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Desenvolvimento e validação de metodologia analítica para determinação de itraconazol em produtos farmacêuticos por CLAE
Edith Cristina Laignier Cazedey1  Roberta De Cássia Pimentel Azevedo1  Érika De Fátima Silva1  Magali Benjamim De Araújo1 
[1] ,Universidade Federal de Alfenas Departamento de Farmácia Alfenas MG ,Brasil
关键词: itraconazole;    validation;    HPLC;   
DOI  :  10.1590/S0100-40422007000400004
来源: SciELO
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【 摘 要 】

Itraconazole is a synthetic antifungal drug administered orally with a broad spectrum of activity against mycotic infections. The present work consists of the development and validation of analytical methodology for evaluation of itraconazole in pharmaceutical products by high performance liquid chromatography. The separation was made using the reversed-phase column LC-18, acetonitrile/diethylamine 0.05% v/v, 60:40 v/v, pH 8.0 as mobile phase, methanol as solvent and detection and quantification at 254 nm. The results here obtained show that the analytical methodology is accurate, reproducible, robust and linear over the concentration range 8.0-12.0 µg/mL of itraconazole. The method was applied to pharmaceutical capsules containg itraconazole pellets and showed to be efficient, yielding good results.

【 授权许可】

CC BY-NC   
 All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License

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