Dissolution, Procedure for a Pooled Sample 711
Medium:
water; 900 mL.
Apparatus 2:
50 rpm.
Time:
20 minutes.
Mobile phase
Prepare a suitable degassed and filtered mixture of pH 3.0, 0.1 M ammonium sulfate and methanol (50:50).
Chromatographic system
(see
Chromatography 621)The liquid chromatograph is equipped with a 220-nm detector and a 4.6-mm × 5-cm column that contains packing L1. The flow rate is about 1.0 mL per minute. Chromatograph the
Standard solution, and record the peak responses as directed under
Procedure: the tailing factor is not more than 1.5, and the relative standard deviation for replicate injections is not more than 2.0%.
Procedure
Separately inject equal volumes (about 20 µL) of the Standard solution and a filtered aliquot of the solution under test into the chromatograph, record the chromatograms, and measure the responses for the major peaks. Calculate the amount of C6H8N2O8 dissolved in comparison with a Standard solution having a known concentration of USP Isosorbide Dinitrate RS, similarly prepared and chromatographed.
Tolerances
Not less than 80% (Q) of the labeled amount of C6H8N2O8 is dissolved in 20 minutes.
Assay
Assay preparation
Weigh and finely powder not fewer than 20 Tablets. Transfer an accurately weighed portion of the powder, equivalent to about 12.5 mg of isosorbide dinitrate, to a 50-mL volumetric flask, add about 30 mL of
Mobile phase, and shake for 30 minutes. Add 8.0 mL of
Internal standard solution, cool to room temperature, add 8 mL of a 1 in 10 dilution of
Buffer solution in water, dilute with
Mobile phase to volume, and mix. Filter a portion through a 0.45-µm filter.
Procedure
Proceed as directed for
Procedure in the
Assay under
Diluted Isosorbide Dinitrate. Calculate the quantity, in mg, of C
6H
8N
2O
8 in the portion of Tablets taken by the formula:
50C(RU / RS),
in which
C is the concentration, in mg per mL, of isosorbide dinitrate from the USP Isosorbide Dinitrate RS taken for the
Standard preparation; and
RU and
RS are the ratios of the peak responses obtained from the
Assay preparation and the
Standard preparation, respectively.