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Clinical Chemistry, Vol 17, 1033-1037, Copyright © 1971 by the American Association for Clinical Chemistry
1 Blodgett Memorial Hospital, Grand Rapids, Mich.
49506 (R.M.N., B.M.N.); U.S. Army Medical Research Laboratory, Fort Knox, Ky. 40121 (F.R.C., N.F.C.); School of Medicine,
Wayne State University, Detroit, Mich. 48207 (R.M.N., J.M.L.,
R.L.H.); and Stanford University Medical Center, Stanford,
Calif. 94305 (P.L.W.).
Automated adaptations of dithionite and ureadithionite tube tests are accurate, reliable, inexpensive methods for detecting hemoglobin S. More than 3,000 individuals have been screened (120 determinations per hour; reagent cost, 2 to 4 cents per test). The dithionite reagent consists of potassium phosphate, sodium dithionite, and saponin. When S hemoglobin contacts this reagent, the red cells lyse, and the hemoglobin deoxygenates and sickles, forming a hydrophobic-bond-dependent nematic liquid crystal system that is manifested as turbidity. The resulting AutoAnalyzer curve is strikingly and diagnostically different from that produced by hemoglobin A in the same reagent. Specificity of the automated dithionite test may be enhanced by use of the automated ureadithionite test, which consists of a specimen set of two aliquots: one traverses a dithionite line, the other a ureadithionite line. A comparison of transmittance in the two lines yields typical diagnostic curves because the urea disperses the sickling, with a consequently increased transmittance over that of the dithionite aliquot. Methods are discussed for recognizing non-S sickling hemoglobins and a few other rare hemoglobinopathies.
Submitted on June 21, 1971
Accepted on July 21, 1971
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