Studies on the Development of Colon Targeted Oral Drug Delivery Systems for Ornidazole in the Treatment of Amoebiasis
The aim of the present study is to develop colon-targeted drug delivery sytems for ornidazole using guar gum as a carrier. The core formulation containing ornidazole was directly compressed. Compression-coated tablets of ornidazole containing various proportions of guar gum in the coat were prepared...
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Veröffentlicht in: | Drug delivery 2003, Vol.10 (2), p.111-117 |
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description | The aim of the present study is to develop colon-targeted drug delivery sytems for ornidazole using guar gum as a carrier. The core formulation containing ornidazole was directly compressed. Compression-coated tablets of ornidazole containing various proportions of guar gum in the coat were prepared. All the formulations were evaluated for hardness and drug content uniformity and were subjected to in vitro drug release studies. The amount of ornidazole released from tablets at different time intervals was estimated by the HPLC method. The compression-coated formulations released less than 8% of ornidazole in the physiological environment of stomach and small intestine. The compression-coated tablets with 85%, 75%, and 65% of guar gum coat released about 21%, 38%, and 73% of ornidazole, respectively, in simulated colonic fluids indicating the susceptibility of the guar gum formulations to the rat caecal contents. The results of the study show that compression-coated ornidazole tablets with either 65% (OLV-65) or 75% (OLV-75) of guar gum coat are most likely to provide targeting of ornidazole for local action in the colon owing to its minimal release of the drug in the first 5 hr. The ornidazole compression-coated tablets showed no change in physical appearance, drug content, or in dissolution pattern after storage at 40°C/75% relative humidity for 6 months. |
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S. R. ; Muzib, Y. Indira ; Rao, G. Srinivasa ; Bhaskar, P. ; Satyanarayana, V.</creator><creatorcontrib>Krishnaiah, Y. S. R. ; Muzib, Y. Indira ; Rao, G. Srinivasa ; Bhaskar, P. ; Satyanarayana, V.</creatorcontrib><description>The aim of the present study is to develop colon-targeted drug delivery sytems for ornidazole using guar gum as a carrier. The core formulation containing ornidazole was directly compressed. Compression-coated tablets of ornidazole containing various proportions of guar gum in the coat were prepared. All the formulations were evaluated for hardness and drug content uniformity and were subjected to in vitro drug release studies. The amount of ornidazole released from tablets at different time intervals was estimated by the HPLC method. The compression-coated formulations released less than 8% of ornidazole in the physiological environment of stomach and small intestine. The compression-coated tablets with 85%, 75%, and 65% of guar gum coat released about 21%, 38%, and 73% of ornidazole, respectively, in simulated colonic fluids indicating the susceptibility of the guar gum formulations to the rat caecal contents. The results of the study show that compression-coated ornidazole tablets with either 65% (OLV-65) or 75% (OLV-75) of guar gum coat are most likely to provide targeting of ornidazole for local action in the colon owing to its minimal release of the drug in the first 5 hr. The ornidazole compression-coated tablets showed no change in physical appearance, drug content, or in dissolution pattern after storage at 40°C/75% relative humidity for 6 months.</description><identifier>ISSN: 0049-8254</identifier><identifier>ISSN: 1071-7544</identifier><identifier>EISSN: 1366-5928</identifier><identifier>EISSN: 1521-0464</identifier><identifier>DOI: 10.1080/713840359</identifier><identifier>PMID: 12746057</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Administration, Oral ; Amebiasis - drug therapy ; Animals ; Cecum - drug effects ; Cecum - metabolism ; Colon - drug effects ; Colon - metabolism ; Colon Targeted ; Compression Coating ; Delayed-Action Preparations ; Drug Carriers ; Drug Delivery Systems ; Drug Stability ; Excipients ; Galactans - administration & dosage ; Galactans - economics ; Galactans - pharmacokinetics ; Guar Gum ; Hardness Tests ; In Vitro Dissolution ; Male ; Mannans - administration & dosage ; Mannans - economics ; Mannans - pharmacokinetics ; Ornidazole ; Ornidazole - administration & dosage ; Ornidazole - chemistry ; Ornidazole - pharmacokinetics ; Plant Gums ; Rats ; Tablets, Enteric-Coated</subject><ispartof>Drug delivery, 2003, Vol.10 (2), p.111-117</ispartof><rights>2003 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-2c0952c3c4974b15bb8ca0537cdd62dfcbe470044b354a97e56bc4893b683fdb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/713840359$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/713840359$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,776,780,4010,27900,27901,27902,59620,60409,61194,61229,61375,61410</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12746057$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krishnaiah, Y. S. R.</creatorcontrib><creatorcontrib>Muzib, Y. Indira</creatorcontrib><creatorcontrib>Rao, G. Srinivasa</creatorcontrib><creatorcontrib>Bhaskar, P.</creatorcontrib><creatorcontrib>Satyanarayana, V.</creatorcontrib><title>Studies on the Development of Colon Targeted Oral Drug Delivery Systems for Ornidazole in the Treatment of Amoebiasis</title><title>Drug delivery</title><addtitle>Drug Deliv</addtitle><description>The aim of the present study is to develop colon-targeted drug delivery sytems for ornidazole using guar gum as a carrier. The core formulation containing ornidazole was directly compressed. Compression-coated tablets of ornidazole containing various proportions of guar gum in the coat were prepared. All the formulations were evaluated for hardness and drug content uniformity and were subjected to in vitro drug release studies. The amount of ornidazole released from tablets at different time intervals was estimated by the HPLC method. The compression-coated formulations released less than 8% of ornidazole in the physiological environment of stomach and small intestine. The compression-coated tablets with 85%, 75%, and 65% of guar gum coat released about 21%, 38%, and 73% of ornidazole, respectively, in simulated colonic fluids indicating the susceptibility of the guar gum formulations to the rat caecal contents. The results of the study show that compression-coated ornidazole tablets with either 65% (OLV-65) or 75% (OLV-75) of guar gum coat are most likely to provide targeting of ornidazole for local action in the colon owing to its minimal release of the drug in the first 5 hr. The ornidazole compression-coated tablets showed no change in physical appearance, drug content, or in dissolution pattern after storage at 40°C/75% relative humidity for 6 months.</description><subject>Administration, Oral</subject><subject>Amebiasis - drug therapy</subject><subject>Animals</subject><subject>Cecum - drug effects</subject><subject>Cecum - metabolism</subject><subject>Colon - drug effects</subject><subject>Colon - metabolism</subject><subject>Colon Targeted</subject><subject>Compression Coating</subject><subject>Delayed-Action Preparations</subject><subject>Drug Carriers</subject><subject>Drug Delivery Systems</subject><subject>Drug Stability</subject><subject>Excipients</subject><subject>Galactans - administration & dosage</subject><subject>Galactans - economics</subject><subject>Galactans - pharmacokinetics</subject><subject>Guar Gum</subject><subject>Hardness Tests</subject><subject>In Vitro Dissolution</subject><subject>Male</subject><subject>Mannans - administration & dosage</subject><subject>Mannans - economics</subject><subject>Mannans - pharmacokinetics</subject><subject>Ornidazole</subject><subject>Ornidazole - administration & dosage</subject><subject>Ornidazole - chemistry</subject><subject>Ornidazole - pharmacokinetics</subject><subject>Plant Gums</subject><subject>Rats</subject><subject>Tablets, Enteric-Coated</subject><issn>0049-8254</issn><issn>1071-7544</issn><issn>1366-5928</issn><issn>1521-0464</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi1ERbeFA38A-YTEIeBvJ8dqCwWpUg_dni3bmXRdOfFiO0XLryewCwipEqc5zDOPZt5B6DUl7ylpyQdNeSsIl90ztKJcqUZ2rH2OVoSIrmmZFKforJQHQoiijL1Ap5RpoYjUKzTf1rkPUHCacN0CvoRHiGk3wlRxGvA6xaWxsfkeKvT4JtuIL_N8v3AxPELe49t9qTAWPKS8tKfQ2-8pAg4H3SaDrb9lF2MCF2wJ5SU6GWws8OpYz9Hdp4-b9efm-ubqy_riuvGCq9owTzrJPPei08JR6VzrLZFc-75XrB-8A6GXI4XjUthOg1TOi7bjTrV86B0_R28P3l1OX2co1YyheIjRTpDmYjRnSkum_wtSLalQv8B3B9DnVEqGwexyGG3eG0rMz2eYP89Y2DdH6exG6P-Sx_QXQByAMC3xjfZbyrE31e5jykO2kw_F8Ke8_J-xLdhYt95mMA9pztOS6BPb_AAth6aO</recordid><startdate>2003</startdate><enddate>2003</enddate><creator>Krishnaiah, Y. S. R.</creator><creator>Muzib, Y. Indira</creator><creator>Rao, G. Srinivasa</creator><creator>Bhaskar, P.</creator><creator>Satyanarayana, V.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>2003</creationdate><title>Studies on the Development of Colon Targeted Oral Drug Delivery Systems for Ornidazole in the Treatment of Amoebiasis</title><author>Krishnaiah, Y. S. R. ; Muzib, Y. Indira ; Rao, G. Srinivasa ; Bhaskar, P. ; Satyanarayana, V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-2c0952c3c4974b15bb8ca0537cdd62dfcbe470044b354a97e56bc4893b683fdb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Administration, Oral</topic><topic>Amebiasis - drug therapy</topic><topic>Animals</topic><topic>Cecum - drug effects</topic><topic>Cecum - metabolism</topic><topic>Colon - drug effects</topic><topic>Colon - metabolism</topic><topic>Colon Targeted</topic><topic>Compression Coating</topic><topic>Delayed-Action Preparations</topic><topic>Drug Carriers</topic><topic>Drug Delivery Systems</topic><topic>Drug Stability</topic><topic>Excipients</topic><topic>Galactans - administration & dosage</topic><topic>Galactans - economics</topic><topic>Galactans - pharmacokinetics</topic><topic>Guar Gum</topic><topic>Hardness Tests</topic><topic>In Vitro Dissolution</topic><topic>Male</topic><topic>Mannans - administration & dosage</topic><topic>Mannans - economics</topic><topic>Mannans - pharmacokinetics</topic><topic>Ornidazole</topic><topic>Ornidazole - administration & dosage</topic><topic>Ornidazole - chemistry</topic><topic>Ornidazole - pharmacokinetics</topic><topic>Plant Gums</topic><topic>Rats</topic><topic>Tablets, Enteric-Coated</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krishnaiah, Y. S. R.</creatorcontrib><creatorcontrib>Muzib, Y. Indira</creatorcontrib><creatorcontrib>Rao, G. Srinivasa</creatorcontrib><creatorcontrib>Bhaskar, P.</creatorcontrib><creatorcontrib>Satyanarayana, V.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Drug delivery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krishnaiah, Y. S. R.</au><au>Muzib, Y. Indira</au><au>Rao, G. Srinivasa</au><au>Bhaskar, P.</au><au>Satyanarayana, V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies on the Development of Colon Targeted Oral Drug Delivery Systems for Ornidazole in the Treatment of Amoebiasis</atitle><jtitle>Drug delivery</jtitle><addtitle>Drug Deliv</addtitle><date>2003</date><risdate>2003</risdate><volume>10</volume><issue>2</issue><spage>111</spage><epage>117</epage><pages>111-117</pages><issn>0049-8254</issn><issn>1071-7544</issn><eissn>1366-5928</eissn><eissn>1521-0464</eissn><abstract>The aim of the present study is to develop colon-targeted drug delivery sytems for ornidazole using guar gum as a carrier. The core formulation containing ornidazole was directly compressed. Compression-coated tablets of ornidazole containing various proportions of guar gum in the coat were prepared. All the formulations were evaluated for hardness and drug content uniformity and were subjected to in vitro drug release studies. The amount of ornidazole released from tablets at different time intervals was estimated by the HPLC method. The compression-coated formulations released less than 8% of ornidazole in the physiological environment of stomach and small intestine. The compression-coated tablets with 85%, 75%, and 65% of guar gum coat released about 21%, 38%, and 73% of ornidazole, respectively, in simulated colonic fluids indicating the susceptibility of the guar gum formulations to the rat caecal contents. The results of the study show that compression-coated ornidazole tablets with either 65% (OLV-65) or 75% (OLV-75) of guar gum coat are most likely to provide targeting of ornidazole for local action in the colon owing to its minimal release of the drug in the first 5 hr. The ornidazole compression-coated tablets showed no change in physical appearance, drug content, or in dissolution pattern after storage at 40°C/75% relative humidity for 6 months.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>12746057</pmid><doi>10.1080/713840359</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Amebiasis - drug therapy Animals Cecum - drug effects Cecum - metabolism Colon - drug effects Colon - metabolism Colon Targeted Compression Coating Delayed-Action Preparations Drug Carriers Drug Delivery Systems Drug Stability Excipients Galactans - administration & dosage Galactans - economics Galactans - pharmacokinetics Guar Gum Hardness Tests In Vitro Dissolution Male Mannans - administration & dosage Mannans - economics Mannans - pharmacokinetics Ornidazole Ornidazole - administration & dosage Ornidazole - chemistry Ornidazole - pharmacokinetics Plant Gums Rats Tablets, Enteric-Coated |
title | Studies on the Development of Colon Targeted Oral Drug Delivery Systems for Ornidazole in the Treatment of Amoebiasis |
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