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Updated: Jun 28, 2026

Autonomously Bioluminescent Mammalian Cells for Continuous and Real-time Monitoring of Cytotoxicity
Published on: October 28, 2013
In situ monitoring of barrier function on-chip via automated, non-invasive luminescence sensing
Bryan G Schellberg1, Abigail N Koppes1,2,3, Ryan A Koppes1,2
1Department of Chemical Engineering, Northeastern University, Boston, Massachusetts, USA. a.koppes@northeastern.edu.
Abstract:
Over the past 30 years, organs-on-a-chip (OOCs) have emerged as a robust alternative to address the technological challenges associated with current in vitro and in vivo options. Although OOCs offer improved bio-relevance and controlled complexity, broad adoption has remained limited. Most approaches to characterize on-chip structure and function require human intervention, limiting device translation and feasibility. Here, we introduce a new fiber optic-based sensing platform that enables automated, temporal luminescence sensing on-chip, validated for real-time readout of epithelial and endothelial barrier function under cytokine-induced inflammation. Our platform, capable of at least 1 μM resolution, tracked paracellular transport in situ for 9 days of culture under perfusion on-chip. These results offer an alternative sensing approach for continuous, non-invasive luminescence monitoring in OOCs.
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