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Methodenentwicklung und Validierung für die Voriconazol-Bestimmung

Methodenentwicklung und Validierung für die Voriconazol-Bestimmung

K. Vara Prasada Rao / Yarguntla Srinivasa Rao

65,80 €
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Editorial:
KS OmniScriptum Publishing
Año de edición:
2025
Materia
Farmacología
ISBN:
9786209077234
65,80 €
IVA incluido
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Für die Bestimmung von Voriconazol wurde eine schnelle, empfindliche und spezifische RP-HPLC-Methode mit UV-Detektion entwickelt und validiert. Die Chromatographie wurde auf einer Enable C18 G-Säule (250 × 4,6 mm) im isokratischen Modus unter Verwendung einer mobilen Phase aus Methanol und Acetonitril (60:40, v/v) durchgeführt. Die Durchflussrate wurde auf 1 mL/min eingestellt, und der Abfluss wurde bei 223 nm überwacht. Die chromatographische Analyse ergab einen Hauptpeak für Voriconazol bei einer Retentionszeit von 2,841 Minuten. Als Lösungsmittel für die Analyse wurde Methanol gewählt, wobei die λmax bei 223 nm bestimmt wurde. Die Methode zeigte Linearität über einen Konzentrationsbereich von 5-30 µg/ml. Die Validierungsparameter, einschließlich Linearität, Bereich, Präzision, Genauigkeit, Nachweisgrenze (LOD) und Bestimmungsgrenze (LOQ), wurden bewertet und entsprachen den erforderlichen Standards.

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Otros libros del autor

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  • Desenvolvimento e validação de métodos para a estimativa do voriconazol
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    Foi desenvolvido e validado um método RP-HPLC rápido, sensível e específico com deteção por UV para a determinação do voriconazol. A cromatografia foi efectuada numa coluna Enable C18 G (250 × 4,6 mm) em modo isocrático, utilizando uma fase móvel de metanol e acetonitrilo (60:40, v/v). O caudal foi fixado em 1 mL/min e o efluente foi monitorizado a 223 nm. A análise cromatográf...
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  • Method Development and Validation for Voriconazole Estimation
    K. Vara Prasada Rao / Yarguntla Srinivasa Rao
    A rapid, sensitive, and specific RP-HPLC method with UV detection was developed and validated for the determination of voriconazole. Chromatography was performed on an Enable C18 G column (250 × 4.6 mm) in isocratic mode, using a mobile phase of methanol and acetonitrile (60:40, v/v). The flow rate was set at 1 mL/min, and the effluent was monitored at 223 nm. Chromatographic a...
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