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Edité par VDM Verlag Dr. Mueller Aktiengesellschaft & Co. KG, 2012
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Langue: anglais
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ISBN 10 : 3659296899 ISBN 13 : 9783659296895
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Ajouter au panierTaschenbuch. Etat : Neu. Analytical Method Development and Validation | Simultaneous Estimation of Esomeprazole and Levosulpiride in Combined Capsule Dosage Form by RP-HPLC | Hardikkumar Patel | Taschenbuch | Englisch | LAP Lambert Academic Publishing | EAN 9783659296895 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Edité par VDM Verlag Dr. Mueller Aktiengesellschaft & Co. KG, 2012
ISBN 10 : 3659296899 ISBN 13 : 9783659296895
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Ajouter au panierEtat : New. Print on Demand pp. 100 2:B&W 6 x 9 in or 229 x 152 mm Perfect Bound on Creme w/Gloss Lam.
Langue: anglais
Edité par VDM Verlag Dr. Mueller Aktiengesellschaft & Co. KG, 2012
ISBN 10 : 3659296899 ISBN 13 : 9783659296895
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Ajouter au panierEtat : New. PRINT ON DEMAND pp. 100.
Langue: anglais
Edité par LAP LAMBERT Academic Publishing, 2012
ISBN 10 : 3659296899 ISBN 13 : 9783659296895
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Ajouter au panierKartoniert / Broschiert. Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Patel HardikkumarHardikkumar Patel is currently working as a Research Associate in Bio-analytical Department at veeda clinical Research, Ahmedabad,Gujarat, India.He graduated in Pharmacy from B.S Patel Pharmacy College Mehsana. He se.
Langue: anglais
Edité par LAP Lambert Academic Publishing, 2012
ISBN 10 : 3659296899 ISBN 13 : 9783659296895
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Ajouter au panierTaschenbuch. Etat : Neu. 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.