Bioengineered articular cartilage biomimetic organ-on-a-chip using microfluidics
Upadhyay U., Maredupaka S., Kancherla R., Srinivasulu K., Chelluri LK.
Laboratory Study on Hip, published in NPJ Biomed Innov (2025) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Laboratory Study
- Journal
- NPJ Biomed Innov (2025)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 42032314
- PMCID
- PMC13055100
- DOI
- 10.1038/s44385-025-00012-2
- Citations
- 1
Abstract (original English)
Cartilage tissue engineering is complex owing to the apt choice of biopolymers, cell source and dynamic simulation. Herein, we elucidate a novel approach to mesenchymal stem cells (MSCs)- induced chondrogenesis using microfluidics on an organ-on-a-chip (OOAC) model, coupled with decellularized extracellular matrix (dECM) as bioink additive, on optimised composite hydrogel. The hydrogel displayed a compression modulus of 0.18 MPa and tensile strength of 0.4 MPa. Microfluidic shear pressures of 150 mbar and 50 mbar were optimised to attain the superficial and middle zones respectively, with a media flow rate of 5 µL min -1 . Gene/protein expression revealed upregulation of collagen type II, aggrecan, and laminin suggestive of chondrogenesis. The OOAC tissue constructs showed non-linear behaviour with tensile strength of 1.01 MPa. The role of microfluidics, bioink and composite hydrogel on MSCs demonstrated notable advancements towards developing hyaline cartilage biomimetics resembling structural and biomechanical properties of native cartilage, thereby serving as a disease model.
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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