2017 Annual Meeting
(267c) Surface Tension-Assisted Additive Manufacturing of Multicomponent Biomaterials
Authors
Tibbitt, M. W. - Presenter, University of Colorado
Ragelle, H., Massachusetts Institute of Technology
Cima, M., Massachusetts Institute of Technology
Langer, R., Massachusetts Institute of Technology
Additive manufacturing, including 3D printing and 3D bio-printing, are enabling the production of geometrically-defined, patient specific biomaterials.1 Despite the many recent advances in additive manufacturing technologies,2 limitations remain to the speed of production, access to a broad range of materials, and easy integration of multiple materials and cells within a single device. Here, we present a facile method to fabricate multicomponent biomaterials with defined geometry incorporating both structural and mechanical support from polymeric constituents (e.g., (meth)acrylates, polycaprolactone, poly(lactic-co-glycolic acid)) as well as cellular and tissue integration from hydrogels (e.g., poly(ethylene glycol) based, collagen/elastin based, gelatin methacryloyl based). The method relies on surface tension-driven surface wetting, which allows for rapid coating of a reticulated frame with suspended films. We have developed a physical understanding of the coating process and demonstrate how it can be exploited to fabricate anisotropic biomaterials. In addition, the process can access a variety of applications on account of its scalability and versatility, with a special emphasis on tracheal replacements. We demonstrate the efficacy of this approach to fabricate mechanically supported and cell-laden biomaterials for ex vivo models of functional tissue as well as for human-scale replacement tissue for regenerative medicine applications. Overall, this presentation will present a facile process of multicomponent biomaterial fabrication and illustrate how this contributes to the emerging field of additive manufacturing in biotechnology and medicine.
References
- Murphy SV et al. Nat Biotech 32 (2014) 773-785
- Kang HW et al. Nat Biotech 34 (2016) 312-319