3D-printed bilayer hydrogel scaffolds incorporating HAP and KGN@Lip for osteochondral regeneration

  • J Mater Chem B. 2026 Jul 1;14(25):7951-7968. doi: 10.1039/d5tb02850g.
Zhenbiao Wangzi  1 Chengcheng Yang  1 Peng Yu  1 Xiubiao Huang  1 Nan Hu  1 Tuo Jiao  1 Hao Qi  2
Affiliations
  • 1. Key Laboratory of Emergency and Trauma of Ministry of Education, Department of Joint Surgery Dept, The First Affiliated Hospital, Hainan Medical University, 31 Longhua Road, Haikou 570102, Hainan, China. [email protected].
  • 2. The Second Affiliated Hospital of Hainan Medical University, 368 YeHaiDaDao Road, Haikou 570145, Hainan, China. [email protected].
Abstract

Osteochondral defects require the simultaneous regeneration of cartilage and subchondral bone, posing a major challenge for current biomaterial strategies. Here, we present a radially oriented 3D-printed bilayer hydrogel scaffold composed of a mechanically reinforced GelMA/HAP osteogenic layer and a compliant, KGN@Lip-loaded GelMA chondrogenic layer, to achieve coordinated osteochondral repair. Structural and physicochemical characterization confirmed the formation of a functionally graded architecture with uniform HAP and KGN@Lip distribution, while mechanical, rheological, swelling, and degradation analyses revealed a layer-dependent gradient that resembles certain structural features of the native osteochondral interface. In vitro, the GelMA/HAP layer promoted robust osteogenic differentiation through ion-mediated activation of osteogenic pathways, whereas the GelMA/KGN@Lip layer sustained chondrogenic stimulation and markedly enhanced SOX9, Col2a1, and Acan expression. The radially oriented microchannels provided an interconnected structure that may support nutrient transport and cell infiltration. In vivo implantation demonstrated substantial subchondral bone regeneration and the formation of cartilage-like tissue with improved matrix organization, along with enhanced integration at the osteochondral interface, confirming the scaffold's ability to provide spatially coordinated biochemical and structural cues. Overall, this anisotropic bilayer hydrogel scaffold offers a promising strategy for integrated and functional osteochondral regeneration.

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