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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of pharmaceutics and biopharmaceutics 2010-02, Vol.74 (2), p.362-370
Hauptverfasser: Yang, Q.W., Flament, M.P., Siepmann, F., Busignies, V., Leclerc, B., Herry, C., Tchoreloff, P., Siepmann, J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 370
container_issue 2
container_start_page 362
container_title European journal of pharmaceutics and biopharmaceutics
container_volume 74
creator Yang, Q.W.
Flament, M.P.
Siepmann, F.
Busignies, V.
Leclerc, B.
Herry, C.
Tchoreloff, P.
Siepmann, J.
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_733557467</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0939641109003270</els_id><sourcerecordid>733557467</sourcerecordid><originalsourceid>FETCH-LOGICAL-c385t-c7717654f7895396927e36ecff5b7ef1a39518f2ac6a36cda4bd3490ced5a0423</originalsourceid><addsrcrecordid>eNp9kE1r3DAQhkVoSTYffyCHokvpyVvJ-rJCLmVpPiDQS3MWsjxKtMhrV_IubH995ey2ufU0MPPMMO-D0DUlS0qo_LpewnpslzUhujSWhKgTtKCNYhXjnH5AC6KZriSn9Ayd57wmhHAlmlN0RnWjRdPIBWpX2xQ2L3jw2P7awrDNeBzivocUHPYh9tgNdipEvsGP_TikyW4czPj0Cn9nOMIOIrabDk_78W06Rpun4MJvSJfoo7cxw9WxXqDnu-8_Vw_V04_7x9W3p8qxRkyVU4oqKbhX5Tempa4VMAnOe9Eq8NQyLWjja-ukZdJ1lrcd45o46IQlvGYX6Mvh7piGEiVPpg_ZQYx2M-cyijEhFJeqkPWBdGnIOYE3Ywq9TXtDiZnVmrWZ1ZpZ7dwrasvSp-P5bdtD975ydFmAz0fAZmejT8VUyP-4uhZEK80Kd3vgoMjYBUgmuwDFahcSuMl0Q_jfH38AJZWYKA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>733557467</pqid></control><display><type>article</type><title>Curing of aqueous polymeric film coatings: Importance of the coating level and type of plasticizer</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Yang, Q.W. ; Flament, M.P. ; Siepmann, F. ; Busignies, V. ; Leclerc, B. ; Herry, C. ; Tchoreloff, P. ; Siepmann, J.</creator><creatorcontrib>Yang, Q.W. ; Flament, M.P. ; Siepmann, F. ; Busignies, V. ; Leclerc, B. ; Herry, C. ; Tchoreloff, P. ; Siepmann, J.</creatorcontrib><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><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 &amp; 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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22509793$$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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 0939-6411
ispartof European journal of pharmaceutics and biopharmaceutics, 2010-02, Vol.74 (2), p.362-370
issn 0939-6411
1873-3441
language eng
recordid cdi_proquest_miscellaneous_733557467
source MEDLINE; Access via ScienceDirect (Elsevier)
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T22%3A52%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Curing%20of%20aqueous%20polymeric%20film%20coatings:%20Importance%20of%20the%20coating%20level%20and%20type%20of%20plasticizer&rft.jtitle=European%20journal%20of%20pharmaceutics%20and%20biopharmaceutics&rft.au=Yang,%20Q.W.&rft.date=2010-02-01&rft.volume=74&rft.issue=2&rft.spage=362&rft.epage=370&rft.pages=362-370&rft.issn=0939-6411&rft.eissn=1873-3441&rft_id=info:doi/10.1016/j.ejpb.2009.10.007&rft_dat=%3Cproquest_cross%3E733557467%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=733557467&rft_id=info:pmid/19895886&rft_els_id=S0939641109003270&rfr_iscdi=true