Use of the dried blood spot sampling process coupled with fast gas chromatography and negative-ion chemical ionization tandem mass spectrometry: application to fluoxetine, norfluoxetine, reboxetine, and paroxetine analysis

被引:48
作者
Deglon, Julien [1 ,2 ]
Lauer, Estelle [1 ,2 ]
Thomas, Aurelien [1 ,2 ]
Mangin, Patrice [1 ]
Staub, Christian [1 ,2 ]
机构
[1] Univ Ctr Legal Med, Toxicol Unit, CH-1211 Geneva 4, Switzerland
[2] Univ Geneva, Swiss Ctr Appl Human Toxicol, CH-1205 Geneva, Switzerland
关键词
DBS; Fast GC; NICI-MS-MS; Antidepressants; Pharmacokinetics; PERFORMANCE LIQUID-CHROMATOGRAPHY; NEW-GENERATION ANTIDEPRESSANTS; SOLID-PHASE EXTRACTION; BIOANALYTICAL METHODS; ACTIVE METABOLITES; HUMAN PLASMA; SFSTP GUIDE; HUMAN HAIR; VALIDATION; ASSAY;
D O I
10.1007/s00216-009-3412-6
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
The objective of this work was to combine the advantages of the dried blood spot (DBS) sampling process with the highly sensitive and selective negative-ion chemical ionization tandem mass spectrometry (NICI-MS-MS) to analyze for recent antidepressants including fluoxetine, norfluoxetine, reboxetine, and paroxetine from micro whole blood samples (i.e., 10 mu L). Before analysis, DBS samples were punched out, and antidepressants were simultaneously extracted and derivatized in a single step by use of pentafluoropropionic acid anhydride and 0.02% triethylamine in butyl chloride for 30 min at 60 A degrees C under ultrasonication. Derivatives were then separated on a gas chromatograph coupled with a triple-quadrupole mass spectrometer operating in negative selected reaction monitoring mode for a total run time of 5 min. To establish the validity of the method, trueness, precision, and selectivity were determined on the basis of the guidelines of the "Soci,t, Fran double dagger aise des Sciences et des Techniques Pharmaceutiques" (SFSTP). The assay was found to be linear in the concentration ranges 1 to 500 ng mL(-1) for fluoxetine and norfluoxetine and 20 to 500 ng mL(-1) for reboxetine and paroxetine. Despite the small sampling volume, the limit of detection was estimated at 20 pg mL(-1) for all the analytes. The stability of DBS was also evaluated at -20 A degrees C, 4 A degrees C, 25 A degrees C, and 40 A degrees C for up to 30 days. Furthermore, the method was successfully applied to a pharmacokinetic investigation performed on a healthy volunteer after oral administration of a single 40-mg dose of fluoxetine. Thus, this validated DBS method combines an extractive-derivative single step with a fast and sensitive GC-NICI-MS-MS technique. Using microliter blood samples, this procedure offers a patient-friendly tool in many biomedical fields such as checking treatment adherence, therapeutic drug monitoring, toxicological analyses, or pharmacokinetic studies.
引用
收藏
页码:2523 / 2532
页数:10
相关论文
共 53 条
[1]
Dried blood spot liquid chromatography assay for therapeutic drug monitoring of metformin [J].
AbuRuz, S ;
Millership, J ;
McElnay, J .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2006, 832 (02) :202-207
[2]
Adson DE, 2001, ANN PHARMACOTHER, V35, P1375
[3]
Determination of rifampicin in human plasma and blood spots by high performance liquid chromatography with UV detection: A potential method for therapeutic drug monitoring [J].
Allanson, A. L. ;
Cotton, M. M. ;
Tettey, J. N. A. ;
Boyter, A. C. .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2007, 44 (04) :963-969
[4]
Paroxetine associated hepatotoxicity: A report of 3 cases and a review of the literature [J].
Azaz-Livshits, T ;
Hershko, A ;
Ben-Chetrit, E .
PHARMACOPSYCHIATRY, 2002, 35 (03) :112-115
[5]
Application of dried blood spots combined with HPLC-MS/MS for the quantification of acetaminophen in toxicokinetic studies [J].
Barfield, Matt ;
Spooner, Neil ;
Lad, Rakesh ;
Parry, Simon ;
Fowles, Susan .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2008, 870 (01) :32-37
[6]
Development and validation of an automated solid-phase extraction and liquid chromatographic method for determination of lumefantrine in capillary blood on sampling paper [J].
Blessborn, D. ;
Roemsing, S. ;
Annerberg, A. ;
Sundquist, D. ;
Bjoerkman, A. ;
Lindegardh, N. ;
Bergqvist, Y. .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2007, 45 (02) :282-287
[7]
An analysis of the SFSTP guide on validation of chromatographic bioanalytical methods: progresses and limitations [J].
Boulanger, B ;
Chiap, P ;
Dewe, W ;
Crommen, J ;
Hubert, P .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2003, 32 (4-5) :753-765
[8]
Determination of Morphine and 6-Acetylmorphine in Blood With Use of Dried Blood Spots [J].
Boy, Regine Garcia ;
Henseler, Joerg ;
Mattern, Rainer ;
Skopp, Gisela .
THERAPEUTIC DRUG MONITORING, 2008, 30 (06) :733-739
[9]
CDC, 1993, GUIDELINES SHIPMENT
[10]
Dried blood spot measurement: application in tacrolimus monitoring using limited sampling strategy and abbreviated AUC estimation [J].
Cheung, Chi Yuen ;
van der Heijden, Jaques ;
Hoogtanders, Karin ;
Christiaans, Maarten ;
Liu, Yan Lun ;
Chan, Yiu Han ;
Choi, Koon Shing ;
van de Plas, Afke ;
Shek, Chi Chung ;
Chau, Ka Foon ;
Li, Chun Sang ;
van Hooff, Johannes ;
Stolk, Leo .
TRANSPLANT INTERNATIONAL, 2008, 21 (02) :140-145