Packaging and storage
Preserve in tight, light-resistant containers. Store at 25
, excursions permitted between 15
and 30
.
Chromatographic purity
[NOTEMake all solutions fresh daily.
]
Mobile phase
Prepare a filtered and degassed mixture of 2,2,4-trimethylpentane,
n-butyl chloride, and methanol (45:4:1). Make adjustments if necessary (see
System Suitability under
Chromatography 621).
Diluting solution
Prepare a filtered and degassed mixture of n-butyl chloride and methanol (5:1).
Test solution
Transfer about 70 mg of Estradiol, accurately weighed, to a 10-mL volumetric flask, dissolve in Diluting solution, shake vigorously to aid dissolution, dilute with Diluting solution to volume, and mix.
Chromatographic system (see Chromatography 621)
The liquid chromatograph is equipped with a 280-nm detector and a 4.6-mm × 25-cm column that contains packing L3. The flow rate is about 2 mL per minute. Chromatograph the
Test solution, and record the peak responses as directed for
Procedure: the resolution,
R, between estradiol and any impurity is not less than 1.0; the column efficiency is not less than 800 theoretical plates; the tailing factor is not more than 1.5; and the relative standard deviation for replicate injections is not more than 2.0%.
Procedure
Inject a volume (about 10 µL) of the
Test solution into the chromatograph, record the chromatogram, and measure the peak responses. Calculate the percentage of each impurity in the portion of Estradiol taken by the formula:
100(ri / rs),
in which
ri is the peak response for each impurity; and
rs is the sum of the responses of all the peaks: not more than 0.5% of any individual impurity is found; and not more than 1.0% of total impurities is found.
Assay
Mobile phase
Prepare a filtered and degassed mixture of acetonitrile and water (55:45). Make adjustments if necessary (see
System Suitability under
Chromatography 621).
Internal standard solution
Transfer about 300 mg of ethylparaben to a 500-mL volumetric flask, add methanol to volume, and mix.
Standard preparation
Dissolve accurately weighed quantities of
USP Estradiol RS and
USP Estrone RS in methanol to obtain a solution containing 0.40 mg and 0.24 mg, respectively, in each mL. Pipet 10 mL of this solution and 5 mL of the
Internal standard solution into a 200-mL volumetric flask. Add 100 mL of methanol, dilute with water to volume, and mix to obtain a solution having a known concentration of about 20 µg of
USP Estradiol RS per mL.
Assay preparation
Transfer about 100 mg of Estradiol, accurately weighed, to a 250-mL volumetric flask, add methanol to volume, and mix. Transfer 10.0 mL of this solution to a 200-mL volumetric flask, add 5.0 mL of Internal standard solution and 100 mL of methanol, dilute with water to volume, and mix.
Chromatographic system (see Chromatography 621)
The liquid chromatograph is equipped with a 205-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 0.7 for the internal standard, about 1.3 for estrone, and 1.0 for estradiol; the resolution,
R, between the analyte and estrone is not less than 2.0; and the relative standard deviation for replicate injections is not more than 2.0%.
Procedure
Separately inject equal volumes (about 25 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 C
18H
24O
2 in the portion of Estradiol taken by the formula:
5C(RU / RS),
in which
C is the concentration, in µg per mL, of
USP Estradiol RS in the
Standard preparation; and
RU and
RS are the peak response ratios obtained from the
Assay preparation and the
Standard preparation, respectively.