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酶制剂质量的研究(十二)——溶菌酶制剂

[Studies on the quality of enzyme preparations (XII)--lysozyme preparations].

作者信息

Yokota I, Ohta M, Tanimoto T, Hayakawa T

出版信息

Eisei Shikenjo Hokoku. 1993(111):75-7.

PMID:7920571
Abstract

This paper was described the results of the weight variation test and the assay for the potency of the commercially available lysozyme preparations (samples: 13 kinds of granules, in which 10 kinds are granules (folded)) collected for the legal sampling inspection in 1992. The potencies of 10 samples were found to be within the range of permissible content, when the all samples extracted with phosphate buffer were determined by the method described in Japanese Standards of Pharmaceutical Ingredients. However, the potencies of 3 samples were not more than 65% of the labeled potencies. These low potency samples showed the potencies of 98-106%, when 0.4M sodium chloride solution or 0.1N hydrochloric acid was used instead of phosphate buffer for enzyme extraction. The weight variation test showed all preparations to be within the permissible JP XII deviation range (10%) for "granules (folded)".

摘要

本文描述了1992年法定抽样检验收集的市售溶菌酶制剂(样品:13种颗粒剂,其中10种为(折叠)颗粒剂)的重量差异试验结果和效价测定结果。当用磷酸盐缓冲液提取所有样品并按照日本药品成分标准中所述方法测定时,10个样品的效价在允许含量范围内。然而,3个样品的效价不超过标示效价的65%。当用0.4M氯化钠溶液或0.1N盐酸代替磷酸盐缓冲液进行酶提取时,这些低效价样品的效价为98 - 106%。重量差异试验表明,所有制剂均在日本药典第十二版“(折叠)颗粒剂”允许偏差范围(10%)内。

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