合作研究新霉素第三项国际标准的制定。

Q4 Medicine
Pharmeuropa bio & scientific notes Pub Date : 2013-01-01
G Rautmann, A Daas, K-H Buchheit
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引用次数: 0

摘要

组织了一项国际合作研究,以建立世界卫生组织(世卫组织)新霉素第三(3)国际标准。来自不同国家的10个实验室参与了合作研究。候选材料的效力,冻干制剂,估计与敏感微生物微生物测定。为了保证连续批次之间的连续性,以新霉素的第2(d) IS作为标准。根据这项研究的结果,2012年世卫组织生物标准化专家委员会(ECBS)会议通过了新霉素的第3份国际标准,指定效力为每瓶19050国际单位。新霉素的第三个IS可从欧洲药品和保健质量理事会(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。
Collaborative study for the establishment of the 3rd international standard for neomycin.

An international collaborative study was organised to establish the World Health Organization (WHO) 3(rd) International Standard (IS) for neomycin. Ten laboratories from different countries participated in the collaborative study. The potency of the candidate material, a freeze-dried preparation, was estimated by microbiological assays with sensitive micro-organisms. To ensure continuity between consecutive batches, the 2(nd) IS for neomycin was used as a standard. Based on the results of the study, the 3(rd) IS for neomycin was adopted at the meeting of the WHO Expert Committee on Biological Standardization (ECBS) in 2012 with an assigned potency of 19,050 IU per vial. The 3(rd) IS for neomycin is available from the European Directorate for the Quality of Medicines & HealthCare (EDQM).

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来源期刊
Pharmeuropa bio & scientific notes
Pharmeuropa bio & scientific notes Medicine-Medicine (all)
CiteScore
0.70
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