[国家卫生科学研究所生长激素参考标准(Control 951)]。

C Yomota, S Okada, E Uchida, K Morimoto, T Hayakawa
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引用次数: 0

摘要

为制备“生长激素标准品”,对生长激素物质进行了检查。候选材料由8个实验室参与的国内合作研究进行评估。经氨基酸分析,蛋白质含量为4.5 mg/瓶。由于有可能作为高效液相色谱法测定的化学参考标准,对候选物质也进行了理化评价。采用高效液相色谱法测定其聚合物含量为0.54%,二聚体含量为0.98%。反相高效液相色谱法测定,早期峰面积占总峰面积的1.07%。对于信息数据,候选材料的效价,通过三种不同的生物学方法,体重增加试验,胫骨试验和脂肪转移试验估计为14.8 IU/瓶。基于以上结果,该候选物被批准为国家卫生科学研究所生长激素参考标准品。
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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[The Somatropin Reference Standard (Control 951) of the National Institute of Health Sciences].

Somatropin material was examined for preparation of the "Somatropin Reference Standard". The candidate material was evaluated by a domestic collaborative study in which eight laboratories participated. The protein content was determined to be 4.5 mg/Vial based on amino acid analysis. Because of the possibility of application as a chemical reference standard for assay by the HPLC method, a physico-chemical evaluation of the candidate material was also performed. By SE-HPLC, the content of polymer, dimer were determined to be 0.54%, 0.98%, respectively. By RP-HPLC, the early peak area ascribed to desamido and sulfoxide form was 1.07% of the total peak area. And for informational data, the potency of the candidate material, being estimated by three different biological methods, weight gain assay, tibia test and adiposeconversion assay is 14.8 IU/vial. Based on the above results, the candidate was authorized as the Somatropin Reference Standard of the National Institute of Health Sciences.

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