Scientific Reports · 2015 · 50 citations · 23 references
Veterinary MedicinePharmacokineticsPhysiologyBioavailabilityClinical PharmacologyTransfusion MedicineBlood ViscosityHemodynamicsHemoglobin PhysiologyRed Blood Cell PhysiologyBlood CompatibilityBlood Component CompatibilityBlood PressureHemoglobin FunctionHemoglobin StructureSystemic Blood Flow Regulation
A hemoglobin (Hb) wrapped covalently by human serum albumins (HSAs), a core-shell structured hemoglobin-albumin cluster designated as "HemoAct", is an O2-carrier designed for use as a red blood cell (RBC) substitute. This report describes the blood compatibility, hemodynamic response, and pharmacokinetic properties of HemoAct, and then explains its preclinical safety. Viscosity and blood cell counting measurements revealed that HemoAct has good compatibility with whole blood. Intravenous administration of HemoAct into anesthetized rats elicited no unfavorable increase in systemic blood pressure by vasoconstriction. The half-life of (125)I-labeled HemoAct in circulating blood is markedly longer than that of HSA. Serum biochemical tests conducted 7 days after HemoAct infusion yielded equivalent values to those observed in the control group with HSA. Histopathologic inspections of the vital organs revealed no marked abnormality in their tissues. All results indicate that HemoAct has sufficient preclinical safety as an alternative material for RBC transfusion.
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Structural Basis of the Drug-binding Specificity of Human Serum Albumin
J. Ghuman, Patricia A. Zunszain, I. Petitpas et al. · Journal of Molecular Biology · 2005 · 1.9K citations
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Kim D. Vandegriff, Ashok Malavalli, Jerod Wooldridge et al. · Transfusion · 2003 · 259 citations