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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Correcting Measurement Errors Using Reference Materials in Method Validation
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Correcting Measurement Errors Using Reference Materials in Method Validation

机译:在方法验证中使用参考材料校正测量误差

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Quality assurance and method validation are needed to reduce false decisions due to measurement errors. In this context accuracy and standard uncertainty for the analytical method need to be considered to ensure that the performance characteristics of the method are understood. Therefore, analytical methods ought to be validated before implementation and controlled on a regular basis during usage. For this purpose reference materials (RMs) are useful to determine the performance characteristics of methods under development. These performance parameters may be documented in the light of a method evaluation study and the documentation related to international standards and guidelines. In a method evaluation study of Pb in blood using reference samples from the Laboratoire Toxicologie du Quebec, Canada, a difference between the systematic errors was observed using a Perkin-Elmer Model 5100 atomic absorption spectrometer and a Perkin-Elmer Model 4100 atomic absorption spectrometer, both with Zeeman background correction. For measurement of blood samples, the performance parameters obtained in the method evaluation studies, i.e. slopes and intercepts of the method evaluation function (MEF), were intended to be used for correcting the systematic errors. However, the number of MEF samples was insufficient to produce an acceptable SD for the MEF slopes to be used for correction. In a method evaluation study on valproate in plasma using the SYVA's EMIT assay on COBAS MIRA S a significant systematic error above the concentration 300 mmol dm"3 was demonstrated (slope 0.9541) and consequently the slope was used for correction of results. For analytes, where certified RMs (CRMs) exist, a systematic error of measurements can be reduced by correcting errors by assessment of the trueness as recommended in international guidelines issued by ISO or the National Institute of Standards and Technology (NIST). When possible, the analysis of several RMs, covering the concentration range of interest, is the most useful way to investigate measurement bias. Unfortunately, until recently only few RMs existed and only few had been produced and certified by specialized organizations such as NIST or the Standards, Measurements and Testing (SMT, previously BCR) programme. Due to the lack of such RMs, network organizations are nowadays established with the aim of supporting the correct use and production of high-quality CRMs.
机译:需要质量保证和方法验证,以减少由于测量错误引起的错误决策。在这种情况下,需要考虑分析方法的准确性和标准不确定性,以确保了解该方法的性能特征。因此,分析方法应在实施之前进行验证,并在使用过程中定期进行控制。为此,参考材料(RM)可用于确定正在开发的方法的性能特征。这些性能参数可以根据方法评估研究以及与国际标准和指南相关的文件进行记录。在使用加拿大魁北克实验室实验室的参考样品进行的血液中铅的方法评估研究中,使用Perkin-Elmer 5100型原子吸收光谱仪和Perkin-Elmer 4100型原子吸收光谱仪观察到系统误差之间的差异,两者均采用塞曼背景校正。为了测量血样,在方法评估研究中获得的性能参数,即方法评估功能(MEF)的斜率和截距,旨在用于校正系统误差。但是,MEF样本的数量不足以产生用于校正的MEF斜率的可接受的SD。在SYVA的EMIT分析中,在COBAS MIRA S上对血浆中丙戊酸的方法评价研究中,证明了浓度超过300 mmol dm·3时存在明显的系统误差(斜率0.9541),因此该斜率用于校正结果。对于分析物,如果存在经过认证的RM(CRM),则可以按照ISO或美国国家标准技术研究院(NIST)发布的国际准则中的建议,通过评估真实性来纠正误差,从而减少系统的测量误差。几个涵盖目标浓度范围的RM是调查测量偏差的最有用方法。不幸的是,直到最近,RM才存在,并且只有少数NRM或NIST或“标准,测量和测试”( SMT(以前称为BCR)计划。由于缺少此类RM,因此如今建立了网络组织,旨在支持相应的功能。 ct使用和生产高质量的CRM。

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