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一种剪切稀化的甲基丙烯酰化黄原胶-明胶复合生物墨水的可打印性和生物功能性。

Printability and bio-functionality of a shear thinning methacrylated xanthan-gelatin composite bioink.

机构信息

Department of Material Science and Engineering, Monash University, Clayton, VIC 3800, Australia.

CSIRO Manufacturing, Clayton, VIC 3168, Australia.

出版信息

Biofabrication. 2021 Apr 8;13(3). doi: 10.1088/1758-5090/abec2d.

Abstract

3D bioprinting is a recent technique that can create complex cell seeded scaffolds and therefore holds great promise to revolutionize the biomedical sector by combining materials and structures that more closely mimic the 3D cell environment in tissues. The most commonly used biomaterials for printing are hydrogels, however, many of the hydrogels used still present issues of printability, stability, or poor cell-material interactions. We propose that bioinks with intrinsic self-assembling and shear thinning properties, such as xanthan gum, can be methacrylated (XGMA) and combined with a bio-functional material such as gelatin methacryloyl (GelMa) to create a stable, cell-interactive bioink with improved properties for 3D bioprinting. These biomaterials have reduced viscosity under high shear and recover their viscosity rapidly after the shear is removed, retaining their shape, which translates to easier extrusion whilst maintaining accurate fidelity after printing. This was confirmed in printing studies, with measured normalized strand widths of 1.2 obtained for high gel concentrations (5+5 % XGMA-GelMA). Furthermore, the introduction of a secondary photo-cross-linking method allowed tuning of the mechanical properties of the hydrogel with stiffness between 15 and 30 kPa, as well as improving the stability of the hydrogel with retention of 75 % of its mass after 90 d. The hydrogel was shown to be biocompatible and bio-active with 97 % cell viability, and cell spreading after 7 d of culture for low gel concentrations (3+3 % XGMA-GelMA). Shear stresses were relatively low while printing (1 kPa) as a result of the shear thinning property of the material, which supported cell viability during extrusion. Finally, printed hydrogels retained high cell viability for lower gel concentrations, and showed improved cell viability for more concentrated hydrogels when compared to cells cultured in bulk hydrogels, presumably due to improved nutrient/oxygen diffusion and cell migration. In conclusion, stability and formulation of a XGMA-GelMA shear thinning composite hydrogel has been optimized to create a bio-functional bioink, with improved printability, andculture stabilitysecondary photo-induced cross-linking, making this composite a promising bioink for 3D bioprinting.

摘要

3D 生物打印是一种新兴技术,可以制造复杂的细胞接种支架,因此通过结合更接近组织中 3D 细胞环境的材料和结构,有望彻底改变生物医学领域。用于打印的最常用生物材料是水凝胶,但是,许多使用的水凝胶仍然存在可打印性、稳定性或与细胞材料相互作用差的问题。我们提出,具有内在自组装和剪切稀化特性的生物墨水,如黄原胶,可以进行甲基丙烯酰化(XGMA),并与生物功能材料如明胶甲基丙烯酰(GelMa)结合,形成一种稳定的、具有细胞相互作用的生物墨水,具有改善的 3D 生物打印性能。这些生物材料在高剪切下粘度降低,在剪切去除后迅速恢复其粘度,保持其形状,这意味着在打印后保持精确保真度的同时,更容易挤出。在打印研究中得到了证实,对于高凝胶浓度(5+5%XGMA-GelMA),测量到的归一化丝宽度为 1.2。此外,引入二次光交联方法可以调整水凝胶的机械性能,使其硬度在 15 和 30 kPa 之间,并且通过在 90 天内保留 75%的质量来提高水凝胶的稳定性。水凝胶表现出生物相容性和生物活性,对于低凝胶浓度(3+3%XGMA-GelMA),细胞活力为 97%,并且在培养 7 天后细胞扩散。由于材料的剪切稀化特性,打印过程中的剪切应力相对较低,这支持了挤出过程中的细胞活力。最后,与在块状水凝胶中培养的细胞相比,对于较低凝胶浓度的打印水凝胶保留了较高的细胞活力,并且对于更浓缩的水凝胶显示出了改善的细胞活力,这可能是由于改善了营养/氧气扩散和细胞迁移。总之,通过优化 XGMA-GelMA 剪切稀化复合水凝胶的稳定性和配方,创建了一种具有生物功能的生物墨水,具有改善的可打印性和培养稳定性,通过二次光诱导交联,使这种复合材料成为 3D 生物打印有前途的生物墨水。

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