Anthralin Cream
» Anthralin Cream is Anthralin in an aqueous (oil-in-water) or oily (water-in-oil) cream vehicle. Anthralin Cream labeled to contain more than 0.1 percent of anthralin contains not less than 90.0 percent and not more than 115.0 percent of the labeled amount of C14H10O3; and Cream labeled to contain 0.1 percent or less of anthralin contains not less than 90.0 percent and not more than 130.0 percent of the labeled amount of C14H10O3.
Packaging and storage— Preserve in tight containers, in a cool place. Protect from light.
Labeling— Label it to indicate whether the cream vehicle is aqueous or oily.
Assay— [note—Use low-actinic glassware.]
Internal standard solution, Mobile phase, System suitability preparation, Solvent blank solution, and Chromatographic system Proceed as directed in the Assay under Anthralin.
Standard preparation— Dissolve an accurately weighed quantity of USP Anthralin RS in dichloromethane to obtain a solution having a known concentration of about 0.25 mg per mL. Pipet 2 mL of this solution and 2 mL of Internal standard solution into a 25-mL volumetric flask, dilute with Mobile phase to volume, and mix.
Assay preparation— Accurately weigh approximately 5 g of Cream into a tared 100-mL beaker. Add about 20 mL of dichloromethane and 10 mL of glacial acetic acid, and stir to disperse the Cream. Transfer the contents of the beaker to a filter paper (Whatman No. 4, or equivalent) with the aid of dichloromethane, and filter into a 100-mL volumetric flask. Thoroughly wash the precipitate with dichloromethane, and allow the washings to drain into the flask. Dilute with dichloromethane to volume, and mix. Pipet a volume of this solution, equivalent to about 0.5 mg of anthralin, and 2 mL of Internal standard solution into a 25-mL volumetric flask, dilute with Mobile phase to volume, and mix.
Procedure— Proceed as directed in the Assay under Anthralin. Calculate the quantity, in mg, of anthralin (C14H10O3) in the portion of Cream taken by the formula:
(200C / V)(RU / RS)
in which C is the concentration, in mg per mL, of USP Anthralin RS in the Standard preparation; V is the volume, in mL, of the filtrate taken for the Assay preparation;, and RU and RS are the response ratios of the anthralin peak to the o-nitroaniline peak obtained from the Assay preparation and the Standard preparation, respectively.
Auxiliary Information— Please check for your question in the FAQs before contacting USP.
Topic/Question Contact Expert Committee
Monograph Feiwen Mao, M.S.
Scientist
1-301-816-8320
(MDOOD05) Monograph Development-Ophthalmics Oncologics and Dermatologicals
Reference Standards Lili Wang, Technical Services Scientist
1-301-816-8129
RSTech@usp.org
USP32–NF27 Page 1560
Chromatographic Column—
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.