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The analysis of solutions of epinephrine and norepinephrine*

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Abstract

A method of analysis is described which is applicable to solutions of epinephrine and norepinephrine, such as epinephrine injection U. S. P. and levarterenol bitartrate injection N. N. R. The method depends on the quantitative conversion of the substances into O3, O4, N‐triacetyl derivatives which may be extracted into chloroform, weighed, identified, and examined polarimetrically for the determination of stereo‐chemical composition. Excellent recoveries of the physiologically potent l‐isomer are obtained, and results of analyses of solutions of epinephrine show very good agreement with potencies determined by the U. S. P. XIV dog bioassay. By supplementing the method with partition chromatography of the acetylation product, the norepinephrine in a solution of U. S. P. epinephrine may be quantitatively isolated as its triacetyl derivative and determined colorimetrically after deacetylation and oxidation to noradrenochrome.

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Cited by (16)

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    Although Markey and colleagues51 found these methods to be effective for tissues, they were not readily applicable to aqueous biologic fluids (CSF, blood, urine). Markey and colleagues were, however, able to use the method developed by Welsh52 to quantitatively separate biogenic amines from aqueous solutions, a method that involved acetylation by acetic anhydride, or by propionic or deuteroacetic anhydride in cases where endogenous N-acetylated serotonin, such as the pineal gland, might be found. This step was followed by extraction into a nonpolar solvent and a second derivatization step with pentafluoropropionic anhydride was performed.51

  • Gas chromatographic analysis of amines in biological systems

    1982, Techniques and Instrumentation in Analytical Chemistry
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*

Department of Health, Education and Welfare, Food and Drug Administration, Division of Pharmaceutical Chemistry, Washington, D.C.

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