High cell density and high-resolution 3D bioprinting for fabricating vascularized tissues

Author:

You Shangting1ORCID,Xiang Yi1,Hwang Henry H.1,Berry David B.12ORCID,Kiratitanaporn Wisarut3ORCID,Guan Jiaao4ORCID,Yao Emmie1,Tang Min1ORCID,Zhong Zheng1ORCID,Ma Xinyue5,Wangpraseurt Daniel16ORCID,Sun Yazhi1,Lu Ting-yu7,Chen Shaochen1347ORCID

Affiliation:

1. Department of NanoEngineering, University of California, San Diego, La Jolla, CA 92093, USA.

2. Department of Orthopedic Surgery, University of California, San Diego, La Jolla, CA 92093, USA.

3. Department of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.

4. Department of Electrical and Computer Engineering, University of California, San Diego, La Jolla, CA 92093, USA.

5. School of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.

6. Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA 92093, USA.

7. Materials Science and Engineering Program, University of California, San Diego, La Jolla, CA 92093, USA.

Abstract

Three-dimensional (3D) bioprinting techniques have emerged as the most popular methods to fabricate 3D-engineered tissues; however, there are challenges in simultaneously satisfying the requirements of high cell density (HCD), high cell viability, and fine fabrication resolution. In particular, bioprinting resolution of digital light processing–based 3D bioprinting suffers with increasing bioink cell density due to light scattering. We developed a novel approach to mitigate this scattering-induced deterioration of bioprinting resolution. The inclusion of iodixanol in the bioink enables a 10-fold reduction in light scattering and a substantial improvement in fabrication resolution for bioinks with an HCD. Fifty-micrometer fabrication resolution was achieved for a bioink with 0.1 billion per milliliter cell density. To showcase the potential application in tissue/organ 3D bioprinting, HCD thick tissues with fine vascular networks were fabricated. The tissues were viable in a perfusion culture system, with endothelialization and angiogenesis observed after 14 days of culture.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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