| Literature DB >> 32700332 |
Ramesh Subbiah1, Christina Hipfinger1, Anthony Tahayeri1, Avathamsa Athirasala1, Sivaporn Horsophonphong1,2, Greeshma Thrivikraman1, Cristiane Miranda França1, Diana Araujo Cunha1, Amin Mansoorifar1, Albena Zahariev1, James M Jones3, Paulo G Coelho4, Lukasz Witek4, Hua Xie3, Robert E Guldberg5,6, Luiz E Bertassoni1,3,6,7.
Abstract
Biomaterial scaffolds have served as the foundation of tissue engineering and regenerative medicine. However, scaffold systems are often difficult to scale in size or shape in order to fit defect-specific dimensions, and thus provide only limited spatiotemporal control of therapeutic delivery and host tissue responses. Here, a lithography-based 3D printing strategy is used to fabricate a novel miniaturized modular microcage scaffold system, which can be assembled and scaled manually with ease. Scalability is based on an intuitive concept of stacking modules, like conventional toy interlocking plastic blocks, allowing for literally thousands of potential geometric configurations, and without the need for specialized equipment. Moreover, the modular hollow-microcage design allows each unit to be loaded with biologic cargo of different compositions, thus enabling controllable and easy patterning of therapeutics within the material in 3D. In summary, the concept of miniaturized microcage designs with such straight-forward assembly and scalability, as well as controllable loading properties, is a flexible platform that can be extended to a wide range of materials for improved biological performance.Keywords: cell migration; growth factor delivery; instructive scaffolds; microgels; vascularization
Year: 2020 PMID: 32700332 DOI: 10.1002/adma.202001736
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849