Alclometasone Dipropionate Cream
»Alclometasone Dipropionate Cream contains not less than 90.0percent and not more than 110.0percent of the labeled amount of alclometasone dipropionate (C28H37ClO7)in a suitable cream base.
Packaging and storage— Preserve in collapsible tubes or tight containers,and store at controlled room temperature.
Identification—
A: The retention time of the major peak in the chromatogram of the Assay preparationcorresponds to that in the chromatogram of the Standard preparation,both relative to the internal standard,as obtained in the Assay.
B: Place a quantity of Cream,equivalent to about 1.25mg of alclometasone dipropionate,in a 50-mLcentrifuge tube,and add 15mLof methanol.Insert a stopper securely into the tube,and place the tube in a water bath maintained at 60until the semisolid components melt.Remove the tube from the bath,shake vigorously until the specimen components resolidify,and place the tube in an ice-methanol bath for 15minutes.Remove the tube from the bath,and centrifuge at 2500rpm for 5minutes.Transfer the clear supernatant to a vial,and allow this test solution to equilibrate to room temperature.Apply separately 20µLof the test solution and 20µLof a Standard solution of USP Alclometasone Dipropionate RSin methanol containing about 0.08mg per mLto a suitable thin-layer chromatographic plate (see Chromatography á621ñ)coated with a 0.25-mm layer of chromatographic silica gel mixture,and dry the applications with the aid of a stream of nitrogen.Position the plate in a saturated,unlined chromatographic chamber,and develop the chromatograms in a solvent system consisting of a mixture of chloroform and acetone (7:1)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 allow the solvent to evaporate.Observe the plate under short-wavelength UVlight:the RFvalue of the principal spot obtained from the test solution corresponds to that obtained from the Standard solution.
Microbial limits á61ñ It meets the requirements of the tests for absence of Staphylococcus aureusand Pseudomonas aeruginosa.
Minimum fill á755ñ: meets the requirements.
Assay—
0.05M Monobasic potassium phosphate— Transfer 3.40g of monobasic potassium phosphate to a 500-mLvolumetric flask,add water to volume,and mix.
Mobile phase— Prepare a filtered and degassed mixture of methanol and 0.05M Monobasic potassium phosphate(2:1).Make adjustments if necessary (see System Suitabilityunder Chromatography á621ñ).
Internal standard solution— Transfer about 20mg of betamethasone dipropionate to a 50-mLvolumetric flask,add methanol to volume,and mix.
Standard preparation— Transfer about 25mg of USP Alclometasone Dipropionate RS,accurately weighed,to a 100-mLvolumetric flask,add methanol to volume,and mix.Transfer 5.0mLof this solution to a small stoppered flask,add 5.0mLof methanol,add 5.0mLof Internal standard solution,and mix to obtain a Standard preparationhaving a known concentration of about 0.08mg of USP Alclometasone Dipropionate RSper mL.
Assay preparation— Transfer an accurately weighed quantity of Cream,equivalent to about 1.25mg of alclometasone dipropionate,to a 50-mLcentrifuge tube,add 5.0mLof Internal standard solution,and add 10.0mLof methanol.Insert a stopper securely into the tube,and place it in a water bath maintained at 60until the semisolid components melt.Remove the tube from the bath,shake vigorously until the specimen components resolidify,and return the tube to the 60water bath until the semisolid components melt.Remove the tube from the bath,shake vigorously until the specimen components resolidify,and place the tube in an ice-methanol bath for 15minutes.Remove the tube from the bath,and centrifuge at 2500rpm for 5minutes.Transfer the clear supernatant to a small stoppered flask,and allow this Assay preparationto equilibrate to room temperature.
Chromatographic system(see Chromatography á621ñ)— The liquid chromatograph is equipped with a 254-nm detector and a 4-mm ×30-cm column that contains packing L1.The flow rate is about 1.2mLper minute.Chromatograph the Standard preparation,and record the peak responses as directed for Procedure:the resolution,R,between the analyte and internal standard peaks is not less than 3.0;and the relative standard deviation for replicate injections is not more than 2%.
Procedure— Separately inject equal volumes (about 20µL)of the Standard preparationand the Assay preparationinto the chromatograph,record the chromatograms,and measure the responses for the major peaks.The relative retention times are about 0.7for alclometasone dipropionate and 1.0for betamethasone dipropionate.Calculate the quantity,in mg,of alclometasone dipropionate (C28H37ClO7)in the portion of Cream taken by the formula:
15C(RU/RS),
in which Cis the concentration,in mg per mL,of USP Alclometasone Dipropionate RSin the Standard preparation;and RUand RSare the peak height ratios obtained from the Assay preparationand the Standard preparation,respectively.
Auxiliary Information— Staff Liaison:Clydewyn M.Anthony,Ph.D.,Scientist
Expert Committee:(PA1)Pharmaceutical Analysis 1
USP28–NF23Page 59
Pharmacopeial Forum:Volume No.27(3)Page 2507
Phone Number:1-301-816-8139