16 research outputs found
International Activities in Metrology in Chemistry
In today's economy goods and information are being exchanged globally, international travel is commonplace as is the cross-boarder transport of livestock and agricultural products, and this trend is set to continue. Just as important are issues that impinge on our quality of life, such
as health care, the environment and food quality. A strong international measurement and standards infrastructure is critical to assure equity in trade and a high quality of life, by ensuring that products and services meet their specifications. In the field of chemical measurements, certified
reference materials (CRMs), measurement standards and reference measurement results provide stated references upon which analytical laboratories can anchor their measurement results. The traceability of measurement results to internationally accepted stated references, together with their
stated measurement uncertainties, as described in ISO/IEC 17025, provides the basis for their comparability and global acceptance. Recent global activities which are succeeding in developing a system for the international acceptance of chemical measurements are described, notably: activities
of the National Metrology Institutes and the BIPM; the Mutual Recognition Arrangement of the International Committee of Weights and Measures (CIPM MRA) for National Calibration Certificates and Measurement Capabilities; the Inter-Laboratory Comparisons organised through the working groups
of the Consultative Committee for Amount of Substance – Metrology in Chemistry (CCQM), and the activities of the Joint Committee for Traceability in Laboratory Medicine (JCTLM)
CCQM-K90, formaldehyde in nitrogen, 2 μmol mol− 1 Final report
The CCQM-K90 comparison is designed to evaluate the level of comparability of national metrology institutes (NMI) or designated institutes (DI) measurement capabilities for formaldehyde in nitrogen at a nominal mole fraction of 2 μmol mol−1.
The comparison was organised by the BIPM using a suite of gas mixtures prepared by a producer of specialty calibration gases. The BIPM assigned the formaldehyde mole fraction in the mixtures by comparison with primary mixtures generated dynamically by permeation coupled with continuous weighing in a magnetic suspension balance. The BIPM developed two dynamic sources of formaldehyde in nitrogen that provide two independent values of the formaldehyde mole fraction: the first one based on diffusion of trioxane followed by thermal conversion to formaldehyde, the second one based on permeation of formaldehyde from paraformaldehyde contained in a permeation tube.
Two independent analytical methods, based on cavity ring down spectroscopy (CRDS) and Fourier transform infrared spectroscopy (FTIR) were used for the assignment procedure.
Each participating institute was provided with one transfer standard and value assigned the formaldehyde mole fraction in the standard based on its own measurement capabilities.
The stability of the formaldehyde mole fraction in transfer standards was deduced from repeated measurements performed at the BIPM before and after measurements performed at participating institutes. In addition, 5 control standards were kept at the BIPM for regular measurements during the course of the comparison.
Temporal trends that approximately describe the linear decrease of the amount-of-substance fraction of formaldehyde in nitrogen in the transfer standards over time were estimated by two different mathematical treatments, the outcomes of which were proposed to participants. The two treatments also differed in the way measurement uncertainties arising from measurements performed at the BIPM were propagated to the uncertainty of the trend parameters, as well as how the dispersion of the dates when measurements were made by the participants was taken into account.
Upon decision of the participants, the Key Comparison Reference Values were assigned by the BIPM using the largest uncertainty for measurements performed at the BIPM, linear regression without weight to calculate the trend parameters, and not taking into account the dispersion of dates for measurements made by the participant. Each transfer standard was assigned its own reference value and associated expanded uncertainty. An expression for the degree of equivalence between each participating institute and the KCRV was calculated from the comparison results and measurement uncertainties submitted by participating laboratories. Results of the alternative mathematical treatment are presented in annex of this report
Report of the CCU/CCQM Workshop on “The Metrology of Quantities Which Can Be Counted”
This article provides a report of the recent workshop on “The metrology of quantities which can be counted” organised jointly by the International Committee for Weights and Measures’ Consultative Committees for Amount of Substance (CCQM) and for Units (CCU). The workshop aimed to trigger a discussion on counting and number quantities across the metrological community so that a common understanding of counting and a common nomenclature could be achieved and there was clarity on the differences between these increasingly important concepts. This article details the background to the workshop, provides a summary of the presentations given and the discussions on the topics raised. It also reports the conclusions, agreed actions and next steps resulting from the workshop
Overcoming challenges regarding reference materials and regulations that influence global standardization of medical laboratory testing results
Background Standardized results for laboratory tests are particularly important when their interpretation depends on fixed medical practice guidelines or common reference intervals. The medical laboratory community has developed a roadmap for an infrastructure to achieve standardized test results described in the International Organization for Standardization standard 17511:2020 In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples. Among the challenges to implementing metrological traceability are the availability of fit-for-purpose matrix-based certified reference materials (CRMs) and requirements for regulatory review that differ among countries. A workshop in December 2021 focused on these two challenges and developed recommendations for improved practices. Discussion The participants agreed that prioritization of measurands for standardization should be based on their impact on medical decisions in a clinical pathway. Ensuring that matrix-based CRMs are globally available for more measurands will enable fit-for-purpose calibration hierarchies for more laboratory tests. Regulation of laboratory tests is important to ensure safety and effectiveness for the populations served. Because regulations are country or region specific, manufacturers must submit recalibration changes intended to standardize results for regulatory review to all areas in which a measuring system is marketed. Recommendations A standardization initiative requires collaboration and planning among all interested stakeholders. Global collaboration should be further developed for prioritization of measurands for standardization, and for coordinating the production and supply of CRMs worldwide. More uniform regulatory submission requirements are desirable when recalibration is implemented to achieve internationally standardized results
Impurity determination for hepcidin by liquid chromatography-high resolution and ion mobility mass spectrometry for the value assignment of candidate primary calibrators
State-of-the-art and trends for the SI traceable value assignment of the purity of peptides using the model compound angiotensin I
CCQM-K120 (Carbon dioxide at background and urban level)
CCQM-K120.a comparison involves preparing standards of carbon dioxide in air which are fit for purpose for the atmospheric monitoring community, with stringent requirements on matrix composition and measurement uncertainty of the CO2 mole fraction. This represents an analytical challenge and is therefore considered as a Track C comparison. The comparison will underpin CMC claims for CO2 in air for standards and calibrations services for the atmospheric monitoring community, matrix matched to real air, over the mole fraction range of 250 μmol/mol to 520 μmol/mol.
CCQM-K120.b comparison tests core skills and competencies required in gravimetric preparation, analytical certification and purity analysis. It is considered as a Track A comparison. It will underpin CO2 in air and nitrogen claims in a mole fraction range starting at the smallest participant's reported expanded uncertainty and ending at 500 mmol/mol. Participants successful in this comparison may use their result in the flexible scheme and underpin claims for all core mixtures
This study has involved a comparison at the BIPM of a suite of 44 gas standards prepared by each of the participating laboratories. Fourteen laboratories took part in both comparisons (CCQM-K120.a, CCQM-K120.b) and just one solely in the CCQM-K120.b comparison.
The standards were sent to the BIPM where the comparison measurements were performed. Two measurement methods were used to compare the standards, to ensure no measurement method dependant bias: GC-FID and FTIR spectroscopic analysis corrected for isotopic variation in the CO2 gases, measured at the BIPM using absorption laser spectroscopy. Following the advice of the CCQM Gas Analysis Working Group, results from the FTIR method were used to calculate the key comparison reference values