Chromatographic purity
Mobile phase
and Chromatographic systemProceed as directed in the Assay.
Test preparation
Transfer about 25 mg of fluocinonide, accurately weighed, to a 10-mL volumetric flask, add acetonitrile to volume, and mix.
Procedure
Inject 30 µL of the Test preparation into the chromatograph, record the chromatogram, and measure the area responses of all peaks. Calculate the area percentage of each peak observed in the chromatogram. The largest secondary peak is not more than 1.0% of the total area, and no other secondary peak is more than 0.5% of the total area. The sum of the areas of all peaks, other than the main peak, does not constitute more than 2.0% of the total area.
Assay
Mobile phase
Prepare a filtered and degassed mixture of acetonitrile and water (1:1). Make adjustments if necessary (see
System Suitability under
Chromatography 621).
Standard preparation
Transfer about 25 mg of
USP Fluocinonide RS, accurately weighed, to a 100-mL volumetric flask, add acetonitrile to volume, and mix. Transfer 10.0 mL of this solution to a 100-mL volumetric flask, dilute with
Mobile phase to volume, and mix to obtain a solution having a known concentration of about 0.025 mg of
USP Fluocinonide RS per mL.
Assay preparation
Using about 25 mg of Fluocinonide, accurately weighed, proceed as directed for Standard preparation.
Chromatographic system
(see
Chromatography 621)The liquid chromatograph is equipped with a 254-nm detector and a 3.9-mm × 30-cm column that contains packing L1. The flow rate is about 2 mL per minute. Chromatograph the
Standard preparation, and record the peak responses as directed for
Procedure: the relative standard deviation for replicate injections is not more than 1.5%.
Procedure
Separately inject equal volumes (about 30 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
26H
32F
2O
7 in the portion of Fluocinonide taken by the formula:
1000C(rU / rS),
in which
C is the concentration, in mg per mL, of
USP Fluocinonide RS in the
Standard preparation; and
rU and
rS are the peak responses due to the fluocinonide obtained from the
Assay preparation and the
Standard preparation, respectively.