Stead D A, Reid R G, Taylor R B
School of Pharmacy, Robert Gordon University, Schoolhill, Aberdeen, UK.
J Chromatogr A. 1998 Mar 6;798(1-2):259-67. doi: 10.1016/s0021-9673(97)00840-6.
A reversed-phase HPLC method previously developed for the analysis of progesterone and its major metabolites has been transferred successfully to a capillary electrochromatography (CEC) system. Procedures for fabricating packed capillaries and the modifications made to the capillary electropherograph which allow operation in the CEC mode without pressurisation are described. The dependence of electroosmotic flow on electric field strength, pH and organic modifier content is discussed. Direct comparison with HPLC shows that CEC provides useful gains in efficiency and speed of analysis and requires vastly reduced amounts of both chromatographic phases and material for analysis. On-line concentration is described which allows the lower sensitivity of CEC to be offset by injecting analytes from a non-eluting solution. Examination of steroids in plasma demonstrates that the superior separation by CEC is maintained in a complex biological matrix.
先前开发的用于分析孕酮及其主要代谢物的反相高效液相色谱法已成功转移至毛细管电色谱(CEC)系统。本文描述了制备填充毛细管的程序以及对毛细管电泳仪进行的改进,这些改进使得在无需加压的情况下以CEC模式运行成为可能。讨论了电渗流对电场强度、pH值和有机改性剂含量的依赖性。与高效液相色谱的直接比较表明,CEC在分析效率和速度方面有显著提高,并且所需的色谱相和分析材料量大大减少。文中还描述了在线浓缩,它可以通过从非洗脱溶液中注入分析物来弥补CEC较低的灵敏度。对血浆中类固醇的检测表明,在复杂的生物基质中,CEC仍能保持出色的分离效果。