Abstract
The administration of extracellular, hemoglobin-based oxygen carriers often elicits an acute increase in blood pressure by vasoconstriction. This side effect is now recognized to be due to the depletion of nitric oxide (endothelial-derived relaxing factor) by the extravasuated hemoglobins. We have recently found that the administration of a recombinant human serum albumin (rHSA)-based oxygen carrier involving synthetic tetraphenyporphinatoiron(II) derivative (FeP) (rHSA-FeP) does not induce such hypertensive action, because of its low permeability through the vascular endothelium. The heart rate responses after the rHSA-FeP injection were also negligibly small. Visualization of the intestinal microcirculatory changes clearly revealed the widths of the venule and arteriole to be fairly constant. The entirely synthetic rHSA-FeP becomes a promising material as a new type of red blood cell substitute.
Original language | English |
---|---|
Pages (from-to) | 257-261 |
Number of pages | 5 |
Journal | Journal of Biomedical Materials Research - Part A |
Volume | 64 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2003 Feb 1 |
Keywords
- Human serum albumin
- Hypertension
- Nitric oxide
- Red blood cell substitute
- Synthetic heme
ASJC Scopus subject areas
- Ceramics and Composites
- Biomaterials
- Biomedical Engineering
- Metals and Alloys