Suppr超能文献

用于监管目的的分析方法的性能特征。I. 药物剂型。B. 气相色谱法。

Performance characteristics of methods of analysis used for regulatory purposes. I. Drug dosage forms. B. Gas chromatographic methods.

作者信息

Horwitz W, Albert R

出版信息

J Assoc Off Anal Chem. 1984 May-Jun;67(3):648-52.

PMID:6746491
Abstract

Gas chromatographic methods for the analysis of drug dosage forms consist of a simple extraction, dilution with an internal standard solution, and injection, or, even simpler, dilution with the internal standard solution and injection. These methods were used in 7 collaborative studies of the determination of 12 pharmaceuticals, published in the Journal of the AOAC during 1973-1983. A total of 43 individual materials consisting of various dosage forms were each analyzed, usually in duplicate, by an average of 8 laboratories, with a total of 582 reported determinations. The average within-laboratory coefficient of variation (CVo) was 1.25% and the average among-laboratories coefficient of variation (CVx) was 2.41%, for a CVo/CVx ratio of 0.52, at an average outlier rate of 1.4% of the reported values. The line of best fit for CVx plotted against concentration increases with decreasing concentration, extending from a CVx of approximately 1.8% at 100% concentration to a CVx of approximately 3.2% at 1% concentration. The change in CVx for a 10-fold decrease in concentration is approximately 0.7% CVx, independent of analyte and matrix.

摘要

用于分析药物剂型的气相色谱方法包括简单的萃取、用内标溶液稀释以及进样,或者更简单的是用内标溶液稀释后直接进样。这些方法用于1973 - 1983年发表在《美国官方分析化学家协会杂志》上的7项关于12种药物测定的协作研究中。总共43种由各种剂型组成的单个材料,通常一式两份,平均由8个实验室进行分析,共报告了582次测定结果。平均实验室内变异系数(CVo)为1.25%,实验室间变异系数(CVx)平均为2.41%,CVo/CVx比值为0.52,报告值的平均异常值率为1.4%。CVx与浓度的最佳拟合线随浓度降低而上升,从100%浓度时的CVx约1.8%延伸至1%浓度时的CVx约3.2%。浓度每降低10倍,CVx的变化约为0.7%CVx,与分析物和基质无关。

相似文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验