Alclometasone Dipropionate Cream
» Alclometasone Dipropionate Cream contains not less than 90.0 percent and not more than 110.0 percent 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.
USP Reference standards 11
USP Alclometasone Dipropionate RS Click to View Structure
Identification—
A: The retention time of the major peak in the chromatogram of the Assay preparation corresponds 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 1.25 mg of alclometasone dipropionate, in a 50-mL centrifuge tube, and add 15 mL of methanol. Insert a stopper securely into the tube, and place the tube in a water bath maintained at 60 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 15 minutes. Remove the tube from the bath, and centrifuge at 2500 rpm for 5 minutes. Transfer the clear supernatant to a vial, and allow this test solution to equilibrate to room temperature. Apply separately 20 µL of the test solution and 20 µL of a Standard solution of USP Alclometasone Dipropionate RS in methanol containing about 0.08 mg per mL to a suitable thin-layer chromatographic plate (see Chromatography 621) 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 UV light: the RF value of the principal spot obtained from the test solution corresponds to that obtained from the Standard solution.
Microbial enumeration tests 61 and Tests for specified microorganisms 62 It meets the requirements of the tests for absence of Staphylococcus aureus and Pseudomonas aeruginosa.
Minimum fill 755: meets the requirements.
Assay—
0.05 M Monobasic potassium phosphate— Transfer 3.40 g of monobasic potassium phosphate to a 500-mL volumetric flask, add water to volume, and mix.
Mobile phase— Prepare a filtered and degassed mixture of methanol and 0.05 M Monobasic potassium phosphate (2:1). Make adjustments if necessary (see System Suitability under Chromatography 621).
Internal standard solution— Transfer about 20 mg of betamethasone dipropionate to a 50-mL volumetric flask, add methanol to volume, and mix.
Standard preparation— Transfer about 25 mg of USP Alclometasone Dipropionate RS, accurately weighed, to a 100-mL volumetric flask, add methanol to volume, and mix. Transfer 5.0 mL of this solution to a small stoppered flask, add 5.0 mL of methanol, add 5.0 mL of Internal standard solution, and mix to obtain a Standard preparation having a known concentration of about 0.08 mg of USP Alclometasone Dipropionate RS per mL.
Assay preparation— Transfer an accurately weighed quantity of Cream, equivalent to about 1.25 mg of alclometasone dipropionate, to a 50-mL centrifuge tube, add 5.0 mL of Internal standard solution, and add 10.0 mL of methanol. Insert a stopper securely into the tube, and place it in a water bath maintained at 60 until the semisolid components melt. Remove the tube from the bath, shake vigorously until the specimen components resolidify, and return the tube to the 60 water 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 15 minutes. Remove the tube from the bath, and centrifuge at 2500 rpm for 5 minutes. Transfer the clear supernatant to a small stoppered flask, and allow this Assay preparation to equilibrate to room temperature.
Chromatographic system (see Chromatography 621)— 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 1.2 mL per 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 20 µL) of the Standard preparation and the Assay preparation into the chromatograph, record the chromatograms, and measure the responses for the major peaks. The relative retention times are about 0.7 for alclometasone dipropionate and 1.0 for 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 C is the concentration, in mg per mL, of USP Alclometasone Dipropionate RS in the Standard preparation; and RU and RS are the peak height ratios obtained from the Assay preparation and the Standard preparation, respectively.
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Topic/Question Contact Expert Committee
Monograph Domenick Vicchio, Ph.D.
Senior Scientific Liaison
1-301-998-6828
(SM42010) Monographs - Small Molecules 4
Reference Standards RS Technical Services
1-301-816-8129
rstech@usp.org
61 Radhakrishna S Tirumalai, Ph.D.
Principal Scientific Liaison
1-301-816-8339
(GCM2010) General Chapters - Microbiology
62 Radhakrishna S Tirumalai, Ph.D.
Principal Scientific Liaison
1-301-816-8339
(GCM2010) General Chapters - Microbiology
USP35–NF30 Page 2087
Pharmacopeial Forum: Volume No. 27(3) Page 2507