ART-BONE · Manufacturing of Artificial Bone for Repair and Regeneration of Large Osseous Defects
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2018-09-03 → 2020-12-05
- EU contribution
- €175,866
- Participants
- 1
- Scheme
- MSCA-IF-EF-CAR
Lines connect the coordinator with its partners.
Results in brief
Manufacturing of Artificial Bone for Repair and Regeneration of Large Osseous Defects
Bone repair and regeneration with postoperative restoration of original structure and functions is a significant clinical goal in traumatology, orthopaedics and oral and maxillofacial surgery. Bone's self-healing capacity can be compromised in the context of large, critical-size osseous defects and non-union fractures caused by trauma, infection, osteoradionecrosis, ablative oncologic surgery, congenital abnormality, or metabolic bone diseases. These defects and fractures often result in long-term aesthetic deformities and/or functional damages which deeply affect patients’ emotional and physical well-being. To treat these defects and promote bone regeneration, there exists an urgent and ever-increasing demand for ‘off-the-shelf’ and cost-effective biomaterial-based therapies to substitute the ever-increasing number of costly and painful autologous bone grafting procedures. Bone grafting is a surgical intervention to reconstruct a damaged or diseased bone with a new bone from the patient′s own body (autografts) or a deceased donor (allografts), a skeletal material of animal origin (xenografts), or a man-made, synthetic substitute (alloplasts, commonly named biomaterials). These biomaterials have evolved through four different generations as follows: bioinert, dense ceramics, metals, alloys, stainless steels and ultra-high-molecular-weight polymers (1st generation); bioactive, dense or porous ceramics, bioglass and cements, or bioresorbable polymers (2nd generation); bioactive and bioresorbable, porous hybrid materials (3rd generation); biomimetic materials so far limited to a handful of second- and third-generation biomaterials functionalized with soluble, secreted signalling polypeptides (or, growth factors) whose role is to trigger new bone formation (4th generation). The goal of the ART-BONE project was to develop and evaluate a new class of fourth generation biomaterials for bone repair. To reach this goal, the fellow achieved three different objectives: the fellow designed (objective 1), characterized (objective 2) and evaluated (objective 3) bone-mimetic biomaterials in the form of inorganic-organic composite materials. The fellow has also compared these bone-mimetic biomaterials with traditional biomaterials for bone repair and regeneration. As a conclusion, this action provides a new mechanistic understanding of the physicochemical processes underlying osteogenesis. Further, this action has had a major impact in the researcher’s career since it allowed him to secure a permanent academic position within less than a year after the end of the action.
Data: CORDIS, © European Union
Project objective
Implant biomaterials currently used for bone repair and regeneration often cause inflammation responses, and possess suboptimal osseointegration capability and osteoconduction ability. These significant clinical problems are due to their chemical, structural and physical properties which differ greatly with respect to a natural bone tissue. ART-BONE aims to overcome these limitations via an innovative, nanotechnology strategy for the manufacturing of a new type of synthetic biomaterial that precisely mimics bone tissue features. This strategy pairs 3D printing technology with a bottom-up process in which the elementary building blocks of bone (hydroxyapatite crystals, collagen fibrils, water molecules, active bioorganic molecules) are combined to reconstruct the overall architecture and chemical composition of a natural bone tissue. In parallel, numerous materials characterization techniques (solid-state nuclear magnetic resonance spectroscopy, scanning helium ion microscopy, cryogenic transmission electron microscopy, etc.) will be applied to scrutinize the finalized synthetic biomaterial; and the experiment conditions will be adjusted accordingly to ensure its biomimicry with native tissues. The novelty of this strategy resides in the fact that the experimental approach is inspired by the latest concepts in bone biomineralization, and enables the design of highly biomimetic, synthetic biomaterials in terms of chemical, structural and physical properties. This strategy must not only guarantee the biocompatibility of the finalized synthetic biomaterial and prevent inflammatory responses, but also insure a good adhesion to the surrounding bone tissue following implantation. Such highly biomimetic, synthetic biomaterial possesses, in theory, optimal osteointegration capacity and osteoconduction ability, and will offer an appealing alternative to the clinical “gold standard” autografts in the future.
Original text from CORDIS.
Participants
- THE PROVOST, FELLOWS, FOUNDATION SCHOLARS & THE OTHER MEMBERS OF BOARD, OF THE COLLEGE OF THE HOLY & UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN · DublinCoordinatorIreland
Links
Data: CORDIS, © European Union
