Study of the properties of the new biodegradable polyurethane PU (TEG-HMDI) as matrix forming excipient for controlled drug delivery
The purpose of this work is to study the ability of a new biodegradable polyurethane PU(TEG-HMDI) obtained by reaction of triethylene glycol (TEG) with 1,6-hexamethylene diisocyanate (HMDI) to act as matrix forming polymer for controlled release tablets and to estimate its percolation threshold in a...
Gespeichert in:
Veröffentlicht in: | Drug development and industrial pharmacy 2013-11, Vol.39 (11), p.1758-1764 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1764 |
---|---|
container_issue | 11 |
container_start_page | 1758 |
container_title | Drug development and industrial pharmacy |
container_volume | 39 |
creator | Campiñez, María Dolores Aguilar-de-Leyva, Ángela Ferris, Cristina de Paz, M. Violante Galbis, Juan Antonio Caraballo, Isidoro |
description | The purpose of this work is to study the ability of a new biodegradable polyurethane PU(TEG-HMDI) obtained by reaction of triethylene glycol (TEG) with 1,6-hexamethylene diisocyanate (HMDI) to act as matrix forming polymer for controlled release tablets and to estimate its percolation threshold in a matrix system. Matrix tablets weighing 250 mg were prepared by direct compression with 10-30% wt/wt of PU(TEG-HMDI) and anhydrous theophylline as model drug. Release studies were carried out using the paddle method. The results were analyzed using the kinetics models of Higuchi, Korsmeyer-Peppas, and Peppas and Sahlin. These studies confirm the existence of an excipient percolation threshold between 10 and 20 % wt/wt of PU(TEG-HMDI) for the different batches prepared. It has been observed that the new biodegradable polyurethane PU(TEG-HMDI) shows adequate compatibility as well as a high ability to control the drug release. |
doi_str_mv | 10.3109/03639045.2012.736516 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_3109_03639045_2012_736516</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1443406612</sourcerecordid><originalsourceid>FETCH-LOGICAL-c418t-365617a8d00a378ba40791b12fb8e8fda8f3d1b5373360b243447f66947b31113</originalsourceid><addsrcrecordid>eNp9kMFu1DAURS0EotPCHyDkZVlksGPHSTYgVEpbqQgk2rVlxy8zrpx4sB3a7PvhOJoOEpuuLD2de5_fQegdJWtGSfuRMMFawqt1SWi5rpmoqHiBVrQqSVHVonyJVgtSLMwROo7xjmSwrarX6KjkpKmbSqzQ4680mRn7Hqct4F3wOwjJQjxMRrjH2noDm6CM0i4z3s1TgLRVI-Cft_j05vyiuPz-9eoDVhEPKgX7gHsfBjtuMDx0dmdhTMsEd35MwTsHBpswbbABZ_9AmN-gV71yEd4-vSfo9tv5zdllcf3j4ursy3XRcdqkIp8oaK0aQ4hidaMVJ3VLNS173UDTG9X0zFBdsZoxQXTJGed1L0TLa80opewEne57852_J4hJDjZ24Fw-xU9RUp4jRAhaZpTv0S74GAP0chfsoMIsKZGLf3nwLxf_cu8_x94_bZj0AOZf6CA8A5_3gB0XR-reB2dkUrPzoQ9q7Gxc6p9d8em_hi0ol7adCiDv_BTGLPD5P_4FOmOnng</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1443406612</pqid></control><display><type>article</type><title>Study of the properties of the new biodegradable polyurethane PU (TEG-HMDI) as matrix forming excipient for controlled drug delivery</title><source>MEDLINE</source><source>EBSCOhost Business Source Complete</source><creator>Campiñez, María Dolores ; Aguilar-de-Leyva, Ángela ; Ferris, Cristina ; de Paz, M. Violante ; Galbis, Juan Antonio ; Caraballo, Isidoro</creator><creatorcontrib>Campiñez, María Dolores ; Aguilar-de-Leyva, Ángela ; Ferris, Cristina ; de Paz, M. Violante ; Galbis, Juan Antonio ; Caraballo, Isidoro</creatorcontrib><description>The purpose of this work is to study the ability of a new biodegradable polyurethane PU(TEG-HMDI) obtained by reaction of triethylene glycol (TEG) with 1,6-hexamethylene diisocyanate (HMDI) to act as matrix forming polymer for controlled release tablets and to estimate its percolation threshold in a matrix system. Matrix tablets weighing 250 mg were prepared by direct compression with 10-30% wt/wt of PU(TEG-HMDI) and anhydrous theophylline as model drug. Release studies were carried out using the paddle method. The results were analyzed using the kinetics models of Higuchi, Korsmeyer-Peppas, and Peppas and Sahlin. These studies confirm the existence of an excipient percolation threshold between 10 and 20 % wt/wt of PU(TEG-HMDI) for the different batches prepared. It has been observed that the new biodegradable polyurethane PU(TEG-HMDI) shows adequate compatibility as well as a high ability to control the drug release.</description><identifier>ISSN: 0363-9045</identifier><identifier>EISSN: 1520-5762</identifier><identifier>DOI: 10.3109/03639045.2012.736516</identifier><identifier>PMID: 24087856</identifier><language>eng</language><publisher>England: Informa Healthcare</publisher><subject>Biodegradable Plastics - chemical synthesis ; Biodegradable Plastics - chemistry ; biopolymer ; Chemical Phenomena ; Cyanates - chemistry ; Delayed-Action Preparations - chemistry ; Diffusion ; Drug Compounding ; Excipients - chemical synthesis ; Excipients - chemistry ; Hydrophilic matrix ; Hydrophobic and Hydrophilic Interactions ; Indicators and Reagents - chemistry ; Isocyanates ; Kinetics ; Mechanical Phenomena ; Models, Molecular ; Molecular Structure ; Molecular Weight ; percolation theory ; Polyethylene Glycols - chemistry ; Polyurethanes - chemical synthesis ; Polyurethanes - chemistry ; Solubility ; sustained release ; Tablets ; Theophylline - chemistry ; theophylline anhydrous ; Vasodilator Agents - chemistry ; Viscosity</subject><ispartof>Drug development and industrial pharmacy, 2013-11, Vol.39 (11), p.1758-1764</ispartof><rights>2013 Informa Healthcare USA, Inc. 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-365617a8d00a378ba40791b12fb8e8fda8f3d1b5373360b243447f66947b31113</citedby><cites>FETCH-LOGICAL-c418t-365617a8d00a378ba40791b12fb8e8fda8f3d1b5373360b243447f66947b31113</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/24087856$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Campiñez, María Dolores</creatorcontrib><creatorcontrib>Aguilar-de-Leyva, Ángela</creatorcontrib><creatorcontrib>Ferris, Cristina</creatorcontrib><creatorcontrib>de Paz, M. Violante</creatorcontrib><creatorcontrib>Galbis, Juan Antonio</creatorcontrib><creatorcontrib>Caraballo, Isidoro</creatorcontrib><title>Study of the properties of the new biodegradable polyurethane PU (TEG-HMDI) as matrix forming excipient for controlled drug delivery</title><title>Drug development and industrial pharmacy</title><addtitle>Drug Dev Ind Pharm</addtitle><description>The purpose of this work is to study the ability of a new biodegradable polyurethane PU(TEG-HMDI) obtained by reaction of triethylene glycol (TEG) with 1,6-hexamethylene diisocyanate (HMDI) to act as matrix forming polymer for controlled release tablets and to estimate its percolation threshold in a matrix system. Matrix tablets weighing 250 mg were prepared by direct compression with 10-30% wt/wt of PU(TEG-HMDI) and anhydrous theophylline as model drug. Release studies were carried out using the paddle method. The results were analyzed using the kinetics models of Higuchi, Korsmeyer-Peppas, and Peppas and Sahlin. These studies confirm the existence of an excipient percolation threshold between 10 and 20 % wt/wt of PU(TEG-HMDI) for the different batches prepared. It has been observed that the new biodegradable polyurethane PU(TEG-HMDI) shows adequate compatibility as well as a high ability to control the drug release.</description><subject>Biodegradable Plastics - chemical synthesis</subject><subject>Biodegradable Plastics - chemistry</subject><subject>biopolymer</subject><subject>Chemical Phenomena</subject><subject>Cyanates - chemistry</subject><subject>Delayed-Action Preparations - chemistry</subject><subject>Diffusion</subject><subject>Drug Compounding</subject><subject>Excipients - chemical synthesis</subject><subject>Excipients - chemistry</subject><subject>Hydrophilic matrix</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Indicators and Reagents - chemistry</subject><subject>Isocyanates</subject><subject>Kinetics</subject><subject>Mechanical Phenomena</subject><subject>Models, Molecular</subject><subject>Molecular Structure</subject><subject>Molecular Weight</subject><subject>percolation theory</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Polyurethanes - chemical synthesis</subject><subject>Polyurethanes - chemistry</subject><subject>Solubility</subject><subject>sustained release</subject><subject>Tablets</subject><subject>Theophylline - chemistry</subject><subject>theophylline anhydrous</subject><subject>Vasodilator Agents - chemistry</subject><subject>Viscosity</subject><issn>0363-9045</issn><issn>1520-5762</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFu1DAURS0EotPCHyDkZVlksGPHSTYgVEpbqQgk2rVlxy8zrpx4sB3a7PvhOJoOEpuuLD2de5_fQegdJWtGSfuRMMFawqt1SWi5rpmoqHiBVrQqSVHVonyJVgtSLMwROo7xjmSwrarX6KjkpKmbSqzQ4680mRn7Hqct4F3wOwjJQjxMRrjH2noDm6CM0i4z3s1TgLRVI-Cft_j05vyiuPz-9eoDVhEPKgX7gHsfBjtuMDx0dmdhTMsEd35MwTsHBpswbbABZ_9AmN-gV71yEd4-vSfo9tv5zdllcf3j4ursy3XRcdqkIp8oaK0aQ4hidaMVJ3VLNS173UDTG9X0zFBdsZoxQXTJGed1L0TLa80opewEne57852_J4hJDjZ24Fw-xU9RUp4jRAhaZpTv0S74GAP0chfsoMIsKZGLf3nwLxf_cu8_x94_bZj0AOZf6CA8A5_3gB0XR-reB2dkUrPzoQ9q7Gxc6p9d8em_hi0ol7adCiDv_BTGLPD5P_4FOmOnng</recordid><startdate>201311</startdate><enddate>201311</enddate><creator>Campiñez, María Dolores</creator><creator>Aguilar-de-Leyva, Ángela</creator><creator>Ferris, Cristina</creator><creator>de Paz, M. Violante</creator><creator>Galbis, Juan Antonio</creator><creator>Caraballo, Isidoro</creator><general>Informa Healthcare</general><general>Taylor & Francis</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>7X8</scope></search><sort><creationdate>201311</creationdate><title>Study of the properties of the new biodegradable polyurethane PU (TEG-HMDI) as matrix forming excipient for controlled drug delivery</title><author>Campiñez, María Dolores ; Aguilar-de-Leyva, Ángela ; Ferris, Cristina ; de Paz, M. Violante ; Galbis, Juan Antonio ; Caraballo, Isidoro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-365617a8d00a378ba40791b12fb8e8fda8f3d1b5373360b243447f66947b31113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Biodegradable Plastics - chemical synthesis</topic><topic>Biodegradable Plastics - chemistry</topic><topic>biopolymer</topic><topic>Chemical Phenomena</topic><topic>Cyanates - chemistry</topic><topic>Delayed-Action Preparations - chemistry</topic><topic>Diffusion</topic><topic>Drug Compounding</topic><topic>Excipients - chemical synthesis</topic><topic>Excipients - chemistry</topic><topic>Hydrophilic matrix</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Indicators and Reagents - chemistry</topic><topic>Isocyanates</topic><topic>Kinetics</topic><topic>Mechanical Phenomena</topic><topic>Models, Molecular</topic><topic>Molecular Structure</topic><topic>Molecular Weight</topic><topic>percolation theory</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Polyurethanes - chemical synthesis</topic><topic>Polyurethanes - chemistry</topic><topic>Solubility</topic><topic>sustained release</topic><topic>Tablets</topic><topic>Theophylline - chemistry</topic><topic>theophylline anhydrous</topic><topic>Vasodilator Agents - chemistry</topic><topic>Viscosity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Campiñez, María Dolores</creatorcontrib><creatorcontrib>Aguilar-de-Leyva, Ángela</creatorcontrib><creatorcontrib>Ferris, Cristina</creatorcontrib><creatorcontrib>de Paz, M. Violante</creatorcontrib><creatorcontrib>Galbis, Juan Antonio</creatorcontrib><creatorcontrib>Caraballo, Isidoro</creatorcontrib><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>Drug development and industrial pharmacy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Campiñez, María Dolores</au><au>Aguilar-de-Leyva, Ángela</au><au>Ferris, Cristina</au><au>de Paz, M. Violante</au><au>Galbis, Juan Antonio</au><au>Caraballo, Isidoro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study of the properties of the new biodegradable polyurethane PU (TEG-HMDI) as matrix forming excipient for controlled drug delivery</atitle><jtitle>Drug development and industrial pharmacy</jtitle><addtitle>Drug Dev Ind Pharm</addtitle><date>2013-11</date><risdate>2013</risdate><volume>39</volume><issue>11</issue><spage>1758</spage><epage>1764</epage><pages>1758-1764</pages><issn>0363-9045</issn><eissn>1520-5762</eissn><abstract>The purpose of this work is to study the ability of a new biodegradable polyurethane PU(TEG-HMDI) obtained by reaction of triethylene glycol (TEG) with 1,6-hexamethylene diisocyanate (HMDI) to act as matrix forming polymer for controlled release tablets and to estimate its percolation threshold in a matrix system. Matrix tablets weighing 250 mg were prepared by direct compression with 10-30% wt/wt of PU(TEG-HMDI) and anhydrous theophylline as model drug. Release studies were carried out using the paddle method. The results were analyzed using the kinetics models of Higuchi, Korsmeyer-Peppas, and Peppas and Sahlin. These studies confirm the existence of an excipient percolation threshold between 10 and 20 % wt/wt of PU(TEG-HMDI) for the different batches prepared. It has been observed that the new biodegradable polyurethane PU(TEG-HMDI) shows adequate compatibility as well as a high ability to control the drug release.</abstract><cop>England</cop><pub>Informa Healthcare</pub><pmid>24087856</pmid><doi>10.3109/03639045.2012.736516</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0363-9045 |
ispartof | Drug development and industrial pharmacy, 2013-11, Vol.39 (11), p.1758-1764 |
issn | 0363-9045 1520-5762 |
language | eng |
recordid | cdi_crossref_primary_10_3109_03639045_2012_736516 |
source | MEDLINE; EBSCOhost Business Source Complete |
subjects | Biodegradable Plastics - chemical synthesis Biodegradable Plastics - chemistry biopolymer Chemical Phenomena Cyanates - chemistry Delayed-Action Preparations - chemistry Diffusion Drug Compounding Excipients - chemical synthesis Excipients - chemistry Hydrophilic matrix Hydrophobic and Hydrophilic Interactions Indicators and Reagents - chemistry Isocyanates Kinetics Mechanical Phenomena Models, Molecular Molecular Structure Molecular Weight percolation theory Polyethylene Glycols - chemistry Polyurethanes - chemical synthesis Polyurethanes - chemistry Solubility sustained release Tablets Theophylline - chemistry theophylline anhydrous Vasodilator Agents - chemistry Viscosity |
title | Study of the properties of the new biodegradable polyurethane PU (TEG-HMDI) as matrix forming excipient for controlled drug delivery |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T04%3A18%3A16IST&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=Study%20of%20the%20properties%20of%20the%20new%20biodegradable%20polyurethane%20PU%20(TEG-HMDI)%20as%20matrix%20forming%20excipient%20for%20controlled%20drug%20delivery&rft.jtitle=Drug%20development%20and%20industrial%20pharmacy&rft.au=Campi%C3%B1ez,%20Mar%C3%ADa%20Dolores&rft.date=2013-11&rft.volume=39&rft.issue=11&rft.spage=1758&rft.epage=1764&rft.pages=1758-1764&rft.issn=0363-9045&rft.eissn=1520-5762&rft_id=info:doi/10.3109/03639045.2012.736516&rft_dat=%3Cproquest_cross%3E1443406612%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=1443406612&rft_id=info:pmid/24087856&rfr_iscdi=true |