Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -In the present day, an attempt was made to formulate and evaluate Microemulsion and Microsphere of Ropinirole Hydrochloride for better treatment of Parkinson¿s disease by improving its solubility profile and drug release of Ropinirole Hydrochloride from its formulations in conventional buffers. It is very poorly available at the site of action for fast and immediate treatment. Thus, formulated Microemulsion and Microsphere of Ropinirole Hydrochloride avoids first pass metabolism. Microemulsion experiment was performed with Ropinirole Hydrochloride as a drug, Sesame Oil, Sunflower Oil, Castrol oil, Elainic Acid (Oleic Acid), Tween 80, Tween 20, Span 20, Span 80, Methanol, Polyethylene glycol 400, Glycerin as surfactant and co-surfactant. For the formulations F1 to F10 diffusion studies i.e. % Cumulative drug release vs. time (mins) were performed and its % cumulative drug release for all formulations was in between 83.57% to 99.93%in pH 6.6 buffer. Out of Ten formulations F2 showed the maximum % cumulative release of 99.93%. The intranasal delivered microemulsion is 0.9334±0.0292¿g/ml than the Intravenous administered PDS 0.1567±0.023 ¿g/ml. 192 pp. Englisch. N° de réf. du vendeur 9786204742960
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Vendeur : moluna, Greven, Allemagne
Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Über den AutorrnrnDr. Shubhrajit Mantry, presently working as an Associate Professor & H.O.D (Pharmaceutics Department) in Sharadchandra Pawar College of Pharmacy, Otur, Pune, Maharashtra, India. He had published more than 60 articles in va. N° de réf. du vendeur 573741100
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Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - In the present day, an attempt was made to formulate and evaluate Microemulsion and Microsphere of Ropinirole Hydrochloride for better treatment of Parkinson's disease by improving its solubility profile and drug release of Ropinirole Hydrochloride from its formulations in conventional buffers. It is very poorly available at the site of action for fast and immediate treatment. Thus, formulated Microemulsion and Microsphere of Ropinirole Hydrochloride avoids first pass metabolism. Microemulsion experiment was performed with Ropinirole Hydrochloride as a drug, Sesame Oil, Sunflower Oil, Castrol oil, Elainic Acid (Oleic Acid), Tween 80, Tween 20, Span 20, Span 80, Methanol, Polyethylene glycol 400, Glycerin as surfactant and co-surfactant. For the formulations F1 to F10 diffusion studies i.e. % Cumulative drug release vs. time (mins) were performed and its % cumulative drug release for all formulations was in between 83.57% to 99.93%in pH 6.6 buffer. Out of Ten formulations F2 showed the maximum % cumulative release of 99.93%. The intranasal delivered microemulsion is 0.9334±0.0292¿g/ml than the Intravenous administered PDS 0.1567±0.023 ¿g/ml. N° de réf. du vendeur 9786204742960
Quantité disponible : 1 disponible(s)
Vendeur : buchversandmimpf2000, Emtmannsberg, BAYE, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -In the present day, an attempt was made to formulate and evaluate Microemulsion and Microsphere of Ropinirole Hydrochloride for better treatment of Parkinson's disease by improving its solubility profile and drug release of Ropinirole Hydrochloride from its formulations in conventional buffers. It is very poorly available at the site of action for fast and immediate treatment. Thus, formulated Microemulsion and Microsphere of Ropinirole Hydrochloride avoids first pass metabolism. Microemulsion experiment was performed with Ropinirole Hydrochloride as a drug, Sesame Oil, Sunflower Oil, Castrol oil, Elainic Acid (Oleic Acid), Tween 80, Tween 20, Span 20, Span 80, Methanol, Polyethylene glycol 400, Glycerin as surfactant and co-surfactant. For the formulations F1 to F10 diffusion studies i.e. % Cumulative drug release vs. time (mins) were performed and its % cumulative drug release for all formulations was in between 83.57% to 99.93%in pH 6.6 buffer. Out of Ten formulations F2 showed the maximum % cumulative release of 99.93%. The intranasal delivered microemulsion is 0.9334±0.0292¿g/ml than the Intravenous administered PDS 0.1567±0.023 ¿g/ml.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 192 pp. Englisch. N° de réf. du vendeur 9786204742960
Quantité disponible : 1 disponible(s)