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Cefonicid Sodium
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[(hydroxyphenylacetyl)amino]-8-oxo-3-[[[1-(sulfomethyl)-1H-tetrazol-5-yl]thio]methyl]disodium salt, [6R-[6 (6R,7R)-[7-[(R)-Mandelamido]-8-oxo-3-[[[1-(sulfomethyl)-1H-tetrazol-5-yl]thio]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, disodium salt » Cefonicid Sodium contains the equivalent of not less than 832 µg and not more than 970 µg of cefonicid (C18H18N6O8S3) per mg, calculated on the anhydrous basis.
Packaging and storage
Preserve in tight containers.
Labeling
Where it is intended for use in preparing injectable dosage forms, the label states that it is sterile or must be subjected to further processing during the preparation of injectable dosage forms.
Identification
A:
The chromatogram of the Assay preparation obtained as directed in the Assay exhibits a major peak for cefonicid, the retention time of which corresponds to that exhibited in the chromatogram of the Standard preparation, as obtained in the Assay.
B:
It responds to the tests for Sodium
pH
Water, Method I
Other requirements
Where the label states that Cefonicid Sodium is sterile, it meets the requirements for Sterility and Bacterial endotoxins under Cefonicid for Injection. Where the label states that Cefonicid Sodium must be subjected to further processing during the preparation of injectable dosage forms, it meets the requirements for Bacterial endotoxins under Cefonicid for Injection.
Assay
Mobile phase
Prepare a mixture of water, methanol, and 0.2 M monobasic ammonium phosphate (33:5:2). Pass through a filter having a 0.5-µm or finer porosity, and degas. Make adjustments if necessary (see System Suitability under Chromatography
Standard preparation
Dissolve an accurately weighed quantity of USP Cefonicid Sodium RS in Mobile phase to obtain a solution having a known concentration of about 200 µg of cefonicid (C18H18N6O8S3) per mL.
Assay preparation
Transfer about 40 mg of Cefonicid Sodium, accurately weighed, to a 200-mL volumetric flask, dissolve in and dilute with Mobile phase to volume, and mix.
Resolution solution
Dissolve a quantity of USP Cefonicid Sodium RS in Mobile phase to obtain a solution containing about 0.2 mg per mL. Heat on a steam bath for 30 minutes, and cool. This Resolution solution contains a mixture of cefonicid and desacetyl cefonicid.
Chromatographic system
(see Chromatography
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 µg, of cefonicid (C18H18N6O8S3) per mg of the Cefonicid Sodium taken by the formula:
200(C / M)(rU / rS)
in which C is the concentration, in µg per mL of cefonicid (C18H18N6O8S3) in the Standard preparation; M is the quantity, in mg, of Cefonicid Sodium taken to prepare the Assay preparation; 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 1839
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.
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