9786139460748 - Method Development & Validation of Diclofenac Sodium and Pantoprazole: Simultaneous Estimation in Bulk Dosage Form de Chaki, Imran; Acharya, Hardik; Pujara, Naisarg... (7 resultados)

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Taschenbuch. Condición: Neu. Method Development & Validation of Diclofenac Sodium and Pantoprazole | Simultaneous Estimation in Bulk Dosage Form | Imran Chaki (u. a.) | Taschenbuch | 120 S. | Englisch | 2019 | LAP LAMBERT Academic Publishing | EAN 9786139460748 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

Condición: Hervorragend. Zustand: Hervorragend | Sprache: Englisch | Produktart: Bücher | The present work describes various methods for the simultaneous estimation of Diclofenac sodium (DICLO) and Pantoprazole (PANTO) in combined Capsule dosage form. A simple, accurate and reproducible RP-HPLC method have been developed and validated for the simultaneous estimation of Diclofenac sodium and Pantoprazole in their marketed formulation. The RP-HPLC methods were validated by Stastically. The retention times of Diclofenac sodium and Pantoprazole were found to be 3.33 ± 0.10 min and 6.66 ± 0.10 min, respectively. Linearity was evaluated over the concentration range of 18.75-56.25 µg/ml for DICLO and 5-15 µg/ml for PANTO by RP-HPLC method. The correlation coefficient and accuracy of both the methods were found to be within the range. The % RSD of precision was found to be NMT 2.0 % for HPLC method. The proposed methods were found to be robust when slight but deliberate changes were made in analytical conditions. Simple, accurate and reproducible RP-HPLC method were developed and validated for the simultaneous estimation of Diclofenac sodium and Pantoprazole in their marketed formulation. The proposed methods can be applied for the routine analysis in quality control laboratory.

Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The present work describes various methods for the simultaneous estimation of Diclofenac sodium (DICLO) and Pantoprazole (PANTO) in combined Capsule dosage form. A simple, accurate and reproducible RP-HPLC method have been developed and validated for the simultaneous estimation of Diclofenac sodium and Pantoprazole in their marketed formulation. The RP-HPLC methods were validated by Stastically. The retention times of Diclofenac sodium and Pantoprazole were found to be 3.33 ± 0.10 min and 6.66 ± 0.10 min, respectively. Linearity was evaluated over the concentration range of 18.75-56.25 µg/ml for DICLO and 5-15 µg/ml for PANTO by RP-HPLC method. The correlation coefficient and accuracy of both the methods were found to be within the range. The % RSD of precision was found to be NMT 2.0 % for HPLC method. The proposed methods were found to be robust when slight but deliberate changes were made in analytical conditions. Simple, accurate and reproducible RP-HPLC method were developed and validated for the simultaneous estimation of Diclofenac sodium and Pantoprazole in their marketed formulation. The proposed methods can be applied for the routine analysis in quality control laboratory. 120 pp. Englisch.

Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Chaki ImranImran A. Chaki, Master of Pharmacy, Pharmaceutical Quality Assurance from Gujarat Technological University. Research Associate at Quantys Clinical Private Limited in Quality Assurance Department.The present work descri.

Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The present work describes various methods for the simultaneous estimation of Diclofenac sodium (DICLO) and Pantoprazole (PANTO) in combined Capsule dosage form. A simple, accurate and reproducible RP-HPLC method have been developed and validated for the simultaneous estimation of Diclofenac sodium and Pantoprazole in their marketed formulation. The RP-HPLC methods were validated by Stastically. The retention times of Diclofenac sodium and Pantoprazole were found to be 3.33 ± 0.10 min and 6.66 ± 0.10 min, respectively. Linearity was evaluated over the concentration range of 18.75-56.25 µg/ml for DICLO and 5-15 µg/ml for PANTO by RP-HPLC method. The correlation coefficient and accuracy of both the methods were found to be within the range. The % RSD of precision was found to be NMT 2.0 % for HPLC method. The proposed methods were found to be robust when slight but deliberate changes were made in analytical conditions. Simple, accurate and reproducible RP-HPLC method were developed and validated for the simultaneous estimation of Diclofenac sodium and Pantoprazole in their marketed formulation. The proposed methods can be applied for the routine analysis in quality control laboratory.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 120 pp. Englisch.

Taschenbuch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The present work describes various methods for the simultaneous estimation of Diclofenac sodium (DICLO) and Pantoprazole (PANTO) in combined Capsule dosage form. A simple, accurate and reproducible RP-HPLC method have been developed and validated for the simultaneous estimation of Diclofenac sodium and Pantoprazole in their marketed formulation. The RP-HPLC methods were validated by Stastically. The retention times of Diclofenac sodium and Pantoprazole were found to be 3.33 ± 0.10 min and 6.66 ± 0.10 min, respectively. Linearity was evaluated over the concentration range of 18.75-56.25 µg/ml for DICLO and 5-15 µg/ml for PANTO by RP-HPLC method. The correlation coefficient and accuracy of both the methods were found to be within the range. The % RSD of precision was found to be NMT 2.0 % for HPLC method. The proposed methods were found to be robust when slight but deliberate changes were made in analytical conditions. Simple, accurate and reproducible RP-HPLC method were developed and validated for the simultaneous estimation of Diclofenac sodium and Pantoprazole in their marketed formulation. The proposed methods can be applied for the routine analysis in quality control laboratory.