Oxygen transport in bioreactors for engineered vascular tissues

Jason W. Bjork, Anton M. Safonov, Robert T. Tranquillo

Research output: Chapter in Book/Report/Conference proceedingChapter

1 Scopus citations

Abstract

Tissue engineered vascular grafts cultured in vitro are often done so under static conditions, which forces a diffusion-only mass transport regime for nutrient delivery and metabolite removal. Some bioreactor culture methods employ mechanical stimulation to improve material strength and stiffness; however, even with mechanical stimulation, engineered tissues are likely to operate in a diffusional transport regime for nutrient delivery and metabolite removal. In this study, we present an analysis of dissolved oxygen (DO) transport limitations that can arise in statically cultured vascular grafts and highlight bioreactor designs that improve transport, particularly by perfusion of medium through the interstitial space by transmural flow. A computational analysis is provided in conjunction with empirical data to support the models. Our goal was to investigate designs that would eliminate nutrient gradients that are evident using static culture methods in order to develop more uniform engineered vascular tissues, which could potentially improve mechanical strength and stiffness.

Original languageEnglish (US)
Title of host publicationStudies in Mechanobiology, Tissue Engineering and Biomaterials
PublisherSpringer
Pages287-306
Number of pages20
DOIs
StatePublished - 2013

Publication series

NameStudies in Mechanobiology, Tissue Engineering and Biomaterials
Volume10
ISSN (Print)1868-2006
ISSN (Electronic)1868-2014

Bibliographical note

Funding Information:
Acknowledgments This work has been supported by National Institutes of Health (NHLBI R01 HL083880 to RTT) and 3M Company (JWB). Furthermore, the technical assistance of Naomi Ferguson and Lee Meier is gratefully acknowledged as well as Dave Hultman for his efforts in machining and design discussions.

Publisher Copyright:
© Springer-Verlag Berlin Heidelberg 2012.

Keywords

  • Axial Flow
  • Dissolve Oxygen
  • Engineer Tissue
  • Nutrient Delivery
  • Oxygen Consumption Rate

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