Procedure
Treat 20.0 mL each of the
Standard preparation and the
Assay preparation in the following manner. To each add 10.0 mL of hexane, and shake for about 15 minutes, then allow the layers to separate, and centrifuge, if necessary. Using a suitable microsyringe or sampling valve, inject equal volumes of lower (acetonitrile) layers obtained from the
Standard preparation and the
Assay preparation into a suitable high-pressure liquid chromatograph (see
Chromatography 621) of the general type equipped with a detector for monitoring UV light absorption at about 254 nm, equipped with a suitable recorder, capable of providing column pressure up to about 1000 psi. The instrument contains a 4-mm × 30-cm stainless steel column that contains packing L3. In a suitable chromatogram, the resolution factor,
R (see
Chromatography 621), is not less than 2.4 between peaks for fluorometholone and the internal standard, and the lowest and highest peak area ratios (
RS) of three replicate injections of the
Standard preparation agree within 2.0%. Calculate the quantity, in mg, of fluorometholone (C
22H
29FO
4) in the portion of Cream taken by the formula:
20C(RU / RS),
in which
C is the concentration, in mg per mL, of
USP Fluorometholone RS in the
Standard preparation; and
RU and
RS are the peak area ratios of the fluorometholone peak and the internal standard peak obtained from the
Assay preparation and the
Standard preparation, respectively.