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关于建立制霉菌素第三国际标准的合作研究。

Collaborative study for the establishment of the third international standard for nystatin.

作者信息

Rautmann G, Charton E, Daas A, Buchheit K-H

机构信息

European Directorate for the Quality of Medicines & HealthCare (EDQM), Council of Europe, Strasbourg, France.

出版信息

Pharmeur Bio Sci Notes. 2010 Oct;2010(2):68-85.

Abstract

Due to the depletion in stocks of the World Health Organization (WHO) 2nd International Standard (IS) for nystatin, an international collaborative study was organised by the European Directorate for the Quality of Medicines & HealthCare (EDQM) to establish a replacement batch. Seventeen laboratories participated in the collaborative study, performing the microbiological diffusion assay to estimate the potency of the candidate 3rd International Standard for nystatin. The 2nd International Standard for nystatin was used as a standard to ensure the continuity of the unitage. Follow-up accelerated degradation studies demonstrated that the IS is stable when at the customary storage temperature of - 20 °C. The 3rd IS for nystatin was adopted by the WHO Expert Committee on Biological Standardization (ECBS) in 2006 with an assigned potency of 5710 International Units per mg (IU/mg). The 3rd IS for nystatin is available from the EDQM.

摘要

由于世界卫生组织(WHO)制霉菌素第二国际标准品(IS)库存告罄,欧洲药品质量管理局(EDQM)组织了一项国际协作研究以建立替代批次。17个实验室参与了该协作研究,采用微生物扩散法测定制霉菌素候选第三国际标准品的效价。以制霉菌素第二国际标准品作为标准来确保单位剂量的连续性。后续加速降解研究表明,该国际标准品在-20°C的常规储存温度下是稳定的。制霉菌素第三国际标准品于2006年被WHO生物标准化专家委员会(ECBS)采用,指定效价为每毫克5710国际单位(IU/mg)。制霉菌素第三国际标准品可从EDQM获得。

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