Literature DB >> 19128911

Quantification of the HIV-integrase inhibitor raltegravir and detection of its main metabolite in human plasma, dried blood spots and peripheral blood mononuclear cell lysate by means of high-performance liquid chromatography tandem mass spectrometry.

R Ter Heine1, M J X Hillebrand, H Rosing, E C M van Gorp, J W Mulder, J H Beijnen, A D R Huitema.   

Abstract

For the quantification of the HIV-integrase inhibitor raltegravir in human plasma, dried blood spots and peripheral blood mononuclear cell (PBMC) lysate, an assay was developed and validated, using liquid chromatography coupled with tandem mass spectrometry. The assay also allowed detection, but no quantification due to absence of reference substance, of the main metabolite, raltegravir-glucuronide. Raltegravir was extracted from plasma by means of protein precipitation with a mixture of methanol and acetonitrile using only 50microL plasma. Extraction from dried blood spots was performed with a simple one-step extraction with a mixture of methanol, acetonitrile and 0.2M zincsulphate in water (1:1:2, v/v/v) and extraction from cell lysate was performed in 50% methanol in water. Chromatographic separation was performed on a reversed phase C18 column (150mmx2.0mm, particle size 5microm) with a quick stepwise gradient using an acetate buffer (pH 5) and methanol, at a flow rate of 0.25mL/min. The analytical run time was 10min. The triple quadrupole mass spectrometer was operated in the positive ion-mode and multiple reaction monitoring was used for drug quantification. The method was validated over a range of 50-10,000ng/mL in plasma and dried blood spots and a range of 1-500ng/mL in PBMC lysate. Dibenzepine was used as the internal standard. The method was proven to be specific, accurate, precise and robust. Accuracies ranged from 104% to 105% in plasma, from 93% to 105% in dried blood spots and from 82% to 113% in PBMC lysate. Precision over the complete concentration range was less than 6%, 11% and 13% in plasma, dried blood spots and PBMC lysate, respectively. The method is now applied for therapeutic drug monitoring and pharmacological research in HIV-infected patients treated with raltegravir.

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Year:  2008        PMID: 19128911     DOI: 10.1016/j.jpba.2008.11.025

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  10 in total

1.  Intracellular and plasma steady-state pharmacokinetics of raltegravir, darunavir, etravirine and ritonavir in heavily pre-treated HIV-infected patients.

Authors:  Rob Ter Heine; Jan Willem Mulder; Eric C M van Gorp; Jiri F P Wagenaar; Jos H Beijnen; Alwin D R Huitema
Journal:  Br J Clin Pharmacol       Date:  2010-05       Impact factor: 4.335

2.  Simultaneous measurement of etravirine, maraviroc and raltegravir in pigtail macaque plasma, vaginal secretions and vaginal tissue using a LC-MS/MS assay.

Authors:  Anna K Blakney; Yonghou Jiang; Dale Whittington; Kim A Woodrow
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2016-05-02       Impact factor: 3.205

3.  Determination of efavirenz in human dried blood spots by reversed-phase high-performance liquid chromatography with UV detection.

Authors:  Justin T Hoffman; Steven S Rossi; Rowena Espina-Quinto; Scott Letendre; Edmund V Capparelli
Journal:  Ther Drug Monit       Date:  2013-04       Impact factor: 3.681

Review 4.  Emerging trends in paper spray mass spectrometry: Microsampling, storage, direct analysis, and applications.

Authors:  Benjamin S Frey; Deidre E Damon; Abraham K Badu-Tawiah
Journal:  Mass Spectrom Rev       Date:  2019-09-06       Impact factor: 10.946

Review 5.  Adherence Measurements in HIV: New Advancements in Pharmacologic Methods and Real-Time Monitoring.

Authors:  Jose R Castillo-Mancilla; Jessica E Haberer
Journal:  Curr HIV/AIDS Rep       Date:  2018-02       Impact factor: 5.071

6.  Incorporation of concentration data below the limit of quantification in population pharmacokinetic analyses.

Authors:  Ron J Keizer; Robert S Jansen; Hilde Rosing; Bas Thijssen; Jos H Beijnen; Jan H M Schellens; Alwin D R Huitema
Journal:  Pharmacol Res Perspect       Date:  2015-03-25

7.  Selective and rapid determination of raltegravir in human plasma by liquid chromatography-tandem mass spectrometry in the negative ionization mode.

Authors:  Ajay Gupta; Swati Guttikar; Priyanka A Shah; Gajendra Solanki; Pranav S Shrivastav; Mallika Sanyal
Journal:  J Pharm Anal       Date:  2014-10-23

8.  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

9.  Development and validation of a multiplex UHPLC-MS/MS assay with stable isotopic internal standards for the monitoring of the plasma concentrations of the antiretroviral drugs bictegravir, cabotegravir, doravirine, and rilpivirine in people living with HIV.

Authors:  Perrine Courlet; Susana Alves Saldanha; Matthias Cavassini; Catia Marzolini; Eva Choong; Chantal Csajka; Huldrych F Günthard; Pascal André; Thierry Buclin; Vincent Desfontaine; Laurent Arthur Decosterd
Journal:  J Mass Spectrom       Date:  2020-03-11       Impact factor: 1.982

10.  Validation of a UHPLC-MS/MS Method to Quantify Twelve Antiretroviral Drugs within Peripheral Blood Mononuclear Cells from People Living with HIV.

Authors:  Amedeo De Nicolò; Alice Ianniello; Micol Ferrara; Valeria Avataneo; Jessica Cusato; Miriam Antonucci; Elisa De Vivo; Catriona Waitt; Andrea Calcagno; Alice Trentalange; Giampiero Muccioli; Stefano Bonora; Giovanni Di Perri; Antonio D'Avolio
Journal:  Pharmaceuticals (Basel)       Date:  2020-12-25
  10 in total

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