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Biomimetic design and fabrication of scaffolds integrating oriented micro-pores with branched channel networks for myocardial tissue engineering

机译:用分支通道网络对微孔与心肌组织工程分支通道网络相结合的仿真设计和制造

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摘要

The ability to fabricate three-dimensional (3D) thick vascularized myocardial tissue could enable scientific and technological advances in tissue engineering and drug screening, and may accelerate its application in myocardium repair. In this study, we developed a novel biomimetic scaffold integrating oriented micro-pores with branched channel networks to mimic the anisotropy and vasculature of native myocardium. The oriented micro-pores were fabricated using an 'Oriented Thermally Induced Phase Separation (OTIPS)' technique, and the channel network was produced by embedding and subsequently dissolving a 3D-printed carbohydrate template after crosslinking. Micro-holes were incorporated on the wall of channels, which greatly enhanced the permeability of channels. The effect of the sacrificial template on the formation of oriented micro- pores was assessed. The mechanical properties of the scaffold were tuned by varying the temperature gradient and chitosan/collagen ratio to match the specific stiffness of native heart tissue. The engineered cardiac tissue achieved synchronized beating with electrical stimulation. Calcium transient results suggested the formation of connection between cardiomyocytes within scaffold. All the results demonstrated that the reported scaffold has the potential to induce formation of a perfusable vascular network and to create thick vascularized cardiac tissue that may advance further clinical applications.
机译:制造三维(3D)厚的血管化心肌组织的能力可以实现组织工程和药物筛查的科技进步,并可以加速其在心肌修复中的应用。在这项研究中,我们开发了一种新的生物仿真支架,其与支化的微孔相结合,具有支链通道网络,以模仿本地心肌的各向异性和脉管系统。使用“取向的热诱导的相分离(otips)”技术制造取向的微孔,并且通过嵌入并随后在交联后溶解3D印刷的碳水化合物模板来产生通道网络。将微孔纳入通道的壁上,这大大提高了通道的渗透性。评估牺牲模板对面向微孔形成的影响。通过改变温度梯度和壳聚糖/胶原蛋白的比率来调节支架的机械性能,以匹配原生心脏组织的比刚度。工程心脏组织实现了电刺激的同步搏动。钙瞬变结果表明脚手架内心肌细胞之间的连接形成。所有结果表明,报告的支架具有诱导灌注血管网络的形成,并产生可能提高进一步临床应用的厚血管化心脏组织。

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