Issue 7, 2024

Next generation microfluidics: fulfilling the promise of lab-on-a-chip technologies

Abstract

Microfluidic lab-on-a-chip technologies enable the analysis and manipulation of small fluid volumes and particles at small scales and the control of fluid flow and transport processes at the microscale, leading to the development of new methods to address a broad range of scientific and medical challenges. Microfluidic and lab-on-a-chip technologies have made a noteworthy impact in basic, preclinical, and clinical research, especially in hematology and vascular biology due to the inherent ability of microfluidics to mimic physiologic flow conditions in blood vessels and capillaries. With the potential to significantly impact translational research and clinical diagnostics, technical issues and incentive mismatches have stymied microfluidics from fulfilling this promise. We describe how accessibility, usability, and manufacturability of microfluidic technologies should be improved and how a shift in mindset and incentives within the field is also needed to address these issues. In this report, we discuss the state of the microfluidic field regarding current limitations and propose future directions and new approaches for the field to advance microfluidic technologies closer to translation and clinical use. While our report focuses on using blood as the prototypical biofluid sample, the proposed ideas and research directions can be extrapolated to other areas of hematology, oncology, biology, and medicine.

Graphical abstract: Next generation microfluidics: fulfilling the promise of lab-on-a-chip technologies

Article information

Article type
Perspective
Submitted
20 sep. 2023
Accepted
04 mar. 2024
First published
05 mar. 2024
This article is Open Access
Creative Commons BY-NC license

Lab Chip, 2024,24, 1867-1874

Next generation microfluidics: fulfilling the promise of lab-on-a-chip technologies

U. A. Gurkan, D. K. Wood, D. Carranza, L. H. Herbertson, S. L. Diamond, E. Du, S. Guha, J. Di Paola, P. C. Hines, I. Papautsky, S. S. Shevkoplyas, N. J. Sniadecki, V. K. Pamula, P. Sundd, A. Rizwan, P. Qasba and W. A. Lam, Lab Chip, 2024, 24, 1867 DOI: 10.1039/D3LC00796K

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements