Department of Chemical Engineering, Technion─Israel Institute of Technology, Haifa 32000, Israel.
The Norman Seiden Multidisciplinary Program for Nanoscience and Nanotechnology, Technion─Israel Institute of Technology, Haifa 32000, Israel.
ACS Biomater Sci Eng. 2024 Oct 14;10(10):6734-6750. doi: 10.1021/acsbiomaterials.4c01136. Epub 2024 Sep 29.
Granular hydrogels, formed by jamming microgels suspension, are promising materials for three-dimensional bioprinting applications. Despite their extensive use as support materials for embedded bioprinting, the influence of the particle's physical properties on the macroscale viscoelasticity on one hand and on the printing performance on the other hand remains unclear. Herein, we investigate the linear and nonlinear rheology of κ-carrageenan granular hydrogel through small- and large-amplitude oscillatory shear measurements. We tuned the granular hydrogel's properties by changing the stiffness (soft, medium, stiff) and the packing density of the individual microgels. Characterizations in the linear viscoelasticity regime revealed that the storage modulus of granular hydrogels is not a simple function of microgel stiffness and depends on the microgel packing density. At larger strains, increasing the microgel stiffness reduced the energy dissipation of the granular beds and increased the solid-fluid transition point. To understand how the different rheological properties of granular support materials influence embedded bioprinting, we examined the printing fidelity and cellular filament shrinkage within the granular beds. We found that microgels with low packing density diminished the printing quality, while stiff microgels promoted filament roughness. In addition, we found that highly packed stiff microgels significantly reduced the postprinting contraction of cellular filaments. Overall, this work provides a comprehensive knowledge of the rheology of granular hydrogels that can be used to rationally design support beds for bioprinting applications with specific characteristics.
颗粒水凝胶通过微凝胶悬浮液的凝胶化形成,是三维生物打印应用的有前途的材料。尽管它们被广泛用作嵌入式生物打印的支撑材料,但颗粒的物理性质对宏观粘弹性的影响以及对打印性能的影响尚不清楚。本文通过小振幅和大振幅振荡剪切测量研究了 κ-卡拉胶颗粒水凝胶的线性和非线性流变特性。通过改变单个微凝胶的刚度(软、中、硬)和堆积密度来调整颗粒水凝胶的性质。在线性粘弹性区的特征研究表明,颗粒水凝胶的储能模量不是微凝胶刚度的简单函数,而是取决于微凝胶堆积密度。在较大应变下,增加微凝胶的刚度会减少颗粒床的能量耗散,并增加固-液转变点。为了了解不同的颗粒支撑材料的流变性能如何影响嵌入式生物打印,我们检查了颗粒床内的打印保真度和细胞丝的收缩。我们发现,堆积密度低的微凝胶会降低打印质量,而硬微凝胶会增加丝的粗糙度。此外,我们发现堆积密度高的硬微凝胶会显著降低细胞丝打印后的收缩。总的来说,这项工作提供了颗粒水凝胶流变学的全面知识,可用于理性设计具有特定特性的生物打印应用的支撑床。