate, or for the selection of a particular maximum tolerated level, as a recent international enquiry demonstrated. Most of the limits for aflatoxins in food were based on rather vague statements of the carcinogenic risk for humans. There was a general consensus that exposure to a potential human carcinogen that could not be totally avoided should be limited to the lowest practical level. Several countries made a claim to a hazard evaluation (Belgium, Canada, India, The Netherlands, Switzerland, South Africa, United Kingdom, United States), although specifics were rather scarce. No rationales for setting limits for other mycotoxins were provided, except for Canada, where risk assessment was done for deoxynivalenol, zearalenone and ochratoxin A. It is apparent that in most countries either the scientific basis for regulation of mycotoxins is non-existent, or the science has not been fully utilized.
目前,50多个国家已经颁布或提议了食品和饲料中霉菌毒素的相关法规。有多种因素可能会影响某些霉菌毒素耐受量的设定,比如毒理学数据的可获取性、膳食暴露数据的可获取性、霉菌毒素在各类商品中的分布情况、与本国存在贸易往来的其他国家的立法情况以及分析方法的可获取性。实际上,正如最近一项国际调查所显示的,只有少数国家正式阐述了进行监管的必要性或选择特定最大耐受水平的理由。食品中黄曲霉毒素的大多数限量是基于对人类致癌风险相当模糊的表述。人们普遍达成共识,即对于无法完全避免的潜在人类致癌物,其暴露量应限制在最低实际水平。一些国家(比利时、加拿大、印度、荷兰、瑞士、南非、英国、美国)要求进行危害评估,不过具体细节相当匮乏。除了加拿大对脱氧雪腐镰刀菌烯醇、玉米赤霉烯酮和赭曲霉毒素A进行了风险评估外,其他霉菌毒素设定限量的理由均未给出。显然,在大多数国家,要么不存在监管霉菌毒素的科学依据,要么就是科学依据未得到充分利用。