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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4709
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dc.contributor.authorHiremath B
dc.contributor.authorMruthyunjayaswamy B.H.M.
dc.date.accessioned2020-06-12T15:04:36Z-
dc.date.available2020-06-12T15:04:36Z-
dc.date.issued2009
dc.identifier.citationAnalytical Letters , Vol. 42 , 14 , p. 2180 - 2191en_US
dc.identifier.uri10.1080/00032710903139802
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4709-
dc.description.abstractA reliable and sensitive RP-HPLC method was developed and validated for the quantitative estimation of ceftriaxone sodium (CFTZ) in pure drug and pharmaceutical dosage forms. The separation of ceftriaxone sodium was achieved on a Waters XTerra RP-18 (5?m, 250 × 4.6mm i.d.) column using photodiode array detector at 240 nm. The mobile phase consisted of 0.1M triethylammoniumacetate-acetonitrile (60:40v/v) mixture delivered at a flow rate of 1.0 ml/min. Accuracy, evaluated by means of the spike recovery method, was excellent, with percent recovery in the range 99.5-102% with precision in the range 0.3-1.2%. © Taylor & Francis Group, LLC.en_US
dc.subjectCeftriaxone sodium
dc.subjectDosage forms
dc.subjectRP-HPLC
dc.titleDevelopment and validation of a high-performance liquid chromatographic determination of ceftriaxone sodium and its application to drug quality controlen_US
dc.typeArticle
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