Liquid-embedded (bio)printing of alginate-free, standalone, ultrafine, and ultrathin-walled cannular structures

Author:

Tang Guosheng12,Luo Zeyu13,Lian Liming1,Guo Jie1,Maharjan Sushila1ORCID,Garciamendez-Mijares Carlos Ezio1,Wang Mian1,Li Wanlu1,Zhang Zhenrui1ORCID,Wang Di1,Xie Maobin1,Ravanbakhsh Hossein1ORCID,Zhou Cuiping1,Kuang Xiao1,Hou Yingying2,Yu Xiyong2,Zhang Yu Shrike1ORCID

Affiliation:

1. Division of Engineering in Medicine, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Cambridge, MA 02139

2. Guangzhou Municipal and Guangdong Provincial Key Laboratory of Molecular Target & Clinical Pharmacology, the NMPA and State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences and the Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou 511436, P. R. China

3. Department of Orthopedics, West China Hospital/West China School of Medicine, Sichuan University, Chengdu 610041, P. R. China

Abstract

While there has been considerable success in the three-dimensional bioprinting of relatively large standalone filamentous tissues, the fabrication of solid fibers with ultrafine diameters or those cannular featuring ultrathin walls remains a particular challenge. Here, an enabling strategy for (bio)printing of solid and hollow fibers whose size ranges could be facilely adjusted across a broad spectrum, is reported, using an aqueous two-phase embedded (bio)printing approach combined with specially designed cross-linking and extrusion methods. The generation of standalone, alginate-free aqueous architectures using this aqueous two-phase strategy allowed freeform patterning of aqueous bioinks, such as those composed of gelatin methacryloyl, within the immiscible aqueous support bath of poly(ethylene oxide). Our (bio)printing strategy revealed the fabrication of standalone solid or cannular structures with diameters as small as approximately 3 or 40 μ m, respectively, and wall thicknesses of hollow conduits down to as thin as <5 μ m. With cellular functions also demonstrated, we anticipate the methodology to serve as a platform that may satisfy the needs for the different types of potential biomedical and other applications in the future, especially those pertaining to cannular tissues of ultrasmall diameters and ultrathin walls used toward regenerative medicine and tissue model engineering.

Funder

BWH | Brigham Research Institute

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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