Carboplatin for Injection
» Carboplatin for Injection is a sterile, lyophilized mixture of Carboplatin and Mannitol. It contains not less than 90.0 percent and not more than 110.0 percent of the labeled amount of C6H12N2O4Pt.
Caution: Great care should be taken in handling Carboplatin because it is a suspected carcinogen.
Packaging and storage Preserve in Containers for Sterile Solids as described under Injections 1, protected from light.
Constituted solution At the time of use, it meets the requirements for Constituted Solutions under Injections 1.
Spray reagent Add 5.6 g of stannous chloride to 10 mL of hydrochloric acid, and stir for 5 minutes. [noteIt is not necessary that all of the solids dissolve.] Add 90 mL of water and 1 g of potassium iodide, and stir. Prepare this solution fresh daily.
Standard solution Prepare a solution in water containing 10 mg of USP Carboplatin RS per mL.
Test solution Dissolve the contents of 1 container in water to obtain a solution containing 10 mg of carboplatin per mL.
Procedure Separately apply 10 µL each of the Standard solution and the Test solution to a thin-layer chromatographic plate (see Chromatography 621) coated with a 0.25-mm layer of chromatographic silica gel. Place the plate in a chromatographic chamber lined with filter paper and equilibrated for 2 hours with a mixture of acetone and water (80:20). Develop the chromatogram until the solvent front has moved about 10 cm from the origin. Remove the plate from the chamber, and air-dry at room temperature for 2 hours. Spray with the Spray reagent, and heat at 110 for 10 minutes: the principal spot from the Test solution corresponds in appearance and RF value to that obtained from the Standard solution.
Sterility 71 It meets the requirements when tested as directed for Membrane Filtration under Test for Sterility of the Product to be Examined.
Bacterial endotoxins 85 It contains not more than 0.54 USP Endotoxin Unit per mg of carboplatin.
pH 791: between 5.0 and 7.0, in a solution constituted as directed in the labeling, Sterile Water for Injection being used.
Water, Method I 921 Proceed as directed in the test for Water under Cisplatin for Injection: not more than 3.0% is found.
Uniformity of dosage units 905: meets the requirements.
Limit of 1,1-cyclobutanedicarboxylic acid
Mobile phase , System suitability solution, and Chromatographic systemProceed as directed for Limit of 1,1-cyclobutanedicarboxylic acid under Carboplatin.
Standard solution Dissolve an accurately weighed quantity of 1,1-cyclobutanedicarboxylic acid in Mobile phase to obtain a solution having a known concentration of about 0.5 mg per mL. Transfer 2.0 mL of this solution to a 100-mL volumetric flask, dilute with Mobile phase to volume, and mix.
Test solution Quantitatively dissolve the contents of 1 container in Mobile phase to obtain a solution having a concentration of 1 mg of carboplatin per mL. [noteComplete the chromatographic analysis of the solution within 2 hours.]
Procedure Separately inject equal volumes (about 100 µL) of the Test solution and the Standard solution into the chromatograph, record the chromatograms, and measure the responses for the 1,1-cyclobutanedicarboxylic acid peaks. Calculate the percentage of 1,1-cyclobutanedicarboxylic acid in the portion of Carboplatin for Injection taken by the formula:
100(CV / L)(rU / rS)in which C is the concentration, in mg per mL, of 1,1-cyclobutanedicarboxylic acid in the Standard solution; V is the volume, in mL, of the constituted container contents; L is the labeled quantity, in mg, of carboplatin per container; and rU and rS are the peak responses for 1,1-cyclobutanedicarboxylic acid obtained from the Test solution and the Standard solution, respectively: not more than 1.0% is found.
Mobile phase , Standard preparation, and Chromatographic systemProceed as directed in the Assay under Carboplatin.
Assay preparation Quantitatively dissolve the contents of 1 container in water to obtain a solution having a concentration of 1 mg per mL. [noteComplete chromatographic analysis of this solution within 2 hours.]
Procedure Separately inject equal volumes (about 10 µL) of the Assay preparation and the Standard preparation into the chromatograph, record the chromatograms, and measure the responses for the major peaks. Calculate the quantity, in mg, of C6H12N2O4Pt in the portion of Carboplatin for Injection taken by the formula:
CV(rU / rS)in which C is the concentration, in mg per mL, of USP Carboplatin RS in the Standard preparation; V is the volume, in mL, of the constituted container contents; and rU and rS are the peak responses obtained from the Assay preparation and the Standard preparation, respectively.
Auxiliary Information Please check for your question in the FAQs before contacting USP.Chromatographic Column
USP32NF27 Page 1800
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.