rp hplc method validation piroxicam von choudhury tirthankar (7 Ergebnisse)

Taschenbuch. Zustand: Neu. 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, 5¿m) 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.Books on Demand GmbH, Überseering 33, 22297 Hamburg 112 pp. Englisch.

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Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Choudhury TirthankarTirthankar Choudhury completed: B. Pharm, M.Pharm, PhD, F.I.C.Teaching, has research experience of 12 years 8 Months. Present Designation: Professor, H.O.D. (Pharmaceutical Chemistry) Award & Achievement:-1) Dis.

Taschenbuch. Zustand: Neu. 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.

Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - 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.

Zustand: New. PRINT ON DEMAND.

Zustand: New. Print on Demand.