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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Using high-performance ~1H NMR (HP-qNMR?) for the certification of organic reference materials under accreditation guidelines-Describing the overall process with focus on homogeneity and stability assessment
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Using high-performance ~1H NMR (HP-qNMR?) for the certification of organic reference materials under accreditation guidelines-Describing the overall process with focus on homogeneity and stability assessment

机译:根据认可指南,使用高性能〜1H NMR(HP-qNMR?)认证有机参考物质-描述整个过程,着重于均质性和稳定性评估

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摘要

Quantitative NMR spectroscopy (qNMR) is gaining interest across both analytical and industrial research applications and has become an essential tool for the content assignment and quantitative determination of impurities.The key benefits of using qNMR as measurement method for the purity determination of organic molecules are discussed, with emphasis on the ability to establish traceability to "The International System of Units" (SI). The work describes a routine certification procedure from the point of view of a commercial producer of certified reference materials (CRM) under ISO/IEC 17025 and ISO Guide 34 accreditation, that resulted in a set of essential references for ~1H qNMR measurements, and the relevant application data for these substances are given. The overall process includes specific selection criteria, pre-tests, experimental conditions, homogeneity and stability studies. The advantages of an accelerated stability study over the classical stability-test design are shown with respect to shelf-life determination and shipping conditions.
机译:定量NMR光谱法(qNMR)在分析和工业研究应用中都引起了人们的兴趣,已成为杂质含量分配和定量测定的重要工具。讨论了将qNMR用作测定有机分子纯度的测量方法的主要好处,着重于建立对“国际单位制”(SI)的追溯能力。这项工作从ISO / IEC 17025和ISO Guide 34认证下的认证参考材料(CRM)的商业生产商的角度描述了一种常规认证程序,该认证过程为〜1 H qNMR测量提供了一组基本参考,并且给出了这些物质的相关应用数据。整个过程包括特定的选择标准,预测试,实验条件,均质性和稳定性研究。就保质期确定和运输条件而言,已显示出加速稳定性研究优于经典稳定性测试设计的优势。

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