The present research works carried out with the aim to prepare suspension dosage form using these microparticles for oral use. Solid Dosage forms are difficult for Pediatric, Geriatric patient & Dysphasic patients so for that patients the suspension dosage form more favorable than other solid dosage form. Albendazole drug has poor oral bioavailability (>5%) & a delayed release microspheric suspension of this drug would improve patient compliance & ease of swallowing. Microencapsulate facilitate the targeting of drug & mask the metallic taste of drug. The % yield was higher in the solvent evaporation method, in the spray drying the % yield was less that was drawback of the spray drying method. The % entrapment efficiency was good in the both method. Spray drying method is more reproducible than the solvent evaporation method. The stability study results show similar values as at the initial time. So, the formulation was stable and had no significant change in drug release profile & drug content on storage for a long time. So the suspension can effectively used for pediatric and geriatric patients. In vivo study will use for confirmatory study.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
The present research works carried out with the aim to prepare suspension dosage form using these microparticles for oral use. Solid Dosage forms are difficult for Pediatric, Geriatric patient & Dysphasic patients so for that patients the suspension dosage form more favorable than other solid dosage form. Albendazole drug has poor oral bioavailability (>5%) & a delayed release microspheric suspension of this drug would improve patient compliance & ease of swallowing. Microencapsulate facilitate the targeting of drug & mask the metallic taste of drug. The % yield was higher in the solvent evaporation method, in the spray drying the % yield was less that was drawback of the spray drying method. The % entrapment efficiency was good in the both method. Spray drying method is more reproducible than the solvent evaporation method. The stability study results show similar values as at the initial time. So, the formulation was stable and had no significant change in drug release profile & drug content on storage for a long time. So the suspension can effectively used for pediatric and geriatric patients. In vivo study will use for confirmatory study.
Mr.Chirag A.PatelM.Pharm,Assistant Professor,Kalol Institute Of Pharmacy,Kalol,Gujarat,India
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Patel Chirag A.Mr.Chirag A.PatelM.Pharm,Assistant Professor,Kalol Institute Of Pharmacy,Kalol,Gujarat,IndiaThe present research works carried out with the aim to prepare suspension dosage form using these microparticles for oral . N° de réf. du vendeur 5519591
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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The present research works carried out with the aim to prepare suspension dosage form using these microparticles for oral use. Solid Dosage forms are difficult for Pediatric, Geriatric patient & Dysphasic patients so for that patients the suspension dosage form more favorable than other solid dosage form. Albendazole drug has poor oral bioavailability (5%) & a delayed release microspheric suspension of this drug would improve patient compliance & ease of swallowing. Microencapsulate facilitate the targeting of drug & mask the metallic taste of drug. The % yield was higher in the solvent evaporation method, in the spray drying the % yield was less that was drawback of the spray drying method. The % entrapment efficiency was good in the both method. Spray drying method is more reproducible than the solvent evaporation method. The stability study results show similar values as at the initial time. So, the formulation was stable and had no significant change in drug release profile & drug content on storage for a long time. So the suspension can effectively used for pediatric and geriatric patients. In vivo study will use for confirmatory study. N° de réf. du vendeur 9783848401321
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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The present research works carried out with the aim to prepare suspension dosage form using these microparticles for oral use. Solid Dosage forms are difficult for Pediatric, Geriatric patient & Dysphasic patients so for that patients the suspension dosage form more favorable than other solid dosage form. Albendazole drug has poor oral bioavailability (5%) & a delayed release microspheric suspension of this drug would improve patient compliance & ease of swallowing. Microencapsulate facilitate the targeting of drug & mask the metallic taste of drug. The % yield was higher in the solvent evaporation method, in the spray drying the % yield was less that was drawback of the spray drying method. The % entrapment efficiency was good in the both method. Spray drying method is more reproducible than the solvent evaporation method. The stability study results show similar values as at the initial time. So, the formulation was stable and had no significant change in drug release profile & drug content on storage for a long time. So the suspension can effectively used for pediatric and geriatric patients. In vivo study will use for confirmatory study. 104 pp. Englisch. N° de réf. du vendeur 9783848401321
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Taschenbuch. Etat : Neu. Neuware -The present research works carried out with the aim to prepare suspension dosage form using these microparticles for oral use. Solid Dosage forms are difficult for Pediatric, Geriatric patient & Dysphasic patients so for that patients the suspension dosage form more favorable than other solid dosage form. Albendazole drug has poor oral bioavailability (>5%) & a delayed release microspheric suspension of this drug would improve patient compliance & ease of swallowing. Microencapsulate facilitate the targeting of drug & mask the metallic taste of drug. The % yield was higher in the solvent evaporation method, in the spray drying the % yield was less that was drawback of the spray drying method. The % entrapment efficiency was good in the both method. Spray drying method is more reproducible than the solvent evaporation method. The stability study results show similar values as at the initial time. So, the formulation was stable and had no significant change in drug release profile & drug content on storage for a long time. So the suspension can effectively used for pediatric and geriatric patients. In vivo study will use for confirmatory study.Books on Demand GmbH, Überseering 33, 22297 Hamburg 104 pp. Englisch. N° de réf. du vendeur 9783848401321
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