Pregn-4-ene-3,20-dione, 11,21-dihydroxy-17-[(1-oxopentyl)oxy]-, (11)-.
11,17,21-Trihydroxypregn-4-ene-3,20-dione 17-valerate [57524-89-7].
» Hydrocortisone Valerate contains not less than 97.0 percent and not more than 102.0 percent of C26H38O6, calculated on the dried basis.
Packaging and storage Preserve in well-closed containers.
Identification, Infrared Absorption 197K.
Specific rotation 781S: between +37 and +43.
Test solution: 10 mg per mL, in dioxane.
Loss on drying 731 Dry it at 105 for 3 hours: it loses not more than 1.0% of its weight.
Mobile phase Prepare a filtered and degassed mixture of water and acetonitrile (55:45). Make adjustments if necessary (see System Suitability under Chromatography 621).
Internal standard solution Prepare a solution of ethyl benzoate in methanol containing about 2.0 mg per mL.
Standard preparation Immediately prior to use, dissolve an accurately weighed quantity of USP Hydrocortisone Valerate RS in methanol to obtain a solution having a known concentration of about 0.5 mg per mL. Pipet 2 mL of this solution and 2 mL of Internal standard solution into a 10-mL volumetric flask. Dilute with methanol to volume, and mix to obtain a Standard preparation having a known concentration of about 100 µg of hydrocortisone valerate per mL.
Assay preparation Transfer about 100 mg of Hydrocortisone Valerate, accurately weighed, to a 100-mL volumetric flask. Dissolve in and dilute with methanol to volume, and mix. Pipet 1 mL of this solution and 2 mL of Internal standard solution into a 10-mL volumetric flask. Dilute with methanol to volume, and mix.
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 1 mL per minute. Chromatograph the Standard preparation, and record the peak responses as directed for Procedure: the relative retention times are about 0.8 for ethyl benzoate and 1.0 for hydrocortisone valerate, the resolution, R, between hydrocortisone valerate and ethyl benzoate is not less than 3.0, and the relative standard deviation for replicate injections is not more than 2.0%.
Procedure Separately inject equal volumes (about 10 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 C26H38O6, in the portion of Hydrocortisone Valerate taken by the formula:
C(RU / RS)in which C is the concentration, in µg per mL, of USP Hydrocortisone Valerate RS in the Standard preparation; and RU and RS are the peak response ratios of the hydrocortisone valerate peak and the internal standard peak obtained from the Assay preparation and the Standard preparation, respectively.
Auxiliary Information Please check for your question in the FAQs before contacting USP.Chromatographic Column
USP32NF27 Page 2585
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.