An Oxygen Transport Model of Human Bone Marrow for Hemolytic Sickle Cell Anemia

Authors

  • MA Islam Department of Chemical Engineering and Applied Chemistry University of Toronto, 200 College Street, Toronto
  • R Kumar Petrofac Engineering, 76-86 Chertsey Road, Woking Surrey, GU21 5BJ

DOI:

https://doi.org/10.3329/jce.v24i0.5577

Keywords:

hemolytic sickle cell anemia

Abstract

The human bone marrow (BM) is a complicated tissue with intricate vascular and heterogeneous
extravascular (tissue) architecture. Oxygen is an important modulator of differentiation and proliferation
of the BM hematopoietic cells under normal and pathological conditions. Currently, due to the
inaccessibility of the BM, it is not possible to measure the spatial distribution of the oxygen tension
(concentration) levels in the tissue. Thus, the present treatise utilizes mathematical modeling to offer a
greater insight on the effects of oxygen on the BM cellular components. Here, we present simulation
results that are correlated with known in vivo data of BM along with proposing a model for the two state
description of allosteric hemoglobin molecule under hemolytic sickle cell anemia condition of BM.

Journal of Chemical Engineering Vol.ChE 24 2006 7-13

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Published

2010-07-21

How to Cite

Islam, M., & Kumar, R. (2010). An Oxygen Transport Model of Human Bone Marrow for Hemolytic Sickle Cell Anemia. Journal of Chemical Engineering, 24, 7–13. https://doi.org/10.3329/jce.v24i0.5577

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Articles