» Metyrosine contains not less than 98.6 percent and not more than 101.0 percent of C10H13NO3, calculated on the dried basis.
Packaging and storage Preserve in well-closed containers.
B: Ultraviolet Absorption 197U
Solution: 15 µg per mL.
Medium: 0.1 N hydrochloric acid.
Absorptivities at 224 nm, calculated on the dried basis, do not differ by more than 3.0%.
Specific rotation 781S: between +185 and +195 (t = 30; = 546 nm; l = 0.5 dm).
Test solution: 5 mg per mL, in Diluent, with the aid of sonication if necessary. Prepare the Diluent as follows.
Solution A Dissolve 20.0 g of anhydrous sodium acetate in about 150 mL of water in a 250-mL volumetric flask. Add 50.0 mL of glacial acetic acid, dilute with water to volume, and mix.
Solution B Dissolve 62.5 g of cupric sulfate in water in a 200-mL volumetric flask, dilute with water to volume, and mix.
Diluent Mix Solution A and Solution B in a 1000-mL volumetric flask, dilute with water to volume, and mix.
Loss on drying 731 Dry it at a pressure not exceeding 5 mm of mercury at 100 for two hours: it loses not more than 1.0% of its weight.
Residue on ignition 281: not more than 0.1%.
Heavy metals, Method II 231: 0.003%.
Standard solutions Dissolve USP Metyrosine RS in a solvent mixture of methanol and ammonium hydroxide (7:3) to obtain a solution having a concentration of 10 mg per mL (Standard solution A). Pipet 1 mL of Standard solution A into a 100-mL volumetric flask, dilute with the same solvent mixture to volume, and mix (Standard solution B). Pipet 5 mL of Standard solution B into a 10-mL volumetric flask, dilute with the same solvent mixture to volume, and mix (Standard solution C). Pipet 5 mL of Standard solution C into a 10-mL volumetric flask, dilute with the same solvent mixture to volume, and mix (Standard solution D).
Test solution Dissolve Metyrosine in the solvent mixture of methanol and ammonium hydroxide (7:3) to obtain a solution having a concentration of 10 mg per mL.
Procedure Apply 10-µL portions of Standard solutions A, B, C, and D and the Test solution to a suitable thin-layer chromatographic plate (see Chromatography 621) coated with a 0.25-mm layer of chromatographic silica gel mixture and previously washed with methanol. Allow the spots to dry, and develop the chromatogram in a solvent system consisting of a mixture of n-propyl alcohol and ammonium hydroxide (7:3) until the solvent front has moved about three-fourths of the length of the plate. Remove the plate from the developing chamber, mark the solvent front, and dry the plate. Expose the plate to iodine vapors, and examine under short-wavelength UV light: the chromatogram shows principal spots at about the same RF value. Estimate the levels of any additional spots observed in the chromatogram of the Test solution by comparison with the spots in the chromatograms of Standard solutions B, C, and D: the sum of the intensities of any spots observed is not greater than that of the principal spot obtained from Standard solution B, corresponding to not more than 1%.
Assay Dissolve about 300 mg of Metyrosine, accurately weighed, in about 100 mL of glacial acetic acid, sonicate for about 5 minutes, and titrate with 0.1 N perchloric acid VS, determining the endpoint potentiometrically, using a platinum ring electrode and a sleeve-type calomel electrode containing 0.1 N lithium perchlorate in glacial acetic acid (see Titrimetry 541). Perform a blank determination, and make any necessary correction. Each mL of 0.1 N perchloric acid is equivalent to 19.52 mg of C10H13NO3.
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USP32NF27 Page 2975
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.