Development and validation of an LC-MS/MS method for quantifying total and unbound doravirine in human plasma.

J Chromatogr B Analyt Technol Biomed Life Sci

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa. Electronic address:

Published: December 2024

A robust LC-MS/MS method was developed to quantify total and unbound doravirine in plasma samples from patients receiving daily doses of 100 mg doravirine, in combination with lamivudine and tenofovir disoproxil fumarate, in a phase 3 clinical trial. The trial is ongoing, and sample analysis is planned to commence once all samples have been collected. The method was validated to quantify both total and unbound doravirine using a single calibration curve. Protein precipitation was used to obtain the total doravirine from plasma and ultrafiltration was used to obtain the unbound doravirine. A Kinetex 1.7 µm EVO C18 100 Å column was used for chromatography using a gradient mobile phase (0.1 % formic acid in water and 0.1 % formic acid acetonitrile) at a flow rate of 250 µL/min during a five minute runtime. The analyte was ionized by positive electrospray ionization and detection was by multiple reaction monitoring on a Sciex API3200 triple quadrupole mass spectrometer. Using calibration standards prepared in whole plasma, the calibration curve fitted a quadratic regression (weighted by 1/x) over a calibration range of 7.00-2000 ng/mL and was applied successfully for the measurement of both total and unbound doravirine. Validation experiments, conducted according to international guidelines, proved the accuracy and precision of the method over three consecutive days. The method demonstrated robustness in the presence of matrix components, different anticoagulants, hemolyzed blood (2 %), and concomitant medications, showing the necessary sensitivity and selectivity for the quantification of both total and unbound doravirine concentrations expected in the study samples.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jchromb.2024.124439DOI Listing

Publication Analysis

Top Keywords

unbound doravirine
24
total unbound
20
lc-ms/ms method
8
doravirine
8
quantify total
8
doravirine plasma
8
calibration curve
8
01 % formic
8
formic acid
8
total
6

Similar Publications

Development and validation of an LC-MS/MS method for quantifying total and unbound doravirine in human plasma.

J Chromatogr B Analyt Technol Biomed Life Sci

December 2024

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa. Electronic address:

A robust LC-MS/MS method was developed to quantify total and unbound doravirine in plasma samples from patients receiving daily doses of 100 mg doravirine, in combination with lamivudine and tenofovir disoproxil fumarate, in a phase 3 clinical trial. The trial is ongoing, and sample analysis is planned to commence once all samples have been collected. The method was validated to quantify both total and unbound doravirine using a single calibration curve.

View Article and Find Full Text PDF

Development and validation of equilibrium dialysis UHPLC-MS/MS measurement procedures for total and unbound concentrations of bictegravir, dolutegravir, darunavir and doravirine in human plasma. Application to patients with HIV.

Clin Chim Acta

January 2024

Human Immunodeficiency Virus (HIV) and Sexually Transmitted Infection (STI) Unit, Department of Infectious Diseases, Bellvitge University Hospital, Bellvitge Biomedical Research Institute (IDIBELL), University of Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain; FLScience, Fight Infections Foundation, Badalona, Spain.

Article Synopsis
  • - The study focuses on developing and validating a method (UHPLC-MS/MS) to measure concentrations of specific antiretroviral drugs in human plasma, highlighting the potential benefits of drug concentration monitoring for HIV treatment.
  • - Equilibrium dialysis and sample preparation were utilized to accurately assess unbound drug concentrations, while successful chromatographic separation was achieved using specialized equipment and specific conditions.
  • - The results demonstrated minimal interferences and strong accuracy in measurement precision, suggesting that this method could enhance research and clinical practices for monitoring HIV medications.
View Article and Find Full Text PDF

Doravirine Concentrations and Human Immunodeficiency Virus Type 1 RNA in the Genital Fluids of Virologically Suppressed Adults Switching to Doravirine Plus Emtricitabine/Tenofovir Alafenamide.

Clin Infect Dis

November 2022

HIV and STI Unit, Department of Infectious Diseases, Bellvitge University Hospital, Bellvitge Biomedical Research Institute (IDIBELL), University of Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.

Doravirine (DOR) concentrations and HIV-1 RNA were evaluated in genital fluids from adults with HIV on stable therapy who switched to DOR + FTC/TAF. High protein-unbound DOR concentrations were observed in both seminal plasma and cervicovaginal fluid. DOR + FTC/TAF maintained viral suppression in genital fluids in all but 1 participant.

View Article and Find Full Text PDF

Total and Unbound Doravirine Concentrations and Viral Suppression in CSF.

Clin Infect Dis

May 2022

HIV and STI Unit, Infectious Disease Service, Hospital Universitari de Bellvitge-IDIBELL, Universitat de Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.

Article Synopsis
  • - We measured the total and unbound levels of doravirine (DOR) in both cerebrospinal fluid and blood plasma.
  • - All patients had DOR levels in their cerebrospinal fluid that were higher than the concentration needed to effectively inhibit the wild-type virus (5.1 ng/mL).
  • - This suggests that doravirine could play a role in reducing viral replication in the cerebrospinal fluid of these patients.
View Article and Find Full Text PDF

Absorption, distribution, metabolism and elimination of doravirine (MK-1439), a novel non-nucleoside reverse transcriptase inhibitor, were investigated. Two clinical trials were conducted in healthy subjects: an oral single dose [C]doravirine (350 mg, ∼200 µCi) trial (n = 6) and an intravenous (IV) single-dose doravirine (100 µg) trial (n = 12). In vitro metabolism, protein binding, apparent permeability and P-glycoprotein (P-gp) transport studies were conducted to complement the clinical trials.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!