Integrating Melt Electrowriting and Fused Deposition Modeling to Fabricate Hybrid Scaffolds Supportive of Accelerated Bone Regeneration

Author:

Eichholz Kian F.123ORCID,Pitacco Pierluca12,Burdis Ross123,Chariyev‐Prinz Farhad12,Barceló Xavier123,Tornifoglio Brooke12,Paetzold Ryan34,Garcia Orquidea5,Kelly Daniel J1236ORCID

Affiliation:

1. Trinity Centre for Biomedical Engineering Trinity Biomedical Sciences Institute Trinity College Dublin 152‐160 Pearse Street Dublin D02 R590 Ireland

2. Department of Mechanical, Manufacturing and Biomedical Engineering School of Engineering Trinity College Dublin Dublin D02 VH29 Ireland

3. Advanced Materials and Bioengineering Research Centre (AMBER) Royal College of Surgeons in Ireland and Trinity College Dublin Dublin D02 CP49 Ireland

4. School of Mechanical and Materials Engineering University College Dublin Dublin D04 E4X0 Ireland

5. Johnson & Johnson 3D Printing Innovation and Customer Solutions Johnson & Johnson Services, Inc. Irvine CA 92618 USA

6. Department of Anatomy and Regenerative ME Royal College of Surgeons in Ireland Dublin D02 YN77 Ireland

Abstract

AbstractEmerging additive manufacturing (AM) strategies can enable the engineering of hierarchal scaffold structures for guiding tissue regeneration. Here, the advantages of two AM approaches, melt electrowriting (MEW) and fused deposition modelling (FDM), are leveraged and integrated to fabricate hybrid scaffolds for large bone defect healing. MEW is used to fabricate a microfibrous core to guide bone healing, while FDM is used to fabricate a stiff outer shell for mechanical support, with constructs being coated with pro‐osteogenic calcium phosphate (CaP) nano‐needles. Compared to MEW scaffolds alone, hybrid scaffolds prevent soft tissue collapse into the defect region and support increased vascularization and higher levels of new bone formation 12 weeks post‐implantation. In an additional group, hybrid scaffolds are also functionalized with BMP2 via binding to the CaP coating, which further accelerates healing and facilitates the complete bridging of defects after 12 weeks. Histological analyses demonstrate that such scaffolds support the formation of well‐defined annular bone, with an open medullary cavity, smooth periosteal surface, and no evidence of abnormal ectopic bone formation. These results demonstrate the potential of integrating different AM approaches for the development of regenerative biomaterials, and in particular, demonstrate the enhanced bone healing outcomes possible with hybrid MEW‐FDM constructs.

Funder

European Regional Development Fund

Johnson and Johnson

Science Foundation Ireland

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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