Abstract

The development of large-scale human liver scaffolds equipped with interconnected flow channels in three-dimensional space offers a promising strategy for the advancement of liver tissue engineering. Tissue-engineered scaffold must be blood-compatible to address the demand for clinical transplantable liver tissue. Here, we demonstrate the construction of 3-D macro scaffold with interconnected flow channels using the selective laser sintering (SLS) fabrication method. The accuracy of the printed flow channels was ensured by the incorporation of polyglycolic acid (PGA) microparticles as porogens over the conventional method of NaCl salt leaching. The fabricated scaffold was populated with Hep G2, followed by endothelization with endothelial cells (ECs) grown under perfusion of culture medium for up to 10 days. The EC covered scaffold was perfused with platelet-rich plasma for the assessment of hemocompatibility to examine its antiplatelet adhesion properties. Both Hep G2-covered scaffolds exhibited a markedly different albumin production, glucose metabolism and lactate production when compared to EC-Hep G2-covered scaffold. Most importantly, EC-Hep G2-covered scaffold retained the antiplatelet adhesion property associated with the perfusion of platelet-rich plasma through the construct. These results show the potential of fabricating a 3-D scaffold with interconnected flow channels, enabling the perfusion of whole blood and circumventing the limitation of blood compatibility for engineering transplantable liver tissue.

Highlights

  • The aim of the present study was to re-establish the fabrication of 3-D macro scaffold with an interconnected network of flow channel in multilayers using the selective laser sintering (SLS) printing method

  • A perfusable 3-D interconnected scaffold was designed as previously reported by our group [12]

  • The computer aided design (CAD) model was designed in such a way to ensure continuity from inlet to outlet using AutoCAD software

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Summary

Introduction

Fabrication of 3-D construct or macro scaffold by additive manufacturing technologies, such as stereolithography [1], deposition and layering [2], silicon micromachining [3], 3-D printing [4], and selective laser sintering (SLS) [5], has garnered interest in recent years. The SLS printing method uses simple operation, adaptation from the patient’s scanned image to the computer aided design (CAD) model, and easier customization of the scaffold for the generation of the CAD model [6,7,8]. SLS printing has made it possible for tissue engineers to fabricate anatomically customized tissues and to develop functional scaffold with enhanced nano-detailed features for efficient cell guidance and growth [9,10,11]. The material selection is critical for structural and mechanical support

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