The revolution of PDMS microfluidics in cellular biology
Abstract
Microfluidics is revolutionizing the way research on cellular biology has been traditionally conducted. The ability to control the cell physicochemical environment by adjusting flow conditions, while performing cellular analysis at single-cell resolution and high-throughput, has made microfluidics the ideal choice to replace traditional in vitro models. However, such a revolution only truly started with the advent of polydimethylsiloxane (PDMS) as a microfluidic structural material and soft-lithography as a rapid manufacturing technology. Indeed, before the "PDMS age," microfluidic technologies were: costly, time-consuming and, more importantly, accessible only to specialized laboratories and users. The simplicity of molding PDMS in various shapes along with its inherent properties (transparency, biocompatibility, and gas permeability) has spread the applications of innovative microfluidic devices to diverse and important biological fields and clinical studies. This review highlights how PDMS-based microfluidic systems are innovating pre-clinical biological research on cells and organs. These devices were able to cultivate different cell lines, enhance the sensitivity and diagnostic effectiveness of numerous cell-based assays by maintaining consistent chemical gradients, utilizing and detecting the smallest number of analytes while being high-throughput. This review will also assist in identifying the pitfalls in current PDMS-based microfluidic systems to facilitate breakthro…
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PDMS, a widely used material for microfluidic chips, has high gas permeability.
“polydimethylsiloxane (PDMS), a widely used material for microfluidic chips, has high gas permeability”
From Material-dependent oxygen transport governs ischemia-reperfusion injury and drug response in a kidney microphysiological system (2026) · cites this paper as Banik et al., 2023
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Kutsuzawa, N., Nakamura, H., Shinha, K., & Kimura, H. (2026) · Frontiers in Toxicology · doi:10.3389/ftox.2026.1854389
- Authors
- Banik, S., Uchil, A., Kalsang, T., Chakrabarty, S., Ali, M. A., Srisungsitthisunti, P., Mahato, K. K., Surdo, S., & Mazumder, N.
- Affiliations
- Manipal Academy of Higher Education (IN)
- Carnegie Mellon University (US)
- King Mongkut's University of Technology North Bangkok (TH)
- Italian Institute of Technology (IT)
- Corresponding author
- Surdo, Salvatore
- Mazumder, Nirmal
- ORCID
- Venue
- Critical Reviews in Biotechnology
- Publisher
- Informa UK Limited
- Published
- 2022-04-11
- Volume
- 43
- Issue
- 3
- Pages
- 465-483
- ISSN
- 0738-8551 (ISSN-L)
- 1549-7801
- OpenAlex
- W4223459119
- Cited by
- 84
- References
- 6
- Citations by year
- 2026: 24 · 2025: 21 · 2024: 19 · 2023: 17 · 2022: 3
- FWCI
- 1.32
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Critical Reviews in Biotechnology (publishedVersion)
- PubMed (publishedVersion)
- CINECA IRIS Institutial research information system (University of Pisa) (submittedVersion)
- Funders
- Indian Council of Medical Research (ICMR), Govt. of India
- Department of Science and Technology, India
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › Microfluidic and Capillary Electrophoresis Applications
- Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
- Physical Sciences › Engineering › Biomedical Engineering › Microfluidic and Bio-sensing Technologies
- Keywords
- PDMS microfluidics, polydimethylsiloxane, soft lithography, cell culture, single-cell analysis, chemical gradients, organ-on-a-chip, biocompatibility, gas permeability
- MeSH terms
- Dimethylpolysiloxanes, Microfluidics, Microfluidic Analytical Techniques, Lab-On-A-Chip Devices, Printing, Three-Dimensional
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