TY - JOUR
T1 - New Mg/Sr phosphate bioresorbable glass system with enhanced sintering properties
AU - Ghanavati, S.
AU - Petit, L.
AU - Massera, J.
N1 - Funding Information:
The authors would like to acknowledge the Academy of Finland (UNIBIO project# 331924) and Jane and Aatos Erkko Foundation (AGATE project) for financial support. The authors would like to also thank the Tampere Microscopy Center and especially, Dr. Turkka Salminen for the SEM/EDX analysis.
Publisher Copyright:
© 2023 The Author(s)
PY - 2023/9/15
Y1 - 2023/9/15
N2 - Phosphate glasses are ideal candidates to substitute traditional silicate bioactive glasses as they can exhibit controlled ion release. Furthermore, phosphate glasses possess congruent dissolution and also resistance to crystallization, two properties that are favorable for the processing of 3D porous scaffolds. However, most of the phosphate glasses also exhibit a fast dissolution rate, which is inappropriate for bone tissue regeneration. In this context, a new bioresorbable phosphate glass within the 45P2O5- 2.5B2O3- 2.5SiO2- 10Na2O- 20CaO- (20-x) SrO- (x)MgO (in %mol) composition was developed. Magnesium is substituted for strontium in order to promote bone formation but in the present study, its role is mainly to favor sintering at lower temperatures without crystallization. The in vitro dissolution in simulated body fluid was assessed for glass particles <38 μm (pH, ICP, SEM-EDS). All glasses were found bioresorbable, rather than bioactive. The newly developed phosphate glasses containing Sr and Mg were found to have a slower dissolution rate when compared to traditional metaphosphate glasses while maintaining their congruent dissolution and hot forming ability. All glasses were 3D printed into scaffolds with controlled pore size and without apparent crystallization. The substitution of SrO for MgO was shown to be highly effective in enhancing the sintering ability of the material by enabling sintering at lower temperatures while avoiding the risk of crystallization leading to the processing of scaffolds with mechanical properties, in compression, above that of the cancellous bone.
AB - Phosphate glasses are ideal candidates to substitute traditional silicate bioactive glasses as they can exhibit controlled ion release. Furthermore, phosphate glasses possess congruent dissolution and also resistance to crystallization, two properties that are favorable for the processing of 3D porous scaffolds. However, most of the phosphate glasses also exhibit a fast dissolution rate, which is inappropriate for bone tissue regeneration. In this context, a new bioresorbable phosphate glass within the 45P2O5- 2.5B2O3- 2.5SiO2- 10Na2O- 20CaO- (20-x) SrO- (x)MgO (in %mol) composition was developed. Magnesium is substituted for strontium in order to promote bone formation but in the present study, its role is mainly to favor sintering at lower temperatures without crystallization. The in vitro dissolution in simulated body fluid was assessed for glass particles <38 μm (pH, ICP, SEM-EDS). All glasses were found bioresorbable, rather than bioactive. The newly developed phosphate glasses containing Sr and Mg were found to have a slower dissolution rate when compared to traditional metaphosphate glasses while maintaining their congruent dissolution and hot forming ability. All glasses were 3D printed into scaffolds with controlled pore size and without apparent crystallization. The substitution of SrO for MgO was shown to be highly effective in enhancing the sintering ability of the material by enabling sintering at lower temperatures while avoiding the risk of crystallization leading to the processing of scaffolds with mechanical properties, in compression, above that of the cancellous bone.
KW - 3D printing
KW - Bioresorbable glasses
KW - In vitro dissolution
KW - Phosphate glasses
KW - Sintering
U2 - 10.1016/j.jnoncrysol.2023.122446
DO - 10.1016/j.jnoncrysol.2023.122446
M3 - Article
AN - SCOPUS:85161937867
SN - 0022-3093
VL - 616
JO - Journal of Non-Crystalline Solids
JF - Journal of Non-Crystalline Solids
M1 - 122446
ER -