UV AND HPLC Method Development and Method Validation of Nevirapine: UV AND HPLC Method Development and Validation of Nevirapine in Bulk and Pharmaceutical dosage forms - Couverture souple

Choudhury, Tirthankar

9786200218094: UV AND HPLC Method Development and Method Validation of Nevirapine: UV AND HPLC Method Development and Validation of Nevirapine in Bulk and Pharmaceutical dosage forms

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ISBN 10 : 6200218099 ISBN 13 : 9786200218094

Editeur : LAP LAMBERT Academic Publishing, 2019

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This research work focused on UV and RP-HPLC method and method validation of Nevirapine accurately and economically. UV spectrophotometric method and mehod development for Nevirapine obeyed Beer's law as depicted by linearity of the developed method. A reverse phase HPLC (RP-HPLC) method is described for the determination of nevirapine in tablet dosage forms. Chromatography was carried on an ODS column using a mixture of methanol and water (89:11 v/v) as the mobile phase at a flow rate of 1 mL/min with detection at 284 nm. The method was validated by determining its sensitivity, accuracy and precision. The proposed method is simple, economical, fast, accurate and precise, hence can be applied for routine quality control of nevirapine in bulk and tablet dosage forms.

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�diteur: LAP LAMBERT Academic Publishing
Date d'�dition: 2019
Langue: anglais
ISBN 10: 6200218099
ISBN 13: 9786200218094
Reliure: Broch�
Nombre de pages: 108
Coordonn�es du fabricant: non disponible
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UV AND HPLC Method Development and Method Validation of Nevirapine

Tirthankar Choudhury

Edit� par LAP LAMBERT Academic Publishing Jun 2019, 2019

ISBN 10 : 6200218099 ISBN 13 : 9786200218094

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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -This research work focused on UV and RP-HPLC method and method validation of Nevirapine accurately and economically. UV spectrophotometric method and mehod development for Nevirapine obeyed Beer's law as depicted by linearity of the developed method. A reverse phase HPLC (RP-HPLC) method is described for the determination of nevirapine in tablet dosage forms. Chromatography was carried on an ODS column using a mixture of methanol and water (89:11 v/v) as the mobile phase at a flow rate of 1 mL/min with detection at 284 nm. The method was validated by determining its sensitivity, accuracy and precision. The proposed method is simple, economical, fast, accurate and precise, hence can be applied for routine quality control of nevirapine in bulk and tablet dosage forms. 108 pp. Englisch. N� de r�f. du vendeur 9786200218094

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UV AND HPLC Method Development and Method Validation of Nevirapine

Tirthankar Choudhury

Edit� par LAP LAMBERT Academic Publishing, 2019

ISBN 10 : 6200218099 ISBN 13 : 9786200218094

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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Choudhury TirthankarDr. (Prof.) Tirthankar Choudhury had his M. Pharm (Pharm. Chemistry) in 2008 and Ph.D.(Pharmaceutical Science) in 2012. Till now he had 11 years of teaching experience along with several paper publications. Now he. N� de r�f. du vendeur 301387468

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UV AND HPLC Method Development and Method Validation of Nevirapine

Tirthankar Choudhury

Edit� par LAP LAMBERT Academic Publishing Jun 2019, 2019

ISBN 10 : 6200218099 ISBN 13 : 9786200218094

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Taschenbuch. Etat : Neu. Neuware -This research work focused on UV and RP-HPLC method and method validation of Nevirapine accurately and economically. UV spectrophotometric method and mehod development for Nevirapine obeyed Beer's law as depicted by linearity of the developed method. A reverse phase HPLC (RP-HPLC) method is described for the determination of nevirapine in tablet dosage forms. Chromatography was carried on an ODS column using a mixture of methanol and water (89:11 v/v) as the mobile phase at a flow rate of 1 mL/min with detection at 284 nm. The method was validated by determining its sensitivity, accuracy and precision. The proposed method is simple, economical, fast, accurate and precise, hence can be applied for routine quality control of nevirapine in bulk and tablet dosage forms.Books on Demand GmbH, �berseering 33, 22297 Hamburg 108 pp. Englisch. N� de r�f. du vendeur 9786200218094

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UV AND HPLC Method Development and Method Validation of Nevirapine : UV AND HPLC Method Development and Validation of Nevirapine in Bulk and Pharmaceutical dosage forms

Tirthankar Choudhury

Edit� par LAP LAMBERT Academic Publishing, 2019

ISBN 10 : 6200218099 ISBN 13 : 9786200218094

Neuf Taschenbuch

impression � la demande

Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne

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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - This research work focused on UV and RP-HPLC method and method validation of Nevirapine accurately and economically. UV spectrophotometric method and mehod development for Nevirapine obeyed Beer's law as depicted by linearity of the developed method. A reverse phase HPLC (RP-HPLC) method is described for the determination of nevirapine in tablet dosage forms. Chromatography was carried on an ODS column using a mixture of methanol and water (89:11 v/v) as the mobile phase at a flow rate of 1 mL/min with detection at 284 nm. The method was validated by determining its sensitivity, accuracy and precision. The proposed method is simple, economical, fast, accurate and precise, hence can be applied for routine quality control of nevirapine in bulk and tablet dosage forms. N� de r�f. du vendeur 9786200218094

Contacter le vendeur