Literature DB >> 6177235

Fetal hemoglobin: optimum conditions for its estimation by alkali denaturation.

D P Molden, N M Alexander, W E Neeley.   

Abstract

Alkali denaturation is the most commonly used technic to estimate fetal hemoglobin in red blood cells. The Betke and colleagues method (Nature 184: 1959; 1877-78) using cyanmethemoglobin (HiCN) was recommended by an International Committee for Standardization in Hematology for fetal hemoglobin levels between 2 and 40%. We showed that precision with samples containing up to 5% fetal hemoglobin can be considerably improved by measuring the absorbance of HiCN at 420 nm rather than at 540 nm because the molar absorptivity is 10 times greater in the Soret band. To determine optimum conditions for the assay, we studied the kinetics and stoichiometry of conversion of hemoglobin to HiCN with various concentrations and mixtures of ferricyanide, kinetics of alkali denaturation, ammonium sulfate precipitation of denatured HiCN, filtration as opposed to centrifugation for separating denatured HiCN, stability of HiCn in water and KCN solutions, and linearity of absorbance in the Soret band. With our modified procedure, the CV with normal amounts (less than 1%) of fetal hemoglobin improved from 28% to 8.7%. The CVs with 6.8% and 55% fetal hemoglobin were 7.0-4.4% respectively, and linear estimates were obtained with cells containing up to 50% fetal hemoglobin. We conclude that our modified alkali denaturation procedure yields reliable and reproducible estimates of fetal hemoglobin over a wide range of concentrations.

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Year:  1982        PMID: 6177235     DOI: 10.1093/ajcp/77.5.568

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  3 in total

1.  Assessment of fetal-maternal haemorrhage in mothers with hereditary persistence of fetal haemoglobin.

Authors:  W N Patton; G S Nicholson; A H Sawers; I M Franklin; F A Ala; A W Simpson
Journal:  J Clin Pathol       Date:  1990-09       Impact factor: 3.411

2.  Polymerization of sickle cell hemoglobin at arterial oxygen saturation impairs erythrocyte deformability.

Authors:  M A Green; C T Noguchi; A J Keidan; S S Marwah; J Stuart
Journal:  J Clin Invest       Date:  1988-06       Impact factor: 14.808

3.  Significantly elevated foetal haemoglobin levels in individuals with glucose 6-phosphate dehydrogenase disease and/or sickle cell trait: a cross-sectional study in Cape Coast, Ghana.

Authors:  Patrick Adu; Essel K M Bashirudeen; Florence Haruna; Edward Morkporkpor Adela; Richard K D Ephraim
Journal:  BMC Hematol       Date:  2017-09-25
  3 in total

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