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REVIEW article

Front. Bioeng. Biotechnol.

Sec. Nanobiotechnology

This article is part of the Research TopicInsights In Nanobiotechnology 2024: Novel Developments, Current Challenges and Future PerspectivesView all 4 articles

Integrating Computational Fluid Dynamics into Organ-on-Chip Systems: A Glioblastoma-Centred Design and Validation Framework

Provisionally accepted
  • 1Teesside University School of Health and Life Sciences, Middlesbrough, United Kingdom
  • 2University of Cumbria, Carlisle, United Kingdom
  • 3Universiteit Twente Technisch Medisch Centrum, Enschede, Netherlands
  • 4Koc Universitesi, Istanbul, Türkiye
  • 5Nacionalni institut za biologijo, Ljubljana, Slovenia

The final, formatted version of the article will be published soon.

Glioblastoma (GBM) remains one of the most lethal and treatment-resistant brain cancers, driven in part by the complexity of its tumour microenvironment (TME). While organ-on-chip (OoC) platforms offer more physiologically relevant models than traditional 2D or static 3D systems, their design remains largely empirical, lacking predictive control over flow conditions, biochemical gradients, and mechanical cues. Computational Fluid Dynamics (CFD) has emerged as a powerful tool to enhance the design, precision, and biological fidelity of OoC platforms. This comprehensive review highlights current limitations in replicating GBM's biological complexity and technical constraints in device fabrication and maintenance, mapping them to specific CFD strategies. It synthesises current strategies into a structured workflow for integrating CFD into the design, optimisation, and validation of microfluidic tumour models—bridging engineering precision with biological complexity. In addition, validation frameworks reported in the literature are highlighted and mapped onto GBM-on-chip applications have been recommended, drawing on widely recognised international standards for engineering validation and regulatory modelling practices. Finally, this review positions CFD as a core component of GBM-on-chip development and explores how its integration with AI-based optimisation can advance the creation of more predictive, scalable, and biologically relevant in vitro tumour models.

Keywords: AI, computational fluid dynamics, Glioblastoma, In silicosimulation, in vitro modelling, Microfluidic perfusion, organ-on-chip, tumour microenvironment

Received: 30 Sep 2025; Accepted: 11 Dec 2025.

Copyright: © 2025 Taleban, Li, Ali, Kalesh, Prakash, Bagci-Onder and Breznik. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Hooman Taleban
Xinzhong Li

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