
Journal of Shanghai Jiao Tong University (Medical Science) ›› 2026, Vol. 46 ›› Issue (9): 1169-1178.doi: 10.3969/j.issn.1674-8115.2026.09.002
• Frontier review • Previous Articles
Yu Meixuan1, Sun Lin2,3, Fu Jingke2,3,#(
), Hao Yongqiang2,3,4,5,6,#(
), Dai Kerong2,3,4,5,6
Received:2026-01-12
Accepted:2026-02-09
Online:2026-09-28
Published:2026-09-28
Contact:
Fu Jingke, Hao Yongqiang
E-mail:fujingke@sjtu.edu.cn;hao_yongqiang@hotmail.com
Supported by:CLC Number:
Yu Meixuan, Sun Lin, Fu Jingke, Hao Yongqiang, Dai Kerong. 3D printing biomimetic periosteum: from structural substitution to functional integration[J]. Journal of Shanghai Jiao Tong University (Medical Science), 2026,(9): 1169-1178.
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URL: https://xuebao.shsmu.edu.cn/EN/10.3969/j.issn.1674-8115.2026.09.002
| Manufacturing | Model | Biomaterial in bioinks | OFC in bioinks | Main effect | Reference |
|---|---|---|---|---|---|
| EBP | Rat cranial defect | Fibrous layer: SFHGMA, SA Formation layer: SFP, SA, MCol | Mg2+ | Simulation of natural periosteal double-layer structure; promotion of cell proliferation and differentiation, angiogenesis, and PC12 cell growth | [ |
| EBP | Regeneration of critical-sized bone defects in long bones | GelMA | G-MBGN, VEGF-loaded liposomes | Simulation of periosteum, endosteum, and intermediate bone matrix; significant promotion of angiogenesis | [ |
| EBP | Critical-sized bone defect | Formation layer: GelMA, GelMA-H-nHA Fibrous layer: P(ACG-GelMA-L)-Mg2+ | Ca2+, Mg2+, nHA | Simulation of natural periosteal double-layer structure, with Mg²⁺-mediated immunomodulation and angiogenesis | [ |
| EBP | Bone defect | PLLA/HA, GelMA | rabBMSCs, rabPDSCs | Excellent cell encapsulation and bioactivity; co-culture of BMSCs and PDSCs | [ |
| EBP | Bone defect | GelMA, SilMA, GelDA | GO nanosheets, BMSCs | Excellent thermosensitivity and printability; high cell viability and adhesion | [ |
| MEW | Critical-sized segmental rat femoral defect | MEW core: PCL FDM Shell: PCL Coating: nnHA | BMP2 | High rigidity, structural integrity, sustained BMP2 release, and significant angiogenesis enhancement | [ |
| MEW | Large bone defect | PCL membrane, PCL sheet | rhBMP-2, PLGA-PEG-COOH microparticles | Controlled rhBMP-2 release and significant enhancement of in vivo bone regeneration | [ |
| SLA | Bone defect | Fibrous layer: PEGDA, TCP Formation layer: GelMA, PEGDA | Mo, Chitosan | Fibrous layer resistance to muscle traction and soft tissue invasion; promotion of osteogenic differentiation by the formation layer | [ |
Tab 1 Representative construction strategies for 3D-printed biomimetic periosteum
| Manufacturing | Model | Biomaterial in bioinks | OFC in bioinks | Main effect | Reference |
|---|---|---|---|---|---|
| EBP | Rat cranial defect | Fibrous layer: SFHGMA, SA Formation layer: SFP, SA, MCol | Mg2+ | Simulation of natural periosteal double-layer structure; promotion of cell proliferation and differentiation, angiogenesis, and PC12 cell growth | [ |
| EBP | Regeneration of critical-sized bone defects in long bones | GelMA | G-MBGN, VEGF-loaded liposomes | Simulation of periosteum, endosteum, and intermediate bone matrix; significant promotion of angiogenesis | [ |
| EBP | Critical-sized bone defect | Formation layer: GelMA, GelMA-H-nHA Fibrous layer: P(ACG-GelMA-L)-Mg2+ | Ca2+, Mg2+, nHA | Simulation of natural periosteal double-layer structure, with Mg²⁺-mediated immunomodulation and angiogenesis | [ |
| EBP | Bone defect | PLLA/HA, GelMA | rabBMSCs, rabPDSCs | Excellent cell encapsulation and bioactivity; co-culture of BMSCs and PDSCs | [ |
| EBP | Bone defect | GelMA, SilMA, GelDA | GO nanosheets, BMSCs | Excellent thermosensitivity and printability; high cell viability and adhesion | [ |
| MEW | Critical-sized segmental rat femoral defect | MEW core: PCL FDM Shell: PCL Coating: nnHA | BMP2 | High rigidity, structural integrity, sustained BMP2 release, and significant angiogenesis enhancement | [ |
| MEW | Large bone defect | PCL membrane, PCL sheet | rhBMP-2, PLGA-PEG-COOH microparticles | Controlled rhBMP-2 release and significant enhancement of in vivo bone regeneration | [ |
| SLA | Bone defect | Fibrous layer: PEGDA, TCP Formation layer: GelMA, PEGDA | Mo, Chitosan | Fibrous layer resistance to muscle traction and soft tissue invasion; promotion of osteogenic differentiation by the formation layer | [ |
| Multi-technology integration | Biomaterial in ink | Bioactive substance in ink | Highlight | Reference |
|---|---|---|---|---|
| Electrospinning+3D printing | Electrospun collagen-dense scaffold, IMCS | BMSCs | Upper-layer blockade of fibrous tissue invasion; lower-layer promotion of BMSC osteogenic differentiation | [ |
| IMT+3D printing | mPCL-TCP | ABG, rhBMP-2, Cerament G®, Cerament V® | Excellent clinical adaptability, superior surgical manoeuvrability, and enhanced angiogenesis and osteogenesis | [ |
| IMT+3D printing | PLA scaffold, dECM | Bone marrow cells, BMP-2 | High-dose, sustained release of BMP-2; reduced fibrosis and macrophage infiltration; optimized BMP-2 loading capacity | [ |
Tab 2 Multi-technology integration for biomimetic periosteum construction
| Multi-technology integration | Biomaterial in ink | Bioactive substance in ink | Highlight | Reference |
|---|---|---|---|---|
| Electrospinning+3D printing | Electrospun collagen-dense scaffold, IMCS | BMSCs | Upper-layer blockade of fibrous tissue invasion; lower-layer promotion of BMSC osteogenic differentiation | [ |
| IMT+3D printing | mPCL-TCP | ABG, rhBMP-2, Cerament G®, Cerament V® | Excellent clinical adaptability, superior surgical manoeuvrability, and enhanced angiogenesis and osteogenesis | [ |
| IMT+3D printing | PLA scaffold, dECM | Bone marrow cells, BMP-2 | High-dose, sustained release of BMP-2; reduced fibrosis and macrophage infiltration; optimized BMP-2 loading capacity | [ |
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