Curing of aqueous polymeric film coatings: Importance of the coating level and type of plasticizer
The aim of this study was to better understand the effects of the curing conditions on the resulting drug release patterns from pellets coated with aqueous polymer dispersions. Diltiazem HCl was used as model drug, ethylcellulose as polymer, triethyl citrate (TEC), dibutyl sebacate (DBS), and distil...
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Veröffentlicht in: | European journal of pharmaceutics and biopharmaceutics 2010-02, Vol.74 (2), p.362-370 |
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description | The aim of this study was to better understand the effects of the curing conditions on the resulting drug release patterns from pellets coated with aqueous polymer dispersions. Diltiazem HCl was used as model drug, ethylcellulose as polymer, triethyl citrate (TEC), dibutyl sebacate (DBS), and distilled acetylated monoglycerides (Myvacet) as plasticizers. Interestingly, the effects of the curing conditions strongly depended on the coating level and the type of plasticizer: in the case of TEC, the drug release rate monotonically decreased with increasing harshness of the curing conditions (time, temperature, and relative humidity), irrespective of the coating level. In contrast, in the case of DBS and Myvacet, this type of relationship was only observed at low coating levels (5%). At intermediate coating levels (around 7.5%), the curing conditions had virtually no effect on drug release. At high coating levels (⩾10%), the release rate initially increased and then decreased with increasing harshness of the curing conditions. This more complex behavior might be attributable to the superposition of two competing phenomena: improved film formation and drug migration into the polymeric membrane. Furthermore, it could be shown that the type of plasticizer had a major effect on drug release in not fully coalesced and equilibrated film coatings, whereas the release profiles were similar for all plasticizers in the case of completely formed and equilibrated film coatings. Importantly, the latter systems were stable for long term even during storage under stress conditions. |
doi_str_mv | 10.1016/j.ejpb.2009.10.007 |
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Diltiazem HCl was used as model drug, ethylcellulose as polymer, triethyl citrate (TEC), dibutyl sebacate (DBS), and distilled acetylated monoglycerides (Myvacet) as plasticizers. Interestingly, the effects of the curing conditions strongly depended on the coating level and the type of plasticizer: in the case of TEC, the drug release rate monotonically decreased with increasing harshness of the curing conditions (time, temperature, and relative humidity), irrespective of the coating level. In contrast, in the case of DBS and Myvacet, this type of relationship was only observed at low coating levels (5%). At intermediate coating levels (around 7.5%), the curing conditions had virtually no effect on drug release. At high coating levels (⩾10%), the release rate initially increased and then decreased with increasing harshness of the curing conditions. This more complex behavior might be attributable to the superposition of two competing phenomena: improved film formation and drug migration into the polymeric membrane. Furthermore, it could be shown that the type of plasticizer had a major effect on drug release in not fully coalesced and equilibrated film coatings, whereas the release profiles were similar for all plasticizers in the case of completely formed and equilibrated film coatings. Importantly, the latter systems were stable for long term even during storage under stress conditions.</description><identifier>ISSN: 0939-6411</identifier><identifier>EISSN: 1873-3441</identifier><identifier>DOI: 10.1016/j.ejpb.2009.10.007</identifier><identifier>PMID: 19895886</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Aqueous ethylcellulose dispersion ; Biological and medical sciences ; Cellulose - analogs & derivatives ; Cellulose - chemistry ; Coating ; Curing ; Diltiazem - pharmacokinetics ; Drug Compounding - methods ; Drug Implants - chemical synthesis ; Drug Implants - chemistry ; Drug Implants - pharmacokinetics ; Drug Stability ; Drug Storage ; Emulsifying Agents - chemistry ; General pharmacology ; Humidity ; In Vitro Techniques ; Medical sciences ; Pellets ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Plasticizer ; Plasticizers - chemistry ; Plasticizers - pharmacokinetics ; Polymers - chemistry ; Polymers - pharmacokinetics ; Surface Properties ; Temperature ; Time Factors ; Wettability</subject><ispartof>European journal of pharmaceutics and biopharmaceutics, 2010-02, Vol.74 (2), p.362-370</ispartof><rights>2009 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright (c) 2009 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-c7717654f7895396927e36ecff5b7ef1a39518f2ac6a36cda4bd3490ced5a0423</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejpb.2009.10.007$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22509793$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19895886$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Q.W.</creatorcontrib><creatorcontrib>Flament, M.P.</creatorcontrib><creatorcontrib>Siepmann, F.</creatorcontrib><creatorcontrib>Busignies, V.</creatorcontrib><creatorcontrib>Leclerc, B.</creatorcontrib><creatorcontrib>Herry, C.</creatorcontrib><creatorcontrib>Tchoreloff, P.</creatorcontrib><creatorcontrib>Siepmann, J.</creatorcontrib><title>Curing of aqueous polymeric film coatings: Importance of the coating level and type of plasticizer</title><title>European journal of pharmaceutics and biopharmaceutics</title><addtitle>Eur J Pharm Biopharm</addtitle><description>The aim of this study was to better understand the effects of the curing conditions on the resulting drug release patterns from pellets coated with aqueous polymer dispersions. Diltiazem HCl was used as model drug, ethylcellulose as polymer, triethyl citrate (TEC), dibutyl sebacate (DBS), and distilled acetylated monoglycerides (Myvacet) as plasticizers. Interestingly, the effects of the curing conditions strongly depended on the coating level and the type of plasticizer: in the case of TEC, the drug release rate monotonically decreased with increasing harshness of the curing conditions (time, temperature, and relative humidity), irrespective of the coating level. In contrast, in the case of DBS and Myvacet, this type of relationship was only observed at low coating levels (5%). At intermediate coating levels (around 7.5%), the curing conditions had virtually no effect on drug release. At high coating levels (⩾10%), the release rate initially increased and then decreased with increasing harshness of the curing conditions. This more complex behavior might be attributable to the superposition of two competing phenomena: improved film formation and drug migration into the polymeric membrane. Furthermore, it could be shown that the type of plasticizer had a major effect on drug release in not fully coalesced and equilibrated film coatings, whereas the release profiles were similar for all plasticizers in the case of completely formed and equilibrated film coatings. Importantly, the latter systems were stable for long term even during storage under stress conditions.</description><subject>Aqueous ethylcellulose dispersion</subject><subject>Biological and medical sciences</subject><subject>Cellulose - analogs & derivatives</subject><subject>Cellulose - chemistry</subject><subject>Coating</subject><subject>Curing</subject><subject>Diltiazem - pharmacokinetics</subject><subject>Drug Compounding - methods</subject><subject>Drug Implants - chemical synthesis</subject><subject>Drug Implants - chemistry</subject><subject>Drug Implants - pharmacokinetics</subject><subject>Drug Stability</subject><subject>Drug Storage</subject><subject>Emulsifying Agents - chemistry</subject><subject>General pharmacology</subject><subject>Humidity</subject><subject>In Vitro Techniques</subject><subject>Medical sciences</subject><subject>Pellets</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Plasticizer</subject><subject>Plasticizers - chemistry</subject><subject>Plasticizers - pharmacokinetics</subject><subject>Polymers - chemistry</subject><subject>Polymers - pharmacokinetics</subject><subject>Surface Properties</subject><subject>Temperature</subject><subject>Time Factors</subject><subject>Wettability</subject><issn>0939-6411</issn><issn>1873-3441</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1r3DAQhkVoSTYffyCHokvpyVvJ-rJCLmVpPiDQS3MWsjxKtMhrV_IubH995ey2ufU0MPPMMO-D0DUlS0qo_LpewnpslzUhujSWhKgTtKCNYhXjnH5AC6KZriSn9Ayd57wmhHAlmlN0RnWjRdPIBWpX2xQ2L3jw2P7awrDNeBzivocUHPYh9tgNdipEvsGP_TikyW4czPj0Cn9nOMIOIrabDk_78W06Rpun4MJvSJfoo7cxw9WxXqDnu-8_Vw_V04_7x9W3p8qxRkyVU4oqKbhX5Tempa4VMAnOe9Eq8NQyLWjja-ukZdJ1lrcd45o46IQlvGYX6Mvh7piGEiVPpg_ZQYx2M-cyijEhFJeqkPWBdGnIOYE3Ywq9TXtDiZnVmrWZ1ZpZ7dwrasvSp-P5bdtD975ydFmAz0fAZmejT8VUyP-4uhZEK80Kd3vgoMjYBUgmuwDFahcSuMl0Q_jfH38AJZWYKA</recordid><startdate>20100201</startdate><enddate>20100201</enddate><creator>Yang, Q.W.</creator><creator>Flament, M.P.</creator><creator>Siepmann, F.</creator><creator>Busignies, V.</creator><creator>Leclerc, B.</creator><creator>Herry, C.</creator><creator>Tchoreloff, P.</creator><creator>Siepmann, J.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20100201</creationdate><title>Curing of aqueous polymeric film coatings: Importance of the coating level and type of plasticizer</title><author>Yang, Q.W. ; Flament, M.P. ; Siepmann, F. ; Busignies, V. ; Leclerc, B. ; Herry, C. ; Tchoreloff, P. ; Siepmann, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-c7717654f7895396927e36ecff5b7ef1a39518f2ac6a36cda4bd3490ced5a0423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Aqueous ethylcellulose dispersion</topic><topic>Biological and medical sciences</topic><topic>Cellulose - analogs & derivatives</topic><topic>Cellulose - chemistry</topic><topic>Coating</topic><topic>Curing</topic><topic>Diltiazem - pharmacokinetics</topic><topic>Drug Compounding - methods</topic><topic>Drug Implants - chemical synthesis</topic><topic>Drug Implants - chemistry</topic><topic>Drug Implants - pharmacokinetics</topic><topic>Drug Stability</topic><topic>Drug Storage</topic><topic>Emulsifying Agents - chemistry</topic><topic>General pharmacology</topic><topic>Humidity</topic><topic>In Vitro Techniques</topic><topic>Medical sciences</topic><topic>Pellets</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Plasticizer</topic><topic>Plasticizers - chemistry</topic><topic>Plasticizers - pharmacokinetics</topic><topic>Polymers - chemistry</topic><topic>Polymers - pharmacokinetics</topic><topic>Surface Properties</topic><topic>Temperature</topic><topic>Time Factors</topic><topic>Wettability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Q.W.</creatorcontrib><creatorcontrib>Flament, M.P.</creatorcontrib><creatorcontrib>Siepmann, F.</creatorcontrib><creatorcontrib>Busignies, V.</creatorcontrib><creatorcontrib>Leclerc, B.</creatorcontrib><creatorcontrib>Herry, C.</creatorcontrib><creatorcontrib>Tchoreloff, P.</creatorcontrib><creatorcontrib>Siepmann, J.</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>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of pharmaceutics and biopharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Q.W.</au><au>Flament, M.P.</au><au>Siepmann, F.</au><au>Busignies, V.</au><au>Leclerc, B.</au><au>Herry, C.</au><au>Tchoreloff, P.</au><au>Siepmann, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Curing of aqueous polymeric film coatings: Importance of the coating level and type of plasticizer</atitle><jtitle>European journal of pharmaceutics and biopharmaceutics</jtitle><addtitle>Eur J Pharm Biopharm</addtitle><date>2010-02-01</date><risdate>2010</risdate><volume>74</volume><issue>2</issue><spage>362</spage><epage>370</epage><pages>362-370</pages><issn>0939-6411</issn><eissn>1873-3441</eissn><abstract>The aim of this study was to better understand the effects of the curing conditions on the resulting drug release patterns from pellets coated with aqueous polymer dispersions. Diltiazem HCl was used as model drug, ethylcellulose as polymer, triethyl citrate (TEC), dibutyl sebacate (DBS), and distilled acetylated monoglycerides (Myvacet) as plasticizers. Interestingly, the effects of the curing conditions strongly depended on the coating level and the type of plasticizer: in the case of TEC, the drug release rate monotonically decreased with increasing harshness of the curing conditions (time, temperature, and relative humidity), irrespective of the coating level. In contrast, in the case of DBS and Myvacet, this type of relationship was only observed at low coating levels (5%). At intermediate coating levels (around 7.5%), the curing conditions had virtually no effect on drug release. At high coating levels (⩾10%), the release rate initially increased and then decreased with increasing harshness of the curing conditions. This more complex behavior might be attributable to the superposition of two competing phenomena: improved film formation and drug migration into the polymeric membrane. Furthermore, it could be shown that the type of plasticizer had a major effect on drug release in not fully coalesced and equilibrated film coatings, whereas the release profiles were similar for all plasticizers in the case of completely formed and equilibrated film coatings. Importantly, the latter systems were stable for long term even during storage under stress conditions.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>19895886</pmid><doi>10.1016/j.ejpb.2009.10.007</doi><tpages>9</tpages></addata></record> |
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subjects | Aqueous ethylcellulose dispersion Biological and medical sciences Cellulose - analogs & derivatives Cellulose - chemistry Coating Curing Diltiazem - pharmacokinetics Drug Compounding - methods Drug Implants - chemical synthesis Drug Implants - chemistry Drug Implants - pharmacokinetics Drug Stability Drug Storage Emulsifying Agents - chemistry General pharmacology Humidity In Vitro Techniques Medical sciences Pellets Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Plasticizer Plasticizers - chemistry Plasticizers - pharmacokinetics Polymers - chemistry Polymers - pharmacokinetics Surface Properties Temperature Time Factors Wettability |
title | Curing of aqueous polymeric film coatings: Importance of the coating level and type of plasticizer |
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