“… Hydrogels | Components | Physicochemical properties | Biofunctions | Ref. |
HA-ADH/d-AHA | HA, adipic dihydrazide, dialdehyde HA | Shear-responsive; boundary lubricated; anti-inflammatory; injectable; self-healing; controlled-release of bioactive molecules | Reducing friction; alleviating the progression of OA; inhibiting inflammation; protecting chondrocytes | [ 141 , 142 ] |
HA-ADH/dextran | HA, adipic dihydrazide, dialdehyde dextran | ROS depletion, sustainable drug release; viscosupplementation | Inhibiting inflammation; alleviating the progression of OA; protecting cartilage | [ 143 ] |
HA-ADH/pectin | HA, adipic dihydrazide, oligopeptide-grafted dialdehyde pectin | Short gel times; controllable mechanical properties and degradation capacity | Providing a suitable microenvironment for the phenotype of chondrocytes and chondrogenesis | [ 144 ] |
HA-Fur/CS-Mal/ACS/ADH | Methylfuran-modified HA, maleimide-modified chondroitin sulfate, adipic dihydrazide, dialdehyde chondroitin sulfate | Double-network; controllable viscoelasticity and stress relaxation; good processability; self-healing ability; high swelling capacity and stability | Negligible inflammatory response | [ 145 ] |
HA-Ad/ β -CD-Ac | HA, adamantane, monoacrylated β -cyclodextrin | Good self-healing properties, compressibility; sustained release of TGF- β 1 | Rapidly integrating with the defect tissue; promoting the chondrogenesis of MSCs and cartilage regeneration | [ 146 ] |
HA-Ad/ β -CD-SH/HA-Mal | HA, adamantane, thiolated β -cyclodextrin, maleimide | Tunable viscoelasticity | Maintaining 3D spreading and intracellular interactions of encapsulated MSCs | [ 147 ] |
HA- β -CD/PAA-Fer | HA, β -cyclodextrin, ferrocene, polyacrylic acid | Magnetic navigation; controlled release of glutathione | Promoting the columnar arrangement of chondrocytes and the repair of cartilage damage | [ 148 ] |
HA-CB [ 6 ]/HA-PA | HA, cucurbit [ |
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