首页> 外文期刊>Macedonian Journal of Chemistry and Chemical Engineering >Study on th method performances for screening and confirmatory analysis of aflatoxin M1 in raw milk according to the mycotoxin regulative requirements
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Study on th method performances for screening and confirmatory analysis of aflatoxin M1 in raw milk according to the mycotoxin regulative requirements

机译:根据霉菌毒素法规要求对生乳中黄曲霉毒素M1进行筛选和确证分析的方法性能研究

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Screning and confirmatory methods for Aflatoxin M 1 (AFM 1 ) analysis were optimized and studied regarding the European Decision 2002/657/EC requirements. The recoveries of AFM 1 from the spiked samples at levels between 0.025 and 0.075 μg kg -1 were 99.6-110.3 % with obtained precision 10.5-13.4 %, confirming the immunochemical method precision and reliability for intensive surveillance studies. According to the regulatory requirements, for confirmation of the obtained positives from the screening, the reference high-performance liquid chromatographic method was evaluated in reference to the performance criteria. The obtained between-day recovery was in the range 67.2-72.8 %, and the precision range 5.4-9.1 %. 205 positives from the screening were subjected to confirmatory analysis. The comparison of the data obtained from the immunoassay and chromatographic method ( R 2 =0.764) revealed a slight overestimation of the screening method, but no cases of false-negative determinations occurred.
机译:黄曲霉毒素M 1(AFM 1)分析的筛选和确认方法已针对欧洲2002/657 / EC要求进行了优化和研究。在0.025和0.075μgkg -1之间的浓度下,加标样品中AFM 1的回收率为99.6-110.3%,精密度为10.5-13.4%,这证实了免疫化学方法在强化监视研究中的准确性和可靠性。根据法规要求,为了确认从筛选中获得的阳性结果,参照性能标准对参考高效液相色谱法进行了评估。获得的日间回收率在67.2-72.8%的范围内,精度在5.4-9.1%的范围内。筛选出的205名阳性患者进行了确认分析。从免疫分析和色谱法获得的数据进行比较(R 2 = 0.764)表明,该筛查方法略有高估,但未发生假阴性测定的情况。

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