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A novel on‐line solid‐phase extraction approach integrated with a monolithic column and tandem mass spectrometry for direct plasma analysis of multiple drugs and metabolites
Author(s) -
Zang Xu,
Luo Rosa,
Song Ning,
Chen Ta Kung,
Bozigian Haig
Publication year - 2005
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.2188
Subject(s) - chemistry , chromatography , analyte , bioanalysis , solid phase extraction , tandem mass spectrometry , mass spectrometry , sample preparation , tandem , extraction (chemistry) , analytical chemistry (journal) , materials science , composite material
An on‐line solid‐phase extraction liquid chromatography/tandem mass spectrometry (SPE LC/MS/MS) assay using a newly developed SPE column and a monolithic column was developed and validated for direct analysis of plasma samples containing multiple analytes. This assay was developed in an effort to increase bioanalysis throughput and reduce the complexity of on‐line SPE LC/MS/MS systems. A simple column‐switching configuration that requires only one six‐port valve and one HPLC pumping system was employed for on‐line plasma sample preparation and subsequent gradient chromatographic separation. The resulting analytical method couples the desired sensitivity with ease of use. The method was found to perform satisfactorily for direct plasma analysis with respect to assay linearity, specificity, sensitivity, precision, accuracy, carryover, and short‐term stability of an eight‐analyte mixture in plasma. A gradient LC condition was applied to separate the eight analytes that cannot be distinctly differentiated by MS/MS. With a run time for every injection of 2.8 min, a minimum of 300 direct plasma injections were made on one on‐line SPE column without noticeable changes in system performance. Due to the ruggedness and simplicity of this system, generic methods can be easily developed and applied to analyze a wide variety of compounds in a high‐throughput manner without laborious off‐line sample preparation. Copyright © 2005 John Wiley & Sons, Ltd.