材料科学
纳米技术
磁性纳米粒子
磁化
模块化设计
生物相容性
计算机科学
纳米颗粒
磁场
量子力学
操作系统
物理
冶金
作者
Tanyong Wei,Ruizhou Zhao,Lijun Fang,Zongze Li,Ming Yang,Zhen Zhan,U Kei Cheang,Chengzhi Hu
标识
DOI:10.1002/adfm.202311908
摘要
Abstract The bottom‐up assembly of premagnetized microgels offers remarkable flexibility in programmability, material selection, and complexity for fabricating programmable magnetic soft machines with discrete 3D magnetization profiles. However, the current microgel bonding encounters challenges due to the utilization of adhesives for attachment, biocompatibility for in vivo applications, and the need for elevated temperature for self‐healing materials. Here, an approach is presented that leverages N‐hydroxysuccinimide ester‐activated sodium alginate (SA‐NHS) and chitosan (CS) to form modular gels for on‐demand assembly through covalent bonding, yielding a tough and durable interface. Photolithography‐based patterning and magnetic maneuverability are imparted by introducing poly(ethylene glycol) diacrylate and ferromagnetic particles into SA‐NHS or CS, resulting in the creation of modularized magnetic or nonmagnetic microgels. Different magnetization profiles of the modular microgel can be achieved by magnetizing the ferromagnetic particles inside the microgel. To prove the versatility of the proposed method, several programmable magnetic soft machines are developed for various application scenarios, including heterogeneous cell‐laden hydrogel assemblies, multisegmented magnetic soft swimmers, programmable magnetic switches for electric circuits, and magnetically triggered release from drug‐encapsulated magnetic capsules. This proposed approach holds great potential to engineer highly intricate and hierarchical architectures, enhancing the functionality, versatility, and adaptability of programmable soft machines.
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