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Pak J Pharm Sci ; 32(2 (Supplementary)): 839-844, 2019 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-31103980

RESUMO

A new method on RP-HPLC is devised and validated, as per ICH guidelines, for the synchronous estimation of cefpodoxime proxetil and H2-receptor antagonits that are Cimetidine, Famotidine and Ranitidine. The method is simple, accurate, expeditious, reproducible, robust and precise. Chromatography was done on a C18 (250 x 4.6mm) column with methanol: water as mobile phae in the ratio of 70:30 (v/v), pumped at a flow rate of 1ml/min and pH was maintained using 85% ortho-phosphoric acid at 3. The λ max 240 nm was preferred for UV detection. A good linear relationship was attained, over the concentration ranges of 20-70 µg/ml and 5-30µg/ml, for cefpodoxime proxetil and H2 blockers respectively, with a correlation coefficient of R= 0.9987 to 0.9992. The method was validated and found precised (i.e. intra day and interday analysis) with RSD <2%. LOD and LOQ observations were under 0.4806 to 2.6069µg/ml which proved the method to be sensitive. The method provided satisfactory results of robustness and reproducibility, when validated and applied successfully for analysis of dosage forms.


Assuntos
Ceftizoxima/análogos & derivados , Cromatografia Líquida de Alta Pressão/métodos , Antagonistas dos Receptores H2 da Histamina/análise , Ceftizoxima/análise , Cromatografia de Fase Reversa/métodos , Cimetidina/análise , Formas de Dosagem , Famotidina/análise , Limite de Detecção , Ranitidina/análise , Comprimidos/análise , Cefpodoxima Proxetil
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