Department of Biomedical Engineering, Duke University.
Departments of Biomedical Engineering, Neurology, and Dermatology, Duke University;
J Vis Exp. 2022 Oct 28(188). doi: 10.3791/64554.
Microgels are the building blocks of microporous annealed particle (MAP) scaffolds, which serve as a platform for both in vitro cell culture and in vivo tissue repair. In these granular scaffolds, the innate porosity generated by the void space between microgels enables cell infiltration and migration. Controlling the void fraction and particle fraction is critical for MAP scaffold design, as porosity is a bioactive cue for cells. Spherical microgels can be generated on a microfluidic device for controlled size and shape and subsequently freeze-dried using methods that prevent fracturing of the polymer network. Upon rehydration, the lyophilized microgels lead to controlled particle fractions in MAP scaffolds. The implementation of these methods for microgel lyophilization has led to reproducible studies showing the effect of particle fraction on macromolecule diffusion and cell spreading. The following protocol will cover the fabrication, lyophilization, and rehydration of microgels for controlling particle fraction in MAP scaffolds, as well as annealing the microgels through bio-orthogonal crosslinking for 3D cell culture in vitro.
微凝胶是微孔退火颗粒(MAP)支架的构建块,可作为体外细胞培养和体内组织修复的平台。在这些颗粒状支架中,微凝胶之间的空隙产生的固有孔隙率允许细胞渗透和迁移。控制空隙率和颗粒分数对于 MAP 支架设计至关重要,因为孔隙率是细胞的生物活性线索。球形微凝胶可以在微流控装置上生成,以控制尺寸和形状,然后使用防止聚合物网络破裂的方法进行冷冻干燥。在复水时,冻干的微凝胶导致 MAP 支架中控制的颗粒分数。这些用于微凝胶冻干的方法的实施导致了可重复的研究,表明颗粒分数对大分子扩散和细胞铺展的影响。以下方案将涵盖微凝胶的制造、冻干和复水,以控制 MAP 支架中的颗粒分数,以及通过生物正交交联对微凝胶进行退火,以进行体外 3D 细胞培养。