The use of cellulose acetate for the electrophoretic separation and quantitation of serum lactic dehydrogenase isozymes in normal and pathologic states

Normal and abnormal lactic dehydrogenase (LDH) isozyme distribution in serum was studied using cellulose acetate electrophoresis with a p-iodonitro tetrazolium violet (INT) stain, and a graphing procedure devised to permit rapid visualization and evaluation of the electrophoretograms. This diagnosti...

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Published inClinica chimica acta Vol. 14; no. 5; pp. 689 - 697
Main Authors Mager, M., Blatt, W.F., Abelmann, W.H.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.11.1966
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Summary:Normal and abnormal lactic dehydrogenase (LDH) isozyme distribution in serum was studied using cellulose acetate electrophoresis with a p-iodonitro tetrazolium violet (INT) stain, and a graphing procedure devised to permit rapid visualization and evaluation of the electrophoretograms. This diagnostic technique was validated by employing the system to analyze sera from 7 patients with acute myocardial infarct and 7 patients with parenchymatous liver disease. In each case elevation was noted in the appropriate tissue specific isozyme (LDH 1 and LDH 5 respectively). LDH isozyme patterns in 5 of 7 patients with pneumonia showed a modest elevation of LDH 1. Serial LDH isozyme patterns of 14 patients with acute pulmonary embolism, in 12 of whom total LDH was elevated, displayed a normal distribution. It is concluded that if tissue-specific LDH isozymes are released by the lung after embolization, their serum concentrations do not reach diagnostically useful levels.
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ISSN:0009-8981
1873-3492
DOI:10.1016/0009-8981(66)90196-3