low blood volume LC‐MS/MS assay for the quantification of fentanyl and its major metabolites norfentanyl and despropionyl fentanyl in children

Preterm and term neonates often require surgical procedures and analgesia. However, our knowledge about neonatal pharmacokinetics of fentanyl, the most commonly used drug for these procedures, and its metabolites is still incomplete. To facilitate pharmacokinetic studies of fentanyl and its metaboli...

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Published inJournal of separation science Vol. 34; no. 24; pp. 3568 - 3577
Main Authors Clavijo, Claudia F, Thomas, James Joseph, Cromie, Meghan, Schniedewind, Björn, Hoffman, Keith L, Christians, Uwe, Galinkin, Jeffrey L
Format Journal Article
LanguageEnglish
Published Weinheim WILEY‐VCH Verlag 01.12.2011
WILEY-VCH Verlag
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Summary:Preterm and term neonates often require surgical procedures and analgesia. However, our knowledge about neonatal pharmacokinetics of fentanyl, the most commonly used drug for these procedures, and its metabolites is still incomplete. To facilitate pharmacokinetic studies of fentanyl and its metabolites in neonates and other children, we developed and validated an LC‐MS/MS method based on minimally invasive, low blood volume sampling. LC‐MS/MS was used for the simultaneous analysis of fentanyl, despropionyl fentanyl (DPF), and norfentanyl from dried blood samples (DBS) collected on filter paper. Positive ions were monitored using multiple reaction monitoring. Since the standard matrix for measuring fentanyl blood concentrations is plasma, the assay was developed and validated in plasma, whole blood, and then DBS. Our method was able to measure clinically relevant levels of fentanyl and its metabolites. In DBS, the lower limits of quantification were 100 pg/mL for fentanyl with a range of reliable response from 0.1 to 100 ng/mL (r2>0.99) and 250 pg/mL for both DPF and norfentanyl with a range of reliable response from 0.25 to 100 ng/mL (r2>0.99). In plasma and in DBS inter‐day accuracy and precisions of fentanyl met predefined acceptance criteria and also indicated comparable assay performance in both matrices.
Bibliography:http://dx.doi.org/10.1002/jssc.201100422
United States National Institutes of Health - No. P30 DK048520
ArticleID:JSSC201100422
istex:B5206EF59CC7B3932AE33D3E1969237F85646FA7
ark:/67375/WNG-QXXWL4C1-7
Mass Spectrometry Core - No. UL1RR025780; No. 3UL1RR025744-02S3
These authors contributed equally to this work.
ObjectType-Article-2
SourceType-Scholarly Journals-1
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ISSN:1615-9306
1615-9314
DOI:10.1002/jssc.201100422