Characterization of a hot-melt fluid bed coating process for fine granules
The equipment modifications and process changes necessary to perform hot-melt particle coating in a fluid bed granulator are reviewed. A specific case is presented in which partially hydrogenated cottonseed oil is coated onto fine granules (mean particle size, 77 microns; range, 10-150 microns; one...
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Veröffentlicht in: | Pharmaceutical research 1990-11, Vol.7 (11), p.1119-1126 |
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description | The equipment modifications and process changes necessary to perform hot-melt particle coating in a fluid bed granulator are reviewed. A specific case is presented in which partially hydrogenated cottonseed oil is coated onto fine granules (mean particle size, 77 microns; range, 10-150 microns; one standard deviation is 10 microns) composed of a hydrophobic drug and sucrose. The major variables were product bed temperature, temperature of the wax, spray rate, and atomization air pressure. The product bed temperature was selected to give the optimum congealing rate, and the latter three variables were varied in a statistically designed experiment. The physical properties of wax-coated granules fabricated using combinations of process variables were examined. Response surface analysis was used to determine the optimum process settings in terms of dissolution, particle size, and density of the coated product. This system proved quite adequate for the production of uniformly coated granules, with the best product being obtained at the optimized conditions using 120 degrees C atomization air and molten coating temperature, 30 g/min as the spray rate, and an atomization air pressure of 5 bar. |
doi_str_mv | 10.1023/A:1015972007342 |
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Response surface analysis was used to determine the optimum process settings in terms of dissolution, particle size, and density of the coated product. This system proved quite adequate for the production of uniformly coated granules, with the best product being obtained at the optimized conditions using 120 degrees C atomization air and molten coating temperature, 30 g/min as the spray rate, and an atomization air pressure of 5 bar.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1023/A:1015972007342</identifier><identifier>PMID: 2293209</identifier><identifier>CODEN: PHREEB</identifier><language>eng</language><publisher>New York, NY: Springer</publisher><subject>Biological and medical sciences ; Capsules ; Chemistry, Pharmaceutical ; Chromatography, High Pressure Liquid ; Cottonseed Oil ; Drug Compounding ; Excipients ; General pharmacology ; Medical sciences ; Microscopy, Electron, Scanning ; Models, Biological ; Particle Size ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. 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M</creatorcontrib><creatorcontrib>FRANZ, R. M</creatorcontrib><title>Characterization of a hot-melt fluid bed coating process for fine granules</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><description>The equipment modifications and process changes necessary to perform hot-melt particle coating in a fluid bed granulator are reviewed. A specific case is presented in which partially hydrogenated cottonseed oil is coated onto fine granules (mean particle size, 77 microns; range, 10-150 microns; one standard deviation is 10 microns) composed of a hydrophobic drug and sucrose. The major variables were product bed temperature, temperature of the wax, spray rate, and atomization air pressure. The product bed temperature was selected to give the optimum congealing rate, and the latter three variables were varied in a statistically designed experiment. The physical properties of wax-coated granules fabricated using combinations of process variables were examined. Response surface analysis was used to determine the optimum process settings in terms of dissolution, particle size, and density of the coated product. This system proved quite adequate for the production of uniformly coated granules, with the best product being obtained at the optimized conditions using 120 degrees C atomization air and molten coating temperature, 30 g/min as the spray rate, and an atomization air pressure of 5 bar.</description><subject>Biological and medical sciences</subject><subject>Capsules</subject><subject>Chemistry, Pharmaceutical</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Cottonseed Oil</subject><subject>Drug Compounding</subject><subject>Excipients</subject><subject>General pharmacology</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Scanning</subject><subject>Models, Biological</subject><subject>Particle Size</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Regression Analysis</subject><subject>Technology, Pharmaceutical</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEtLxDAUhYMo4zi6diVko7vqvXk0iTsZfDLgRsFdSdNkptLH2LQL_fUGLK7u4vs4nHMJOUe4RmD85u4WAaVRDEBxwQ7IEqXimQHxcUiWoJjItBJ4TE5i_AQAjUYsyIIxwxmYJXlZ7-xg3eiH-seOdd_RPlBLd_2Ytb4ZaWimuqKlr6jrE--2dD_0zsdIQz_QUHeebgfbTY2Pp-Qo2Cb6s_muyPvD_dv6Kdu8Pj6v7zaZY5qNGQZfQV46CFxjJXleldqkomVpmTLCKpUjOmmM9hLRoHYuQEiyKJ1UCvmKXP3lpiZfk49j0dbR-aaxne-nWGhgKoXIJF7M4lS2vir2Q93a4buYxyd-OXMbnW1C2uHq-K-lT-VCcsl_AeOpZ8E</recordid><startdate>19901101</startdate><enddate>19901101</enddate><creator>JOZWIAKOWSKI, M. J</creator><creator>JONES, D. M</creator><creator>FRANZ, R. 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J</creatorcontrib><creatorcontrib>JONES, D. M</creatorcontrib><creatorcontrib>FRANZ, R. M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>JOZWIAKOWSKI, M. J</au><au>JONES, D. M</au><au>FRANZ, R. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of a hot-melt fluid bed coating process for fine granules</atitle><jtitle>Pharmaceutical research</jtitle><addtitle>Pharm Res</addtitle><date>1990-11-01</date><risdate>1990</risdate><volume>7</volume><issue>11</issue><spage>1119</spage><epage>1126</epage><pages>1119-1126</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><coden>PHREEB</coden><abstract>The equipment modifications and process changes necessary to perform hot-melt particle coating in a fluid bed granulator are reviewed. A specific case is presented in which partially hydrogenated cottonseed oil is coated onto fine granules (mean particle size, 77 microns; range, 10-150 microns; one standard deviation is 10 microns) composed of a hydrophobic drug and sucrose. The major variables were product bed temperature, temperature of the wax, spray rate, and atomization air pressure. The product bed temperature was selected to give the optimum congealing rate, and the latter three variables were varied in a statistically designed experiment. The physical properties of wax-coated granules fabricated using combinations of process variables were examined. Response surface analysis was used to determine the optimum process settings in terms of dissolution, particle size, and density of the coated product. This system proved quite adequate for the production of uniformly coated granules, with the best product being obtained at the optimized conditions using 120 degrees C atomization air and molten coating temperature, 30 g/min as the spray rate, and an atomization air pressure of 5 bar.</abstract><cop>New York, NY</cop><pub>Springer</pub><pmid>2293209</pmid><doi>10.1023/A:1015972007342</doi><tpages>8</tpages></addata></record> |
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subjects | Biological and medical sciences Capsules Chemistry, Pharmaceutical Chromatography, High Pressure Liquid Cottonseed Oil Drug Compounding Excipients General pharmacology Medical sciences Microscopy, Electron, Scanning Models, Biological Particle Size Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Regression Analysis Technology, Pharmaceutical |
title | Characterization of a hot-melt fluid bed coating process for fine granules |
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