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首页> 外文期刊>Accreditation and quality assurance >Provision of proficiency testing for histamine mass fraction in canned tuna to improve the capability of chemical laboratories in the Philippines
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Provision of proficiency testing for histamine mass fraction in canned tuna to improve the capability of chemical laboratories in the Philippines

机译:罐装金枪鱼中组胺质量分数的能力检测,以提高菲律宾化学实验室的能力

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摘要

In this work, two reference materials (RMs) for mass fraction of histamine in canned tuna were developed to address the need of local testing laboratories for matrix RMs and a PT scheme for histamine. A validated method using HPLC with fluorescence detector (340nm for excitation and 445nm for emission) was applied with post-column derivatization for the RM's homogeneity and stability studies. Acceptable results were obtained after statistical evaluation of homogeneity and stability according to IUPAC Harmonized Protocol and ISO Guide 35, respectively. Two PT exercises for histamine determination based on ISO/IEC 17043 were organized in 2014 and 2015 with the assigned values of 148 and 65mg/kg, respectively. These reference values were obtained using exact matching liquid chromatography-isotope dilution mass spectrometry (LC-IDMS) with gravimetric sample preparation. The corresponding uncertainty of the reference value was obtained by ISO GUM approach where the characterization of the sample gave the highest contribution (41%). The satisfactory z-score performance evaluated from the 12 laboratories was 50% and 58.3% in the first and second PT round, respectively. Most of the laboratories used AOAC Official Method 977.13 but not all conducted method validation. The 50% decrease in unsatisfactory results in the second PT round is a significant improvement in the local laboratory performance for histamine analysis. However, the provision of more PT schemes and the increased use of CRMs in the future are still needed by these laboratories for external quality assurance and method validation to enhance the present capability.
机译:在这项工作中,开发了两种用于组胺的组胺的参考材料(RMS),以解决局部测试实验室的基质RMS和组胺的PT方案的需要。使用HPLC具有荧光检测器的验证方法(用于激发340nm,发射445nm),具有用于RM的均匀性和稳定性研究的柱柱衍生化。根据Iupac协调方案和ISO指南35分别在统计统计评估后获得可接受的结果。基于ISO / IEC 17043的两种PT练习为2014年和2015年组织,分别为148%和65mg / kg的分配值。使用精确匹配的液相色谱 - 同位素稀释质谱(LC-IDMS)获得这些参考值,以重量样品制备。参考值的相应不确定度是通过ISO胶质方法获得的,其中样品的表征给出了最高贡献(41%)。从12个实验室评估的令人满意的Z评分性能分别在第一和第二PT圆形中的50%和58.3%。大多数实验室使用了AOAC官方方法977.13但并非所有进行的方法验证。第二PT循环中不令人满意的结果下降50%,是组胺分析局部实验室性能的显着改善。然而,这些实验室仍然需要提供更多PT方案和增加CRM的使用,以便外部质量保证和方法验证,以提高目前的能力。

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