Chromatographic purity
Phosphate buffer, Mobile phase, and Chromatographic system
Proceed as directed in the Assay.
Test solution
Transfer about 300 mg of Diethylcarbamazine Citrate, accurately weighed, to a 100-mL volumetric flask, add 100 mL of Phosphate buffer, and mix. Filter or centrifuge, and use the clear filtrate or supernatant.
Procedure
Separately inject equal volumes (about 20 µL) of the
Standard solution and the
Test solution into the chromatograph, record the chromatograms, and measure the responses for all the peaks. Calculate the percentage of each impurity in the portion of Diethylcarbamazine Citrate taken by the formula:
10,000(C / W)(ri / rS),
in which
C is the concentration, in mg per mL, of
USP Diethylcarbamazine Citrate RS in the
Standard solution; W is the weight, in mg, of Diethylcarbamazine Citrate taken to prepare the
Test solution; ri is the peak response for each impurity obtained from the
Test solution; and
rS is the peak response for diethylcarbamazine citrate obtained from the
Standard solution. Not more than 0.1% of any individual impurity is found.
Assay
Phosphate buffer
Dissolve 31.24 g of monobasic potassium phosphate in 1000 mL of water.
Mobile phase
Dissolve 10 g of monobasic potassium phosphate in 1000 mL of water. Prepare a filtered and degassed mixture of 900 mL of this solution and 100 mL of methanol.
Standard preparation
Transfer about 5 mg of
USP Diethylcarbamazine Citrate RS, accurately weighed, to a 50-mL volumetric flask, dissolve in and dilute with
Phosphate buffer to volume, and mix.
Assay preparation
Transfer about 5 mg of Diethylcarbamazine Citrate, accurately weighed, to a 50-mL volumetric flask, dissolve in and dilute with Phosphate buffer to volume, and mix.
Chromatographic system
The liquid chromatograph is equipped with a 220-nm detector and a 3.9-mm × 15-cm column that contains 5-µm packing L1. The flow rate is about 0.8 mL per minute. Chromatograph the Standard preparation, and record the peak responses as directed for Procedure: the relative standard deviation for replicate injections is not more than 2.0%.
Procedure
Separately inject equal volumes (about 20 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
10H
21N
3O·C
6H
8O
7 in the portion of Diethylcarbamazine Citrate taken by the formula:
50C(rU / rS),
in which
C is the concentration, in mg per mL, of
USP Diethylcarbamazine Citrate RS in the
Standard preparation; and
rU and
rS are the peak responses obtained from the
Assay preparation and the
Standard preparation, respectively.