Identification
A:
The chromatogram of the
Assay preparation obtained as directed in the
Assay exhibits a major peak for dihydrocodeine, the retention time of which corresponds to that in the chromatogram of the
Standard preparation similarly determined.
B:
It responds to the tests for
Tartrate 191.
C:
To a solution of 20 mg in 5 mL of sulfuric acid in a test tube add 1 drop of
ferric chloride TS, and heat in a boiling water bath for 2 minutes: although the solution may darken, no blue color is produced (
distinction from codeine and morphine).
Ordinary impurities 466
Test solution:
water.
Standard solution:
water.
Eluant:
a mixture of methylene chloride, methanol, and ammonium hydroxide (90:10:1).
Visualization:
17, and view under short-wavelength UV light.
Assay
Mobile phase
Prepare a mixture of acetonitrile, water, and diethylamine (800:4:1). Prepare a suitable mixture of this solution and methanol (55:45). Make adjustments if necessary (see
System Suitability under
Chromatography 621).
Resolution solution
Prepare a solution in methanol containing about 0.4 mg of
USP Dihydrocodeine Bitartrate RS and 0.6 mg of hydrocodone bitartrate per mL. Prepare a mixture of this solution and water (1:1).
Standard preparation
Transfer about 20 mg of
USP Dihydrocodeine Bitartrate RS, accurately weighed, to a 50-mL volumetric flask, add 25 mL of methanol, swirl to dissolve, dilute with water to volume, and mix.
Assay preparation
Transfer about 20 mg of Dihydrocodeine Bitartrate, accurately weighed, to a 50-mL volumetric flask, add 25 mL of methanol, swirl to dissolve, dilute with water to volume, and mix.
Chromatographic system
(see
Chromatography 621)The liquid chromatograph is equipped with a 280-nm detector and a 4.6-mm × 25-cm column that contains 5-µm packing L3. The flow rate is about 1.5 mL per minute. Chromatograph the
Resolution solution, and record the responses as directed under
Procedure: the relative retention times are about 0.8 for hydrocodone and 1.0 for dihydrocodeine, and the resolution,
R, between the hydrocodone and dihydrocodeine peaks is not less than 1.8. Chromatograph the
Standard preparation, and record the responses as directed under
Procedure: the column efficiency determined from the dihydrocodeine peak is not less than 900 theoretical plates, the tailing factor for the dihydrocodeine peak is not more than 1.7, and the relative standard deviation for replicate injections is not more than 2.0%.
Procedure
Separately inject equal volumes (about 25 µL) of the
Standard preparation and the
Assay preparation into the chromatograph, record the chromatograms, and measure the responses for the major peaks. Calculate the quantity, in mg, of C
18H
23NO
3·C
4H
6O
6 in the portion of Dihydrocodeine Bitartrate taken by the formula:
50C(rU / rS),
in which
C is the concentration, in mg per mL, of
USP Dihydrocodeine Bitartrate RS in the
Standard preparation, and
rU and
rS are the peak responses obtained from the
Assay preparation and the
Standard preparation, respectively.