Abstract
The Morgan-Elson reaction, a method for the detn. of hyaluronidase activity, was optimized for the quantitation of the enzyme in biol. material. Based on HPLC and spectrometric (UV-Vis, LC-MS) studies, the structure of the red-colored product (mesomeric forms of N3-protonated 3-acetylimino-2-(4-dimethylaminophenyl)methylidene-5-(1,2-dihydroxyethyl)furane) formed by condensation of chromogen III ...
Abstract
The Morgan-Elson reaction, a method for the detn. of hyaluronidase activity, was optimized for the quantitation of the enzyme in biol. material. Based on HPLC and spectrometric (UV-Vis, LC-MS) studies, the structure of the red-colored product (mesomeric forms of N3-protonated 3-acetylimino-2-(4-dimethylaminophenyl)methylidene-5-(1,2-dihydroxyethyl)furane) formed by condensation of chromogen III with p-dimethylaminobenzaldehyde is proposed. Activities corresponding to ³0.1 IU of endogenous and therapeutically administered hyaluronidase can be detected in 50 ml samples. Application of the method for the detn. of the enzyme in plasma of tumor patients revealed no difference in activity levels, interindividual variability and pH profile compared to healthy volunteers.
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