Dimino Michael L, Palmer Andre F
Department of Chemical and Biomolecular Engineering, University of Notre Dame, 182 Fitzpatrick Hall, Notre Dame, Indiana 46556, USA.
Biotechnol Prog. 2007 Jul-Aug;23(4):921-31. doi: 10.1021/bp0700298. Epub 2007 Jun 8.
Hemopure (Biopure; Cambridge, MA) and PolyHeme (Northfield Laboratories; Evanston, IL) are two acellular hemoglobin-based O2 carriers (HBOCs) currently in phase III clinical trials for use as red blood cell substitutes. The most common adverse side effect that these HBOCs exhibit is increased vasoconstriction. Autoregulatory theory has been presented as a possible explanation for this physiological effect, where it is hypothesized that low-affinity HBOCs over-deliver O2 to tissues surrounding arterioles, thereby eliciting vasoconstriction. In this paper, we wanted to investigate HBOC oxygenation of tissue surrounding a capillary, which is the smallest element of the circulatory system. An a priori model has been developed in which the performance of mixtures of acellular HBOCs (synthesized by our group and others) and human red blood cells (hRBCs) has been simulated using a Krogh tissue cylinder model (KTCM) comprising a capillary surrounded by a capillary membrane and skeletal muscle tissue in cylindrical coordinates with specified tissue O2 consumption rates and Michaelis-Menten kinetics. In this study, the total hemoglobin (hRBCs and HBOCs) concentration was kept constant. The HBOCs studied possessed O2 affinities that were higher and lower compared to hRBCs (P50's spanned 5-55 mmHg), and the equilibrium binding/release of oxygen to/from the HBOCs was modeled using the Adair equation. At normoxic inlet pO2's, there was no correlation between O2 flux out of the capillary and the O2 affinity of the HBOC. However, a correlation was found between the average pO2 tension in the capillary and the O2 affinity of the HBOC. Additionally, we studied the change in the O2 equilibrium curve of HBOCs with different O2 affinities over a wide range of inlet pO2's and found that changing the inlet pO2 greatly affected which HBOC, having a unique O2 affinity, best delivered O2 to the surrounding tissue. The analysis of oxygen transport presented could lead to a better prediction of which acellular HBOC is best suited for a specific transfusion application that many times depends on the capillary inlet pO2 tension.
血红蛋白替代品Hemopure(Biopure公司;马萨诸塞州剑桥)和PolyHeme(Northfield Laboratories公司;伊利诺伊州埃文斯顿)是两种基于脱细胞血红蛋白的氧载体(HBOCs),目前正处于III期临床试验阶段,用作红细胞替代品。这些HBOCs表现出的最常见不良副作用是血管收缩增强。自调节理论被提出作为这种生理效应的一种可能解释,该理论假设低亲和力的HBOCs向小动脉周围组织过度输送氧气,从而引发血管收缩。在本文中,我们想要研究毛细血管周围组织的HBOC氧合情况,毛细血管是循环系统的最小组成部分。我们开发了一个先验模型,其中使用Krogh组织圆柱体模型(KTCM)模拟了脱细胞HBOCs(由我们团队和其他团队合成)与人红细胞(hRBCs)混合物的性能,该模型在柱坐标中包含一个被毛细血管膜和骨骼肌组织包围的毛细血管,并具有指定的组织氧消耗率和米氏动力学。在本研究中,总血红蛋白(hRBCs和HBOCs)浓度保持恒定。所研究的HBOCs与hRBCs相比,具有更高和更低的氧亲和力(P50范围为5 - 55 mmHg),并且使用Adair方程对氧气与HBOCs的平衡结合/释放进行了建模。在正常氧分压入口条件下,毛细血管输出的氧通量与HBOC的氧亲和力之间没有相关性。然而,发现毛细血管中的平均氧分压与HBOC的氧亲和力之间存在相关性。此外,我们研究了在广泛的入口氧分压范围内,具有不同氧亲和力的HBOCs的氧平衡曲线变化,发现改变入口氧分压极大地影响了哪种具有独特氧亲和力的HBOC最能向周围组织输送氧气。所呈现的氧运输分析可能会更好地预测哪种脱细胞HBOC最适合特定的输血应用,而这种应用很多时候取决于毛细血管入口氧分压。