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QUALITY ASSURANCE IN MYCOTOXIN ANALYSIS

机译:霉菌毒素分析的质量保证

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摘要

Mycotoxin analysis in food and biological fluids is receiving more and more concern, in view also of increasing involvement by the European Union regarding legislation. Basically all the analytical steps regarding mycotoxin analysis have to be performed according to accurate criteria which are strictly connected to the quality of results in terms of reliability. The only rationale for reducing this difficulty is to apply quality assurance principles. Quality assurance principles define, in fact, the rules to be observed for performing this analysis with a degree of uncertainty that is as low as may be possible. In particular sampling techniques, if carried out improperly, give rise to uncertainty concerning the representativeness of samples that is so critical as to induce a dramatic source of errors in the final analysis. Therefore it seems appropriate to plan training courses for personnel on the various side-effects related to the available sampling and subsampling techniques depending on the commodity. Other contributions to the overall error derive from improper methodologies used by technicians in the pre-treatment step of the samples (incorrect use of glassware, standard solutions, etc.), and finally from the operations involved in the whole analytical procedure. In addition, the use of reference materials and certified reference materials together with the utilization of validated methods of analysis will be dealt with as concrete procedures for obtaining the certainty of final results of good quality. This aspect takes on a relevant outcome if applied to official control activities from authorized bodies acting at a national level. (C) 1996 Academic Press, Inc. [References: 5]
机译:鉴于欧洲联盟越来越多地参与立法,食品和生物体液中的霉菌毒素分析越来越受到关注。基本上,所有有关霉菌毒素分析的分析步骤都必须根据准确的标准执行,就可靠性而言,这些标准与结果的质量严格相关。减少这种困难的唯一理由是应用质量保证原则。实际上,质量保证原则定义了要执行的分析要遵循的规则,其不确定性程度应尽可能低。在特定的采样技术中,如果执行不当,会导致有关样品代表性的不确定性,这一不确定性至关重要,以至于在最终分析中引起巨大的误差来源。因此,似乎计划针对人员计划培训课程,这些培训涉及与取决于商品的可用采样和二次采样技术相关的各种副作用。造成总误差的其他原因还在于技术人员在样品的预处理步骤中使用的方法不正确(玻璃器皿,标准溶液等的使用不正确),最后是整个分析过程中涉及的操作。此外,参考材料和认证参考材料的使用以及经过验证的分析方法的使用,将作为获得确定的高质量最终结果的具体程序进行处理。如果将其应用于国家一级授权机构的官方控制活动,这方面将产生重要的结果。 (C)1996 Academic Press,Inc. [参考:5]

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