FORMULATION AND IN VITROEVALUATION OF FLOATING TABLETS OF CEFPODOXIME PROXETIL
Objective: The objective of research work was to formulate and evaluate the floating drug delivery system containing Cefpodoxime Proxetil using polymer HPMC K4M, Guar Gum.Methods: Effervescent floating tablets containing Cefpodoxime proxetil were prepared by direct compression technique using varyin...
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Veröffentlicht in: | International journal of current pharmaceutical research 2017-11, Vol.9 (6), p.18 |
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creator | Tekade, Bharat W. Jadhao, Umesh T. Patil, Shruti G. Patil, Vijay R. |
description | Objective: The objective of research work was to formulate and evaluate the floating drug delivery system containing Cefpodoxime Proxetil using polymer HPMC K4M, Guar Gum.Methods: Effervescent floating tablets containing Cefpodoxime proxetil were prepared by direct compression technique using varying concentrations of different grades of polymer.Results: Physical parameters like hardness, weight variation, thickness and friability were within pharmacopoeial limit. Percentage drug content in all floating tablet formulations was found to be 90% to 110%. The floating time was found to be more than 12 H. floating lag time was found to be 10±2.99 second. Formulation batch F8 was selected as an optimum formulation, as possessing less disintegration time, higher water absorption ratio and good content uniformity i.e. within acceptable limit.% drug release of formulation batch F8 was found to be 96.66% in 0.1 N HCL.Conclusion: The FT-IR studies of batch F8 was carried out which showed the peak values within the spectrum corresponding to the peak values of pure drug. |
doi_str_mv | 10.22159/ijcpr.2017v9i6.23422 |
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Percentage drug content in all floating tablet formulations was found to be 90% to 110%. The floating time was found to be more than 12 H. floating lag time was found to be 10±2.99 second. Formulation batch F8 was selected as an optimum formulation, as possessing less disintegration time, higher water absorption ratio and good content uniformity i.e. within acceptable limit.% drug release of formulation batch F8 was found to be 96.66% in 0.1 N HCL.Conclusion: The FT-IR studies of batch F8 was carried out which showed the peak values within the spectrum corresponding to the peak values of pure drug.</description><identifier>ISSN: 0975-7066</identifier><identifier>EISSN: 0975-7066</identifier><identifier>DOI: 10.22159/ijcpr.2017v9i6.23422</identifier><language>eng</language><ispartof>International journal of current pharmaceutical research, 2017-11, Vol.9 (6), p.18</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Tekade, Bharat W.</creatorcontrib><creatorcontrib>Jadhao, Umesh T.</creatorcontrib><creatorcontrib>Patil, Shruti G.</creatorcontrib><creatorcontrib>Patil, Vijay R.</creatorcontrib><title>FORMULATION AND IN VITROEVALUATION OF FLOATING TABLETS OF CEFPODOXIME PROXETIL</title><title>International journal of current pharmaceutical research</title><description>Objective: The objective of research work was to formulate and evaluate the floating drug delivery system containing Cefpodoxime Proxetil using polymer HPMC K4M, Guar Gum.Methods: Effervescent floating tablets containing Cefpodoxime proxetil were prepared by direct compression technique using varying concentrations of different grades of polymer.Results: Physical parameters like hardness, weight variation, thickness and friability were within pharmacopoeial limit. Percentage drug content in all floating tablet formulations was found to be 90% to 110%. The floating time was found to be more than 12 H. floating lag time was found to be 10±2.99 second. Formulation batch F8 was selected as an optimum formulation, as possessing less disintegration time, higher water absorption ratio and good content uniformity i.e. within acceptable limit.% drug release of formulation batch F8 was found to be 96.66% in 0.1 N HCL.Conclusion: The FT-IR studies of batch F8 was carried out which showed the peak values within the spectrum corresponding to the peak values of pure drug.</description><issn>0975-7066</issn><issn>0975-7066</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqdjtEKwiAARSUKGtUnBP7Allqb7XGVlmAay2JvMqJgURQKQX9frYKee7qHAxcOAH2MIkJwnA6q4-7qIoIwvaVVEpHhiJAGCFBK45CiJGn-cBv0vD8ihAimKU3GAVBc58uNzIzQCmZqBoWCW2FyzbaZ3Ly15pBL_WQ1hyabSGbWLzdlfKVnuhBLBle5LpgRsgtah_Lk973PdkDMmZkuwp27eO_2B3t11bl0d4uRrftt3W-__bbuH_77ewAdg0tE</recordid><startdate>20171114</startdate><enddate>20171114</enddate><creator>Tekade, Bharat W.</creator><creator>Jadhao, Umesh T.</creator><creator>Patil, Shruti G.</creator><creator>Patil, Vijay R.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20171114</creationdate><title>FORMULATION AND IN VITROEVALUATION OF FLOATING TABLETS OF CEFPODOXIME PROXETIL</title><author>Tekade, Bharat W. ; Jadhao, Umesh T. ; Patil, Shruti G. ; Patil, Vijay R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-crossref_primary_10_22159_ijcpr_2017v9i6_234223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Tekade, Bharat W.</creatorcontrib><creatorcontrib>Jadhao, Umesh T.</creatorcontrib><creatorcontrib>Patil, Shruti G.</creatorcontrib><creatorcontrib>Patil, Vijay R.</creatorcontrib><collection>CrossRef</collection><jtitle>International journal of current pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tekade, Bharat W.</au><au>Jadhao, Umesh T.</au><au>Patil, Shruti G.</au><au>Patil, Vijay R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FORMULATION AND IN VITROEVALUATION OF FLOATING TABLETS OF CEFPODOXIME PROXETIL</atitle><jtitle>International journal of current pharmaceutical research</jtitle><date>2017-11-14</date><risdate>2017</risdate><volume>9</volume><issue>6</issue><spage>18</spage><pages>18-</pages><issn>0975-7066</issn><eissn>0975-7066</eissn><abstract>Objective: The objective of research work was to formulate and evaluate the floating drug delivery system containing Cefpodoxime Proxetil using polymer HPMC K4M, Guar Gum.Methods: Effervescent floating tablets containing Cefpodoxime proxetil were prepared by direct compression technique using varying concentrations of different grades of polymer.Results: Physical parameters like hardness, weight variation, thickness and friability were within pharmacopoeial limit. Percentage drug content in all floating tablet formulations was found to be 90% to 110%. The floating time was found to be more than 12 H. floating lag time was found to be 10±2.99 second. Formulation batch F8 was selected as an optimum formulation, as possessing less disintegration time, higher water absorption ratio and good content uniformity i.e. within acceptable limit.% drug release of formulation batch F8 was found to be 96.66% in 0.1 N HCL.Conclusion: The FT-IR studies of batch F8 was carried out which showed the peak values within the spectrum corresponding to the peak values of pure drug.</abstract><doi>10.22159/ijcpr.2017v9i6.23422</doi></addata></record> |
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