Identification
A:
Place a quantity of finely powdered Tablets, equivalent to about 50 mg of anileridine, in a 250-mL volumetric flask, add 100 mL of water, and heat on a steam bath. Cool, dilute with water to volume, mix, and filter: five mL of the filtrate responds to
Identification test
C under
Anileridine Hydrochloride.
B:
Transfer to a 100-mL volumetric flask a quantity of finely powdered Tablets, equivalent to about 50 mg of anileridine. Add about 30 mL of water, and heat on a steam bath. Cool, dilute with water to volume, mix, and filter (
Stock solution): the filtrate responds to
Identification test
B under
Anileridine Hydrochloride, beginning with Transfer 4.0 mL of this solution.
Dissolution 711
Medium:
0.01 N hydrochloric acid; 900 mL.
Apparatus 1:
100 rpm.
Time:
45 minutes.
Procedure
Determine the amount of anileridine (C
22H
28N
2O
2) dissolved, employing the procedure set forth in the
Assay, using a filtered portion of the solution under test as the
Assay preparation in comparison with a Standard solution having a known concentration of
USP Anileridine Hydrochloride RS in the same
Medium.
Tolerances
Not less than 65% (Q) of the labeled amount of C22H28N2O2 is dissolved in 45 minutes.
Assay
Assay preparation
Weigh and finely powder not fewer than 20 Tablets. Transfer an accurately weighed portion of the powder, equivalent to about 50 mg of anileridine, to a 250-mL volumetric flask. Add 25 mL of 1 N hydrochloric acid and 100 mL of water, and heat on a water bath. Cool, dilute with water to volume, and mix. Filter the solution, discarding the first 25 mL of the filtrate.
Procedure
Proceed as directed for
Procedure in the
Assay under
Anileridine Injection. Calculate the quantity, in mg, of C
22H
28N
2O
2 in the portion of Tablets taken by the formula:
(352.48/425.40)(0.25C)(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; and
AU and
AS are the absorbances of the solutions from the
Assay preparation and the
Standard preparation, respectively.