Development and validation of a dried blood spot assay for the quantification of ribavirin using liquid chromatography coupled to mass spectrometry
Autor: | Jia-Hua Zheng, Peter L. Anderson, Lane R. Bushman, Leah C. Jimmerson, Christine E. MacBrayne, Jennifer J. Kiser |
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Rok vydání: | 2013 |
Předmět: |
Analyte
Chromatography Chemistry Coefficient of variation Clinical Biochemistry Reproducibility of Results Cell Biology General Medicine Tandem mass spectrometry Mass spectrometry Biochemistry Sensitivity and Specificity Article Analytical Chemistry Dried blood spot Matrix (chemical analysis) Drug Stability Liquid chromatography–mass spectrometry Tandem Mass Spectrometry Ribavirin Linear Models Humans Dried Blood Spot Testing Chromatography Liquid |
Zdroj: | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 944 |
ISSN: | 1873-376X |
Popis: | Efficient, inexpensive and sensitive assays for the measurement of drugs are of interest for pharmacokinetic and pharmacodynamics (PK–PD) analysis. Dried blood spots (DBS) are a unique bioanaltyical matrix with the potential to fulfill this interest for the measurement of numerous analytes. Here we describe the development and validation of a reversed-phase high performance liquid chromatographic (LC), tandem mass spectrometry (MS/MS) assay for the determination of ribavirin (RBV) in DBS. A 3 mm punch from spotted and dried whole blood was extracted in methanol utilizing isotopically labeled internal standard for LC–MS/MS analysis. Validation was performed over a range of 0.05 μg/mL to 10.0 μg/mL and the method was shown to be precise (coefficient of variation ≤15%) and accurate (within ±15% of control). These acceptance criteria were met for hematocrit ranges of 20–54%, for center versus edge punches and for spot volumes from 10 to 60 μL. RBV was stable for up to 140 days at room temperature and −20 °C as well as for three freeze/thaw cycles. Correlation of RBV in DBS versus in plasma yielded r2 ≥ 0.98 demonstrating that DBS can be used as an alternative to plasma for PK–PD studies in human subjects. |
Databáze: | OpenAIRE |
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