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一项旨在研究巴比妥类药物在高效液相色谱法中保留重现性的合作研究,目的是建立用于药物鉴定的保留数据库。

A collaborative study to investigate the retention reproducibility of barbiturates in HPLC with a view to establishing retention databases for drug identification.

作者信息

Gill R, Moffat A C, Smith R M, Hurdley T G

出版信息

J Chromatogr Sci. 1986 Apr;24(4):153-9. doi: 10.1093/chromsci/24.4.153.

Abstract

A collaborative study among 10 laboratories has been undertaken to investigate the interlaboratory reproducibility of retention measurements in a high performance liquid chromatographic (HPLC) system for separating barbiturates. The system involved an ODS-Hypersil column with an eluent of methanol:phosphate buffer (40:60, v/v) at pH 8.5; all laboratories used the same batch of packing material. The conventional methods of recording retention properties (retention times and capacity factors) gave poor interlaboratory reproducibility. Better results were obtained by expressing the retentions relative to a standard barbiturate (quinalbarbitone); relative adjusted retention times proved to be more effective than straightforward relative retention times. Retention indices based on the alkylarylketone scale were not as reproducible as the methods based on a single closely related compound. The best reproducibility was obtained using corrected capacity factors based on the retention of four barbiturates in a standard mixture. The results of the study are discussed with a view to selecting the best methods of recording retention in HPLC when considering the establishment of databases for drug identification.

摘要

10个实验室开展了一项合作研究,以调查用于分离巴比妥类药物的高效液相色谱(HPLC)系统中保留值测量的实验室间再现性。该系统采用ODS- Hypersil柱,流动相为甲醇:磷酸盐缓冲液(40:60,v/v),pH值为8.5;所有实验室使用同一批次的填充材料。记录保留特性(保留时间和容量因子)的传统方法在实验室间的再现性较差。将保留值相对于标准巴比妥类药物(速可巴比妥)表示可获得更好的结果;相对调整保留时间被证明比直接的相对保留时间更有效。基于烷基芳基酮标度的保留指数不如基于单一密切相关化合物的方法具有再现性。使用基于标准混合物中四种巴比妥类药物保留值的校正容量因子可获得最佳再现性。考虑到建立药物鉴定数据库,对该研究结果进行了讨论,以选择HPLC中记录保留值的最佳方法。

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