Assay
Citric acid buffer
Transfer 2.5 g of citric acid to a 500-mL volumetric flask, add 400 mL of water, and swirl to dissolve. Adjust the solution with 2 N sodium hydroxide to a pH of 6.0, dilute with water to volume, and mix.
Mobile phase
Dissolve 930 mg of sodium octyl sulfate in 740 mL of water, add 8 mL of 3.6 N sulfuric acid, mix, and pass through a 1-µm or finer porosity filter. To the filtrate add 250 mL of acetonitrile, mix, and degas. Make adjustments if necessary (see
System Suitability under
Chromatography 621).
Standard preparation
Transfer about 50 mg of
USP Atenolol RS to a 100-mL volumetric flask, add 80 mL of
Citric acid buffer, and sonicate for about 30 seconds to achieve dissolution. Dilute with
Citric acid buffer to volume, and mix. Transfer 4.0 mL of this solution to a 10-mL volumetric flask, dilute with
Citric acid buffer to volume, and mix. This solution contains about 0.2 mg of
USP Atenolol RS per mL.
Assay preparation
Transfer an accurately measured volume of Injection, equivalent to 2 mg of atenolol, to a 10-mL volumetric flask, dilute with Citric acid buffer to volume, and mix.
Chromatographic system
(see
Chromatography 621)The liquid chromatograph is equipped with a 275-nm detector and a 4.6-mm × 25-cm column that contains 5-µm packing L1. The flow rate is about 1.7 mL per minute. Chromatograph the
Standard preparation, and record the peak responses as directed for
Procedure: the tailing factor is not more than 2, 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 areas for the major peaks. Calculate the quantity, in mg, of C
14H
22N
2O
3 in each mL of the Injection taken by the formula:
10(C / V)(rU / rS),
in which
C is the concentration, in mg per mL, of
USP Atenolol RS in the
Standard preparation; V is the volume, in mL, of Injection taken; and
rU and
rS are the atenolol peak responses obtained from the
Assay preparation and the
Standard preparation, respectively.