Issue 20, 2022

Integrated biosensors for monitoring microphysiological systems

Abstract

Microphysiological systems (MPSs), also known as organ-on-a-chip models, aim to recapitulate the functional components of human tissues or organs in vitro. Over the last decade, with the advances in biomaterials, 3D bioprinting, and microfluidics, numerous MPSs have emerged with applications to study diseased and healthy tissue models. Various organs have been modeled using MPS technology, such as the heart, liver, lung, and blood–brain barrier. An important aspect of in vitro modeling is the accurate phenotypical and functional characterization of the modeled organ. However, most conventional characterization methods are invasive and destructive and do not allow continuous monitoring of the cells in culture. On the other hand, microfluidic biosensors enable in-line, real-time sensing of target molecules with an excellent limit of detection and in a non-invasive manner, thereby effectively overcoming the limitation of the traditional techniques. Consequently, microfluidic biosensors have been increasingly integrated into MPSs and used for in-line target detection. This review discusses the state-of-the-art microfluidic biosensors by providing specific examples, detailing their main advantages in monitoring MPSs, and highlighting current developments in this field. Finally, we describe the remaining challenges and potential future developments to advance the current state-of-the-art in integrated microfluidic biosensors.

Graphical abstract: Integrated biosensors for monitoring microphysiological systems

Associated articles

Article information

Article type
Critical Review
Submitted
21 Mar 2022
Accepted
22 Aug 2022
First published
25 Aug 2022

Lab Chip, 2022,22, 3801-3816

Author version available

Integrated biosensors for monitoring microphysiological systems

L. Mou, K. Mandal, M. M. Mecwan, A. L. Hernandez, S. Maity, S. Sharma, R. D. Herculano, S. Kawakita, V. Jucaud, M. R. Dokmeci and A. Khademhosseini, Lab Chip, 2022, 22, 3801 DOI: 10.1039/D2LC00262K

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