Influence of blood proteins on biomedical analysis. VIII. Attempts at purification of gliclazide-degrading factor in human serum

Life Sci. 1985 Nov 25;37(21):2015-9. doi: 10.1016/0024-3205(85)90032-3.

Abstract

Gliclazide(hypoglycemic drug having sulfonylurea structure)-degrading activity was found in fraction M(macroglobulin, Fr. M) obtained from pooled human serum by gel filtration using a Sephadex G-150 column. The main degrading activity was in the fraction eluted from the Fr. M-subjected DEAE-cellulose column with 0.4 M phosphate buffer (pH 5.2), and the gliclazide-degrading protein localized around alpha 2 to beta-globulin on an electrophoretic pattern using a cellulose acetate membrane. The degrading activity was enhanced about two-fold by lyophilizing Fr. M solution containing a higher sodium phosphate (Na2HPO4-NaH2PO4), over 0.27 M. This indicates that the appearance and enhancement of the degrading activity required the combination of the lyophilization of the sample solution and a certain initial concentration of sodium phosphate prior to lyophilization.

MeSH terms

  • Alpha-Globulins / isolation & purification
  • Beta-Globulins / isolation & purification
  • Chromatography, DEAE-Cellulose
  • Chromatography, Gel
  • Electrophoresis, Cellulose Acetate
  • Freeze Drying
  • Gliclazide / blood*
  • Gliclazide / metabolism
  • Humans
  • Phosphates / pharmacology
  • Protein Conformation
  • Sulfonylurea Compounds / blood*
  • Ultrafiltration

Substances

  • Alpha-Globulins
  • Beta-Globulins
  • Phosphates
  • Sulfonylurea Compounds
  • Gliclazide
  • sodium phosphate