4.7 Article

Mineralizing Coating on 3D Printed Scaffolds for the Promotion of Osseointegration

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fbioe.2022.836386

Keywords

biomineralization; elastin-like recombinamers; bone regeneration; 3D printing; nylon; tissueimplant integration

Funding

  1. AO foundation [AOCMF - 17-19M]
  2. ERC Starting Grant (STROFUNSCAFF)
  3. Engineering and Physical Sciences Research Council [EP/N006615/1]
  4. Medical Research Council (United Kingdom Regenerative Medicine Platform Hub Acellular Smart Materials 3D Architecture) [MR/R015651/1]
  5. Spanish Government [PID2019 - 110709RB - 100, RED2018 - 102417 - T]
  6. Junta de Castilla y Leon [VA317P18, Infrared 2018 - UVA06]
  7. Interreg V Espana Portugal POCTEP [0624_2IQBIONEURO_6_E]
  8. Centro en Red de Medicina Regenerativa y Terapia Celular de Castilla y Leon
  9. ERC Proof-of-concept Grant (MINGRAFT)

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This study reports the development of acellular mineralizing 3D printed scaffolds for hard tissue regeneration using a combination of additive manufacturing and supramolecular chemistry. The pre-mineralized scaffolds showed improved bone ingrowth and tissue-implant integration in an in vivo model.
Design and fabrication of implants that can perform better than autologous bone grafts remain an unmet challenge for the hard tissue regeneration in craniomaxillofacial applications. Here, we report an integrated approach combining additive manufacturing with supramolecular chemistry to develop acellular mineralizing 3D printed scaffolds for hard tissue regeneration. Our approach relies on an elastin-like recombinamer (ELR) coating designed to trigger and guide the growth of ordered apatite on the surface of 3D printed nylon scaffolds. Three test samples including a) uncoated nylon scaffolds (referred to as Uncoated), b) ELR coated scaffolds (referred to as ELR only), and c) ELR coated and in vitro mineralized scaffolds (referred to as Pre-mineralized) were prepared and tested for in vitro and in vivo performance. All test samples supported normal human immortalized mesenchymal stem cell adhesion, growth, and differentiation with enhanced cell proliferation observed in the Pre-mineralized samples. Using a rabbit calvarial in vivo model, 'Pre-mineralized' scaffolds also exhibited higher bone ingrowth into scaffold pores and cavities with higher tissue-implant integration. However, the coated scaffolds (ELR only and Pre-mineralized) did not exhibit significantly more new bone formation compared to Uncoated scaffolds. Overall, the mineralizing coating offers an opportunity to enhance integration of 3D printed bone implants. However, there is a need to further decipher and tune their immunologic response to develop truly osteoinductive/conductive surfaces.

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