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

Q4 Medicine
Pharmeuropa bio & scientific notes Pub Date : 2010-10-01
G Rautmann, E Charton, A Daas, K-H Buchheit
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引用次数: 0

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.

制霉菌素第三个国际标准的联合研究。
由于世界卫生组织(世卫组织)制霉菌素第二国际标准(IS)的库存耗尽,欧洲药品和保健质量理事会(EDQM)组织了一项国际合作研究,以建立替代批次。17个实验室参与了合作研究,进行微生物扩散试验以估计制霉菌素候选第三国际标准的效价。以制霉菌素第二版国际标准为标准,保证单位的连续性。随后的加速降解研究表明,在- 20℃的常规储存温度下,IS是稳定的。2006年,世卫组织生物标准化专家委员会(ECBS)通过了制霉菌素第三版标准,指定效价为每毫克5710国际单位(IU/mg)。制霉菌素的第三个IS可从EDQM获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmeuropa bio & scientific notes
Pharmeuropa bio & scientific notes Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
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0
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