A novel colonic drug delivery system of ibuprofen
The present endeavor was directed towards fabrication of the novel colonic drug delivery system of ibuprofen. To begin with, the hydroxypropyl methylcellulose capsules containing adsorbate of eutectic mixture of ibuprofen and menthol and pregelatinized starch were coated with ethyl cellulose. These...
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Veröffentlicht in: | Asian journal of pharmaceutics 2009-07, Vol.3 (3), p.233 |
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description | The present endeavor was directed towards fabrication of the novel colonic drug delivery system of ibuprofen. To begin with, the hydroxypropyl methylcellulose capsules containing adsorbate of eutectic mixture of ibuprofen and menthol and pregelatinized starch were coated with ethyl cellulose. These ethyl cellulose coated capsules were filled in another capsule and the capsules were coated with a Eudragit ; S100. The in vitro drug release study was conducted using sequential dissolution technique at pH 1.2 (two hour), 6.0 (1hr), 7.2 (two hour) and 6.4 (three hour) mimicking different regions of gastrointestinal tract. The optimized batch with two per cent and 6.5% weight gain of ethyl cellulose and Eudragit ; S100 showed less than eight per cent drug release in stomach and intestinal pH. The remaining 92% drug release was obtained thereafter from the optimized batch within two hours in colonic pH. Scanning electron microscopy study of the optimized batch confirmed presence of ibuprofen crystals (rod shape) in the formulation. The infrared spectroscopy study of the optimized batch indicated stability of ibuprofen during processing of the formulation. |
doi_str_mv | 10.4103/0973-8398.56304 |
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To begin with, the hydroxypropyl methylcellulose capsules containing adsorbate of eutectic mixture of ibuprofen and menthol and pregelatinized starch were coated with ethyl cellulose. These ethyl cellulose coated capsules were filled in another capsule and the capsules were coated with a Eudragit ; S100. The in vitro drug release study was conducted using sequential dissolution technique at pH 1.2 (two hour), 6.0 (1hr), 7.2 (two hour) and 6.4 (three hour) mimicking different regions of gastrointestinal tract. The optimized batch with two per cent and 6.5% weight gain of ethyl cellulose and Eudragit ; S100 showed less than eight per cent drug release in stomach and intestinal pH. The remaining 92% drug release was obtained thereafter from the optimized batch within two hours in colonic pH. Scanning electron microscopy study of the optimized batch confirmed presence of ibuprofen crystals (rod shape) in the formulation. The infrared spectroscopy study of the optimized batch indicated stability of ibuprofen during processing of the formulation.</description><identifier>ISSN: 0973-8398</identifier><identifier>EISSN: 1998-409X</identifier><identifier>DOI: 10.4103/0973-8398.56304</identifier><language>eng</language><publisher>Mandsaur: Medknow Publications and Media Pvt. Ltd</publisher><subject>Chemical properties ; Colon ; Dosage and administration ; Drug delivery systems ; Drug therapy ; Drugs ; Ibuprofen ; Inflammatory bowel disease ; Methods ; Methylcellulose ; Scanning electron microscopy ; Scholarships & fellowships ; Vehicles</subject><ispartof>Asian journal of pharmaceutics, 2009-07, Vol.3 (3), p.233</ispartof><rights>COPYRIGHT 2009 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications & Media Pvt Ltd Jul 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c296t-3874eb482acb5d59003bbea07cf815b1522f7a4b23ef2b5fc0a62d4072e6f6303</citedby></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>Gohel, MC</creatorcontrib><creatorcontrib>Nagori, SA</creatorcontrib><title>A novel colonic drug delivery system of ibuprofen</title><title>Asian journal of pharmaceutics</title><description>The present endeavor was directed towards fabrication of the novel colonic drug delivery system of ibuprofen. To begin with, the hydroxypropyl methylcellulose capsules containing adsorbate of eutectic mixture of ibuprofen and menthol and pregelatinized starch were coated with ethyl cellulose. These ethyl cellulose coated capsules were filled in another capsule and the capsules were coated with a Eudragit ; S100. The in vitro drug release study was conducted using sequential dissolution technique at pH 1.2 (two hour), 6.0 (1hr), 7.2 (two hour) and 6.4 (three hour) mimicking different regions of gastrointestinal tract. The optimized batch with two per cent and 6.5% weight gain of ethyl cellulose and Eudragit ; S100 showed less than eight per cent drug release in stomach and intestinal pH. The remaining 92% drug release was obtained thereafter from the optimized batch within two hours in colonic pH. Scanning electron microscopy study of the optimized batch confirmed presence of ibuprofen crystals (rod shape) in the formulation. The infrared spectroscopy study of the optimized batch indicated stability of ibuprofen during processing of the formulation.</description><subject>Chemical properties</subject><subject>Colon</subject><subject>Dosage and administration</subject><subject>Drug delivery systems</subject><subject>Drug therapy</subject><subject>Drugs</subject><subject>Ibuprofen</subject><subject>Inflammatory bowel disease</subject><subject>Methods</subject><subject>Methylcellulose</subject><subject>Scanning electron microscopy</subject><subject>Scholarships & fellowships</subject><subject>Vehicles</subject><issn>0973-8398</issn><issn>1998-409X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNo9kEtLAzEUhYMoWKtrt0HX0948JpMsS_EFBTcK7kKSScqU6aQmM4X-e2esuLqL-3EO50PonsCCE2BLUBUrJFNyUQoG_ALNiFKy4KC-LtHs_3uNbnLeAQjBFMwQWeEuHn2LXWxj1zhcp2GLa982R59OOJ9y7_c4BtzY4ZBi8N0tugqmzf7u787R5_PTx_q12Ly_vK1Xm8JRJfqCyYp7yyU1zpZ1qQCYtd5A5YIkpSUlpaEy3FLmA7VlcGAErTlU1IswDmBz9HDOHWu_B597vYtD6sZKLcW4hkE1QY9naGtar5suxD4Zt2-y0ysKiiuhKBmp5ZlyKeacfNCH1OxNOmkCepKnJz160qN_5bEfCuRfXg</recordid><startdate>20090701</startdate><enddate>20090701</enddate><creator>Gohel, MC</creator><creator>Nagori, SA</creator><general>Medknow Publications and Media Pvt. 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To begin with, the hydroxypropyl methylcellulose capsules containing adsorbate of eutectic mixture of ibuprofen and menthol and pregelatinized starch were coated with ethyl cellulose. These ethyl cellulose coated capsules were filled in another capsule and the capsules were coated with a Eudragit ; S100. The in vitro drug release study was conducted using sequential dissolution technique at pH 1.2 (two hour), 6.0 (1hr), 7.2 (two hour) and 6.4 (three hour) mimicking different regions of gastrointestinal tract. The optimized batch with two per cent and 6.5% weight gain of ethyl cellulose and Eudragit ; S100 showed less than eight per cent drug release in stomach and intestinal pH. The remaining 92% drug release was obtained thereafter from the optimized batch within two hours in colonic pH. Scanning electron microscopy study of the optimized batch confirmed presence of ibuprofen crystals (rod shape) in the formulation. The infrared spectroscopy study of the optimized batch indicated stability of ibuprofen during processing of the formulation.</abstract><cop>Mandsaur</cop><pub>Medknow Publications and Media Pvt. Ltd</pub><doi>10.4103/0973-8398.56304</doi></addata></record> |
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source | EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Chemical properties Colon Dosage and administration Drug delivery systems Drug therapy Drugs Ibuprofen Inflammatory bowel disease Methods Methylcellulose Scanning electron microscopy Scholarships & fellowships Vehicles |
title | A novel colonic drug delivery system of ibuprofen |
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