TY - JOUR
T1 - Highly degradable porous melt-derived bioactive glass foam scaffolds for bone regeneration
AU - Nommeots-nomm, Amy
AU - Labbaf, Sheyda
AU - Devlin, Aine
AU - Todd, Naomi
AU - Geng, Hua
AU - Solanki, Anu K.
AU - Tang, Hok Man
AU - Perdika, Polytimi
AU - Pinna, Alessandra
AU - Ejeian, Fatemeh
AU - Tsigkou, Olga
AU - Lee, Peter D.
AU - Esfahani, Mohammad Hossein Nasr
AU - Mitchell, Christopher A.
AU - Jones, Julian R.
PY - 2017/7/15
Y1 - 2017/7/15
N2 - A challenge in using bioactive melt-derived glass in bone regeneration is to produce scaffolds with interconnected pores while maintaining the amorphous nature of the glass and its associated bioactivity. Here we introduce a method for creating porous melt-derived bioactive glass foam scaffolds with low silica content and report in vitro and preliminary in vivo data. The gel-cast foaming process was adapted, employing temperature controlled gelation of gelatin, rather than the in situ acrylic polymerisation used previously. To form a 3D construct from melt derived glasses, particles must be fused via thermal processing, termed sintering. The original Bioglass® 45S5 composition crystallises upon sintering, altering its bioactivity, due to the temperature difference between the glass transition temperature and the crystallisation onset being small. Here, we optimised and compared scaffolds from three glass compositions, ICIE16, PSrBG and 13–93, which were selected due to their widened sintering windows. Amorphous scaffolds with modal pore interconnect diameters between 100–150 µm and porosities of 75% had compressive strengths of 3.4 ± 0.3 MPa, 8.4 ± 0.8 MPa and 15.3 ± 1.8 MPa, for ICIE16, PSrBG and 13–93 respectively. These porosities and compressive strength values are within the range of cancellous bone, and greater than previously reported foamed scaffolds. Dental pulp stem cells attached to the scaffold surfaces during in vitro culture and were viable. In vivo, the scaffolds were found to regenerate bone in a rabbit model according to X-ray micro tomography imaging.
AB - A challenge in using bioactive melt-derived glass in bone regeneration is to produce scaffolds with interconnected pores while maintaining the amorphous nature of the glass and its associated bioactivity. Here we introduce a method for creating porous melt-derived bioactive glass foam scaffolds with low silica content and report in vitro and preliminary in vivo data. The gel-cast foaming process was adapted, employing temperature controlled gelation of gelatin, rather than the in situ acrylic polymerisation used previously. To form a 3D construct from melt derived glasses, particles must be fused via thermal processing, termed sintering. The original Bioglass® 45S5 composition crystallises upon sintering, altering its bioactivity, due to the temperature difference between the glass transition temperature and the crystallisation onset being small. Here, we optimised and compared scaffolds from three glass compositions, ICIE16, PSrBG and 13–93, which were selected due to their widened sintering windows. Amorphous scaffolds with modal pore interconnect diameters between 100–150 µm and porosities of 75% had compressive strengths of 3.4 ± 0.3 MPa, 8.4 ± 0.8 MPa and 15.3 ± 1.8 MPa, for ICIE16, PSrBG and 13–93 respectively. These porosities and compressive strength values are within the range of cancellous bone, and greater than previously reported foamed scaffolds. Dental pulp stem cells attached to the scaffold surfaces during in vitro culture and were viable. In vivo, the scaffolds were found to regenerate bone in a rabbit model according to X-ray micro tomography imaging.
KW - Bioactive glass
KW - Bioglass
KW - Bone regeneration
KW - Rabbit model
KW - Scaffold
UR - https://pure.ulster.ac.uk/en/publications/highly-degradable-porous-melt-derived-bioactive-glass-foam-scaffo-2
UR - https://linkinghub.elsevier.com/retrieve/pii/S1742706117302775
U2 - 10.1016/j.actbio.2017.04.030
DO - 10.1016/j.actbio.2017.04.030
M3 - Article
C2 - 28457960
SN - 1742-7061
VL - 57
SP - 449
EP - 461
JO - Acta Biomaterialia
JF - Acta Biomaterialia
ER -