PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
September 12, 2025Advanced Healthcare Materials0 citationsOpen Access

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

View Full Paper
DMDaniel MinahanKNKatherine M. NelsonFRFilipa Ribeiro

Key Points

  • The modular microphysiological system supports long-term culture for up to 14 days, enhancing research capabilities.
  • Validation involved dual epithelial and endothelial cell co-culture under both static and perfused conditions.
  • Material testing ensured biocompatibility, and manufacturing fidelity was confirmed through vinyl cutting reproducibility.
  • The system is designed for ease of use, aiming to democratize access to advanced in vitro model systems.

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.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Minahan et al. (2025) studied this question.

synapsesocial.com/papers/68d44b3831b076d99fa54b4fhttps://doi.org/10.1002/adhm.202502202
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1A Pumpless, High‐Throughput Microphysiological System to Mimic Enteric Innervation of Duodenal Epithelium and the Impact on Barrier Function2024 · 15 citations
  2. 2Modulation of tight junction properties relevant to fluid transport across rabbit corneal endothelium2007 · 34 citations
  3. 3From the cellular perspective: exploring differences in the cellular baseline in macroscale and microfluidic cultures2009 · 136 citations
  4. 4A Microfluidic Biomaterial2005 · 235 citations
  5. 5Endothelial Cell Orientation and Polarity Are Controlled by Shear Stress and VEGF Through Distinct Signaling Pathways2021 · 110 citations