Bj. Berger et al., HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF BIOLOGICAL AND CHEMICAL HEME POLYMERIZATION, Analytical biochemistry, 231(1), 1995, pp. 151-156
Free hematin can be converted to a stable polymer both chemically, by
heating hematin in acid suspensions, or biologically, in the food vacu
oles of malaria. A high-performance liquid chromatographic assay has b
een developed which can separate and quantitate both free hematin and
the polymer (beta-hematin), based on the differential solubility of th
e two compounds. Ion-pair reverse-phase chromatography, utilizing tetr
amethylammonium chloride and heptane sulfonate as the ion-pair agents
in the presence of 40% acetonitrile, was performed on a polymeric-resi
n-based column with a phenyl bonded phase. Initiating the runs at pH 2
.5 led to elution only of the free hematin, and a subsequent shift to
pH 12.0 converted the beta-hematin back to hematin which then eluted s
eparately. The method was found to have a linear range of detection fr
om 78 pmol to 20 nmol injected hematin and intra- and interday variati
ons of 9.71 and 12.46%, respectively. The assay was used to study seve
ral basic aspects of heme polymerization in vitro, including effects o
f hematin and beta-hematin concentration on the rate of polymerization
. (C) 1995 Academic Press, Inc.