Development of a new taurine purity certified reference material

In this work, a new taurine purity CRM (GBW(E)100594) was developed based on the principles of the ISO Guide. The whole procession included sample preparation, structural analysis, homogeneity assessment, stability study, characterization and uncertainty assessment. The CRM was purified by recrystal...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Microchemical journal 2022-10, Vol.181, p.107761, Article 107761
Hauptverfasser: Chen, Weizhu, Jin, Wenhui, Fang, Hua, Chen, Hui, Chen, Xiaoying, Zhang, Yiping, Hong, Zhuan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:In this work, a new taurine purity CRM (GBW(E)100594) was developed based on the principles of the ISO Guide. The whole procession included sample preparation, structural analysis, homogeneity assessment, stability study, characterization and uncertainty assessment. The CRM was purified by recrystallization from commercial taurine. The purity of the CRM was verified through q NMR and MB methods. The purity was 99.8 % with a relative expanded uncertainty of 0.6 % (k = 2) at a confidence level of 95 %. [Display omitted] •A new purity certified reference material (CRM) of taurine (GBW(E)100594) was developed.•Mass balance method and q NMR were simultaneously used for certification of the CRM.•A highly sensitive HPLC-UV with pre‐column derivatization was developed to determine the main content of the CRM.•Homogeneity and stability of the CRM were evaluated. Taurine (2-aminoethanesulfonic acid) is a conditionally necessary amino acid with valuable physiological functions. This paper describes the development of a taurine purity certified reference material (CRM) based on the principle of ISO. The characterization was carried out using mass balance and quantitative nuclear magnetic resonance spectroscopy. The mass balance method involved measuring the main component, as well as moisture, volatile impurities, and inorganic impurities. The main component of the CRM was determined by high-performance liquid chromatography with ultraviolet detection and pre-column derivatization. The homogeneity assessment, stability study and uncertainty assessment were also examined. The purity of the CRM was sufficiently homogeneous. It remained stable for 24 months at room temperature and for 28 days at 60 °C. The definite value was 99.8 % with the relative expanded uncertainty of 0.6 % (k = 2) at a confidence level of 95 %. The CRM is capable of validating the analytical measurements in laboratories, to ensure the accuracy, traceability, reliability, and comparability of analytical results from different laboratories.
ISSN:0026-265X
DOI:10.1016/j.microc.2022.107761