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The rapid identification of drug metabolites using capillary liquid chromatography coupled to an ion trap mass spectrometer
Capillary liquid chromatography (LC) using a 320 µm column and a flow rate of 10 µL/min has been coupled to an ion trap mass spectrometer using electrospray ionisation (ESI) to enable the rapid and effective identification of metabolites in urine, following oral administration of a novel human neutr...
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Published in: | Rapid communications in mass spectrometry 1999-01, Vol.13 (5), p.456-463 |
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creator | Dear, G. J. Ayrton, J. Plumb, R. Fraser, I. J. |
description | Capillary liquid chromatography (LC) using a 320 µm column and a flow rate of 10 µL/min has been coupled to an ion trap mass spectrometer using electrospray ionisation (ESI) to enable the rapid and effective identification of metabolites in urine, following oral administration of a novel human neutrophil elastase inhibitor, GW311616. Metabolites were identified from their mass (MS) spectra and tandem (MS/MS) mass spectra using minimal sample (1 µL of urine) and no sample pretreatment. Sensitivity assessment has shown that both molecular weight and structural information is obtainable on as little as 5 pg of compound, making the capillary LC/ion trap system as described an ideal analytical tool for the detection and characterisation of low level metabolites in biofluids (particularly when sample volume is limited). This level of detection was unattainable using a triple quadrupole mass spectrometer operating in full‐scan mode, although 200 fg on column was detected using selected reaction monitoring target analysis. Copyright © 1999 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/(SICI)1097-0231(19990315)13:5<456::AID-RCM508>3.0.CO;2-T |
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Sensitivity assessment has shown that both molecular weight and structural information is obtainable on as little as 5 pg of compound, making the capillary LC/ion trap system as described an ideal analytical tool for the detection and characterisation of low level metabolites in biofluids (particularly when sample volume is limited). This level of detection was unattainable using a triple quadrupole mass spectrometer operating in full‐scan mode, although 200 fg on column was detected using selected reaction monitoring target analysis. Copyright © 1999 John Wiley & Sons, Ltd.</description><subject>Animals</subject><subject>Biotransformation</subject><subject>Chromatography, Ion Exchange</subject><subject>Chromatography, Liquid</subject><subject>Enzyme Inhibitors - metabolism</subject><subject>Humans</subject><subject>Leukocyte Elastase - antagonists & inhibitors</subject><subject>Mass Spectrometry</subject><subject>Molecular Weight</subject><subject>Piperidines - metabolism</subject><subject>Rats</subject><issn>0951-4198</issn><issn>1097-0231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkVtv0zAYhiMEYmXwF5Cv0HaR4kMdxwUhpsBGpbFyKBri5pPjOK0hp8WOoOLP4yhlQgKJK0v26-c7PFH0kuA5wZg-Pfm4ylanBEsRY8rICZFSYkb4KWFL_nzBk-XybPUq_pC95Th9weZ4nq2f0XhzJ5rdfrobzbDkJF4QmR5FD5z7ijEhnOL70RHBFMtUiFn0c7MzqFedLZAtTONtabXytm1QW6KiH7aoNl7lbWW9cWhwttkiHeJVpfo9quzNEH7qXd_WyrfbANrtkW6HrjIF8i1SDRpZPjygWjmHXGe0D2njTf8wuleqyplHh_M4-nT-epO9iS_XF6vs7DLWi9BlXBBGtRJUhOaFpEotpCIypyxNypyVRBnMS6mJTPKc8VzTRGBVCqwpYbxIBTuOnkzcrm9vBuM81NZpE0ZoTDs4SKTAC5wmIfh5Cuq-da43JXS9rcOgQDCMYgBGMTDuGMYdw28xQBhwCGIAghiYxAADDNkaKGwC-vGhhyGvTfEHeDIRAl-mwHdbmf1fhf9b959lDzcBHk9w67z5cQtX_TdIBBMcrq8u4P3VOXt3vUmAs1-Zsbsb</recordid><startdate>19990101</startdate><enddate>19990101</enddate><creator>Dear, G. 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source | Wiley-Blackwell Read & Publish Collection |
subjects | Animals Biotransformation Chromatography, Ion Exchange Chromatography, Liquid Enzyme Inhibitors - metabolism Humans Leukocyte Elastase - antagonists & inhibitors Mass Spectrometry Molecular Weight Piperidines - metabolism Rats |
title | The rapid identification of drug metabolites using capillary liquid chromatography coupled to an ion trap mass spectrometer |
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