Optimisation and routine use of generic ultra-high flow-rate liquid chromatography with mass spectrometric detection for the direct on-line analysis of pharmaceuticals in plasma

The use of ultra-high flow-rate chromatography coupled to mass spectrometry offers great potential for the rapid, on-line analysis of pharmaceutical c ompounds in plasma as it permits high throughput direct analysis of plasma samples without any time-consuming sample preparation such as solid-phase e xtraction. The coupling of mass spectrometry with high performance liquid c hromatography often results in enhanced selectivity and sensitivity compare d to, for example, ultraviolet absorbance detection. This can remove the ne ed for complete resolution of the analyte from endogenous materials in the matrix. The use of large particle size stationary phases, and therefore, th e ability to use large porosity column end frits, coupled with the added se lectivity and sensitivity of the mass spectrometer allows an on-line analys is approach to be used for the direct analysis of pharmaceuticals in biolog ical matrices with extremely high throughput. This paper presents an overvi ew of the manner in which we have optimised this technique for the analysis of plasma samples, in terms of gradient profile, system configuration and optimal injection volume for maximum throughput and robustness. The nature of the mobile phase flow is also discussed. (C) 1998 Published by Elsevier Science B.V. All rights reserved.