Granular Biphasic Colloidal Hydrogels for 3D Bioprinting

Author:

Deo Kaivalya A.1ORCID,Murali Aparna1ORCID,Tronolone James J.1ORCID,Mandrona Cole1ORCID,Lee Hung Pang1ORCID,Rajput Satyam1ORCID,Hargett Sarah E.1ORCID,Selahi Amirali1ORCID,Sun Yuxiang2ORCID,Alge Daniel L.13ORCID,Jain Abhishek145ORCID,Gaharwar Akhilesh K.13567ORCID

Affiliation:

1. Biomedical Engineering College of Engineering Texas A&M University College Station TX 77843 USA

2. Nutrition College of Agriculture Texas A&M University College Station TX 77843 USA

3. Material Science and Engineering College of Engineering Texas A&M University College Station TX 77843 USA

4. Medical Physiology School of Medicine Texas A&M Health Science Center Bryan TX USA

5. Cardiovascular Sciences Houston Methodist Research Institute Houston TX 77030 USA

6. Interdisciplinary Graduate Program in Genetics & Genomics Texas A&M University College Station TX 77843 USA

7. Center for Remote Health Technologies and Systems Texas A&M University College Station TX 77843 USA

Abstract

AbstractGranular hydrogels composed of hydrogel microparticles are promising candidates for 3D bioprinting due to their ability to protect encapsulated cells. However, to achieve high print fidelity, hydrogel microparticles need to jam to exhibit shear‐thinning characteristics, which is crucial for 3D printing. Unfortunately, this overpacking can significantly impact cell viability, thereby negating the primary advantage of using hydrogel microparticles to shield cells from shear forces. To overcome this challenge, a novel solution: a biphasic, granular colloidal bioink designed to optimize cell viability and printing fidelity is introduced. The biphasic ink consists of cell‐laden polyethylene glycol (PEG) hydrogel microparticles embedded in a continuous gelatin methacryloyl (GelMA)‐nanosilicate colloidal network. Here, it is demonstrated that this biphasic bioink offers outstanding rheological properties, print fidelity, and structural stability. Furthermore, its utility for engineering complex tissues with multiple cell types and heterogeneous microenvironments is demonstrated, by incorporating β‐islet cells into the PEG microparticles and endothelial cells in the GelMA‐nanosilicate colloidal network. Using this approach, it is possible to induce cell patterning, enhance vascularization, and direct cellular function. The proposed biphasic bioink holds significant potential for numerous emerging biomedical applications, including tissue engineering and disease modeling.

Funder

National Institute of Dental and Craniofacial Research

National Institute of Biomedical Imaging and Bioengineering

National Science Foundation

American Heart Association

Biomedical Advanced Research and Development Authority

U.S. Food and Drug Administration

National Institutes of Health

Texas A and M University

National Aeronautics and Space Administration

Publisher

Wiley

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