Aminocaproic Acid Injection
» Aminocaproic Acid Injection is a sterile solution of Aminocaproic Acid in Water for Injection. It contains not less than 95.0 percent and not more than 107.5 percent of the labeled amount of aminocaproic acid (C6H13NO2).
Packaging and storage Preserve in single-dose or multiple-dose containers, preferably of Type I glass.
Identification Mix 2 mL of Injection, added dropwise, with 100 mL of acetone, rapidly stirring the mixture with a glass rod to induce crystallization. Allow the mixture to stand for 15 minutes, and pass through a medium-porosity, sintered-glass filter. Wash the crystals with 25 mL of acetone, apply vacuum to remove the solvent, dry at 105 for 30 minutes, and cool: the residue so obtained responds to the Identification test under Aminocaproic Acid.
Bacterial endotoxins 85 It contains not more than 0.05 USP Endotoxin Unit per mg of aminocaproic acid.
pH 791: between 6.0 and 7.6.
Other requirements It meets the requirements under Injections 1.
Mobile phase Transfer 11 g of sodium 1-pentanesulfonate and 40 g of anhydrous sodium sulfate to a 2-L volumetric flask, and dissolve in about 500 mL of water. Add 20 mL of 1 N sulfuric acid and 30 mL of acetonitrile, dilute with water to volume, and mix. Filter and degas. Make adjustments if necessary (see System Suitability under Chromatography 621).
Standard preparation Dissolve an accurately weighed quantity of USP Aminocaproic Acid RS in Mobile phase to obtain a solution having a known concentration of about 2.5 mg per mL.
Resolution solution Mix 20 µL of benzyl alcohol with 100 mL of water. Dilute 1.0 mL of this solution with the Standard preparation to 10 mL.
Assay preparation Transfer an accurately measured volume of Injection, equivalent to about 1.25 g of aminocaproic acid, to a 50-mL volumetric flask, dilute with water to volume, and mix. Transfer 5.0 mL of the resulting solution to a 50-mL volumetric flask, dilute with Mobile phase to volume, and mix.
Chromatographic system (see Chromatography 621) The liquid chromatograph is equipped with a 210-nm detector and a 4-mm × 30-cm column that contains packing L1. The flow rate is about 2 mL per minute. Chromatograph the Resolution solution as directed for Procedure: the resolution, R, between benzyl alcohol and aminocaproic acid is not less than 7.0. The aminocaproic acid peak elutes prior to the benzyl alcohol peak. Chromatograph the Standard preparation, and record the peak responses as directed for Procedure: the relative standard deviation for replicate injections is not more than 1.0%.
Procedure Separately inject equal volumes (about 50 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 aminocaproic acid (C6H13NO2) in each mL of the Injection taken by the formula:
500(C / V)(rU / rS)in which C is the concentration, in mg per mL, of USP Aminocaproic Acid RS in the Standard preparation; V is the volume, in mL, of Injection taken; and rU and rS are the aminocaproic acid peak areas obtained from the Assay preparation and the Standard preparation, respectively.
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USP32NF27 Page 1518
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.