A: Infrared Absorption 197M. The IR absorption spectrum exhibits maxima at about 3.0–3.1, 5.9, 6.2, and 13.6 µm.

B: The retention time of the major peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation, as obtained in the Assay.

Test solution: 10 mg per mL, in water.

Solution A— Dissolve 0.54 g of monobasic potassium phosphate and 2.79 g of dibasic potassium phosphate in 2 L of water.

Solution B— Use acetonitrile.

Diluent— Prepare a mixture of Solution A and Solution B (1:1).

Mobile phase— Use variable mixtures of Solution A and Solution B as directed for Chromatographic system. Make adjustments if necessary (see System Suitability under Chromatography 621).

System suitability solution— Transfer about 40 mg of USP Indinavir System Suitability RS to a 100-mL volumetric flask, dissolve in and dilute with Diluent to volume, and mix.

Test solution— Transfer about 50 mg of Indinavir Sulfate, accurately weighed, to a 100-mL volumetric flask, dissolve in and dilute with Diluent to volume, and mix.

Chromatographic system (see Chromatography 621)— The liquid chromatograph is equipped with a 220-nm detector and a 4.6-mm × 25-cm column that contains 5-µm packing L1. The flow rate is about 1.0 mL per minute. The chromatograph is programmed as follows. Chromatograph the System suitability solution, and record the peak responses as directed for Procedure: the relative retention times, based on the indinavir peak at about 21 to 26 minutes, are listed in Table 1; the resolution, R, between indinavir and related compound C is greater than 1.8; and the tailing factor, determined from the indinavir peak, is greater than 0.95 and less than 2.0.

Procedure— Inject about 20 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 Indinavar Sulfate taken by the formula: in which ri is the peak area response for each impurity; and rs is the sum of the responses of all the peaks: not more than 0.1% of any individual impurity specified in Table 1 is found; and not more than 0.5% of total impurities is found.

Standard solution— Transfer 1.0 mL of dehydrated alcohol, at 20, to a 100-mL volumetric flask, dilute with water to volume, and mix. Dilute an accurately measured volume of the resulting solution quantitatively, and stepwise if necessary, with water to obtain a solution having a known concentration of about 0.001 mL of alcohol per mL of solution.

Test solution— Transfer about 400 mg of Indinavir Sulfate, accurately weighed, to a 100-mL volumetric flask, dissolve in and dilute with water to volume, and mix.

Chromatographic system (see Chromatography 621)— The gas chromatograph is equipped with a flame-ionization detector and a 0.53-mm × 30-m capillary column coated with a 1.0-µm film of phase G14. The carrier gas is helium, flowing at a rate of 10 mL per minute. The chromatograph is programmed as follows. The temperature of the column is maintained at 35, the injection port temperature is maintained at 140, and the detector temperature is maintained at 220. At the end of each five-minute isothermal run, the oven temperature is increased to 200 before adjusting the column temperature to 35 for the next injection. Chromatograph the Standard solution, 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 0.1 µL) of the Standard solution and the Test solution into the chromatograph, record the chromatograms, and measure the responses for the major peaks. Calculate the percentage of alcohol, in mg, in the portion of Indinavir Sulfate taken by the formula: in which CS is the concentration, in mL per mL, of dehydrated alcohol in the Standard solution; CU is the concentration, in mg per mL, of Indinavir Sulfate in the Test solution; and rU and rS are the peak areas for alcohol obtained from the Test solution and the Standard solution, respectively: between 5.0% and 8.0% is found. [NOTE—The value 79,000 = conversion to percent (100%) × density of alcohol at 20 (790 mg/mL).]

Methanolic formaldehyde solution— Transfer 1000 mL of methanol to a suitable container, add 300 µL of formaldehyde, and mix.

Diluent— Prepare a mixture of Methanolic formaldehyde solution and water (50:50).

Test solution— Dissolve about 500 mg of Indinavir Sulfate, accurately weighed, in about 80 mL of Diluent.

Procedure— Titrate with 0.1 M lead perchlorate VS, determining the endpoint potentiometrically, using a lead-specific electrode in conjunction with a suitable reference electrode. Each mL of 0.1 M lead perchlorate VS is equivalent to 9.604 mg of sulfate: between 13.2% and 14.4% is found, calculated on the anhydrous and solvent-free basis.

(Official January 1, 2007)

Dibutylammonium phosphate buffer— Transfer 20 mL of dibutyl ammonium phosphate to 1000 mL of water. While stirring, adjust with sodium hydroxide TS to a pH of 6.5 ± 0.05.

Mobile phase— Prepare a filtered and degassed mixture of Dibutylammonium phosphate buffer and acetonitrile (11:9). Make adjustments if necessary (see System Suitability under Chromatography 621).

Standard preparation— Dissolve a suitable quantity of USP Indinavir RS, accurately weighed, in Mobile phase to obtain a solution having a known concentration of about 0.5 mg per mL.

Assay preparation— Transfer about 60 mg of Indinavir Sulfate, accurately weighed, to a 100-mL volumetric flask, dissolve in and dilute with Mobile phase to volume, and mix.

Chromatographic system (see Chromatography 621)— The liquid chromatograph is equipped with a 260-nm detector and a 4.6-mm × 25-cm column that contains 5-µm packing L7. The flow rate is about 1.0 mL per minute. The column temperature is maintained at 40. Chromatograph the Standard preparation, and record the peak responses as directed for Procedure: the column efficiency is not less than 4000 theoretical plates; the tailing factor is less than 2.0; and the relative standard deviation for replicate injections is not more than 1.0%.

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 responses for the major peaks. Calculate the quantity, in mg, of C36H47N5O4·H2SO4 in the portion of Indinavir Sulfate taken by the formula: in which D is the dilution factor, in mL, for the Assay preparation; C is the concentration, in mg per mL, of USP Indinavir RS in the Standard preparation; and rU and rS are the peak responses obtained from the Assay preparation and the Standard preparation, respectively. [NOTE—1.1598 = Indinavir Sulfate MW (711.87 g/mol)/Indinavir MW (613.80 g/mol).]