Development of an Emulsion-Solvent Evaporation Technique for Microencapsulation of Drus-Resin complexes
Abstract Chlorpheniramine maleate was complexed with a carboxylic acid cation-exchange resin and the complexes were microencapsulated with polymethyl methacrylate using an emulsion-solvent evaporation technique. Microcapsules of larger mean diameters resulted from polymer solutions of increased visc...
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Veröffentlicht in: | Drug development and industrial pharmacy 1990, Vol.16 (2), p.361-376 |
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creator | Sprockel, Omar L. Price, James C. |
description | Abstract
Chlorpheniramine maleate was complexed with a carboxylic acid cation-exchange resin and the complexes were microencapsulated with polymethyl methacrylate using an emulsion-solvent evaporation technique. Microcapsules of larger mean diameters resulted from polymer solutions of increased viscosities. Addition of 3% finely divided solids to the encapsulation vehicle resulted in smaller microcapsules, whereas a 6% concentration had the opposite effect, an increased capsule mean diameter. Emulsion stabilizers, such as magnesium stearate, up to a 1% concentration reduced microcapsule size by as much as 50%. The process efficiency ranged from 73% to 99%, depending on the formulation and manufacturing conditions used. The rate of drug release from the microcapsules was directly related to the amount of polymer deposited and inversely proportional to the capsule size. |
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Chlorpheniramine maleate was complexed with a carboxylic acid cation-exchange resin and the complexes were microencapsulated with polymethyl methacrylate using an emulsion-solvent evaporation technique. Microcapsules of larger mean diameters resulted from polymer solutions of increased viscosities. Addition of 3% finely divided solids to the encapsulation vehicle resulted in smaller microcapsules, whereas a 6% concentration had the opposite effect, an increased capsule mean diameter. Emulsion stabilizers, such as magnesium stearate, up to a 1% concentration reduced microcapsule size by as much as 50%. The process efficiency ranged from 73% to 99%, depending on the formulation and manufacturing conditions used. The rate of drug release from the microcapsules was directly related to the amount of polymer deposited and inversely proportional to the capsule size.</description><identifier>ISSN: 0363-9045</identifier><identifier>EISSN: 1520-5762</identifier><identifier>DOI: 10.3109/03639049009114891</identifier><language>eng</language><publisher>Informa UK Ltd</publisher><ispartof>Drug development and industrial pharmacy, 1990, Vol.16 (2), p.361-376</ispartof><rights>1990 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1990</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c263t-5339ca2449dfb8a21a5959653ac22f5790fa2a77c77205bdc2548203e28a3c273</citedby><cites>FETCH-LOGICAL-c263t-5339ca2449dfb8a21a5959653ac22f5790fa2a77c77205bdc2548203e28a3c273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.3109/03639049009114891$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.3109/03639049009114891$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,780,784,4024,27923,27924,27925,59647,59753,60436,60542,61221,61256,61402,61437</link.rule.ids></links><search><creatorcontrib>Sprockel, Omar L.</creatorcontrib><creatorcontrib>Price, James C.</creatorcontrib><title>Development of an Emulsion-Solvent Evaporation Technique for Microencapsulation of Drus-Resin complexes</title><title>Drug development and industrial pharmacy</title><description>Abstract
Chlorpheniramine maleate was complexed with a carboxylic acid cation-exchange resin and the complexes were microencapsulated with polymethyl methacrylate using an emulsion-solvent evaporation technique. Microcapsules of larger mean diameters resulted from polymer solutions of increased viscosities. Addition of 3% finely divided solids to the encapsulation vehicle resulted in smaller microcapsules, whereas a 6% concentration had the opposite effect, an increased capsule mean diameter. Emulsion stabilizers, such as magnesium stearate, up to a 1% concentration reduced microcapsule size by as much as 50%. The process efficiency ranged from 73% to 99%, depending on the formulation and manufacturing conditions used. The rate of drug release from the microcapsules was directly related to the amount of polymer deposited and inversely proportional to the capsule size.</description><issn>0363-9045</issn><issn>1520-5762</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EEqXwAez8AwE_4iQWbFBbHlIREpR1NHVtmsqxg50U-vckKhuEYDXSnTkzcy9C55RccErkJeEZlySVhEhK00LSAzSigpFE5Bk7RKOhn_QD4hidxLghhDIpxAi9TfVWW9_U2rXYGwwOz-rOxsq75MXb7SDPttD4AG2v4YVWa1e9dxobH_BjpYLXTkETO7sf6HdMQxeTZx0rh5WvG6s_dTxFRwZs1GffdYxeb2eLyX0yf7p7mNzME8Uy3iaCc6mApalcmWUBjIKQQmaCg2LMiFwSAwzyXOU5I2K5UkykBSNcswK4YjkfI7rf2z8WY9CmbEJVQ9iVlJRDUuWvpHrmes9UrjdVw4cPdlW2sLM-mABOVXFA_8avfuBrDbZdKwi63PguuN7uP8e_ANmkgiQ</recordid><startdate>1990</startdate><enddate>1990</enddate><creator>Sprockel, Omar L.</creator><creator>Price, James C.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>1990</creationdate><title>Development of an Emulsion-Solvent Evaporation Technique for Microencapsulation of Drus-Resin complexes</title><author>Sprockel, Omar L. ; Price, James C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c263t-5339ca2449dfb8a21a5959653ac22f5790fa2a77c77205bdc2548203e28a3c273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sprockel, Omar L.</creatorcontrib><creatorcontrib>Price, James C.</creatorcontrib><collection>CrossRef</collection><jtitle>Drug development and industrial pharmacy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sprockel, Omar L.</au><au>Price, James C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of an Emulsion-Solvent Evaporation Technique for Microencapsulation of Drus-Resin complexes</atitle><jtitle>Drug development and industrial pharmacy</jtitle><date>1990</date><risdate>1990</risdate><volume>16</volume><issue>2</issue><spage>361</spage><epage>376</epage><pages>361-376</pages><issn>0363-9045</issn><eissn>1520-5762</eissn><abstract>Abstract
Chlorpheniramine maleate was complexed with a carboxylic acid cation-exchange resin and the complexes were microencapsulated with polymethyl methacrylate using an emulsion-solvent evaporation technique. Microcapsules of larger mean diameters resulted from polymer solutions of increased viscosities. Addition of 3% finely divided solids to the encapsulation vehicle resulted in smaller microcapsules, whereas a 6% concentration had the opposite effect, an increased capsule mean diameter. Emulsion stabilizers, such as magnesium stearate, up to a 1% concentration reduced microcapsule size by as much as 50%. The process efficiency ranged from 73% to 99%, depending on the formulation and manufacturing conditions used. The rate of drug release from the microcapsules was directly related to the amount of polymer deposited and inversely proportional to the capsule size.</abstract><pub>Informa UK Ltd</pub><doi>10.3109/03639049009114891</doi><tpages>16</tpages></addata></record> |
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title | Development of an Emulsion-Solvent Evaporation Technique for Microencapsulation of Drus-Resin complexes |
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