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一套定量核磁共振内标物的独立认证:确保在广泛应用中的计量溯源性。

Independent certification of a suite of qNMR internal standards: ensuring metrological traceability in a wide range of applications.

作者信息

Wollinger Wagner, Fernandes Jane Luiza Nogueira, do Rego Eliane Cristina Pires, de Aquino Neto Francisco Radler, Garrido Bruno Carius

机构信息

Divisão de Metrologia Química, Laboratório de Análise Orgânica, Instituto Nacional de Metrologia, Qualidade E Tecnologia (Inmetro), 50 N. Sra. das Graças Av., Duque de Caxias, RJ, 25250-020, Brazil.

Universidade Federal Do Rio de Janeiro (UFRJ), Instituto de Química, LADETEC, 1281 Horácio Macedo Av., Rio de Janeiro, RJ, 21941-598, Brazil.

出版信息

Anal Bioanal Chem. 2025 May;417(12):2473-2487. doi: 10.1007/s00216-024-05671-5. Epub 2024 Nov 29.

Abstract

The Brazilian National Metrology Institute produced a suite of certified reference materials (CRMs) intended as internal standards (ISs) for quantitative nuclear magnetic resonance (qNMR). Being a ratio primary method, the use of qNMR in organic chemistry has already crossed the borders of research laboratories, despite the cost of instrumentation. The International Bureau of Weights and Measures (BIPM) proposed eight potential qNMR ISs. Four candidate materials were selected for their solubility in various solvents and distinct chemical shifts, making them suitable for qNMR analysis of diverse analytes. The certification process compared orthogonal primary methods such as mass balance, qNMR, freezing-point depression, and coulometry, to ensure independent value assignment. Different approaches were compared to assess batch homogeneity and stability. While directly comparing the main compound's chromatographic area proved to be a quick and fit-for-purpose approach, the determination of individual impurities provided lower uncertainties but required more laborious work. CRM batches of maleic acid, dimethyl sulfone, potassium hydrogen phthalate, and dimethyl terephthalate were delivered with over 999.8 mg g purity and uncertainty in the range of 0.6 to 3 mg g (k = 2). The literature shows certification procedures for qNMR ISs whose traceability chain is exclusively based on qNMR measurements. As opposed to that, the methodology presented here provides robust certified values assigned by methods independent of qNMR, in accordance with BIPM recommendations and less prone to qNMR biases. The CRMs developed in this work have already been used for SI-traceable purity evaluation of compounds such as drugs and pesticides, by laboratories in Brazil and abroad.

摘要

巴西国家计量研究所制备了一套认证参考物质(CRM),用作定量核磁共振(qNMR)的内标(IS)。作为一种比率基本方法,尽管仪器成本高昂,但qNMR在有机化学中的应用已经跨越了研究实验室的范畴。国际计量局(BIPM)提出了八种潜在的qNMR内标。选择了四种候选物质,因其在各种溶剂中的溶解性和独特的化学位移,使其适用于多种分析物的qNMR分析。认证过程比较了质量平衡、qNMR、冰点降低和库仑法等正交基本方法,以确保独立赋值。比较了不同方法来评估批次均匀性和稳定性。虽然直接比较主要化合物的色谱面积被证明是一种快速且适用的方法,但测定单个杂质的不确定性较低,但需要更繁琐的工作。马来酸、二甲基砜、邻苯二甲酸氢钾和对苯二甲酸二甲酯的CRM批次以纯度超过999.8 mg/g且不确定度在0.6至3 mg/g范围内(k = 2)交付。文献显示了qNMR内标的认证程序,其溯源链仅基于qNMR测量。与此相反,本文提出的方法根据BIPM的建议,通过独立于qNMR的方法提供可靠的认证值,且不易受到qNMR偏差的影响。这项工作中开发的CRM已经被巴西和国外的实验室用于对药物和农药等化合物进行可溯源至国际单位制(SI)的纯度评估。

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