Biomedical Engineering Department, Rensselaer Polytechnic Institute, 110 Eighth Street, Troy, NY 12180.
Rensselaer Polytechnic Institute, Biomedical Engineering Department, 110 Eighth Street, Troy, NY 12180.
J Biomech Eng. 2023 Mar 1;145(3). doi: 10.1115/1.4055757.
Hydrogel microbeads are engineered spherical microgels widely used for biomedical applications in cell cultures, tissue engineering, and drug delivery. Their mechanical and physical properties (i.e., modulus, porosity, diffusion) heavily influence their utility by affecting encapsulated cellular behavior, biopayload elution kinetics, and stability for longer term cultures. There is a need to quantify these properties to guide microbead design for effective application. However, there are few techniques with the μN-level resolution required to evaluate these relatively small, compliant constructs. To circumvent mechanically testing individual microbeads, researchers often approximate microbead properties by characterizing larger bulk gel analogs of the same material formulation. This approach provides some insight into the hydrogel properties. However, bulk gels possess key structural and mechanical differences compared to their microbead equivalents, which may limit their accuracy and utility as analogs for estimating microbead properties. Herein, we explore how microbead properties are influenced by hydrogel formulation (i.e., alginate concentration, divalent cation crosslinker, and crosslinker concentration), and whether these trends are accurately reflected in bulk gel analogs. To accomplish this, we utilize laser direct-write bioprinting to create 12 × 12 arrays of alginate microbeads and characterize all 144 microbeads in parallel using a commercially available microcompression system. In this way, the compressive load is distributed across a large number of beads, thus amplifying sample signal. Comparing microbead properties to those of their bulk gel analogs, we found that their trends in modulus, porosity, and diffusion with hydrogel formulation are consistent, yet bulk gels exhibit significant discrepancies in their measured values.
水凝胶微球是一种工程化的球形微凝胶,广泛应用于细胞培养、组织工程和药物输送等生物医学领域。其力学和物理性质(如模量、孔隙率、扩散率)对其应用有很大影响,会影响包封细胞的行为、生物有效载荷洗脱动力学以及更长期培养的稳定性。因此,需要定量这些性质以指导微球设计,实现有效应用。然而,目前只有少数技术具有评估这些相对较小、顺应性构建体所需的 μN 级分辨率。为了避免对单个微球进行力学测试,研究人员通常通过对相同材料配方的较大块状凝胶类似物进行特征化来近似微球的性质。这种方法提供了一些关于水凝胶性质的见解。然而,与微球等效物相比,块状凝胶具有关键的结构和力学差异,这可能会限制其作为估计微球性质的类似物的准确性和实用性。在此,我们探讨了水凝胶配方(即藻酸盐浓度、二价阳离子交联剂和交联剂浓度)如何影响微球性质,以及这些趋势在块状凝胶类似物中是否得到准确反映。为了实现这一目标,我们利用激光直写生物打印技术创建藻酸盐微球的 12×12 阵列,并使用市售的微压缩系统并行表征所有 144 个微球。通过这种方式,压缩负载分布在大量微球上,从而放大了样品信号。将微球性质与其块状凝胶类似物进行比较,我们发现它们的模量、孔隙率和扩散率随水凝胶配方的趋势是一致的,但块状凝胶在测量值上存在显著差异。