Affiliation:
1. Univ. Polytechnique Hauts‐de‐France—CERAMATHS‐DMP Valenciennes France
2. CIRIMAT Université de Toulouse, CNRS Toulouse France
3. Univ. Lyon, UCBL, INSA Lyon, CNRS, MATEIS, UMR5510 Lyon France
Abstract
Abstractβ‐tricalcium phosphate (β‐TCP, β‐Ca3(PO4)2) is an attractive biomaterial for bone repair applications. However, its sintering and mechanical properties are limited by a problematic phase transition to α‐TCP. Cationic doping of β‐TCP is able to postpone the formation of α‐TCP allowing higher sintering temperatures and better mechanical properties. The co‐doping of β‐TCP with Mg2+ and Sr2+ has already been studied in detail, but the addition of antibacterial cations (Ag+ and Cu2+) on the Mg–Sr β‐TCP co‐doped composition remains unexplored. Thus, two co‐doped β‐TCP compositions were realized by aqueous precipitation technique without any secondary phase and compared with undoped β‐TCP: Mg–Sr (2.0–2.0 mol%) and Mg–Sr–Ag–Cu (2.0–2.0–0.1–0.1 mol%). Differential thermal analysis and dilatometry analyses showed a slight decrease of the β‐TCP → α‐TCP phase transition temperature for the Mg–Sr–Ag–Cu (2.0–2.0–0.1–0.1% mol) composition as compared to the Mg–Sr (2.0–2.0 mol%). However, both exhibited much higher transition temperatures than undoped β‐TCP. The addition of Ag+ and Cu2+ slightly reduces the grain size after sintering compared to the Mg–Sr (2.0–2.0 mol%) and the undoped compositions. The co‐doped compositions also exhibited improved mechanical properties, specifically a higher Vickers hardness and elastic modulus. Finally, cell proliferation assays showed that the presence of dopants, even Ag+ and Cu2+, does not affect the survival and proliferation of cells. Thus, the use of Mg2+, Sr2+, Ag+, and Cu2+ co‐doped β‐TCP could be very promising for biomedical applications due to the improvements of these dopants on the thermal stability and mechanical and biological properties.
Subject
Materials Chemistry,Ceramics and Composites
Cited by
6 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献