pH-Sensitive polymer blends used as coating materials to control drug release from spherical beads: elucidation of the underlying mass transport mechanisms
To elucidate the drug release mechanisms from pellets coated with pH-sensitive polymer blends. Verapamil hydrochloride-loaded beads were coated with various blends of a water-insoluble and an enteric polymer, ethylcellulose:Eudragit L and Eudragit NE:Eudragit L, respectively. Both experimental and t...
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Veröffentlicht in: | Pharmaceutical research 2005-07, Vol.22 (7), p.1129-1141 |
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creator | Lecomte, Florence Siepmann, Juergen Walther, Mathias MacRae, Ross J Bodmeier, Roland |
description | To elucidate the drug release mechanisms from pellets coated with pH-sensitive polymer blends.
Verapamil hydrochloride-loaded beads were coated with various blends of a water-insoluble and an enteric polymer, ethylcellulose:Eudragit L and Eudragit NE:Eudragit L, respectively. Both experimental and theoretical techniques were used to characterize the systems before and upon exposure to 0.1 M HCl and phosphate buffer (pH 7.4).
Using analytical solutions of Fick's second law of diffusion, optical and scanning electron microscopy, and mechanical and gravimetric analysis, new insight into the underlying drug release mechanisms could be gained. More importantly, the latter can be effectively altered by varying the type of polymer blend and blend ratio. For example, at low pH drug release is primarily controlled by diffusion through the intact film coatings in Eudragit NE:Eudragit L blends, whereas crack formation is of major importance in ethylcellulose:Eudragit L-coated systems. At high pH, the (partial) leaching of the enteric polymer out of the coatings plays an important role. In all cases, the observed drug release profiles could be explained based on the occurring mass transport processes.
The obtained new knowledge can be used to effectively adjust desired drug release mechanisms and, thus, release patterns. |
doi_str_mv | 10.1007/s11095-005-5421-2 |
format | Article |
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Verapamil hydrochloride-loaded beads were coated with various blends of a water-insoluble and an enteric polymer, ethylcellulose:Eudragit L and Eudragit NE:Eudragit L, respectively. Both experimental and theoretical techniques were used to characterize the systems before and upon exposure to 0.1 M HCl and phosphate buffer (pH 7.4).
Using analytical solutions of Fick's second law of diffusion, optical and scanning electron microscopy, and mechanical and gravimetric analysis, new insight into the underlying drug release mechanisms could be gained. More importantly, the latter can be effectively altered by varying the type of polymer blend and blend ratio. For example, at low pH drug release is primarily controlled by diffusion through the intact film coatings in Eudragit NE:Eudragit L blends, whereas crack formation is of major importance in ethylcellulose:Eudragit L-coated systems. At high pH, the (partial) leaching of the enteric polymer out of the coatings plays an important role. In all cases, the observed drug release profiles could be explained based on the occurring mass transport processes.
The obtained new knowledge can be used to effectively adjust desired drug release mechanisms and, thus, release patterns.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1007/s11095-005-5421-2</identifier><identifier>PMID: 16028014</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Acrylic Resins - chemistry ; Cellulose - analogs & derivatives ; Cellulose - chemistry ; Delayed-Action Preparations - chemistry ; Drug Compounding ; Drug delivery systems ; Drug dosages ; Hydrogen-Ion Concentration ; Methacrylates - chemistry ; Microscopy, Electron, Scanning ; Permeability ; Pharmacy ; Polymer blends ; Polymers - chemistry ; Protective coatings ; Solubility ; Time Factors ; Verapamil - administration & dosage ; Verapamil - chemistry ; Water - analysis ; Water - chemistry</subject><ispartof>Pharmaceutical research, 2005-07, Vol.22 (7), p.1129-1141</ispartof><rights>Springer Science + Business Media, Inc. 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c326t-ad26745229a8986669bd1a834241ae8b956cdad7d9b40e4940599c252686a0903</citedby><cites>FETCH-LOGICAL-c326t-ad26745229a8986669bd1a834241ae8b956cdad7d9b40e4940599c252686a0903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16028014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lecomte, Florence</creatorcontrib><creatorcontrib>Siepmann, Juergen</creatorcontrib><creatorcontrib>Walther, Mathias</creatorcontrib><creatorcontrib>MacRae, Ross J</creatorcontrib><creatorcontrib>Bodmeier, Roland</creatorcontrib><title>pH-Sensitive polymer blends used as coating materials to control drug release from spherical beads: elucidation of the underlying mass transport mechanisms</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><description>To elucidate the drug release mechanisms from pellets coated with pH-sensitive polymer blends.
Verapamil hydrochloride-loaded beads were coated with various blends of a water-insoluble and an enteric polymer, ethylcellulose:Eudragit L and Eudragit NE:Eudragit L, respectively. Both experimental and theoretical techniques were used to characterize the systems before and upon exposure to 0.1 M HCl and phosphate buffer (pH 7.4).
Using analytical solutions of Fick's second law of diffusion, optical and scanning electron microscopy, and mechanical and gravimetric analysis, new insight into the underlying drug release mechanisms could be gained. More importantly, the latter can be effectively altered by varying the type of polymer blend and blend ratio. For example, at low pH drug release is primarily controlled by diffusion through the intact film coatings in Eudragit NE:Eudragit L blends, whereas crack formation is of major importance in ethylcellulose:Eudragit L-coated systems. At high pH, the (partial) leaching of the enteric polymer out of the coatings plays an important role. In all cases, the observed drug release profiles could be explained based on the occurring mass transport processes.
The obtained new knowledge can be used to effectively adjust desired drug release mechanisms and, thus, release patterns.</description><subject>Acrylic Resins - chemistry</subject><subject>Cellulose - analogs & derivatives</subject><subject>Cellulose - chemistry</subject><subject>Delayed-Action Preparations - chemistry</subject><subject>Drug Compounding</subject><subject>Drug delivery systems</subject><subject>Drug dosages</subject><subject>Hydrogen-Ion Concentration</subject><subject>Methacrylates - chemistry</subject><subject>Microscopy, Electron, Scanning</subject><subject>Permeability</subject><subject>Pharmacy</subject><subject>Polymer blends</subject><subject>Polymers - chemistry</subject><subject>Protective coatings</subject><subject>Solubility</subject><subject>Time Factors</subject><subject>Verapamil - administration & dosage</subject><subject>Verapamil - chemistry</subject><subject>Water - analysis</subject><subject>Water - chemistry</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkcGKFDEQQIMo7rj6AV4kePDWWkkn6Y43WdRdWPCggreQ7tTs9JJO2lS3MN_iz5plBhY8BYpXrwKPsdcC3guA7gMJAVY3ALrRSopGPmE7obu2saB-PWU76KRq-k6JC_aC6B4AemHVc3YhDMgehNqxv8t18x0TTev0B_mS43HGwoeIKRDfCAP3xMfs1ynd8dmvWCYfia-5DtNacuShbHe8YERPyPclz5yWQ8VGH_mAPtBHjnEbp1AdOfG85-sB-ZYClng8WakKi0-05LLyGceDTxPN9JI929dj-Or8XrKfXz7_uLpubr99vbn6dNuMrTRr44M0ndJSWt_b3hhjhyB83yqphMd-sNqMwYcu2EEBKqtAWztKLU1vPFhoL9m7k3cp-feGtLp5ohFj9AnzRs70oLVtTQXf_gfe562k-jcnZdW19X6FxAkaSyYquHdLmWZfjk6Ae8jmTtlczeYesjlZd96cxdswY3jcOHdq_wEKvZU6</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Lecomte, Florence</creator><creator>Siepmann, Juergen</creator><creator>Walther, Mathias</creator><creator>MacRae, Ross J</creator><creator>Bodmeier, Roland</creator><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20050701</creationdate><title>pH-Sensitive polymer blends used as coating materials to control drug release from spherical beads: elucidation of the underlying mass transport mechanisms</title><author>Lecomte, Florence ; Siepmann, Juergen ; Walther, Mathias ; MacRae, Ross J ; Bodmeier, Roland</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-ad26745229a8986669bd1a834241ae8b956cdad7d9b40e4940599c252686a0903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acrylic Resins - chemistry</topic><topic>Cellulose - analogs & derivatives</topic><topic>Cellulose - chemistry</topic><topic>Delayed-Action Preparations - chemistry</topic><topic>Drug Compounding</topic><topic>Drug delivery systems</topic><topic>Drug dosages</topic><topic>Hydrogen-Ion Concentration</topic><topic>Methacrylates - chemistry</topic><topic>Microscopy, Electron, Scanning</topic><topic>Permeability</topic><topic>Pharmacy</topic><topic>Polymer blends</topic><topic>Polymers - chemistry</topic><topic>Protective coatings</topic><topic>Solubility</topic><topic>Time Factors</topic><topic>Verapamil - administration & dosage</topic><topic>Verapamil - chemistry</topic><topic>Water - analysis</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lecomte, Florence</creatorcontrib><creatorcontrib>Siepmann, Juergen</creatorcontrib><creatorcontrib>Walther, Mathias</creatorcontrib><creatorcontrib>MacRae, Ross J</creatorcontrib><creatorcontrib>Bodmeier, Roland</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lecomte, Florence</au><au>Siepmann, Juergen</au><au>Walther, Mathias</au><au>MacRae, Ross J</au><au>Bodmeier, Roland</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>pH-Sensitive polymer blends used as coating materials to control drug release from spherical beads: elucidation of the underlying mass transport mechanisms</atitle><jtitle>Pharmaceutical research</jtitle><addtitle>Pharm Res</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>22</volume><issue>7</issue><spage>1129</spage><epage>1141</epage><pages>1129-1141</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><abstract>To elucidate the drug release mechanisms from pellets coated with pH-sensitive polymer blends.
Verapamil hydrochloride-loaded beads were coated with various blends of a water-insoluble and an enteric polymer, ethylcellulose:Eudragit L and Eudragit NE:Eudragit L, respectively. Both experimental and theoretical techniques were used to characterize the systems before and upon exposure to 0.1 M HCl and phosphate buffer (pH 7.4).
Using analytical solutions of Fick's second law of diffusion, optical and scanning electron microscopy, and mechanical and gravimetric analysis, new insight into the underlying drug release mechanisms could be gained. More importantly, the latter can be effectively altered by varying the type of polymer blend and blend ratio. For example, at low pH drug release is primarily controlled by diffusion through the intact film coatings in Eudragit NE:Eudragit L blends, whereas crack formation is of major importance in ethylcellulose:Eudragit L-coated systems. At high pH, the (partial) leaching of the enteric polymer out of the coatings plays an important role. In all cases, the observed drug release profiles could be explained based on the occurring mass transport processes.
The obtained new knowledge can be used to effectively adjust desired drug release mechanisms and, thus, release patterns.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>16028014</pmid><doi>10.1007/s11095-005-5421-2</doi><tpages>13</tpages></addata></record> |
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subjects | Acrylic Resins - chemistry Cellulose - analogs & derivatives Cellulose - chemistry Delayed-Action Preparations - chemistry Drug Compounding Drug delivery systems Drug dosages Hydrogen-Ion Concentration Methacrylates - chemistry Microscopy, Electron, Scanning Permeability Pharmacy Polymer blends Polymers - chemistry Protective coatings Solubility Time Factors Verapamil - administration & dosage Verapamil - chemistry Water - analysis Water - chemistry |
title | pH-Sensitive polymer blends used as coating materials to control drug release from spherical beads: elucidation of the underlying mass transport mechanisms |
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