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Study of Hydroxyapatite-coated High-strength Biodegradable Magnesium-based Alloy in Repairing Fracture Damage in Rats
Ding Ma1,2, Kui Zhang2, Bingchen Dong2
1Department of Orthopaedics, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, P.R. China.
In Vivo (Athens, Greece)
|January 2, 2023
Summary
Hydroxyapatite coating on ultrafine-grained WE43 magnesium implants enhances bone fracture repair. This novel HA/UFG-WE43 Mg implant shows improved biodegradation and biological activity, promoting efficient healing with minimal inflammation.
Area of Science:
- Biomaterials Engineering
- Orthopedic Implants
- Tissue Regeneration
Background:
- Hydroxyapatite (HA) coating enhances metallic implant properties, including degradation rate and biological activity.
- Biodegradable magnesium (Mg) alloys are promising for orthopedic applications due to their biocompatibility and mechanical properties.
- WE43 magnesium alloy is a suitable candidate for biodegradable implants, but its surface properties require optimization.
Purpose of the Study:
- To fabricate a hydroxyapatite-coated ultrafine-grained WE43 magnesium (HA/UFG-WE43 Mg) implant for bone fracture repair.
- To evaluate the physicochemical and biological properties of the developed HA/UFG-WE43 Mg implant.
- To assess the efficacy of the HA/UFG-WE43 Mg implant in promoting tibial fracture healing in a rat model.
Main Methods:
- A hybrid fabrication approach combining parallel tubular-channel angular pressing (PTCAP) and physical vapour deposition (PVD) magnetron sputtering was utilized.
- The microstructure, phase composition, and surface characteristics of the HA/UFG-WE43 Mg samples were analyzed.
- In vitro cell adhesion, morphology, and proliferation assays using rat skeletal muscle cells were performed.
- In vivo studies assessed Mg ion concentration in blood and histological analysis of tibial fracture healing in rats.
Main Results:
- PTCAP processing resulted in ultrafine microstructures with improved uniformity in the WE43 Mg samples.
- The HA coating exhibited characteristic peaks, confirming successful deposition on the UFG-WE43 Mg implant.
- In vitro studies demonstrated good cell adhesion, morphology, and proliferation on the HA/UFG-WE43 Mg specimens.
- In vivo results indicated reduced Mg ion concentration after HA deposition and efficient biodegradation with moderate inflammatory response during tibial fracture healing.
Conclusions:
- The combination of PTCAP processing and HA surface modification successfully created a functional HA/UFG-WE43 Mg implant.
- The developed implant demonstrated efficient biodegradation and promoted tibial fracture healing with a moderate inflammatory reaction.
- This HA/UFG-WE43 Mg implant shows significant potential for orthopedic applications in bone fracture repair.

