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.
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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
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
Identifiers
What Socratic holds
Registered trials
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.