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1.
Biomed Sci Instrum ; 33: 535-40, 1997.
Article in English | MEDLINE | ID: mdl-9731417

ABSTRACT

A useful decontaminant for mustard would be one which is readily available in large quantities, inexpensive and potentially biodegradable. Currently one that is being investigated consists of a mixture containing bovine hemoglobin, gelatin and poi. Two of them, gelatin and poi, are common foodstuffs in the diet on the mainland of the United States and in the Hawaiian culture, respectively. Various combinations of these substances have unusual flow properties since the physical states change from a liquid to a gel form. The hydrolytic kinetics of the mustard simulants, 2-chloroethyl ethyl, 2-chloroethyl methyl and 2-bromoethyl phenyl sulfide are reported. The kinetic mechanisms and rate constants are dependent upon the mixtures' concentration and viscosity.


Subject(s)
Chemical Warfare Agents , Decontamination/methods , Mustard Gas/analogs & derivatives , Biodegradation, Environmental , Chemical Phenomena , Chemistry, Physical , Gelatin/chemistry , Hemoglobins/chemistry , Hydrolysis , Starch/chemistry
2.
Article in English | MEDLINE | ID: mdl-8907693

ABSTRACT

A resuscitative compound in freeze-dried form has been synthesized between a modified starch and a tetremerically stabilized hemoglobin. In order to complex the hemoglobin, the starch has been prepared in mono-, di-, tri-, and tetra-aldehyde moieties. The hemoglobin was stabilized with low molecular weight diacids. Electrophoretic densitometric patterns indicate compound formation. The resulting polymers were characterized with respect to oxygen transport (biotonometry), Hill constant and P50. The in vivo evaluation indicates that these compounds are effective in exchange-transfusion experiments with rats to a level of about 85% replacement of whole blood. The final product is a cost-effective acellular resuscitative compound which can be stored in freeze-dried form at room temperature for extended periods of time. This artificial blood substitute can be reconstituted upon the addition of water.


Subject(s)
Blood Substitutes , Hemoglobins/chemistry , Resuscitation/methods , Starch , Animals , Blood Transfusion , Cost-Benefit Analysis , Freeze Drying , Molecular Structure , Rats , Resuscitation/economics , Temperature
3.
Article in English | MEDLINE | ID: mdl-7994384

ABSTRACT

To evaluate the biophysical properties of two acellular resuscitative fluids, experiments were performed using mixtures of these with suspensions of red blood cells. Two acellular resuscitative fluids were synthesized using a diacid to tetramerically stabilized hemoglobin and then complexing it with either a hydroxyethyl starch or a Tetronic Polyol. The new polymers were characterized with respect to the molecular weight, second virial coefficient and intrinsic viscosity. These fluids were then combined with red cells and the following measurements were made: non-Newtonian flow properties, malonamide induced hemolytic kinetics, sedimentation rates and oxygen transport. The in vitro evaluation indicates that these compounds are effective hemodiluents, offer protection to the red cell membrane and do not cause erythrocyte aggregation. The oxygen transport was satisfactory.


Subject(s)
Blood Substitutes/chemistry , Erythrocytes/physiology , Animals , Biophysical Phenomena , Biophysics , Blood Sedimentation , Blood Substitutes/metabolism , Exchange Transfusion, Whole Blood , Hemodilution , Hemoglobins/chemistry , Hemoglobins/metabolism , Hemolysis , Humans , In Vitro Techniques , Molecular Weight , Oxygen/metabolism , Rats , Viscosity
4.
Article in English | MEDLINE | ID: mdl-1391448

ABSTRACT

This study reports some recent work dealing with the stabilization of the tetramers of hemoglobin. It is shown that by using a variety of diacids, it is possible to increase the P50 above that of stroma free hemoglobin. In order to lengthen the retention times in the circulatory system, the stabilized hemoglobins were complexed with both hydroxyethyl starch polymers and polyol tetronic polymers. The resulting hemoglobin-polymer compounds were then freeze-dried. It was possible to reconstitute the powder by the addition of physiological saline when needed. The methods presented here appear to be appear to be as effective as using pyridoxal phosphate but at a fraction of the cost.


Subject(s)
Blood Substitutes/chemical synthesis , Hemoglobins/chemical synthesis , Animals , Blood Substitutes/chemistry , Blood Substitutes/toxicity , Drug Stability , Hemoglobins/chemistry , Humans , Polymers , Protein Conformation , Resuscitation
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