Evidence map›Paper›PMID 33182761›Full record

ArticlePharmaceutics2020

A Physiologically-Based Pharmacokinetic Model of Trimethoprim for MATE1, OCT1, OCT2, and CYP2C8 Drug-Drug-Gene Interaction Predictions.

Denise Türk, Nina Hanke, Thorsten Lehr

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 28% of its field
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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Denise TürkClinical Pharmacy, Saarland University, 66123 Saarbrücken, Germany.
Nina HankeClinical Pharmacy, Saarland University, 66123 Saarbrücken, Germany.ORCID 0000-0001-6166-8838
Thorsten LehrClinical Pharmacy, Saarland University, 66123 Saarbrücken, Germany.ORCID 0000-0002-8372-1465
Saarland University · DE

Funding

Bundesministerium für Bildung und Forschung 031L0161C ("OSMOSES")Deutsche Forschungsgemeinschaft (DFG) and Saarland University Funding program "Open Access Publishing"
6 · The paper itself

Abstract

Trimethoprim is a frequently-prescribed antibiotic and therefore likely to be co-administered with other medications, but it is also a potent inhibitor of multidrug and toxin extrusion protein (MATE) and a weak inhibitor of cytochrome P450 (CYP) 2C8. The aim of this work was to develop a physiologically-based pharmacokinetic (PBPK) model of trimethoprim to investigate and predict its drug-drug interactions (DDIs). The model was developed in PK-Sim

Indexed as

cytochrome P450 2C8 (CYP2C8)drug–drug interaction (DDI)multidrug and toxin extrusion protein (MATE)organic cation transporter (OCT)physiologically-based pharmacokinetic (PBPK) modelingtrimethoprim

Identifiers

PMID33182761
PMCPMC7696733
OpenAlexW3106016925

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.