自愈水凝胶
材料科学
纳米技术
药物输送
明胶
磁性纳米粒子
生物相容性材料
纳米颗粒
化学工程
生物医学工程
化学
高分子化学
医学
生物化学
工程类
作者
Maria C. Mendes,João E. Pereira,Ana Sofia Silva,João F. Mano
标识
DOI:10.1002/adma.202402988
摘要
Abstract The inclusion of hollow channels in tissue‐engineered hydrogels is crucial for mimicking the natural physiological conditions and facilitating the delivery of nutrients and oxygen to cells. Although bio‐fabrication techniques provide diverse strategies to create these channels, many require sophisticated equipment and time‐consuming protocols. Herein, collagenase, a degrading agent for methacrylated gelatin hydrogels, and magnetic nanoparticles (MNPs) are combined and processed into enzymatically active spherical structures using a straightforward oil bath emulsion methodology. The generated microgels are then used to microfabricate channels within biomimetic hydrogels via a novel sculpturing approach that relied on the precise coupling of protein‐enzyme pairs (for controlled local degradation) and magnetic actuation (for directional control). Results show that the sculpting velocity can be tailored by adjusting the magnetic field intensity or concentration of MNPs within the microgels. Additionally, varying the magnetic field position or microgel size generated diverse trajectories and channels of different widths. This innovative technology improves the viability of encapsulated cells through enhanced medium transport, outperforming non‐sculpted hydrogels and offering new perspectives for hydrogel vascularization and drug/biomolecule administration. Ultimately, this novel concept can help design fully controlled channels in hydrogels or soft materials, even those with complex tortuosity, in a single wireless top‐down biocompatible step.
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