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Engineering biomimetic tissue barrier models on chips: From design and fabrication to applications in disease modeling and drug screening
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Nano Biotechnology. KTH, Centres, Science for Life Laboratory, SciLifeLab. AIMES, Center for the Advancement of Integrated Medical and Engineering Sciences, Department of Neuroscience, Karolinska Institute, Solna, Sweden; Division of Medical Physics, Department of Radiation Oncology, Stanford University, Stanford, CA, USA.ORCID iD: 0000-0002-8245-692X
School of Engineering and Sciences, Tecnologico de Monterrey, Ave. Eugenio Garza Sada 2501, Monterrey 64849, NL, Mexico.
Edwin L Steele Laboratories, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114 USA.
Department of Bioengineering, Graduate School of Natural and Applied Sciences, Ege University, Turkey.
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2026 (English)In: Biomaterials, ISSN 0142-9612, E-ISSN 1878-5905, Vol. 327, article id 123739Article, review/survey (Refereed) Published
Abstract [en]

Replicating the in vitro properties of tissue barriers—such as the blood-brain barrier, gut, skin, lung, kidney, retina, nasal epithelium, and placenta—is crucial for many applications, including drug screening, studying molecular transport, drug delivery, and disease modeling in preclinical studies. Organ-on-a-chip (OoC) platforms are advanced three-dimensional (3D) in vitro models that aim to replicate various aspects of organ functionality within microfluidic systems by providing microenvironments akin to native tissue. When used to model the interface between two different tissue compartments, OoC technology offers a promising platform for more accurately replicating the physiology and pathophysiology of various tissue barriers in the body. This review focuses on the state-of-the-art biomimetic tissue barrier models, ranging from two-channel tissue barrier-on-a-chip systems with a thin porous membrane to hydrogel-based membrane models. Specifically, it explores the engineering of tissue barrier-on-a-chip platforms, highlighting various fabrication techniques for microfluidic chips and membranes, as well as methods for functional characterization of the engineered tissue barriers. Additionally, we discuss the development of organ-specific barrier models and multi-organ-on-a-chip systems for studying inter-organ communication. Finally, we highlight the current challenges in the field and future directions in advancing tissue barrier modeling using OoC technology.

Place, publisher, year, edition, pages
Elsevier BV , 2026. Vol. 327, article id 123739
Keywords [en]
Disease modeling, Drug screening, Drug transport, Membrane, Microfabrication, Microfluidics, Organ-on-a-chip, Tissue-tissue interface
National Category
Nanotechnology for/in Life Science and Medicine Medical Biotechnology (Focus on Cell Biology, (incl. Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy)
Identifiers
URN: urn:nbn:se:kth:diva-372606DOI: 10.1016/j.biomaterials.2025.123739ISI: 001596123400001PubMedID: 41072391Scopus ID: 2-s2.0-105019211938OAI: oai:DiVA.org:kth-372606DiVA, id: diva2:2013043
Note

QC 20251111

Available from: 2025-11-11 Created: 2025-11-11 Last updated: 2025-11-11Bibliographically approved

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Nasiri, RohollahJain, SaumeyEnrico, AlessandroHerland, Anna

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Nasiri, RohollahVan Gastel, DirkjeJain, SaumeyEnrico, AlessandroHerland, Anna
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Nanotechnology for/in Life Science and MedicineMedical Biotechnology (Focus on Cell Biology, (incl. Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy)

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