Evidence map›Paper›PMID 34680836›Full record

ArticleAntibiotics (Basel, Switzerland)2021

Experimental Validation of a Mathematical Framework to Simulate Antibiotics with Distinct Half-Lives Concurrently in an In Vitro Model.

Brianna M Eales, Cole S Hudson, Iordanis Kesisoglou, Weiqun Wang, Michael Nikolaou, Vincent H Tam

Open access · goldAbstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. DynamicAntibiotics (Basel, Switzerland) · 2024
    Review
  2. In vitro model to simulate multiple drugs with distinct elimination half-lives.International journal of antimicrobial agents · 2023
    Article
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 at 1 institution in 1 country.

Brianna M EalesDepartment of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX 77204, USA.
Cole S HudsonDepartment of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX 77204, USA.
Iordanis KesisoglouDepartment of Chemical and Biomolecular Engineering, University of Houston, Houston, TX 77204, USA.ORCID 0000-0003-0109-0215
Weiqun WangDepartment of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX 77204, USA.
Michael NikolaouDepartment of Chemical and Biomolecular Engineering, University of Houston, Houston, TX 77204, USA.ORCID 0000-0003-0241-6600
Vincent H TamDepartment of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX 77204, USA.ORCID 0000-0001-7071-5376
University of Houston · US

Funding

Personalized Antimicrobial Combinations to Combat ResistanceR01AI140287 · NIAID · UNIVERSITY OF HOUSTON · PI VINCENT H TAM · 2018 to 2026
$5.9M
NIAID NIH HHS R01 AI140287NIH HHS 5R01AI140287-04
6 · The paper itself

Abstract

Antimicrobial resistance has been steadily increasing in prevalence, and combination therapy is commonly used to treat infections due to multidrug resistant bacteria. Under certain circumstances, combination therapy of three or more drugs may be necessary, which makes it necessary to simulate the pharmacokinetic profiles of more than two drugs concurrently in vitro. Recently, a general theoretical framework was developed to simulate three drugs with distinctly different half-lives. The objective of the study was to experimentally validate the theoretical model. Clinically relevant exposures of meropenem, ceftazidime, and ceftriaxone were simulated concurrently in a hollow-fiber infection model, with the corresponding half-lives of 1, 2.5, and 8 h, respectively. Serial samples were obtained over 24 h and drug concentrations were assayed using validated LC-MS/MS methods. A one-compartment model with zero-order input was used to characterize the observed concentration-time profiles. The experimentally observed half-lives corresponding to exponential decline of all three drugs were in good agreement with the respective values anticipated at the experiment design stage. These results were reproducible when the experiment was repeated on a different day. The validated benchtop setup can be used as a more flexible preclinical tool to explore the effectiveness of various drug combinations against multidrug resistant bacteria.

Indexed as

antimicrobial agentsexperimental therapeuticspharmacodynamicspharmacokinetics

Identifiers

PMID34680836
PMCPMC8532833
OpenAlexW3205454273

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.