Advances in Gelatin Bioinks to Optimize Bioprinted Cell Functions

Author:

Asim Saad1,Tabish Tanveer A.2,Liaqat Usman3,Ozbolat Ibrahim T.4567,Rizwan Muhammad18ORCID

Affiliation:

1. Department of Biomedical Engineering Michigan Technological University Houghton MI 49931 USA

2. Cardiovascular Division Radcliff Department of Medicine University of Oxford Oxford OX3 9DU UK

3. Department of Materials Engineering School of Chemical and Materials Engineering (SCME) National University of Sciences and Technology (NUST) Islamabad 44000 Pakistan

4. Engineering Science and Mechanics Pennsylvania State University University Park PA 16802 USA

5. Department of Biomedical Engineering Pennsylvania State University University Park PA 16802 USA

6. Department of Neurosurgery Pennsylvania State University Hershey PA 16802 USA

7. Department of Medical Oncology Cukurova University Adana 01330 Turkey

8. Health Research Institute Michigan Technological University Houghton MI 49931 USA

Abstract

AbstractGelatin is a widely utilized bioprinting biomaterial due to its cell‐adhesive and enzymatically cleavable properties, which improve cell adhesion and growth. Gelatin is often covalently cross‐linked to stabilize bioprinted structures, yet the covalently cross‐linked matrix is unable to recapitulate the dynamic microenvironment of the natural extracellular matrix (ECM), thereby limiting the functions of bioprinted cells. To some extent, a double network bioink can provide a more ECM‐mimetic, bioprinted niche for cell growth. More recently, gelatin matrices are being designed using reversible cross‐linking methods that can emulate the dynamic mechanical properties of the ECM. This review analyzes the progress in developing gelatin bioink formulations for 3D cell culture, and critically analyzes the bioprinting and cross‐linking techniques, with a focus on strategies to optimize the functions of bioprinted cells. This review discusses new cross‐linking chemistries that recapitulate the viscoelastic, stress‐relaxing microenvironment of the ECM, and enable advanced cell functions, yet are less explored in engineering the gelatin bioink. Finally, this work presents the perspective on the areas of future research and argues that the next generation of gelatin bioinks should be designed by considering cell–matrix interactions, and bioprinted constructs should be validated against currently established 3D cell culture standards to achieve improved therapeutic outcomes.

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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