Literature DB >> 19919036

Direct quantitative bioanalysis of drugs in dried blood spot samples using a thin-layer chromatography mass spectrometer interface.

Paul Abu-Rabie1, Neil Spooner.   

Abstract

The CAMAG thin-layer chromatography mass spectrometer (TLC-MS) interface has been assessed as a tool for the direct quantitative bioanalysis of drugs from dried blood spot (DBS) samples, using an MS detector, with or without high-performance liquid chromatography (HPLC) separation. The approach gave acceptable sensitivity, linearity, accuracy, and precision data for bioanalytical validations with and without the inclusion of HPLC separation. In addition, the direct elution technique was shown to increase assay sensitivity for a range of analytes representing a wide "chemical space" for pharmaceutical-type molecules over that obtained by conventional manual extraction of samples (punching of DBS and elution with solvent prior to HPLC-MS analysis). Investigations were performed to optimize extraction time, minimize sample-to-sample carry-over, and compare chromatographic performance. On the basis of this preliminary assessment, it has been demonstrated that the TLC-MS interface has the potential to be an effective tool for the direct analysis of drugs in DBS samples at physiologically relevant concentrations, an approach that could provide significant time and cost savings and greatly simplify bioanalytical procedures compared to current manual practices. Further, the increased sensitivity compared to that of manual extraction may enable the analysis of analytes not currently amenable to DBS sampling due to limitations in assay sensitivity.

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Year:  2009        PMID: 19919036     DOI: 10.1021/ac901985e

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  6 in total

1.  Quantitation of Fentanyl Analogs in Dried Blood Spots by Flow-Through Desorption Coupled to Online Solid Phase Extraction Tandem Mass Spectrometry.

Authors:  Rebecca L Shaner; Nicholas D Schulze; Craig Seymour; Elizabeth I Hamelin; Jerry D Thomas; Rudolph C Johnson
Journal:  Anal Methods       Date:  2017-06-16       Impact factor: 2.896

Review 2.  Quantitative mass spectrometry methods for pharmaceutical analysis.

Authors:  Glenn Loos; Ann Van Schepdael; Deirdre Cabooter
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2016-10-28       Impact factor: 4.226

Review 3.  Therapeutic drug monitoring by dried blood spot: progress to date and future directions.

Authors:  Abraham J Wilhelm; Jeroen C G den Burger; Eleonora L Swart
Journal:  Clin Pharmacokinet       Date:  2014-11       Impact factor: 6.447

4.  Advantages and Challenges of Dried Blood Spot Analysis by Mass Spectrometry Across the Total Testing Process.

Authors:  Rosita Zakaria; Katrina J Allen; Jennifer J Koplin; Peter Roche; Ronda F Greaves
Journal:  EJIFCC       Date:  2016-12-01

5.  The development and validation of a fast and robust dried blood spot based lipid profiling method to study infant metabolism.

Authors:  Albert Koulman; Philippa Prentice; Max C Y Wong; Lee Matthews; Nicholas J Bond; Michael Eiden; Julian L Griffin; David B Dunger
Journal:  Metabolomics       Date:  2014-02-11       Impact factor: 4.290

6.  Combining lipidomics and machine learning to measure clinical lipids in dried blood spots.

Authors:  Stuart G Snowden; Aniko Korosi; Susanne R de Rooij; Albert Koulman
Journal:  Metabolomics       Date:  2020-07-24       Impact factor: 4.290

  6 in total

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