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Jordan Journal of Pharmaceutical Sciences. 2013; 6 (2): 188-202
em Inglês | IMEMR | ID: emr-143066

RESUMO

This study develops and validates an efficient, sensitive and simple method for the simultaneous determination of cetirizine dihydrochloride and pseudoephedrine combined in tablet dosage form by high performance liquid chromatography [HPLC] with an ultraviolet [UV] detector.The validation of this method was carried out according to ICH and USP guidelines. In this study, the mobile phase used was acetonitrile: water [530:470 [v/v]] with 200mg sodium heptane sulfonic acid and the pH value was adjusted to 2.5 with sulfuric acid. The limit of detection and quantification for cetirizinedihydrochloride were 0.805 and 2.685 microg/mL, respectively, and the limit of detection and quantification for pseudoephedrine were 17.976 and 59.921 microg/mL, respectively. The linearity was studied in the concentration range of 12.2 and 36.5 microg/mL forcetirizinedihydrochloride and 295.91 and 861.73 microg/mL for pseudoephedrine. The recovered amounts of cetirizinedihydrochloride and pseudoephedrine were 98.2% -102.9% and 99.5%- 102.4%, respectively.


Assuntos
Cromatografia Líquida de Alta Pressão , Piperazinas/química , Sensibilidade e Especificidade , Reprodutibilidade dos Testes , Formas de Dosagem
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