Rocha Luiz Maria Eduarda, Carreira Mariana, Nadine Sara, Tognato Riccardo, Parolini Romedi, Bakht Syeda M, Serra Tiziano, Mano João F
CICECO - Aveiro Institute of Materials, Department of Chemistry, University of Aveiro, Campus Universitário de Santiago, 3810-193, Aveiro, Portugal.
AO Research Institute Davos, Clavadelerstrasse 8, 7270, Davos, Switzerland.
Biomaterials. 2026 Feb;325:123555. doi: 10.1016/j.biomaterials.2025.123555. Epub 2025 Jul 12.
In recent years, considerable efforts have been directed towards developing systems that replicate native tissue microarchitecture, enhancing cell viability and achieving close-to-native cellular organization. Despite advancements in various assembly methods, scalability and cell viability remain challenging due to the time consuming nature of certain approaches. Acoustic assembly has emerged as a powerful technology for modular units' assembly, leveraging sound waves to achieve rapid, contactless spatial arrangement by fine-tuning parameters such as frequency, amplitude, and chamber geometry. Here we present a system that employs acoustic waves to generate spatial patterns of liquid-core microcapsules, encapsulating poly-caprolactone surface-functionalized microparticles and umbilical cord-derived mesenchymal stem cells. The microcapsules were produced using electrohydrodynamic atomization in conjugation with an aqueous two-phase system and subsequently embedded in gelatin methacrylate. Acoustic waves were then applied to assemble the liquid-core microcapsules in well-defined patterns within the hydrogel precursor followed by crosslinking for structural stability. This approach allows us to define spatial patterns with precision, aligning with simulation predictions. The liquid nature of the microcapsules' core permits the organization of cells within the space towards the formation of microtissues decoupled from the external environment. The patterned constructs maintained cell viability for 14 days, facilitating the formation of microaggregates within liquid-core microcapsules and maintained organized microstructures. To explore the versatility of this system, we successfully patterned and stacked multiple layers of microcapsules, increasing structural complexity. Furthermore, we demonstrated its ability to support co-culture by seeding human umbilical vein endothelial cells onto the constructs as a proof of concept for promoting enhanced cellular interactions. This platform offers a scalable, versatile solution for developing tissue-mimetic multiscale constructs with tunable complexity, enabling rapid and non-contact assembly, making it a valuable tool for advancing in vitro models and studying complex cellular interactions.
近年来,人们付出了巨大努力来开发能够复制天然组织微结构、提高细胞活力并实现接近天然细胞组织的系统。尽管各种组装方法取得了进展,但由于某些方法耗时的特性,可扩展性和细胞活力仍然具有挑战性。声学组装已成为一种用于模块化单元组装的强大技术,它利用声波通过微调频率、振幅和腔室几何形状等参数来实现快速、非接触式的空间排列。在此,我们展示了一种利用声波生成液芯微胶囊空间图案的系统,该微胶囊包裹着聚己内酯表面功能化的微粒和脐带间充质干细胞。微胶囊是通过电液动力雾化结合水两相系统制备的,随后嵌入甲基丙烯酸明胶中。然后施加声波,将液芯微胶囊以明确的图案组装在水凝胶前体中,随后进行交联以实现结构稳定性。这种方法使我们能够精确地定义空间图案,与模拟预测结果相符。微胶囊核心的液体性质允许细胞在空间内组织起来,形成与外部环境解耦的微组织。图案化构建体在14天内保持细胞活力,促进了液芯微胶囊内微聚集体的形成,并维持了有组织的微观结构。为了探索该系统的多功能性,我们成功地对多层微胶囊进行了图案化和堆叠,增加了结构复杂性。此外,作为促进增强细胞相互作用概念验证,我们通过将人脐静脉内皮细胞接种到构建体上,展示了其支持共培养的能力。该平台为开发具有可调复杂性的组织模拟多尺度构建体提供了一种可扩展、多功能的解决方案,实现了快速和非接触式组装,使其成为推进体外模型和研究复杂细胞相互作用的宝贵工具。