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The mechanical properties and cytotoxicity of cell-laden double-network hydrogels based on photocrosslinkable gelatin and gellan gum biomacromolecules

机译:基于可光交联明胶和结冷胶生物大分子的载有细胞的双网络水凝胶的力学性能和细胞毒性

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摘要

A major goal in the application of hydrogels for tissue engineering scaffolds, especially for load-bearing tissues such as cartilage, is to develop hydrogels with high mechanical strength. In this study, a double-network (DN) strategy was used to engineer strong hydrogels that can encapsulate cells. We improved upon previously studied double-network (DN) hydrogels by using a processing condition compatible with cell survival. The DN hydrogels were created by a two-step photocrosslinking using gellan gum methacrylate (GGMA) for the rigid and brittle first network, and gelatin methacrylamide (GelMA) for the soft and ductile second network. We controlled the degree of methacrylation of each polymer so that they obtain relevant mechanical properties as each network. The DN was formed by photocrosslinking the GGMA, diffusing GelMA into the first network, and photocrosslinking the GelMA to form the second network. The formation of the DN was examined by diffusion tests of the large GelMA molecules into the GGMA network, the resulting enhancement in the mechanical properties, and the difference in mechanical properties between GGMA/GelMA single networks (SN) and DNs. The resulting DN hydrogels exhibited the compressive failure stress of up to 6.9 MPa, which approaches the strength of cartilage. It was found that there is an optimal range of the crosslink density of the second network for high strength of DN hydrogels. DN hydrogels with a higher mass ratio of GelMA to GGMA exhibited higher strength, which shows promise in developing even stronger DN hydrogels in the future. Three dimensional (3D) encapsulation of NIH-3T3 fibroblasts and the following viability test showed the cell-compatibility of the DN formation process. Given the high strength and the ability to encapsulate cells, the DN hydrogels made from photocrosslinkable macromolecules could be useful for the regeneration of load-bearing tissues.
机译:将水凝胶用于组织工程支架,特别是用于承重组织如软骨的水凝胶的主要目的是开发具有高机械强度的水凝胶。在这项研究中,使用了双网络(DN)策略来设计可以封装细胞的强力水凝胶。通过使用与细胞存活相容的加工条件,我们改进了先前研究的双网络(DN)水凝胶。 DN水凝胶是通过两步光交联生成的,其中第二步使用刚性和脆性的吉兰胶甲基丙烯酸酯(GGMA),第二次使用软性和延展性的明胶甲基丙烯酰胺(GelMA)。我们控制了每种聚合物的甲基丙烯酸酯化程度,以使它们在每个网络中都获得相关的机械性能。 DN是通过将GGMA光交联,将GelMA扩散到第一个网络中,然后将GelMA光交联以形成第二个网络而形成的。通过大的GelMA分子向GGMA网络中的扩散测试,机械性能的增强以及GGMA / GelMA单网络(SN)和DN之间机械性能的差异来检查DN的形成。所得的DN水凝胶表现出高达6.9 MPa的压缩破坏应力,接近软骨的强度。发现对于DN水凝胶的高强度,第二网络的交联密度存在最佳范围。质量比更高的GelMA与GGMA的DN水凝胶显示出更高的强度,这在将来开发出更坚固的DN水凝胶方面显示出了希望。 NIH-3T3成纤维细胞的三维(3D)封装和随后的生存力测试显示了DN形成过程的细胞相容性。鉴于其高强度和封装细胞的能力,由可光交联的大分子制成的DN水凝胶可用于承重组织的再生。

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