Adjustment of Micro- and Macroporosity of ss-TCP Scaffolds Using Solid-Stabilized Foams as Bone Replacement

被引:5
作者
Dufner, Lukas [1 ]
Osswald, Bettina [1 ]
Eberspaecher, Jan [1 ]
Riedel, Bianca [2 ]
Kling, Chiara [2 ]
Kern, Frank [1 ]
Seidenstuecker, Michael [2 ]
机构
[1] Univ Stuttgart, Inst Mfg Technol Ceram Components & Composites, D-70569 Stuttgart, Germany
[2] Albert Ludwigs Univ Freiburg, GERN Ctr Tissue Replacement Regenerat & Neogenesis, Med Ctr, Fac Med,Dept Orthoped & Trauma Surg, Hugstetter Str 55, D-79106 Freiburg, Germany
来源
BIOENGINEERING-BASEL | 2023年 / 10卷 / 02期
关键词
capillary suspension; bioceramics; foaming; polymer particles; sacrificial templating;
D O I
10.3390/bioengineering10020256
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To enable rapid osteointegration in bioceramic implants and to give them osteoinductive properties, scaffolds with defined micro- and macroporosity are required. Pores or pore networks promote the integration of cells into the implant, facilitating the supply of nutrients and the removal of metabolic products. In this paper, scaffolds are created from ss-tricalciumphosphate (ss-TCP) and in a novel way, where both the micro- and macroporosity are adjusted simultaneously by the addition of pore-forming polymer particles. The particles used are 10-40 wt%, spherical polymer particles of polymethylmethacrylate (PMMA) (o = 5 mu m) and alternatively polymethylsilsesquioxane (PMSQ) (o = 2 mu m), added in the course of ss-TCP slurry preparation. The arrangement of hydrophobic polymer particles at the interface of air bubbles was incorporated during slurry preparation and foaming of the slurry. The foam structures remain after sintering and lead to the formation of macro-porosity in the scaffolds. Furthermore, decomposition of the polymer particles during thermal debindering results in the formation of an additional network of interconnecting micropores in the stabilizing structures. It is possible to adjust the porosity easily and quickly in a range of 1.2-140 mu m with a relatively low organic fraction. The structures thus prepared showed no cytotoxicity nor negative effects on the biocompatibility.
引用
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页数:19
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