Highlights of our work
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Developed a decellularized extracellular matrix (dECM)–based bioink supporting chondrogenesis.
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Optimized composite alginate–chitosan hydrogels achieving compression modulus of 0.18 MPa and tensile strength of 0.4 MPa.
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Dynamic microfluidic perfusion (150 mbar & 50 mbar) enabled formation of superficial and middle cartilage zones.
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MSCs-derived chondrocytes in bioink showed upregulation of COL2A1, Aggrecan, and Laminin — hallmark features of hyaline cartilage.
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The resulting constructs exhibited non-linear mechanical behavior similar to native cartilage, positioning them as models for drug testing.
 
This study represents a step forward in tissue-engineered biomimetics, integrating material science, stem cell biology, and microfluidic mechanics to emulate native cartilage physiology in vitro.