Evidence map›Paper›PMID 40716709›Full record

ArticleJournal of pharmaceutical sciences2025

Novel liquid chromatography-tandem mass spectrometry method for simultaneous detection of three anti-HIV drugs tenofovir, lamivudine, and dolutegravir in plasma.

Luqi Duan, Shreshtha Dash, Masa Eguchi, Rachele Delle Fratte, Zachary R Stephen, Rodney Jy Ho

Abstract read
In one paragraph

Article in Journal of pharmaceutical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Luqi DuanDepartment of Pharmaceutics, University of Washington, Seattle, Washington, USA.
Shreshtha DashDepartment of Pharmaceutics, University of Washington, Seattle, Washington, USA.
Masa EguchiDepartment of Pharmaceutics, University of Washington, Seattle, Washington, USA.
Rachele Delle FratteDepartment of Pharmaceutics, University of Washington, Seattle, Washington, USA.
Zachary R StephenDepartment of Pharmaceutics, University of Washington, Seattle, Washington, USA.
Rodney Jy HoDepartment of Pharmaceutics, University of Washington, Seattle, Washington, USA. Electronic address: rodneyho@u.washington.edu.

Funding

Targeted Long-acting Combination Antiretroviral Therapy (TLC-ART)UM1AI120176 · NIAID · UNIVERSITY OF WASHINGTON · PI COLLIER, ANN CORNWALL, HO, RODNEY J.Y. · 2015 to 2019
$15.0M
NextGen Long-acting and targeted combination ART for Children with HIVR33AI149665 · NIAID · UNIVERSITY OF WASHINGTON · PI HO, RODNEY J.Y. · 2022 to 2025
$4.1M
Long-acting Antiviral Treatment for HBVR01AI179309 · NIAID · UNIVERSITY OF WASHINGTON · PI RODNEY J.Y. HO, Hyang Nina Kim · 2024 to 2026
$2.4M
NextGen Long-acting and targeted combination ART for Children with HIVR61AI149665 · NIAID · UNIVERSITY OF WASHINGTON · PI HO, RODNEY J.Y., MELVIN, ANN JORNS · 2020 to 2021
$2.1M
NIAID NIH HHS R01 AI179309NIAID NIH HHS R33 AI149665NIAID NIH HHS R61 AI149665NIAID NIH HHS UM1 AI120176
6 · The paper itself

Abstract

Currently, the world health organization (WHO) recommends a fixed-dose combination therapy called TLD, composed of tenofovir, lamivudine, and dolutegravir (TLD) for human immunodeficiency virus (HIV) treatment. About 23 of 39 million people living with HIV/AIDS (PLWHA) are on a daily TLD pill. In this study, we successfully developed a simple, efficient, and sensitive method to extract and enable the simultaneous quantification of tenofovir, lamivudine, and dolutegravir in rats, non-human primates (NHP), and human plasma samples. The 3 HIV drugs in small volume, 100 µL plasma were extracted after protein precipitation, and all the analytes were quantified using a novel liquid chromatography-tandem mass spectrometry. The assay provided analysis of all three analytes in rat, NHP, and human plasma. This method was used to evaluate time-plasma drug concentrations in two NHPs (Macaca nemestrina). The reported bioanalytical method demonstrated high sensitivity, reproducibility, and robustness for quantifying the 3 HIV drugs with efficiency. Lower limit of quantification (LLOQ) for tenofovir (TFV), lamivudine (3TC) and dolutegravir (DTG) were between 0.3 - 2.6 ng/mL equivalent to 30 - 260 pg in 100 µL of rats, NHPs, or human plasma samples. This assay may be adapted for evaluating drug concentrations across multiple species to support preclinical, clinical, and translational studies for developing long-acting products.

Indexed as

Anti-HIV AgentsHeterocyclic Compounds, 3-RingLamivudineTenofovirAnimalsChromatography, LiquidDolutegravirHIV InfectionsHumansMaleOxazinesPiperazinesPyridonesRatsRats, Sprague-DawleyReproducibility of ResultsAnti-HIV AgentsDolutegravirHeterocyclic Compounds, 3-RingLamivudineOxazinesPiperazinesPyridonesTenofovirAntiinfective(s)BioanalysisChromatographyDrug-combination particle(s)HIV/AIDSInjectable(s)Liquid chromatography-mass spectrometry (LC-MS)LongactingMass spectrometryPreclinical pharmacokinetics

Identifiers

PMID40716709
PMCPMC13215559

What Socratic holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.