RP-HPLC METHOD AND METHOD VALIDATION OF PIROXICAM

Tirthankar Choudhury

ISBN 10: 6204184016 / ISBN 13: 9786204184012

Verlag: LAP LAMBERT Academic Publishing Jul 2021, 2021

Beschreibung

This item is printed on demand - it takes 3-4 days longer - Neuware -A rapid and precise Reverse Phase High Performance Liquid Chromatographic method has been developed for the validated of Piroxicam, in its pure form as well as in tablet dosage form. Chromatography was carried out on X-terra C18 (4.6 x 250mm, 5mim) column using a mixture of Acetonitrile and Water (40:60 v/v) as the mobile phase at a flow rate of 0.9ml/min, the detection was carried out at 227nm. The retention time of the Piroxicam was 5.430 ±0.02min respectively. The method produce linear responses in the concentration range of 10-50mg/ml of Piroxicam.The method precision for the determination of assay was below 2.0%RSD. The method is useful in the quality control of bulk and pharmaceutical formulations. 112 pp. Englisch. Bestandsnummer des Verkäufers 9786204184012

Bibliografische Details

Titel: RP-HPLC METHOD AND METHOD VALIDATION OF ...

Verlag: LAP LAMBERT Academic Publishing Jul 2021

Erscheinungsdatum: 2021

Einband: Taschenbuch

Zustand: Neu

Zustand des Schutzumschlags: Schutzumschlag

Über diesen Titel

Inhaltsangabe:

A rapid and precise Reverse Phase High Performance Liquid Chromatographic method has been developed for the validated of Piroxicam, in its pure form as well as in tablet dosage form. Chromatography was carried out on X-terra C18 (4.6 x 250mm, 5μm) column using a mixture of Acetonitrile and Water (40:60 v/v) as the mobile phase at a flow rate of 0.9ml/min, the detection was carried out at 227nm. The retention time of the Piroxicam was 5.430 ±0.02min respectively. The method produce linear responses in the concentration range of 10-50mg/ml of Piroxicam.The method precision for the determination of assay was below 2.0%RSD. The method is useful in the quality control of bulk and pharmaceutical formulations.