Stability Indicating Assay Method by Shingade Sunil (5 results)

Taschenbuch. Condition: Neu. Stability Indicating Assay Method Development of Fingolimod | Sunil Shingade (u. a.) | Taschenbuch | 100 S. | Englisch | 2017 | LAP LAMBERT Academic Publishing | EAN 9783659692758 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.…

Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Stress testing of Fingolimod capsules was carried out under acidic, alkaline, peroxide, photolytic, and dry heat conditions. The stressed sample and standard drug were subjected to chromatographic separation and the conditions required for resolving the drug peak from any potential degradation products were optimized. The HPLC analysis of Fingolimod Capsules was carried out using X-Bridge (250mm x 4.6 mm, 5µm) during the stress studies Fingolimod Capsules were found to be stable degrade under acidic, alkaline, peroxide, photolytic and heat conditions. The degradation products and tablet excipients were well resolved from the drug using mobile phase comprising of Buffer:ACN (30:70v/v). The detection wavelength was 220 nm. The developed method was validated as per ICH Guide lines. The method was found to be accurate, precise, robust and linear in the range of 2-14µg/ml. Accuracy was calculated at three levels:50 %, 100%, 150% and recovery was found to be between 95-105%. It can be concluded that the HPLC method developed for Fingolimod Capsules is capable of discriminating between the drug and degradation products. 100 pp. Englisch.…

Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Stress testing of Fingolimod capsules was carried out under acidic, alkaline, peroxide, photolytic, and dry heat conditions. The stressed sample and standard drug were subjected to chromatographic separation and the conditions required for resolving the drug peak from any potential degradation products were optimized. The HPLC analysis of Fingolimod Capsules was carried out using X-Bridge (250mm x 4.6 mm, 5µm) during the stress studies Fingolimod Capsules were found to be stable degrade under acidic, alkaline, peroxide, photolytic and heat conditions. The degradation products and tablet excipients were well resolved from the drug using mobile phase comprising of Buffer:ACN (30:70v/v). The detection wavelength was 220 nm. The developed method was validated as per ICH Guide lines. The method was found to be accurate, precise, robust and linear in the range of 2-14µg/ml. Accuracy was calculated at three levels:50 %, 100%, 150% and recovery was found to be between 95-105%. It can be concluded that the HPLC method developed for Fingolimod Capsules is capable of discriminating between the drug and degradation products.…

Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Shingade SunilDr. Sunil G. Shingade obtained his M. Pharm. degree from Rajiv Gandhi University of Health Sciences, Bangalore, India and Ph. D. in Pharmacy from North Maharashtra University, Jalgaon, India. He is Assistant Professor o.…

Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Stress testing of Fingolimod capsules was carried out under acidic, alkaline, peroxide, photolytic, and dry heat conditions. The stressed sample and standard drug were subjected to chromatographic separation and the conditions required for resolving the drug peak from any potential degradation products were optimized. The HPLC analysis of Fingolimod Capsules was carried out using X-Bridge (250mm x 4.6 mm, 5µm) during the stress studies Fingolimod Capsules were found to be stable degrade under acidic, alkaline, peroxide, photolytic and heat conditions. The degradation products and tablet excipients were well resolved from the drug using mobile phase comprising of Buffer:ACN (30:70v/v). The detection wavelength was 220 nm. The developed method was validated as per ICH Guide lines. The method was found to be accurate, precise, robust and linear in the range of 2-14µg/ml. Accuracy was calculated at three levels:50 %, 100%, 150% and recovery was found to be between 95-105%. It can be concluded that the HPLC method developed for Fingolimod Capsules is capable of discriminating between the drug and degradation products.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 100 pp. Englisch.…