Analiza Usp(3)
This document was uploaded by user and they confirmed that they have the permission to share it. If you are author or own the copyright of this book, please report to us by using this DMCA report form. Report DMCA
Overview
Download & View Analiza Usp(3) as PDF for free.
More details
- Words: 714
- Pages: 2
Phenazopyridine Hydrochloride Tablets
» Phenazopyridine Hydrochloride Tablets contain not less than 90.0 percent and not more than 110.0 percent of the labeled amount of phenazopyridine hydrochloride (C11H11N5·HCl). Packaging and storage— Preserve in tight containers. USP Reference standards 11 — USP Phenazopyridine Hydrochloride RS. Identification— Transfer a quantity of finely ground Tablets, equivalent to about 50 mg of phenazopyridine hydrochloride, to a 125-mL separator, add 50 mL of water, 1 mL of 1 N hydrochloric acid, and 5 mL of a saturated sodium chloride solution, and shake to dissolve. Extract with two 25-mL portions of chloroform, and discard the chloroform. Add 5 mL of 1 N sodium hydroxide to the aqueous solution, and extract with one 50-mL portion of chloroform. Transfer the chloroform layer to a second 125-mL separator, and wash with one 50-mL portion of 0.1 N sodium hydroxide. Filter the chloroform layer through a pledget of cotton previously washed with chloroform. Add 5 drops of hydrochloric acid to the filtrate, and evaporate under a current of air on a steam bath to dryness. Add 5 mL of alcohol, and evaporate. Dry the residue at 105 for 4 hours: the IR absorption spectrum of a potassium bromide dispersion of the dried residue so obtained exhibits maxima only at the same wavelengths as that of a similar preparation of USP Phenazopyridine Hydrochloride RS. Dissolution
711 —
Medium: water; 900 mL. Apparatus 2: 50 rpm. Time: 45 minutes. Procedure— Determine the amount of C11H11N5·HCl dissolved from UV absorbances at the wavelength of maximum absorbance at about 422 nm on filtered portions of the solution under test, suitably diluted with Dissolution Medium in comparison with a Standard solution having a known concentration of USP Phenazopyridine Hydrochloride RS in the same Medium. Tolerances— Not less than 75% (Q) of the labeled amount of C11H11N5.HCl is dissolved in 45 minutes. Uniformity of dosage units
905 : meet the requirements.
Assay— Phosphate buffer— Dissolve 2.64 g of dibasic ammonium phosphate in about 900 mL of water. Adjust with phosphoric acid to a pH of 3.0, dilute with water to 1000 mL, and mix. Mobile phase— Prepare a mixture of Phosphate buffer and methanol (50:50). Make adjustments if necessary (see System Suitability under Chromatography
621 ).
Standard preparation— Transfer about 50 mg of USP Phenazopyridine Hydrochloride RS, accurately weighed, to a 100-mL volumetric flask. Add 50 mL of methanol, and swirl to dissolve. Dilute with Phosphate buffer to volume, mix, and pass through a filter having a 0.5-µm or finer porosity.
Assay preparation— Weigh and finely powder not fewer than 20 Tablets. Transfer an accurately weighed portion of the powder, equivalent to about 100 mg of phenazopyridine hydrochloride, to a 200-mL volumetric flask. Add 100 mL of methanol, and sonicate for 10 minutes. Add about 75 mL of Phosphate buffer, and sonicate for an additional 10 minutes, with occasional mixing. Dilute with Phosphate buffer to volume, and mix. Pass this solution through a filter having a 0.5-µm or finer porosity. Chromatographic system (see Chromatography 621 )— The liquid chromatograph is equipped with a 220-nm detector and a 3.9-mm × 30-cm column that contains packing L1. The flow rate is about 1.5 mL per minute. Chromatograph the Standard preparation, and record the responses as directed for Procedure: the column efficiency is not less than 1400 theoretical plates; the tailing factor for the analyte peak is not more than 2.0; and the relative standard deviation for replicate injections is not more than 2.0%. 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 C11H11N5. HCl in the portion of Tablets taken by the formula: 200C(rU / rS) in which C is the concentration, in mg per mL, of USP Phenazopyridine Hydrochloride RS in the Standard preparation; and rU and rS are the phenazopyridine 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. Topic/Question Monograph Reference Standards
711
Contact Clydewyn M. Anthony, Ph.D. Scientist 1-301-816-8139 Lili Wang, Technical Services Scientist 1-301-816-8129 [email protected] Margareth R.C. Marques, Ph.D. Senior Scientist 1-301-816-8106
USP32–NF27 Page 3265
Expert Committee (MDCCA05) Monograph Development-Cough Cold and Analgesics
(BPC05) Biopharmaceutics05
» Phenazopyridine Hydrochloride Tablets contain not less than 90.0 percent and not more than 110.0 percent of the labeled amount of phenazopyridine hydrochloride (C11H11N5·HCl). Packaging and storage— Preserve in tight containers. USP Reference standards 11 — USP Phenazopyridine Hydrochloride RS. Identification— Transfer a quantity of finely ground Tablets, equivalent to about 50 mg of phenazopyridine hydrochloride, to a 125-mL separator, add 50 mL of water, 1 mL of 1 N hydrochloric acid, and 5 mL of a saturated sodium chloride solution, and shake to dissolve. Extract with two 25-mL portions of chloroform, and discard the chloroform. Add 5 mL of 1 N sodium hydroxide to the aqueous solution, and extract with one 50-mL portion of chloroform. Transfer the chloroform layer to a second 125-mL separator, and wash with one 50-mL portion of 0.1 N sodium hydroxide. Filter the chloroform layer through a pledget of cotton previously washed with chloroform. Add 5 drops of hydrochloric acid to the filtrate, and evaporate under a current of air on a steam bath to dryness. Add 5 mL of alcohol, and evaporate. Dry the residue at 105 for 4 hours: the IR absorption spectrum of a potassium bromide dispersion of the dried residue so obtained exhibits maxima only at the same wavelengths as that of a similar preparation of USP Phenazopyridine Hydrochloride RS. Dissolution
711 —
Medium: water; 900 mL. Apparatus 2: 50 rpm. Time: 45 minutes. Procedure— Determine the amount of C11H11N5·HCl dissolved from UV absorbances at the wavelength of maximum absorbance at about 422 nm on filtered portions of the solution under test, suitably diluted with Dissolution Medium in comparison with a Standard solution having a known concentration of USP Phenazopyridine Hydrochloride RS in the same Medium. Tolerances— Not less than 75% (Q) of the labeled amount of C11H11N5.HCl is dissolved in 45 minutes. Uniformity of dosage units
905 : meet the requirements.
Assay— Phosphate buffer— Dissolve 2.64 g of dibasic ammonium phosphate in about 900 mL of water. Adjust with phosphoric acid to a pH of 3.0, dilute with water to 1000 mL, and mix. Mobile phase— Prepare a mixture of Phosphate buffer and methanol (50:50). Make adjustments if necessary (see System Suitability under Chromatography
621 ).
Standard preparation— Transfer about 50 mg of USP Phenazopyridine Hydrochloride RS, accurately weighed, to a 100-mL volumetric flask. Add 50 mL of methanol, and swirl to dissolve. Dilute with Phosphate buffer to volume, mix, and pass through a filter having a 0.5-µm or finer porosity.
Assay preparation— Weigh and finely powder not fewer than 20 Tablets. Transfer an accurately weighed portion of the powder, equivalent to about 100 mg of phenazopyridine hydrochloride, to a 200-mL volumetric flask. Add 100 mL of methanol, and sonicate for 10 minutes. Add about 75 mL of Phosphate buffer, and sonicate for an additional 10 minutes, with occasional mixing. Dilute with Phosphate buffer to volume, and mix. Pass this solution through a filter having a 0.5-µm or finer porosity. Chromatographic system (see Chromatography 621 )— The liquid chromatograph is equipped with a 220-nm detector and a 3.9-mm × 30-cm column that contains packing L1. The flow rate is about 1.5 mL per minute. Chromatograph the Standard preparation, and record the responses as directed for Procedure: the column efficiency is not less than 1400 theoretical plates; the tailing factor for the analyte peak is not more than 2.0; and the relative standard deviation for replicate injections is not more than 2.0%. 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 C11H11N5. HCl in the portion of Tablets taken by the formula: 200C(rU / rS) in which C is the concentration, in mg per mL, of USP Phenazopyridine Hydrochloride RS in the Standard preparation; and rU and rS are the phenazopyridine 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. Topic/Question Monograph Reference Standards
711
Contact Clydewyn M. Anthony, Ph.D. Scientist 1-301-816-8139 Lili Wang, Technical Services Scientist 1-301-816-8129 [email protected] Margareth R.C. Marques, Ph.D. Senior Scientist 1-301-816-8106
USP32–NF27 Page 3265
Expert Committee (MDCCA05) Monograph Development-Cough Cold and Analgesics
(BPC05) Biopharmaceutics05
