海藻酸-明胶混合生物3d打印用聚己内酯(PCL)支架的力学性能

F. Koch, Ole Thaden, Stefan Conrad, Kevin Tröndle, G. Finkenzeller, R. Zengerle, Sabrina Kartmann, S. Zimmermann, P. Koltay
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引用次数: 10

摘要

近年来,利用生物3d打印技术生成人造人体组织作为临床相关的研究课题得到了显著扩展。然而,为了生产一个复杂和可行的组织,深入的生物学理解和先进的打印技术需要大量的工艺参数。在这里,我们系统地评估了基于热塑性材料的熔融沉积建模(FDM)和细胞负载水凝胶的微挤压的混合生物打印工艺的相关工艺参数。首先,我们研究了聚己内酯(PCL)的打印温度对单个融合丝之间连接强度的影响,以及对海藻酸-明胶-水凝胶中永生化间充质干细胞(iMSC)活力的影响。结果表明,当打印温度为140°C,纤维之间的键角为90°时,纤维的键合强度和周围细胞的活力之间得到了很好的平衡。利用从单个熔丝中获得的这些工艺参数,我们打印了体积为10 × 10 × 10 mm3的立方体测试结构,并设计了不同的填充图案。这些立方体的机械强度变化被测量为仅由PCL制成的支架,以及由PCL和水凝胶交替混合生物打印打印的水凝胶填充的PCL支架,一层一层。裸露支架的压缩模量可达6 MPa,接近人体硬组织,与水凝胶一起打印PCL后压缩模量降至4 MPa左右。最适合混合打印的支架设计与细胞负载的水凝胶一起孵育,其机械强度没有下降,长达28天。
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Mechanical properties of polycaprolactone (PCL) scaffolds for hybrid 3D-bioprinting with alginate-gelatin hydrogel.
The generation of artificial human tissue by 3D-bioprinting has expanded significantly as a clinically relevant research topic in recent years. However, to produce a complex and viable tissue, in-depth biological understanding and advanced printing techniques are required with a high number of process parameters. Here, we systematically evaluate the process parameters relevant for a hybrid bioprinting process based on fused-deposition modeling (FDM) of thermoplastic material and microextrusion of a cell-laden hydrogel. First, we investigated the effect of the printing temperature of polycaprolactone (PCL), on the junction strength between individual fused filaments and on the viability of immortalized mesenchymal stem cells (iMSC) in the surrounding alginate-gelatin-hydrogel. It was found that a printing temperature of 140 °C and bonds with an angle of 90° between the filaments provided a good compromise between bonding strength of the filaments and the viability of the surrounding cells. Using these process parameters obtained from individual fused filaments, we then printed cubic test structures with a volume of 10 × 10 × 10 mm3 with different designs of infill patterns. The variations in mechanical strength of these cubes were measured for scaffolds made of PCL-only as well as for hydrogel-filled PCL scaffolds printed by alternating hybrid bioprinting of PCL and hydrogel, layer by layer. The bare scaffolds showed a compressive modulus of up to 6 MPa, close to human hard tissue, that decreased to about 4 MPa when PCL was printed together with hydrogel. The scaffold design suited best for hybrid printing was incubated with cell-laden hydrogel and showed no degradation of its mechanical strength for up to 28 days.
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