In vitro bioactivity of Polyurethane/85S Bioglass composite scaffolds

被引:12
作者
Radev, Lachezar [1 ]
Zheleva, Darina [2 ]
Michailova, Irena [3 ]
机构
[1] Univ Chem Technol & Met, Dept Fundamental Chem Technol, BU-1756 Sofia, Bulgaria
[2] Univ Chem Technol & Met, Text & Leather Dept, BU-1756 Sofia, Bulgaria
[3] Univ Chem Technol & Met, Dept Silicate Technol, BU-1756 Sofia, Bulgaria
来源
CENTRAL EUROPEAN JOURNAL OF CHEMISTRY | 2013年 / 11卷 / 09期
关键词
Scaffolds; Polyurethane; Bioglass; In vitro bioactivity; HYDROXYAPATITE; GLASSES; BIOCOMPATIBILITY; SPECTROSCOPY; DEGRADATION; CARBONATE; MECHANISM; MODEL; FTIR; IR;
D O I
10.2478/s11532-013-0273-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the present work Polyurethane (PU)/Bioglass (BG) composite materials were synthesized with different content of BG (10 and 20 mol.%) as filler. The 85S Bioglass was synthesized via polystep sol-gel method. The chemical composition of BG is 85SiO(2)-10CaO-5P(2)O(5) (wt.%). The synthesis of PU was carried out by a two-step polyaddition reaction. The 85S BG was added in situ during the polymerization reaction. In vitro bioactivity of the prepared composites was examined in the presence of 1.5 SBF for 7 days in static conditions. The structure of synthesized PU/BG composites before and after in vitro test was determined by XRD, FTIR and SEM. XRD of the samples before in vitro test proved that the phase of gamma Ca2P2O7 in the PU/20BG is visible. FTIR revealed the presence of urethane bond between OH-(from BG) and NCO groups (from PU). Based on FTIR results after in vitro test in 1.5 SBF solutions, A/B-carbonate containing hydroxyapatite (CO(3)HA) was formed. XRD proved that HA was formed on the surface of the samples, but Ca2P2O7 does not undergo any changes in the 1.5 SBF solution. SEM depicted the nano-HA agglomerated in spherical particles after immersion in 1.5 SBF for 7 days.
引用
收藏
页码:1439 / 1446
页数:8
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