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Collaborative study for the establishment of Ph. Eur. Human albumin (molecular size) Biological Reference Preparation batches 1, 2 and 3.
Sinitskaya, N; Regourd, E; Wierer, M; Behr-Gross, M-E; Lièvre, V.
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  • Sinitskaya N; European Directorate for the Quality of Medicines & HealthCare (EDQM), Department of Biological Standardisation, OMCL Network & HealthCare (DBO), Council of Europe, 7 allée Kastner, 67000 Strasbourg, France.
  • Regourd E; European Directorate for the Quality of Medicines & HealthCare (EDQM), Department of Biological Standardisation, OMCL Network & HealthCare (DBO), Council of Europe, 7 allée Kastner, 67000 Strasbourg, France.
  • Wierer M; European Directorate for the Quality of Medicines & HealthCare (EDQM), Department of Biological Standardisation, OMCL Network & HealthCare (DBO), Council of Europe, 7 allée Kastner, 67000 Strasbourg, France.
  • Behr-Gross ME; European Directorate for the Quality of Medicines & HealthCare (EDQM), Department of Biological Standardisation, OMCL Network & HealthCare (DBO), Council of Europe, 7 allée Kastner, 67000 Strasbourg, France.
  • Lièvre V; Agence Nationale de Sécurité du Médicament et des produits de santé (ANSM-CTROL), 143-147 bvd Anatole France, 93285 Saint-Denis, France.
Pharmeur Bio Sci Notes ; 2021: 184-198, 2021.
Article en En | MEDLINE | ID: mdl-34913434
To comply with European Pharmacopoeia (Ph. Eur.) monograph Human albumin solution (0255), albumin solutions have to be tested for molecular-size distribution by size-exclusion chromatography (SEC). However, differences in interpretation of the test results continue to be observed among albumin manufacturers in Europe. A collaborative study was run by the European Directorate for the Quality of Medicines & HealthCare (EDQM), under the aegis of the Biological Standardisation Programme (BSP), to support the revision of Ph. Eur. monograph 0255 and to establish a Biological Reference Preparation (BRP) for use in the molecular-size distribution test. In 2019, Ph. Eur. Expert Group 6B proposed to include an analytical improvement of the SEC procedure in the monograph, which was then submitted for public enquiry. This publication describes the evaluation of three candidate BRPs to serve as a tool for both the system suitability test (SST) and albumin monomer and dimer peak identification according to the proposed revised methodology. Three Official Medicines Control Laboratories (OMCLs) involved in the official batch release of human albumin solution took part in the study. Based on the study results, the candidate BRPs were found suitable for purpose and were adopted by the Ph. Eur. Commission as Ph. Eur. Human albumin (molecular size) BRP batches 1, 2 and 3 concomitantly with the revised monograph Human albumin solution (0255) in November 2020.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Albúminas / Albúmina Sérica Humana Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Pharmeur Bio Sci Notes Asunto de la revista: FARMACOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Francia
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Albúminas / Albúmina Sérica Humana Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Pharmeur Bio Sci Notes Asunto de la revista: FARMACOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Francia