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首页> 外文期刊>Lab on a chip >Engineering interconnected 3D vascular networks in hydrogels using molded sodium alginate lattice as the sacrificial template
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Engineering interconnected 3D vascular networks in hydrogels using molded sodium alginate lattice as the sacrificial template

机译:使用模制海藻酸钠晶格作为牺牲模板设计水凝胶中的互连3D血管网络

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摘要

Engineering 3D perfusable vascular networks in vitro and reproducing the physiological environment of blood vessels is very challenging for tissue engineering and investigation of blood vessel function. Here, we engineer interconnected 3D microfluidic vascular networks in hydrogels using molded sodium alginate lattice as sacrificial templates. The sacrificial templates are rapidly replicated in polydimethylsiloxane (PDMS) microfluidic chips via Ca~(2+)-crosslinking and then fully encapsulated in hydrogels. Interconnected channels with well controlled size and morphology are obtained by dissolving the monolayer or multilayer templates with EDTA solution. The human umbilical vein endothelial cells (HUVECs) are cultured on the channel linings and proliferated to form vascular lumens. The strong cell adhesion capability and adaptive response to shear stress demonstrate the excellent cytocompatibility of both the template and template-sacrificing process. Furthermore, the barrier function of the endothelial layer is characterized and the results show that a confluent endothelial monolayer is fully developed. Taken together, we develop a facile and rapid approach to engineer a vascular model that could be potentially used in physiological studies of vascular functions and vascular tissue engineering.
机译:对于组织工程和血管功能研究,在体外工程化3D可灌注血管网络并重现血管的生理环境非常具有挑战性。在这里,我们使用模塑海藻酸钠晶格作为牺牲模板来设计水凝胶中的互连3D微流体血管网络。牺牲模板通过Ca〜(2+)交联在聚二甲基硅氧烷(PDMS)微流控芯片中快速复制,然后完全封装在水凝胶中。通过用EDTA溶液溶解单层或多层模板,可以获得大小和形态得到很好控制的互连通道。将人脐静脉内皮细胞(HUVEC)培养在通道衬里上并增殖形成血管腔。强大的细胞粘附能力和对剪应力的适应性反应证明了模板和模板牺牲过程均具有出色的细胞相容性。此外,表征了内皮层的屏障功能,并且结果表明融合的内皮单层被完全显影。综上所述,我们开发了一种简便而快速的方法来设计血管模型,该模型可潜在地用于血管功能和血管组织工程的生理研究。

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