On-line desorption of dried blood spots coupled to hydrophilic interaction/reversed-phase LC/MS/MS system for the simultaneous analysis of drugs and their polar metabolites
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作者:
Thomas, Aurelien
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Univ Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, Switzerland
Univ Geneva, Swiss Ctr Appl Human Toxicol, Geneva, SwitzerlandUniv Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, Switzerland
Thomas, Aurelien
[1
,4
]
Deglon, Julien
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Univ Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, Switzerland
Univ Geneva, Swiss Ctr Appl Human Toxicol, Geneva, SwitzerlandUniv Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, Switzerland
Deglon, Julien
[1
,4
]
Steimer, Thierry
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Univ Hosp Geneva, Clin Psychopharmacol Unit, Geneva, SwitzerlandUniv Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, Switzerland
Steimer, Thierry
[2
]
Mangin, Patrice
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Univ Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, SwitzerlandUniv Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, Switzerland
Mangin, Patrice
[1
]
Daali, Youssef
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Univ Hosp Geneva, Div Clin Pharmacol & Toxicol, Geneva, SwitzerlandUniv Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, Switzerland
Daali, Youssef
[3
]
Staub, Christian
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Univ Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, Switzerland
Univ Geneva, Swiss Ctr Appl Human Toxicol, Geneva, SwitzerlandUniv Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, Switzerland
An assay for the simultaneous analysis of pharmaceutical compounds and their metabolites from micro-whole blood samples (i.e. 5 mu L) was developed using an on-line dried blood spot (on-line DBS) device coupled with hydrophilic interaction/reversed-phase (HILIC/RP) LC/MS/MS. Filter paper is directly integrated to the LC device using a homemade inox desorption cell. Without any sample pretreatment, analytes are desorbed from the paper towards an automated system of valves linking a zwitterionic-HILIC column to an RP C18 column. In the same run, the polar fraction is separated by the zwitterionic-HILIC column while the non-polar fraction is eluted on the RP C18. Both fractions are detected by IT-MS operating in full scan mode for the survey scan and in product ion mode for the dependant scan using an ESI source. The procedure was evaluated by the simultaneous qualitative analysis of four probes and their relative phase I and II metabolites spiked in whole blood. In addition, the method was successfully applied to the in vivo monitoring of buprenorphine metabolism after the administration of an intraperitoneal injection of 30 mg/kg on adult female Wistar rat.