4.7 Article

High Resolution Dual Material Stereolithography for Monolithic Microdevices

期刊

ADVANCED MATERIALS TECHNOLOGIES
卷 7, 期 6, 页码 -

出版社

WILEY
DOI: 10.1002/admt.202101180

关键词

3D printing; additive manufacturing; advanced cell culture; dual material stereolithography; hydrogels; monolithic devices

资金

  1. Independent Research Fund Denmark [7017-00366B]

向作者/读者索取更多资源

A high-resolution dual-material 3D printing concept is developed, allowing for the production of distinct materials locally based on orthogonal chemical reactions depending on the illumination wavelength. The resulting devices have micrometer-scale precision in tissue modeling.
Functional 3D components such as perfusion channels and mechanical actuation elements at cellular length scales can support cell survival and tissue maturation in tissue modeling devices. These advanced requirements call for increasingly complex materials and 3D fabrication methods. Here, a high-resolution dual-material 3D printing concept is developed, where distinct materials are produced locally by orthogonal chemical reactions depending on the illumination wavelength. A tough, stiff epoxy network results from cationic polymerization in UV light, while a soft and diffusion-open hydrogel forms by free-radical polymerization initiated by blue light. Thus, dual-exposure allows for selection of material properties in every voxel, while retaining the 3D design flexibility associated with stereolithography. This enables single-process fabrication of devices integrating mechanically stable chip-to-world interconnects and compliant, diffusion-open perfusable channel components of 150 mu m in width and height, while also allowing structural and mechanical feature dimensions down to 60 mu m. A perfusion chip capable of creating a stable uniaxial chemical gradient by passive dye diffusion through hydrogel sections, and a negative Poisson ratio structure based on the interplay between stiff rotators and compliant hinges, are manufactured as proof-of-concept microdevices. Lastly, week-long culture of hydrogel-encapsulated human liver cells demonstrates the cytocompatibility of both materials.

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