Sensitive determination of a pharmaceutical compound and its metabolites in human plasma by ultra-high performance liquid chromatography-tandem mass spectrometry with on-line solid-phase extraction |
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Authors: | Heinig K Wirz T Bucheli F Monin V Gloge A |
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Affiliation: | Pharma Research, Non-clinical Safety, DMPK Development, F. Hoffmann-La Roche Ltd., Grenzacherstrasse 124, Basel, Switzerland. katja.heinig@roche.com |
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Abstract: | This paper describes the determination of a drug candidate and two metabolites in human plasma by column-switching LC-MS/MS after protein precipitation. Starting from a standard method with a quantitation limit of 0.5 ng/mL, a highly sensitive assay was developed, employing UHPLC separation and detection on an API 5000 mass spectrometer. The injected plasma equivalent was increased from 6 to 20 μL; conventional column trapping for compound enrichment and removal of matrix constituents was combined with high-pressure analytical separation using small particle columns to improve resolution and signal-to-noise ratio. Quantitation limits were thus lowered to between 5 and 20 pg/mL, offering the possibility to provide bioanalytical support for microdosing studies in humans. Excellent assay quality and robustness were achieved by both methods. |
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Keywords: | UHPLC LC–MS/MS On-line SPE Human plasma Microdosing |
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