A quantitative framework for the design of acellular hemoglobins as blood substitutes: Implications of dynamic flow conditions

被引:19
作者
Cole, Russell H.
Vandegriff, Kim D.
Szeri, Andrew J.
Savas, Omer
Baker, Dale A.
Winslow, Robert M.
机构
[1] Univ Calif Berkeley, Dept Mech Engn, Berkeley, CA 94720 USA
[2] Sangart Inc, San Diego, CA 92121 USA
[3] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
关键词
facilitated diffusion; O-2; affinity; transport simulation; vasoconstriction; blood substitutes;
D O I
10.1016/j.bpc.2007.03.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The delivery of oxygen to tissue by cell-firee carriers eliminates intraluminal barriers associated with red blood cells. This is important in arterioles, since arteriolar tone controls capillary perfusion. We describe a mathematical model for O-2 transport by hemoglobin solutions and red blood cells flowing through arteriolar-sized tubes to optimize values of p50, Hill number, hemoglobin molecular diffusivity and concentration. Oxygen release is evaluated by including an extra-luminal resistance term to reflect tissue oxygen consumption. For low consumption (i.e., high resistance to O-2 release) a hemoglobin solution with p50 = 15 mmHg, n = 1, D-HBO2 = 3 x 10(-7) cm(2)/s delivers O-2 at a rate similar to that of red blood cells. For high consumption, the p50 must be decreased to 5 mmHg. The model predicts that regardless of size, hemoglobin solutions with higher p50 will present excess O-2 to arteriolar walls. Oversupply of O-2 to arteriolar walls may cause constriction and paradoxically reduced capillary perfusion. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 74
页数:12
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