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Annals of Biomedical Engineering

, Volume 47, Issue 5, pp 1223–1236 | Cite as

Transport Analysis of Engineered Liver Tissue Fabricated Using a Capsule-Based, Modular Approach

  • Ramkumar T. Annamalai
  • Howard W. T. MatthewEmail author
Article
  • 84 Downloads

Abstract

The bioinspired, microscale tissue engineering approach has emerged in recent years as a promising alternative to preformed scaffolds. Using this approach, complex tissues and organs can be efficiently engineered from microscale modules to replicate the intricate architecture and physiology of vascularized organs and tissues. Previously, we demonstrated assembly of a prototype, engineered liver tissue, formed by the fusion of hepatocyte-containing capsules. Here, we analyzed the effects of various controllable system parameters with the aim of predicting the operating limits of our modular tissue in high cell density, perfused cultures. Both the capsule diameter and construct height were limited by mass transfer requirements, while the shear stress on the capsule wall and the pressure drop across the packed capsule bed were dictated by the capsule diameter and permissible flow rates of the system. Our analysis predicts that capsules with a 200 µm radius can efficiently maintain hepatocytes at cell densities comparable to liver tissue. Some model predictions were validated by packed bed perfusion cultures. Flow-induced bed compaction hysteresis was tested experimentally and found to have minimal effect on flow characteristics. The effectiveness factor (η) for the overall oxygen transfer within packed beds of capsule modules was estimated to be 0.72 for all conditions. Primary hepatocytes encapsulated in the capsules exhibited normal metabolism and formed spheroids during a 7-day culture. The model predictions can be useful to study mass transfer and shear stress in high-density perfusion cultures. Overall, analysis of a perfused, capsule-based, modular tissue demonstrated the feasibility of the technology as a platform for fabrication of highly metabolic solid organs.

Keywords

Hepatocyte encapsulation Perfusion bioreactor Mass transfer Shear stress Pre-vascularization Modular tissue engineering 

Notes

Acknowledgments

Funding for these studies was provided by a DRICTR award from Wayne State University, and a grant award from the National Science Foundation (CBET-1067323).

Conflict of interest

Authors have no conflict of interest to declare.

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Copyright information

© Biomedical Engineering Society 2019

Authors and Affiliations

  • Ramkumar T. Annamalai
    • 1
  • Howard W. T. Matthew
    • 1
    • 2
    Email author
  1. 1.Department of Biomedical EngineeringWayne State UniversityDetroitUSA
  2. 2.Department of Chemical Engineering and Materials ScienceWayne State UniversityDetroitUSA

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