Volume 3, 2024

Versatile, in-line optical oxygen tension sensors for continuous monitoring during ex vivo kidney perfusion

Abstract

Integration of physiological sensing modalities within tissue and organ perfusion systems is becoming a steadily expanding field of research, aimed at achieving technological breakthrough innovations that will expand the sites and clinical settings at which such systems can be used. This is becoming possible in part due to the advancement of user-friendly optical sensors in recent years, which rely both on synthetic, luminescent sensor molecules and inexpensive, low-power electronic components for device engineering. In this article we report a novel approach towards enabling automated, continuous monitoring of oxygenation during ex vivo organ perfusion, by combining versatile flow cell components and low-power, programmable electronic readout devices. The sensing element comprises a 3D printed, miniature flow cell with tubing connectors and an affixed oxygen-sensing thin film material containing in-house developed, brightly-emitting metalloporphyrin phosphor molecules embedded within a polymer matrix. Proof-of-concept validation of this technology is demonstrated through integration within the tubing circuit of a transportable medical device for hypothermic oxygenated machine perfusion of extracted kidneys as a model for organs to be preserved as transplants.

Graphical abstract: Versatile, in-line optical oxygen tension sensors for continuous monitoring during ex vivo kidney perfusion

Supplementary files

Article information

Article type
Communication
Submitted
15 Sep 2023
Accepted
19 Feb 2024
First published
27 Feb 2024
This article is Open Access
Creative Commons BY license

Sens. Diagn., 2024,3, 1014-1019

Versatile, in-line optical oxygen tension sensors for continuous monitoring during ex vivo kidney perfusion

E. Roussakis, J. P. Cascales, D. Yoeli, A. Cralley, A. Goss, A. Wiatrowski, M. Carvalho, H. B. Moore, E. E. Moore, C. A. Huang and C. L. Evans, Sens. Diagn., 2024, 3, 1014 DOI: 10.1039/D3SD00240C

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