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Determination of albuterol concentrations in human plasma using solid-phase extraction and high-performance liquid
R E Bland1, R J Tanner, W H Chern
1Department of Biochemical Pharmacology, Glaxo Group Research Ltd, Ware, Herts, UK.
Abstract:
A fast, simple, and accurate method for determining albuterol concentrations in human plasma has been developed and validated for use in routine clinical analyses. This method involves a solid-phase extraction procedure using silica cartridges and normal-phase high-performance liquid chromatography with fluorescence detection. Regression analysis showed the method was linear over the standard curve range 1-16 ng ml-1. The percent recovery for albuterol and the internal standard, bamethane, at 5 ng ml-1 was found to be greater than 90%. The newly developed method has been applied in the analysis of plasma samples from patients and healthy volunteers.