Stroma-free hemoglobin from bovine blood

Artif Cells Blood Substit Immobil Biotechnol. 2007;35(4):431-47. doi: 10.1080/10731190701460333.

Abstract

Isolation and purification of bovine hemoglobin (HbBv) was carried out after reaction of whole blood with carbon monoxide. Washing/centrifugation steps were used to eliminate leukocytes, platelets, and plasma proteins. Hypotonic media and ultrasound radiation were used to lyse red blood cells. Lyse by ultrasound was shown to lead to solutions at the highest concentrations in HbBv, and the least concentrations in major phospholipids contaminants. Additional purification procedures were performed to remove membrane proteins and phospholipids. In the first case, proteins were denatured by thermal treatment, and filtered. To eliminate phospholipids, liquid chromatography was used with strong anion exchangers. Purity of HbBv was evaluated by normal phase high performance liquid chromatography (HPLC), electrophoresis, and size-exclusion HPLC.

MeSH terms

  • Animals
  • Blood
  • Blood Proteins
  • Carbon Monoxide
  • Cattle
  • Chromatography, High Pressure Liquid / methods*
  • Chromatography, Ion Exchange / methods*
  • Hemoglobins / isolation & purification*
  • Phospholipids

Substances

  • Blood Proteins
  • Hemoglobins
  • Phospholipids
  • Carbon Monoxide