Combining method validation data with additional information for measurement uncertainty evaluation - determination of melatonin content in tea.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-10-28 DOI:10.1039/d4ay01468e
Lucía Gutiérrez-Fernández, Cristina M Oliveira, Ana M Díez-Pascual, María Paz San Andrés, Ricardo J N Bettencourt da Silva
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Abstract

The evaluation of measurement uncertainty involves combining available experimental data with additional knowledge on the impact of sources of uncertainty on the measured value to quantify combined uncertainty. This uncertainty should express the impact of relevant random and systematic effects on the measured value to allow an objective interpretation of the performed quantification. This research discusses how to assess and account for the impact on measurement uncertainty evaluation of uncontrolled high temperature of sample preparation and of supporting experimental validation data on a single calibration of the instrumental method of analysis used. After the detailed inspection of the measurand and measurement process, the various uncertainty components were quantified from experimental data and/or additional information. This research illustrates that experimental limitations can be overcome by a detailed and quantitative understanding of the measurement process. Melatonin content in tea was quantified between 3.7 g kg-1 and 196 g kg-1 with a relative expanded uncertainty between 28% and 40%, lower than the target or maximum admissible relative expanded uncertainty of 40%. The use of HPLC-FD calibration several days before sample analysis is the major uncertainty component responsible for up to 82.7% of the measurement uncertainty.

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将方法验证数据与用于测量不确定性评估的附加信息相结合--测定茶叶中的褪黑素含量。
测量不确定性的评估涉及将可用的实验数据与不确定性来源对测量值影响的其他知识相结合,以量化综合不确定性。这种不确定性应表达相关随机和系统效应对测量值的影响,以便对所进行的量化进行客观解释。本研究讨论了如何评估和说明样品制备过程中不受控制的高温对测量不确定度评估的影响,以及对所用仪器分析方法单一校准的支持性实验验证数据的影响。在对测量材料和测量过程进行详细检查后,根据实验数据和/或其他信息对各种不确定性成分进行了量化。这项研究表明,通过对测量过程进行详细和定量的了解,可以克服实验上的局限性。茶叶中褪黑素含量的定量范围在 3.7 g kg-1 至 196 g kg-1 之间,相对扩展不确定度在 28% 至 40% 之间,低于 40% 的目标或最大允许相对扩展不确定度。在样品分析前几天使用高效液相色谱-荧光定量法进行校准是造成测量不确定度高达 82.7% 的主要不确定因素。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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