Evidence map›Paper›PMID 40931573›Full record

ArticleAdvanced healthcare materials2026

Democratizing Organ-On-Chip Technologies With a Modular, Reusable, and Perfusion-Ready Microphysiological System.

Daniel J Minahan, Katherine M Nelson, Filipa Ribeiro, Bryan J Ferrick, Alexandra M Zurzolo, Kira Byers, Victoria Mckeown, Jason P Gleghorn

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Daniel J MinahanDepartment of Biomedical Engineering, University of Delaware, Newark, DE, 19716, USA.
Katherine M NelsonDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE, 19716, USA.ORCID 0000-0002-1070-1551
Filipa RibeiroDepartment of Biomedical Engineering, University of Delaware, Newark, DE, 19716, USA.
Bryan J FerrickDepartment of Biomedical Engineering, University of Delaware, Newark, DE, 19716, USA.ORCID 0000-0001-6767-3988
Alexandra M ZurzoloDepartment of Mechanical Engineering, University of Delaware, Newark, DE, 19716, USA.
Kira ByersDepartment of Biomedical Engineering, University of Delaware, Newark, DE, 19716, USA.
Victoria MckeownDepartment of Biomedical Engineering, University of Delaware, Newark, DE, 19716, USA.
Jason P GleghornDepartment of Biomedical Engineering, University of Delaware, Newark, DE, 19716, USA.ORCID 0000-0003-1283-2966

Funding

The Effects of Sex Hormones on Chlamydia InfectionU19AI158930 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI CRISS, ALISON K · 2021 to 2025
$7.7M
Chemistry-Biology Interface Predoctoral Training Grant 2024-2029T32GM133395 · NIGMS · UNIVERSITY OF DELAWARE · PI Catherine Leimkuhler Grimes · 2019 to 2026
$3.7M
The impact of the physical microenvironment on trophoblast functionF31HD105398 · NICHD · UNIVERSITY OF DELAWARE · PI NELSON, KATHERINE · 2021 to 2023
$122k
Division of Intramural Research, National Institute of Allergy and Infectious Diseases U19AI158930National Institute of Child Health and Human Development F31HD105398National Science Foundation ART 2331440NIAID NIH HHS U19 AI158930NICHD NIH HHS F31 HD105398NIGMS NIH HHS T32 GM133395NIGMS NIH HHS T32GM133395University of Delaware - Insitutue for Engineering Driven Health
6 · The paper itself

Abstract

Organ-on-chip (OOC) technologies, also called microphysiological systems (MPS), offer dynamic microenvironments that improve upon static culture systems, yet widespread adoption has been hindered by fabrication complexity, reliance on polydimethylsiloxane (PDMS), and limited modularity. Here, a modular MPS platform is presented, designed for ease of use, reproducibility, and broad applicability. The system comprises layered elastomeric inserts for dual monolayer cell culture, which is clamped within a reusable acrylic cassette for perfusion studies. This enables researchers to decouple model establishment from flow experiments and streamline their workflows. The system is validated using dual epithelial and endothelial cell co-culture under static and perfused conditions, including shear-induced alignment of HUVECs. Material testing confirmed biocompatibility, while vinyl cutting reproducibility demonstrated high manufacturing fidelity. The platform reliably supported long-term culture (up to 14 days), and the open insert format facilitated uniform seeding and imaging access. This approach enables parallelized experimentation, minimizes pump usage, and is well-suited for labs without microfabrication infrastructure. By combining fabrication flexibility with biological robustness, this work establishes a generalizable platform for modular tissue-chip development adapted to diverse organ systems and serves as a foundational framework for democratizing advanced in vitro model systems.

Indexed as

Lab-On-A-Chip DevicesCell Culture TechniquesCoculture TechniquesDimethylpolysiloxanesHumansHuman Umbilical Vein Endothelial CellsMicrophysiological SystemsPerfusionbaysilonDimethylpolysiloxanesin vitro tissue modelslow‐resourcemicrophysiological system (MPS)modular microfluidicsorgan‐on‐chip (OOC)

Identifiers

PMID40931573
PMCPMC12914553

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.