Formulation research is oriented towards safty, efficiency and quick onset of action of existing drug molecule through novel concepts of drug delivery. Metformin hydrochloride is an oral antidiabetic biguinide agent, used in the management of non-insulin dependent (type-2) diabetes Mellitus. Orodispersible tablets of Metformin Hcl were prepared by direct compression method. About nine formulations for the present study were carried out based on combination of two superdisintegrants. Croscarmellose sodium, crosspovidone and sodium starch glycolate were used as superdisintegrant. The prepared batches of tablets were evaluated for weight variation, hardness, friability, wetting time, invitro dispersion time, drug content and invitro dissolution studies. The formulation containing combination of croscarmellose sodium and sodium starch glycolate showed rapid invitro dispersion time as compared to other formulations. The optimized formulation dispersed in 28 seconds. It also showed a higher water absorption ratio and 98.37% of drug is released within 30 minutes.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
Formulation research is oriented towards safty, efficiency and quick onset of action of existing drug molecule through novel concepts of drug delivery. Metformin hydrochloride is an oral antidiabetic biguinide agent, used in the management of non-insulin dependent (type-2) diabetes Mellitus. Orodispersible tablets of Metformin Hcl were prepared by direct compression method. About nine formulations for the present study were carried out based on combination of two superdisintegrants. Croscarmellose sodium, crosspovidone and sodium starch glycolate were used as superdisintegrant. The prepared batches of tablets were evaluated for weight variation, hardness, friability, wetting time, invitro dispersion time, drug content and invitro dissolution studies. The formulation containing combination of croscarmellose sodium and sodium starch glycolate showed rapid invitro dispersion time as compared to other formulations. The optimized formulation dispersed in 28 seconds. It also showed a higher water absorption ratio and 98.37% of drug is released within 30 minutes.
I am Pramod Kumar Biswal, currently working as Assistant Professor in Kunuwar Haribansh Singh college of Pharmacy, Jaunpur, U.P., India.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
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 -Formulation research is oriented towards safty, efficiency and quick onset of action of existing drug molecule through novel concepts of drug delivery. Metformin hydrochloride is an oral antidiabetic biguinide agent, used in the management of non-insulin dependent (type-2) diabetes Mellitus. Orodispersible tablets of Metformin Hcl were prepared by direct compression method. About nine formulations for the present study were carried out based on combination of two superdisintegrants. Croscarmellose sodium, crosspovidone and sodium starch glycolate were used as superdisintegrant. The prepared batches of tablets were evaluated for weight variation, hardness, friability, wetting time, invitro dispersion time, drug content and invitro dissolution studies. The formulation containing combination of croscarmellose sodium and sodium starch glycolate showed rapid invitro dispersion time as compared to other formulations. The optimized formulation dispersed in 28 seconds. It also showed a higher water absorption ratio and 98.37% of drug is released within 30 minutes. 88 pp. Englisch. N° de réf. du vendeur 9783659626999
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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Formulation research is oriented towards safty, efficiency and quick onset of action of existing drug molecule through novel concepts of drug delivery. Metformin hydrochloride is an oral antidiabetic biguinide agent, used in the management of non-insulin dependent (type-2) diabetes Mellitus. Orodispersible tablets of Metformin Hcl were prepared by direct compression method. About nine formulations for the present study were carried out based on combination of two superdisintegrants. Croscarmellose sodium, crosspovidone and sodium starch glycolate were used as superdisintegrant. The prepared batches of tablets were evaluated for weight variation, hardness, friability, wetting time, invitro dispersion time, drug content and invitro dissolution studies. The formulation containing combination of croscarmellose sodium and sodium starch glycolate showed rapid invitro dispersion time as compared to other formulations. The optimized formulation dispersed in 28 seconds. It also showed a higher water absorption ratio and 98.37% of drug is released within 30 minutes. N° de réf. du vendeur 9783659626999
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Biswal Pramod KumarI am Pramod Kumar Biswal, currently working as Assistant Professor in Kunuwar Haribansh Singh college of Pharmacy, Jaunpur, U.P., India.Formulation research is oriented towards safty, efficiency and quick onset. N° de réf. du vendeur 5169373
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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Formulation research is oriented towards safty, efficiency and quick onset of action of existing drug molecule through novel concepts of drug delivery. Metformin hydrochloride is an oral antidiabetic biguinide agent, used in the management of non-insulin dependent (type-2) diabetes Mellitus. Orodispersible tablets of Metformin Hcl were prepared by direct compression method. About nine formulations for the present study were carried out based on combination of two superdisintegrants. Croscarmellose sodium, crosspovidone and sodium starch glycolate were used as superdisintegrant. The prepared batches of tablets were evaluated for weight variation, hardness, friability, wetting time, invitro dispersion time, drug content and invitro dissolution studies. The formulation containing combination of croscarmellose sodium and sodium starch glycolate showed rapid invitro dispersion time as compared to other formulations. The optimized formulation dispersed in 28 seconds. It also showed a higher water absorption ratio and 98.37% of drug is released within 30 minutes.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 88 pp. Englisch. N° de réf. du vendeur 9783659626999
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Taschenbuch. Etat : Neu. Anti Diabetics Fast Dissolving Tablet | Pramod Kumar Biswal (u. a.) | Taschenbuch | 88 S. | Englisch | 2014 | LAP LAMBERT Academic Publishing | EAN 9783659626999 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. N° de réf. du vendeur 104975811
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