Evidence map›Paper›PMID 34075381›Full record

ArticlebioRxiv : the preprint server for biology2021

Quantitation of tizoxanide in multiple matrices to support cell culture, animal and human research.

Megan Neary, Usman Arshad, Lee Tatham, Henry Pertinez, Helen Box, Rajith Kr Rajoli, Anthony Valentijn, Joanne Sharp, Steve P Rannard, Giancarlo A Biagini and 2 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2021. 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, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Megan NearyDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, L7 3NY, UK.
Usman ArshadDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, L7 3NY, UK.
Lee TathamDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, L7 3NY, UK.
Henry PertinezDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, L7 3NY, UK.
Helen BoxDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, L7 3NY, UK.
Rajith Kr RajoliDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, L7 3NY, UK.
Anthony ValentijnDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, L7 3NY, UK.
Joanne SharpDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, L7 3NY, UK.
Steve P RannardDepartment of Chemistry, University of Liverpool, Liverpool, L69 3BX, UK.
Giancarlo A BiaginiCentre for Drugs and Diagnostics, Liverpool School of Tropical Medicine, Liverpool L3 5QA, UK.
Paul CurleyDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, L7 3NY, UK.
Andrew OwenDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, L7 3NY, UK.
University of Liverpool · GBLiverpool School of Tropical Medicine · GB

Funding

The Long-Acting/Extended Release Antiretroviral Resource Program (LEAP)R24AI118397 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Charles W. Flexner · 2015 to 2026
$9.4M
Long acting NRTI therapies for HIVR01AI134091 · NIAID · JOHNS HOPKINS UNIVERSITY · PI FREEL MEYERS, CAREN L., RANNARD, STEVE · 2017 to 2021
$3.1M
Medical Research Council MC_PC_17167Medical Research Council MR/S00467X/1Medical Research Council MR/W004356/1NIAID NIH HHS R01 AI134091NIAID NIH HHS R24 AI118397
6 · The paper itself

Abstract

Currently nitazoxanide is being assessed as a candidate therapeutic for SARS-CoV-2. Unlike many other candidates being investigated, tizoxanide (the active metabolite of nitazoxanide) plasma concentrations achieve antiviral levels after administration of the approved dose, although higher doses are expected to be needed to maintain these concentrations across the dosing interval in the majority of patients. Here an LC-MS/MS assay is described that has been validated in accordance with Food and Drug Administration (FDA) guidelines. Fundamental parameters have been evaluated, and these included accuracy, precision and sensitivity. The assay was validated for human plasma, mouse plasma and Dulbeccos Modified Eagles Medium (DMEM) containing varying concentrations of Foetal Bovine Serum (FBS). Matrix effects are a well-documented source of concern for chromatographic analysis, with the potential to impact various stages of the analytical process, including suppression or enhancement of ionisation. Therefore, a robustly validated LC-MS/MS analytical method is presented capable of quantifying tizoxanide in multiple matrices with minimal impact of matrix effects. The validated assay presented here was linear from 15.6ng/mL to 1000ng/mL. Accuracy and precision ranged between 102.2% and 113.5%, 100.1% and 105.4%, respectively. The presented assay here has applications in both pre-clinical and clinical research and may be used to facilitate further investigations into the application of nitazoxanide against SARS-CoV-2.

Identifiers

PMID34075381
PMCPMC8168394
OpenAlexW3165734231

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 OpenQuestion graph.