Abstract

Hydrogel-based scaffolds have been widely used to fabricate artificial tissues capable of replacing tissues and organs. However, several challenges inherent in fabricating tissues of large size and complex morphology using such scaffolds while ensuring cell viability remain. To address this problem, we synthesized gelatin methacryloyl (GelMA) based bioink with cells for fabricating a scaffold with superior characteristics. The bioink was grafted onto a Z-stacking bioprinter that maintained the cells at physiological temperature during the printing process, without exerting any physical pressure on the cells. Various parameters, such as the bioink composition and light exposure time, were optimized. The printing accuracy of the scaffolds was evaluated using photorheological studies. The internal morphology of the scaffolds at different time points was analyzed using electron microscopy. The Z-stacked scaffolds were fabricated using high-speed printing, with the conditions optimized to achieve high model reproducibility. Stable adhesion and high proliferation of cells encapsulated within the scaffold were confirmed. We introduced various strategies to improve the accuracy and reproducibility of Z-stack GelMA bioprinting while ensuring that the scaffolds facilitated cell adhesion, encapsulation, and proliferation. Our results demonstrate the potential of the present method for various applications in tissue engineering.

Highlights

  • The purpose of tissue engineering is to develop artificial tissues using functional biomaterials that can replace damaged tissues and organs [1,2,3]

  • The peaks at around 5.3 and 5.5 ppm chemical shifts were assigned to the acrylic protons of the grafted methacryloyl group, and the peak at 1.9 ppm was attributed to the methyl group of the grafted methacryloyl group

  • We optimized the reactivity of the light source and the extent of polymerization of the Z-stack bioprinter by adding a photoabsorber, thereby improving the printing accuracy through light exposure time optimization

Read more

Summary

Introduction

The purpose of tissue engineering is to develop artificial tissues using functional biomaterials that can replace damaged tissues and organs [1,2,3]. Methods for the rapid fabrication of sophisticated tissues with guaranteed cell viability in actual size are a major challenge. Many studies have reported the fabrication of complex hydrogel-based scaffolds using 3D printers with bioinks composed of a mixture of biomaterials and cells [7,8]. In a typical extrusion-type 3D bioprinting method, a bioink that maintains structural integrity is extruded based on a three-dimensional (3D). This approach is widely used because it allows intuitive movement and permits simple user adjustment [9,10]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call