Please use this identifier to cite or link to this item: http://10.9.150.37:8080/dspace//handle/atmiyauni/1126
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dc.contributor.authorGarala, Kevin-
dc.contributor.authorShinde, Anil-
dc.contributor.authorShah, Pratik-
dc.date.accessioned2023-05-27T04:03:52Z-
dc.date.available2023-05-27T04:03:52Z-
dc.date.issued2009-12-
dc.identifier.citationGarala, Kevin & Shinde, Anilkumar & Shah, Pratik. (2009). Formulation and in-vitro characterization of monolithic matrix transdermal systems using HPMC/Eudragit S 100 polymer blends. International Journal of Pharmacy and Pharmaceutical Sciences. 1.en_US
dc.identifier.issn0975-1491-
dc.identifier.urihttp://10.9.150.37:8080/dspace//handle/atmiyauni/1126-
dc.description.abstractIn the present work, monolithic matrix transdermal systems containing tramadol HCl were prepared using various ratios of the polymer blends of hydroxy propyl methyl cellulose (HPMC) and Eudragit S 100 (ES) with triethyl citrate as a plasticizer. A 32 full factorial design was employed. The concentration of HPMC and ES were used as independent variables, while percentage drug release was selected as dependent variable. Physical evaluation was performed such as moisture content, moisture uptake, tensile strength, flatness and folding endurance. In-vitro diffusion studies were performed using cellulose acetate membrane (pore size 0.45 μ) in a Franz’s diffusion cell. The concentration of diffused drug was measured using UV-visible spectrophotometer (Jasco V-530) at λ max 272 nm. The experimental results shows that the transdermal drug delivery system (TDDS) containing ES in higher proportion gives sustained the release of drug.en_US
dc.language.isoenen_US
dc.publisherInternational Journal of Pharmacy and Pharmaceutical Sciencesen_US
dc.subjectHPMCen_US
dc.subjectEudragit S 100en_US
dc.subjectTramadol HClen_US
dc.subjectTransdermal Deliveryen_US
dc.titleFormulation and in-vitro characterization of monolithic matrix Transdermal systems using hpmc/eudragit s 100 polymer blendsen_US
dc.typeArticleen_US
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