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Structural and Redox Behavior of OxyVita™, a Zero-linked Polymeric Hemoglobin: Comparison with Natural Acellular Polymeric Hemoglobins.

Authors :
Harrington, John P.
Orlig, Kseniya
Zito, Samantha L.
Wollocko, Jacek
Wollocko, Hanna
Source :
Artificial Cells, Blood Substitutes & Biotechnology. Apr2010, Vol. 38 Issue 2, p64-68. 5p. 2 Charts, 3 Graphs.
Publication Year :
2010

Abstract

A zero-linked polymeric hemoglobin (OxyVita Hb) has been developed for application as an acellular therapeutic hemoglobin-based-oxygen-carrier (HBOC). For effective and safe oxygen binding, transport and delivery, an HBOC must meet essential molecular requirements related to its structural integrity and redox stability. OxyVita™ is a super polymer possessing an average M.wt. of 17 × 106 Da. Structural integrity was determined by unfolding studies of OxyVita™ in the presence of increasing concentrations of urea. The unfolding midpoints (D1/2) of different preparations of OxyVita™ (solution and powder forms) were compared to Lumbricus Hb (LtHb) and Arenicola Hb (ArHb), natural acellular polymeric hemoglobins, which are serving as models for an effective and safe acellular HBOC. Reduction studies of OxyVita Hb using endogenous reducing agents were also investigated. Results from these studies indicate that: 1) OxyVita Hb exhibits greater resistance to conformational change than either LtHb or ArHb in the reduced (oxyHb) state; and 2) the reduction of met OxyVita Hb to oxyHb occurs slowly in the presence of either ascorbic acid (70% reduction in 560 min.) or β-NADH (40% reduction in 90 min.). These studies provide consistent evidence that OxyVita Hb possesses physiochemical properties that exhibit structural integrity and redox behavior necessary for functioning as an effective and safe HBOC within clinical applications. These results are in agreement with observations made by other investigators as to the reduction in heme-loss of OxyVita Hb, essential for the reversible binding/release of molecular oxygen within the circulatory system. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10731199
Volume :
38
Issue :
2
Database :
Academic Search Index
Journal :
Artificial Cells, Blood Substitutes & Biotechnology
Publication Type :
Academic Journal
Accession number :
48558487
Full Text :
https://doi.org/10.3109/10731191003634562