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建立医学实验室中小分子测量指标的计量溯源性。

Establishing metrological traceability for small molecule measurands in laboratory medicine.

机构信息

Labordiagnostic St. Gallen West AG, St. Gallen, Switzerland.

Institute of Pharmacy, CCB - Centrum of Chemistry and Biomedicine, CMBI - Center for Molecular Biosciences, University of Innsbruck, Innsbruck, Austria.

出版信息

Clin Chem Lab Med. 2023 Jan 9;61(11):1890-1901. doi: 10.1515/cclm-2022-0995. Print 2023 Oct 26.

Abstract

For molecules that can be well described metrologically in the sense of the definition of measurands, and which can also be recorded analytically as individual substances, reference measurement service traceability to a metrologically sound foundation is a necessity. The establishment of traceability chains must be initiated by National Metrology Institutes (NMIs) according to applicable standards; they are at the top and leading position in this concept. If NMIs are not in the position to take up this task, alternative approaches must be sought. Traceability initiatives established by device industry or academia must meet the quality standards of NMIs. Adherence to International Organization for Standardization (ISO) procedure 15193 must be a matter of course for the establishment of reference measurement procedures (RMPs). Certified reference material (CRM) characterization must be thorough, e.g., by the application of quantitative nuclear magnetic resonance measurements and by adherence to ISO 15194. Both for RMPs and CRMs Joint Committee for Traceability in Laboratory Medicine (JCTLM) listing must be the ultimate goal. Results must be shared in a transparent manner to allow other stakeholders including NMIs to reproduce and disseminate the reference measurement procedures.

摘要

对于那些在可测量的定义意义上可以得到很好的计量描述、并且可以作为单个物质进行分析记录的分子来说,参考测量服务向计量可靠基础的可追溯性是必要的。可追溯链的建立必须由国家计量院(NMIs)根据适用标准发起;它们在这个概念中处于最高和领导地位。如果 NMIs 无法承担这项任务,就必须寻求替代方法。由设备行业或学术界发起的可追溯性计划必须符合 NMIs 的质量标准。参考测量程序(RMPs)的建立必须遵循国际标准化组织(ISO)程序 15193,这是理所当然的。对于参考物质(CRM)的特性描述,必须彻底,例如,应用定量核磁共振测量,并遵守 ISO 15194。对于 RMPs 和 CRMs,联合实验室医学可追溯性委员会(JCTLM)的清单必须是最终目标。结果必须以透明的方式共享,以使包括 NMIs 在内的其他利益相关者能够复制和传播参考测量程序。

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