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Fabrication of three-dimensional porous cell-laden hydrogel for tissue engineering

机译:用于组织工程的三维多孔多孔水凝胶的制备

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摘要

For tissue engineering applications, scaffolds should be porous to enable rapid nutrient and oxygen transfer while providing a three-dimensional (3D) microenvironment for the encapsulated cells. This dual characteristic can be achieved by fabrication of porous hydrogels that contain encapsulated cells. In this work, we developed a simple method that allows cell encapsulation and pore generation inside alginate hydrogels simultaneously. Gelatin beads of 150-300 mu m diameter were used as a sacrificial porogen for generating pores within cell-laden hydrogels. Gelation of gelatin at low temperature (4 degrees C) was used to form beads without chemical crosslinking and their subsequent dissolution after cell encapsulation led to generation of pores within cell-laden hydrogels. The pore size and porosity of the scaffolds were controlled by the gelatin bead size and their volume ratio, respectively. Fabricated hydrogels were characterized for their internal microarchitecture, mechanical properties and permeability. Hydrogels exhibited a high degree of porosity with increasing gelatin bead content in contrast to nonporous alginate hydrogel. Furthermore, permeability increased by two to three orders while compressive modulus decreased with increasing porosity of the scaffolds. Application of these scaffolds for tissue engineering was tested by encapsulation of hepatocarcinoma cell line (HepG2). All the scaffolds showed similar cell viability; however, cell proliferation was enhanced under porous conditions. Furthermore, porous alginate hydrogels resulted in formation of larger spheroids and higher albumin secretion compared to nonporous conditions. These data suggest that porous alginate hydrogels may have provided a better environment for cell proliferation and albumin production. This may be due to the enhanced mass transfer of nutrients, oxygen and waste removal, which is potentially beneficial for tissue engineering and regenerative medicine applications.
机译:对于组织工程应用,支架应该是多孔的,以实现快速的营养和氧气传输,同时为封装的细胞提供三维(3D)微环境。这种双重特性可以通过制造包含被囊封的细胞的多孔水凝胶来实现。在这项工作中,我们开发了一种简单的方法,该方法可以同时在藻酸盐水凝胶内封装细胞和产生孔。使用直径为150-300微米的明胶珠作为牺牲性致孔剂,以在充满细胞的水凝胶中产生孔。明胶在低温(4℃)下的凝胶化作用用于形成没有化学交联的珠子,并且在细胞包封后其随后的溶解导致在充满细胞的水凝胶中产生孔。支架的孔径和孔隙率分别由明胶珠的大小和它们的体积比控制。制备的水凝胶具有内部微结构,机械性能和渗透性的特点。与无孔藻酸盐水凝胶相反,水凝胶显示出较高的孔隙度,明胶珠含量增加。此外,随着支架孔隙率的增加,渗透率增加了2到3个数量级,而压缩模量却降低了。这些支架在组织工程中的应用通过封装肝癌细胞系(HepG2)进行了测试。所有的支架都显示出相似的细胞活力。然而,在多孔条件下细胞增殖得以增强。此外,与无孔条件相比,多孔藻酸盐水凝胶导致形成更大的球体和更高的白蛋白分泌。这些数据表明多孔藻酸盐水凝胶可能为细胞增殖和白蛋白产生提供了更好的环境。这可能是由于营养素,氧气和废物去除的质量传递增强,这可能对组织工程和再生医学应用有益。

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