Thiabendazole Chewable Tablets
(Monograph under this new titleto become official February 1, 2010)
(Current monograph title is Thiabendazole Tablets)
» Thiabendazole Chewable Tablets contain not less than 90.0 percent and not more than 110.0 percent of the labeled amount of thiabendazole (C10H7N3S).
Packaging and storage Preserve in tight containers.
Labeling Label the Chewable Tablets to indicate that they are to be chewed before swallowing.
A: Triturate a quantity of powdered Chewable Tablets, equivalent to about 0.5 g of thiabendazole, with about 20 mL of water, and filter. Wash the residue with 20 mL of water, discard the washing, dissolve the residue in 30 mL of 0.1 N hydrochloric acid, and filter. Collect the filtrate in a separator, render it alkaline with 1 N sodium hydroxide, and extract with 10 mL of carbon disulfide. Pass the carbon disulfide layer through a dry filter, collecting the filtrate in an evaporating dish. Evaporate the solvent with the aid of gentle heat and a stream of nitrogen. [CautionDo not overheat the residue.] The residue so obtained meets the requirements for Identification test A under Thiabendazole.
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.
Uniformity of dosage units 905: meet the requirements.
procedure for content uniformity
Standard preparation Dissolve an accurately weighed quantity of USP Thiabendazole RS in 0.1 N hydrochloric acid, and dilute quantitatively and stepwise with 0.1 N hydrochloric acid to obtain a solution having a known concentration of about 5 µg per mL.
Test preparation Transfer 1 Chewable Tablet to a 1000-mL volumetric flask, add about 75 mL of 0.1 N hydrochloric acid, and heat on a steam bath for about 1 hour. Cool to room temperature, dilute with 0.1 N hydrochloric acid to volume, mix, and filter a portion of the solution, discarding the first 20 mL of the filtrate. Pipet 5 mL of the filtrate into a 500-mL volumetric flask, dilute with 0.1 N hydrochloric acid to volume, and mix.
Procedure Concomitantly determine the absorbances of the Standard preparation and the Test preparation at the wavelength of maximum absorbance at about 302 nm, with a suitable spectrophotometer, using 0.1 N hydrochloric acid as the blank. Calculate the quantity, in mg, of C10H7N3S in the Chewable Tablet taken by the formula:
(TC/D)(AU / AS)in which T is the labeled quantity, in mg, of thiabendazole in the Chewable Tablet; C is the concentration, in µg per mL, of USP Thiabendazole RS in the Standard preparation; D is the concentration, in µg per mL, of thiabendazole in the Test preparation, based upon the labeled quantity per Chewable Tablet and the extent of dilution; and AU and AS are the absorbances of the Test preparation and the Standard preparation, respectively.
Standard preparation and Chromatographic system Prepare as directed in the Assay under Thiabendazole Oral Suspension.
pH 3.5 Phosphate buffer Dissolve 13.8 g of monobasic sodium phosphate in water to obtain 2000 mL of solution. Adjust this solution with phosphoric acid to a pH of 3.5 ± 0.05.
Mobile phase Prepare a filtered and degassed mixture of pH 3.5 Phosphate buffer and methanol (54:46). Make adjustments if necessary (see System Suitability under Chromatography 621).
Assay preparation Weigh and finely powder not fewer than 20 Chewable Tablets. Transfer an accurately weighed portion of the powder, equivalent to about 200 mg of thiabendazole, to a 1000-mL volumetric flask, add 100 mL of 0.1 N hydrochloric acid, mix, and warm the solution for a minimum of 30 minutes. Allow to cool to room temperature, dilute with water to volume, mix, and filter, discarding the first 20 mL of the filtrate.
Procedure Proceed as directed for Procedure in the Assay under Thiabendazole Oral Suspension. Calculate the quantity, in mg, of thiabendazole (C10H7N3S) in the portion of Chewable Tablets taken by the formula:
1000C(rU / rS)in which C is the concentration, in mg per mL, of USP Thiabendazole RS in the Standard preparation; and rU and rS are the peak responses obtained from the Assay preparation and the Standard preparation, respectively.
(Official February 1, 2010)
Auxiliary Information Please check for your question in the FAQs before contacting USP.Chromatographic Column
USP32NF27 Page 3717Pharmacopeial Forum: Volume No. 29(6) Page 1991
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.