4.7 Article

Patient-Specific Bioimplants and Reconstruction Plates for Mandibular Defects: Production Workflow and In Vivo Large Animal Model Study

Journal

MACROMOLECULAR BIOSCIENCE
Volume 22, Issue 4, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/mabi.202100398

Keywords

additive manufacturing; bone reconstructions; calcium phosphates; continuity defects; Gottingen minipigs; poly(trimethylene carbonate)

Funding

  1. Business Finland [CraMaxS 557/31/2016]
  2. Helsinki University [Y1149SUL30, Y1014SL015, Y1014SULE1, TYH2018225, TYH2019117]

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A major challenge in extensive craniomaxillofacial bone reconstruction is the limited availability of donor sites. This study tested patient-specific composite bioimplants in an animal model and found that they can induce bone growth but also have issues with resorption and infection.
A major challenge with extensive craniomaxillofacial bone reconstruction is the limited donor-site availability to reconstruct defects predictably and accurately according to the anatomical shape of the patient. Here, patient-specific composite bioimplants, consisting of cross-linked poly(trimethylene carbonate) (PTMC) networks and beta-tricalcium phosphate (beta-TCP), are tested in vivo in twelve Gottingen minipigs in a large mandibular continuity defect model. The 25 mm defects are supported by patient-specific titanium reconstruction plates and receive either osteoconductive composite bioimplants (PTMC+TCP), neat polymer network bioimplants (PTMC), autologous bone segments (positive control), or are left empty (negative control). Postoperatively, defects treated with bioimplants show evident ossification at 24 weeks. Histopathologic evaluation reveals that neat PTMC bioimplant surfaces are largely covered with fibrous tissue, while in the PTMC+TCP bioimplants, bone attached directly to the implant surface shows good osteoconduction and histological signs of osteoinductivity. However, PTMC+TCP bioimplants are associated with high incidence of necrosis and infection, possibly due to rapid resorption and/or particle size of the used beta-TCP. The study highlights the importance of testing bone regeneration implants in a clinically relevant large animal model and at the in situ reconstruction site, since results on small animal models and studies in nonloadbearing areas do not translate directly.

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