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. 1985 Dec 4;348(2):407-15.
doi: 10.1016/s0021-9673(01)92479-3.

Determination of phenylethanolamine N-methyltransferase by high-performance liquid chromatography with fluorescence detection

Determination of phenylethanolamine N-methyltransferase by high-performance liquid chromatography with fluorescence detection

M Lee et al. J Chromatogr. .

Abstract

A highly sensitive assay method for phenylethanolamine N-methyltransferase in rat adrenal medulla and brain is described which employs high-performance liquid chromatography with fluorescence detection. Epinephrine formed enzymatically from the substrate norepinephrine and isoproterenol (internal standard), after chromatography on a small cartridge of a cation exchanger, Toyopak SP, are converted into the corresponding fluorescent compounds by reaction with 1,2-diphenylethylenediamine, a selective fluorescence derivatization reagent for catechol compounds. The derivatives are separated by reversed-phase chromatography on TSK gel ODS-120T. The detection limit for epinephrine formed enzymatically is 0.66 pmol per assay tube.

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