Quantification of porogen effect on the drug release from single- and multi-layered ethylcellulose coated pellets containing single or combined drugs
[Display omitted] The aim of this work was to develop a mathematical model to estimate the drug release from a conventional single-compartment reservoir pellet and extend its applicability to multi-compartment reservoir pellets. Conventional pellets were prepared by layering the drug onto starter-co...
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Veröffentlicht in: | International journal of pharmaceutics 2020-03, Vol.577, p.119050-119050, Article 119050 |
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container_start_page | 119050 |
container_title | International journal of pharmaceutics |
container_volume | 577 |
creator | Chaerunisaa, Anis Yohana Ali, Rebaz Körber, Martin Bodmeier, Roland |
description | [Display omitted]
The aim of this work was to develop a mathematical model to estimate the drug release from a conventional single-compartment reservoir pellet and extend its applicability to multi-compartment reservoir pellets. Conventional pellets were prepared by layering the drug onto starter-core then applying various ethylcellulose/HPC coatings for drug release control. Multi-layered pellets comprised a first drug layer of propranolol HCl (D1) followed by a first controlled release coating (C1) and consecutively a second drug layer of carbamazepine or caffeine (D2) and then a second controlled-release coating (C2). Drug release from single- and multi-compartment pellets generally increased with an increase of the water-soluble HPC in the coatings. The response described a sigmoidal curve, which agreed with a cumulative normal distribution function. The developed mathematical model facilitated quantification of the drug release of pellets as a function of the porogen content and the coating level. Additionally, the model was applied successfully in multi-compartment pellets to calculate theses effects on the release of drugs with a broad range of aqueous solubility. |
doi_str_mv | 10.1016/j.ijpharm.2020.119050 |
format | Article |
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The aim of this work was to develop a mathematical model to estimate the drug release from a conventional single-compartment reservoir pellet and extend its applicability to multi-compartment reservoir pellets. Conventional pellets were prepared by layering the drug onto starter-core then applying various ethylcellulose/HPC coatings for drug release control. Multi-layered pellets comprised a first drug layer of propranolol HCl (D1) followed by a first controlled release coating (C1) and consecutively a second drug layer of carbamazepine or caffeine (D2) and then a second controlled-release coating (C2). Drug release from single- and multi-compartment pellets generally increased with an increase of the water-soluble HPC in the coatings. The response described a sigmoidal curve, which agreed with a cumulative normal distribution function. The developed mathematical model facilitated quantification of the drug release of pellets as a function of the porogen content and the coating level. Additionally, the model was applied successfully in multi-compartment pellets to calculate theses effects on the release of drugs with a broad range of aqueous solubility.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2020.119050</identifier><identifier>PMID: 31991186</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Coated pellets ; Drug combination ; Mathematical model ; Porogen</subject><ispartof>International journal of pharmaceutics, 2020-03, Vol.577, p.119050-119050, Article 119050</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright © 2020 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-5a96ac9c896352a642a06e93bae6066901e5dbe3b2c4670512d4fbd5976f8b693</citedby><cites>FETCH-LOGICAL-c365t-5a96ac9c896352a642a06e93bae6066901e5dbe3b2c4670512d4fbd5976f8b693</cites><orcidid>0000-0001-7647-7241</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijpharm.2020.119050$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31991186$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chaerunisaa, Anis Yohana</creatorcontrib><creatorcontrib>Ali, Rebaz</creatorcontrib><creatorcontrib>Körber, Martin</creatorcontrib><creatorcontrib>Bodmeier, Roland</creatorcontrib><title>Quantification of porogen effect on the drug release from single- and multi-layered ethylcellulose coated pellets containing single or combined drugs</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>[Display omitted]
The aim of this work was to develop a mathematical model to estimate the drug release from a conventional single-compartment reservoir pellet and extend its applicability to multi-compartment reservoir pellets. Conventional pellets were prepared by layering the drug onto starter-core then applying various ethylcellulose/HPC coatings for drug release control. Multi-layered pellets comprised a first drug layer of propranolol HCl (D1) followed by a first controlled release coating (C1) and consecutively a second drug layer of carbamazepine or caffeine (D2) and then a second controlled-release coating (C2). Drug release from single- and multi-compartment pellets generally increased with an increase of the water-soluble HPC in the coatings. The response described a sigmoidal curve, which agreed with a cumulative normal distribution function. The developed mathematical model facilitated quantification of the drug release of pellets as a function of the porogen content and the coating level. Additionally, the model was applied successfully in multi-compartment pellets to calculate theses effects on the release of drugs with a broad range of aqueous solubility.</description><subject>Coated pellets</subject><subject>Drug combination</subject><subject>Mathematical model</subject><subject>Porogen</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkVGP1CAUhYnRuLOrP0HDoy8doRRanozZrK7JJsZEnwmFywyTFipQk_kh_l9pZvTVJ8LJd-65cBB6Q8meEiren_b-tBx1mvctaatGJeHkGdrRoWcN63rxHO0I64eG057doNucT4QQ0VL2Et0wKiWlg9ih399WHYp33ujiY8DR4SWmeICAwTkwBVexHAHbtB5wggl0BuxSnHH24TBBg3WweF6n4ptJnyGBxVCO58nANK1TrLSJulR1qQKUXK-haB-q-zoCx1TFefShUltOfoVeOD1leH0979CPTw_f7x-bp6-fv9x_fGoME7w0XEuhjTSDFIy3WnStJgIkGzUIIoQkFLgdgY2t6URPOG1t50bLZS_cMArJ7tC7y9wlxZ8r5KJmn7fFdYC4ZtWybmgZ43JD-QU1KeacwKkl-Vmns6JEbY2ok7o2orZG1KWR6nt7jVjHGew_198KKvDhAkB96C8PSWXjIRiwPtX_Vzb6_0T8ASpQolc</recordid><startdate>20200315</startdate><enddate>20200315</enddate><creator>Chaerunisaa, Anis Yohana</creator><creator>Ali, Rebaz</creator><creator>Körber, Martin</creator><creator>Bodmeier, Roland</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7647-7241</orcidid></search><sort><creationdate>20200315</creationdate><title>Quantification of porogen effect on the drug release from single- and multi-layered ethylcellulose coated pellets containing single or combined drugs</title><author>Chaerunisaa, Anis Yohana ; Ali, Rebaz ; Körber, Martin ; Bodmeier, Roland</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-5a96ac9c896352a642a06e93bae6066901e5dbe3b2c4670512d4fbd5976f8b693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Coated pellets</topic><topic>Drug combination</topic><topic>Mathematical model</topic><topic>Porogen</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chaerunisaa, Anis Yohana</creatorcontrib><creatorcontrib>Ali, Rebaz</creatorcontrib><creatorcontrib>Körber, Martin</creatorcontrib><creatorcontrib>Bodmeier, Roland</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chaerunisaa, Anis Yohana</au><au>Ali, Rebaz</au><au>Körber, Martin</au><au>Bodmeier, Roland</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantification of porogen effect on the drug release from single- and multi-layered ethylcellulose coated pellets containing single or combined drugs</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2020-03-15</date><risdate>2020</risdate><volume>577</volume><spage>119050</spage><epage>119050</epage><pages>119050-119050</pages><artnum>119050</artnum><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted]
The aim of this work was to develop a mathematical model to estimate the drug release from a conventional single-compartment reservoir pellet and extend its applicability to multi-compartment reservoir pellets. Conventional pellets were prepared by layering the drug onto starter-core then applying various ethylcellulose/HPC coatings for drug release control. Multi-layered pellets comprised a first drug layer of propranolol HCl (D1) followed by a first controlled release coating (C1) and consecutively a second drug layer of carbamazepine or caffeine (D2) and then a second controlled-release coating (C2). Drug release from single- and multi-compartment pellets generally increased with an increase of the water-soluble HPC in the coatings. The response described a sigmoidal curve, which agreed with a cumulative normal distribution function. The developed mathematical model facilitated quantification of the drug release of pellets as a function of the porogen content and the coating level. Additionally, the model was applied successfully in multi-compartment pellets to calculate theses effects on the release of drugs with a broad range of aqueous solubility.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31991186</pmid><doi>10.1016/j.ijpharm.2020.119050</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-7647-7241</orcidid></addata></record> |
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subjects | Coated pellets Drug combination Mathematical model Porogen |
title | Quantification of porogen effect on the drug release from single- and multi-layered ethylcellulose coated pellets containing single or combined drugs |
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