Standard preparation
[NOTEPrepare on the day of the assay.
] Dissolve an accurately weighed quantity of
USP Anileridine Hydrochloride RS in 0.1 N hydrochloric acid, and quantitatively dilute with the same solvent to obtain a solution having a known concentration of about 250 µg per mL. (Each mg of anileridine hydrochloride is equivalent to 0.8286 mg of anileridine.)
Procedure
Transfer 5.0 mL each of the
Standard preparation, the
Assay preparation, and 0.1 N hydrochloric acid to provide the blank to separate 200-mL volumetric flasks. To each flask add 25 mL of water, 5 mL of 1 N hydrochloric acid, and 5 mL of sodium nitrite solution (1 in 1000), and mix. Allow to stand for 2 minutes, then add to each flask 5 mL of ammonium sulfamate solution (1 in 200), and mix. Allow to stand for 3 minutes, then add 5 mL of N-(1-naphthyl)ethylenediamine dihydrochloride solution (1 in 1000), and mix. Allow to stand for 1 hour, dilute with water to volume, and mix. Determine the absorbances of the solutions in 1-cm cells at the wavelength of maximum absorbance at about 560 nm, with a suitable spectrophotometer, using the reagent blank to set the instrument. Calculate the quantity, in mg, of anileridine (C
22H
28N
2O
2) in each mL of the Injection taken by the formula:
(352.48 / 425.40)(0.5C / V)(AU / AS),
in which 352.48 and 425.40 are the molecular weights of anileridine and anileridine hydrochloride, respectively;
C is the concentration, in µg per mL, of
USP Anileridine Hydrochloride RS in the
Standard preparation; V is the volume, in mL, of Injection taken; and
AU and
AS are the absorbances of the solutions from the
Assay preparation and the
Standard preparation, respectively.