Custom-made macroporous bioceramic implants based on triply-periodic minimal surfaces for bone defects in load-bearing sites.


Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
06 2020
Historique:
received: 04 10 2019
revised: 05 03 2020
accepted: 11 03 2020
pubmed: 21 3 2020
medline: 16 4 2021
entrez: 21 3 2020
Statut: ppublish

Résumé

The architectural features of synthetic bone grafts are key parameters for regulating cell functions and tissue formation for the successful repair of bone defects. In this regard, macroporous structures based on triply-periodic minimal surfaces (TPMS) are considered to have untapped potential. In the present study, custom-made implants based on a gyroid structure, with (GPRC) and without (GP) a cortical-like reinforcement, were specifically designed to fit an intended bone defect in rat femurs. Sintered hydroxyapatite implants were produced using a dedicated additive manufacturing technology and their morphological, physico-chemical and mechanical features were characterized. The implants' integrity and ability to support bone ingrowth were assessed after 4, 6 and 8 weeks of implantation in a 3-mm-long, femoral defect in Lewis rats. GP and GPRC implants were manufactured with comparable macro- to nano-architectures. Cortical-like reinforcement significantly improved implant effective stiffness and resistance to fracture after implantation. This cortical-like reinforcement also concentrated new bone formation in the core of the GPRC implants, without affecting newly formed bone quantity or maturity. This study showed, for the first time, that custom-made TPMS-based bioceramic implants could be produced and successfully implanted in load-bearing sites. Adding a cortical-like reinforcement (GPRC implants) was a relevant solution to improve implant mechanical resistance, and changed osteogenic mechanism compared to the GP implants. STATEMENT OF SIGNIFICANCE: Architectural features are known to be key parameters for successful bone repair using synthetic bioceramic bone graft. So far, conventional manufacturing techniques, lacking reproducibility and complete control of the implant macro-architecture, impeded the exploration of complex architectures, such as triply periodic minimal surfaces (TPMS), which are foreseen to have an unrivaled potential for bone repair. Using a new additive manufacturing process, macroporous TPMS-based bioceramics implants were produced in calcium phosphate, characterized and implanted in a femoral defect in rats. The results showed, for the first time, that such macroporous implants can be successfully implanted in anatomical load-bearing sites when a cortical-like outer shell is added. This outer shell also concentrated new bone formation in the implant center, without affecting new bone quantity or maturity.

Identifiants

pubmed: 32194263
pii: S1742-7061(20)30148-3
doi: 10.1016/j.actbio.2020.03.016
pii:
doi:

Substances chimiques

Durapatite 91D9GV0Z28

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

254-266

Informations de copyright

Copyright © 2020 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Author disclosure statement The authors wish to confirm that there are no known conflicts of interest associated with this publication and that there was no significant financial support for this work that could have influenced its outcome.

Auteurs

Baptiste Charbonnier (B)

Mines Saint-Etienne, Univ Lyon, Univ Jean Monnet, INSERM, U 1059 Sainbiose, Centre CIS, F-42023 Saint-Etienne, France.

Mathieu Manassero (M)

Université de Paris, CNRS, INSERM, B3OA, F-75010 Paris, France; Ecole Nationale Vétérinaire d'Alfort, B3OA, F-94700 Maisons-Alfort, France. Electronic address: mathieu.manassero@vet-alfort.fr.

Marianne Bourguignon (M)

Université de Paris, CNRS, INSERM, B3OA, F-75010 Paris, France; Ecole Nationale Vétérinaire d'Alfort, B3OA, F-94700 Maisons-Alfort, France.

Adeline Decambron (A)

Université de Paris, CNRS, INSERM, B3OA, F-75010 Paris, France; Ecole Nationale Vétérinaire d'Alfort, B3OA, F-94700 Maisons-Alfort, France. Electronic address: adeline.decambron@vet-alfort.fr.

Hanane El-Hafci (H)

Université de Paris, CNRS, INSERM, B3OA, F-75010 Paris, France; Ecole Nationale Vétérinaire d'Alfort, B3OA, F-94700 Maisons-Alfort, France. Electronic address: hanane.el-hafci@univ-paris-diderot.fr.

Claire Morin (C)

Mines Saint-Etienne, Univ Lyon, Univ Jean Monnet, INSERM, U 1059 Sainbiose, Centre CIS, F-42023 Saint-Etienne, France. Electronic address: claire.morin@emse.fr.

Diego Leon (D)

Mines Saint-Etienne, Univ Lyon, Univ Jean Monnet, INSERM, U 1059 Sainbiose, Centre CIS, F-42023 Saint-Etienne, France.

Morad Bensidoum (M)

Université de Paris, CNRS, INSERM, B3OA, F-75010 Paris, France; Ecole Nationale Vétérinaire d'Alfort, B3OA, F-94700 Maisons-Alfort, France. Electronic address: morad.bensidhoum@univ-paris-diderot.fr.

Simon Corsia (S)

Université de Paris, CNRS, INSERM, B3OA, F-75010 Paris, France; Ecole Nationale Vétérinaire d'Alfort, B3OA, F-94700 Maisons-Alfort, France.

Hervé Petite (H)

Université de Paris, CNRS, INSERM, B3OA, F-75010 Paris, France; Ecole Nationale Vétérinaire d'Alfort, B3OA, F-94700 Maisons-Alfort, France. Electronic address: herve.petite@univ-paris-diderot.fr.

David Marchat (D)

Mines Saint-Etienne, Univ Lyon, Univ Jean Monnet, INSERM, U 1059 Sainbiose, Centre CIS, F-42023 Saint-Etienne, France. Electronic address: marchat@emse.fr.

Esther Potier (E)

Université de Paris, CNRS, INSERM, B3OA, F-75010 Paris, France; Ecole Nationale Vétérinaire d'Alfort, B3OA, F-94700 Maisons-Alfort, France. Electronic address: esther.potier@cnrs.fr.

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Classifications MeSH