Analytical Method Development and Validation : Simultaneous Estimation of Esomeprazole and Levosulpiride in Combined Capsule Dosage Form by RP-HPLC

Language: English

Published by LAP Lambert Academic Publishing, 2012

3659296899 / 9783659296895

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Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH

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nach der Bestellung gedruckt Neuware - Printed after ordering - A new simple, accurate, rapid and precise isocratic Reverse Phase High performance liquid chromatographic (HPLC) method was developed and validated for the determination of Esomeprazole (ESO), and Levosulpiride (LEVO) in capsule formulation. The Method employs Shimadzu HPLC system on Hypercil BDS C18 (25 cm × 4.6 mm i.e., 5 µm) and flow rate of 1 ml/min with a load of 20µl. Acetonitrile and Phosphate buffer was used as mobile phase in the composition of 50:50 at 3.5 PH. The Detection was carried out at 240 nm. Linearity ranges for Esomeprazole and Levosulpiride were 20-60 µg/ml, 37.5-225 µg/ml respectively. Retention Time of Levosulpiride and Esomeprazole were found to be 3.367 min, 4.320 min respectively. Percent Recovery study values of Esomeprazole and Levosulpiride were found to be within 98-102%. This newly developed method was successfully utilized for the Quantitative estimation of Esomeprazole and Levosulpiride in pharmaceutical dosage forms. This method was validated for accuracy, precision, linearity and Robustness as per ICH guidelines.…

Seller Inventory # 9783659296895

Title
Analytical Method Development and Validation : Simultaneous Estimation of Esomeprazole and Levosulpiride in Combined Capsule Dosage Form by RP-HPLC
Author
Hardikkumar Patel
Publisher
LAP Lambert Academic Publishing
Publication year
2012
Condition
Neu
Binding
Taschenbuch
Language
English
ISBN 10
3659296899
ISBN 13
9783659296895
Item weight
151 grams
Dimensions
220x150x6 mm

AHA-BUCH GmbH

Einbeck, Germany

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