Thermoplastic polyurethanes for the manufacturing of highly dosed oral sustained release matrices via hot melt extrusion and injection molding
[Display omitted] •Thermoplastic polyurethanes (TPUR) were evaluated as matrix excipients to produce high drug load solid dosage forms.•A high drug load (65wt.%) was achieved in combination with an in vitro and in vivo controlled release capacity.•Oral administration of TPUR did not affect the GI ec...
Gespeichert in:
Veröffentlicht in: | European journal of pharmaceutics and biopharmaceutics 2015-02, Vol.90, p.44-52 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 52 |
---|---|
container_issue | |
container_start_page | 44 |
container_title | European journal of pharmaceutics and biopharmaceutics |
container_volume | 90 |
creator | Claeys, Bart Vervaeck, Anouk Hillewaere, Xander K.D. Possemiers, Sam Hansen, Laurent De Beer, Thomas Remon, Jean Paul Vervaet, Chris |
description | [Display omitted]
•Thermoplastic polyurethanes (TPUR) were evaluated as matrix excipients to produce high drug load solid dosage forms.•A high drug load (65wt.%) was achieved in combination with an in vitro and in vivo controlled release capacity.•Oral administration of TPUR did not affect the GI ecosystem.
This study evaluated thermoplastic polyurethanes (TPUR) as matrix excipients for the production of oral solid dosage forms via hot melt extrusion (HME) in combination with injection molding (IM). We demonstrated that TPURs enable the production of solid dispersions – crystalline API in a crystalline carrier – at an extrusion temperature below the drug melting temperature (Tm) with a drug content up to 65% (wt.%). The release of metoprolol tartrate was controlled over 24h, whereas a complete release of diprophylline was only possible in combination with a drug release modifier: polyethylene glycol 4000 (PEG 4000) or Tween 80. No burst release nor a change in tablet size and geometry was detected for any of the formulations after dissolution testing. The total matrix porosity increased gradually upon drug release. Oral administration of TPUR did not affect the GI ecosystem (pH, bacterial count, short chain fatty acids), monitored via the Simulator of the Human Intestinal Microbial Ecosystem (SHIME). The high drug load (65wt.%) in combination with (in vitro and in vivo) controlled release capacity of the formulations, is noteworthy in the field of formulations produced via HME/IM. |
doi_str_mv | 10.1016/j.ejpb.2014.11.003 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1664205081</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0939641114003208</els_id><sourcerecordid>1664205081</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-b6f894205c94c61c6c877cb7bb3695cfce0c5b03ccfec873e2ca7e45c92cd6e83</originalsourceid><addsrcrecordid>eNp9kc1q3TAQRkVJaW7TvkAWQcts7Eq2LNuQTQnpDwS6SddCHo9jGdlyJDn0vkSfuTI3zTIrMeh8B2Y-Qi45yznj8suU47R2ecG4yDnPGSvfkQNv6jIrheBn5MDass2k4PycfAxhYoyJumo-kPOiEqJhdXUgfx9G9LNbrQ7RAF2dPW4e46gXDHRwnsYR6ayXbdAQN2-WR-oGOprH0R5p7wL21HltadhC1GZJo0eLOuyh6A0ky7PRdHSRzmgjxT_Rb8G4heqlp2aZEOI-zc72Sf6JvB-0Dfj55b0gv7_dPdz-yO5_ff95-_U-A8FYzDo5NK0oWAWtAMlBQlPX0NVdV8q2ggGQQdWxEmDA9FViAbpGkfACeolNeUGuT97Vu6cNQ1SzCYDWpr3dFhSXctezhie0OKHgXQgeB7V6M2t_VJypvQc1qb0HtfegOFephxS6evFv3Yz9a-T_4RNwcwIwbfls0KsABhfA3vh0EtU785b_H-0Qnhc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1664205081</pqid></control><display><type>article</type><title>Thermoplastic polyurethanes for the manufacturing of highly dosed oral sustained release matrices via hot melt extrusion and injection molding</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Claeys, Bart ; Vervaeck, Anouk ; Hillewaere, Xander K.D. ; Possemiers, Sam ; Hansen, Laurent ; De Beer, Thomas ; Remon, Jean Paul ; Vervaet, Chris</creator><creatorcontrib>Claeys, Bart ; Vervaeck, Anouk ; Hillewaere, Xander K.D. ; Possemiers, Sam ; Hansen, Laurent ; De Beer, Thomas ; Remon, Jean Paul ; Vervaet, Chris</creatorcontrib><description>[Display omitted]
•Thermoplastic polyurethanes (TPUR) were evaluated as matrix excipients to produce high drug load solid dosage forms.•A high drug load (65wt.%) was achieved in combination with an in vitro and in vivo controlled release capacity.•Oral administration of TPUR did not affect the GI ecosystem.
This study evaluated thermoplastic polyurethanes (TPUR) as matrix excipients for the production of oral solid dosage forms via hot melt extrusion (HME) in combination with injection molding (IM). We demonstrated that TPURs enable the production of solid dispersions – crystalline API in a crystalline carrier – at an extrusion temperature below the drug melting temperature (Tm) with a drug content up to 65% (wt.%). The release of metoprolol tartrate was controlled over 24h, whereas a complete release of diprophylline was only possible in combination with a drug release modifier: polyethylene glycol 4000 (PEG 4000) or Tween 80. No burst release nor a change in tablet size and geometry was detected for any of the formulations after dissolution testing. The total matrix porosity increased gradually upon drug release. Oral administration of TPUR did not affect the GI ecosystem (pH, bacterial count, short chain fatty acids), monitored via the Simulator of the Human Intestinal Microbial Ecosystem (SHIME). The high drug load (65wt.%) in combination with (in vitro and in vivo) controlled release capacity of the formulations, is noteworthy in the field of formulations produced via HME/IM.</description><identifier>ISSN: 0939-6411</identifier><identifier>EISSN: 1873-3441</identifier><identifier>DOI: 10.1016/j.ejpb.2014.11.003</identifier><identifier>PMID: 25448075</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject><![CDATA[Administration, Oral ; Chemistry, Pharmaceutical - methods ; Controlled release ; Delayed-Action Preparations - administration & dosage ; Delayed-Action Preparations - chemistry ; Dosage Forms ; Drug Carriers - administration & dosage ; Drug Carriers - chemistry ; Drug Compounding - methods ; Drug delivery systems ; Dyphylline - administration & dosage ; Dyphylline - chemistry ; Excipients - chemistry ; Extrusion ; Hot Temperature ; Humans ; Injection molding ; Metoprolol - administration & dosage ; Metoprolol - chemistry ; Polyethylene Glycols - administration & dosage ; Polyethylene Glycols - chemistry ; Polymers ; Polyurethane ; Polyurethanes - administration & dosage ; Polyurethanes - chemistry ; Porosity ; Tablets - administration & dosage ; Tablets - chemistry]]></subject><ispartof>European journal of pharmaceutics and biopharmaceutics, 2015-02, Vol.90, p.44-52</ispartof><rights>2014 Elsevier B.V.</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-b6f894205c94c61c6c877cb7bb3695cfce0c5b03ccfec873e2ca7e45c92cd6e83</citedby><cites>FETCH-LOGICAL-c400t-b6f894205c94c61c6c877cb7bb3695cfce0c5b03ccfec873e2ca7e45c92cd6e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0939641114003208$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25448075$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Claeys, Bart</creatorcontrib><creatorcontrib>Vervaeck, Anouk</creatorcontrib><creatorcontrib>Hillewaere, Xander K.D.</creatorcontrib><creatorcontrib>Possemiers, Sam</creatorcontrib><creatorcontrib>Hansen, Laurent</creatorcontrib><creatorcontrib>De Beer, Thomas</creatorcontrib><creatorcontrib>Remon, Jean Paul</creatorcontrib><creatorcontrib>Vervaet, Chris</creatorcontrib><title>Thermoplastic polyurethanes for the manufacturing of highly dosed oral sustained release matrices via hot melt extrusion and injection molding</title><title>European journal of pharmaceutics and biopharmaceutics</title><addtitle>Eur J Pharm Biopharm</addtitle><description>[Display omitted]
•Thermoplastic polyurethanes (TPUR) were evaluated as matrix excipients to produce high drug load solid dosage forms.•A high drug load (65wt.%) was achieved in combination with an in vitro and in vivo controlled release capacity.•Oral administration of TPUR did not affect the GI ecosystem.
This study evaluated thermoplastic polyurethanes (TPUR) as matrix excipients for the production of oral solid dosage forms via hot melt extrusion (HME) in combination with injection molding (IM). We demonstrated that TPURs enable the production of solid dispersions – crystalline API in a crystalline carrier – at an extrusion temperature below the drug melting temperature (Tm) with a drug content up to 65% (wt.%). The release of metoprolol tartrate was controlled over 24h, whereas a complete release of diprophylline was only possible in combination with a drug release modifier: polyethylene glycol 4000 (PEG 4000) or Tween 80. No burst release nor a change in tablet size and geometry was detected for any of the formulations after dissolution testing. The total matrix porosity increased gradually upon drug release. Oral administration of TPUR did not affect the GI ecosystem (pH, bacterial count, short chain fatty acids), monitored via the Simulator of the Human Intestinal Microbial Ecosystem (SHIME). The high drug load (65wt.%) in combination with (in vitro and in vivo) controlled release capacity of the formulations, is noteworthy in the field of formulations produced via HME/IM.</description><subject>Administration, Oral</subject><subject>Chemistry, Pharmaceutical - methods</subject><subject>Controlled release</subject><subject>Delayed-Action Preparations - administration & dosage</subject><subject>Delayed-Action Preparations - chemistry</subject><subject>Dosage Forms</subject><subject>Drug Carriers - administration & dosage</subject><subject>Drug Carriers - chemistry</subject><subject>Drug Compounding - methods</subject><subject>Drug delivery systems</subject><subject>Dyphylline - administration & dosage</subject><subject>Dyphylline - chemistry</subject><subject>Excipients - chemistry</subject><subject>Extrusion</subject><subject>Hot Temperature</subject><subject>Humans</subject><subject>Injection molding</subject><subject>Metoprolol - administration & dosage</subject><subject>Metoprolol - chemistry</subject><subject>Polyethylene Glycols - administration & dosage</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Polymers</subject><subject>Polyurethane</subject><subject>Polyurethanes - administration & dosage</subject><subject>Polyurethanes - chemistry</subject><subject>Porosity</subject><subject>Tablets - administration & dosage</subject><subject>Tablets - chemistry</subject><issn>0939-6411</issn><issn>1873-3441</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1q3TAQRkVJaW7TvkAWQcts7Eq2LNuQTQnpDwS6SddCHo9jGdlyJDn0vkSfuTI3zTIrMeh8B2Y-Qi45yznj8suU47R2ecG4yDnPGSvfkQNv6jIrheBn5MDass2k4PycfAxhYoyJumo-kPOiEqJhdXUgfx9G9LNbrQ7RAF2dPW4e46gXDHRwnsYR6ayXbdAQN2-WR-oGOprH0R5p7wL21HltadhC1GZJo0eLOuyh6A0ky7PRdHSRzmgjxT_Rb8G4heqlp2aZEOI-zc72Sf6JvB-0Dfj55b0gv7_dPdz-yO5_ff95-_U-A8FYzDo5NK0oWAWtAMlBQlPX0NVdV8q2ggGQQdWxEmDA9FViAbpGkfACeolNeUGuT97Vu6cNQ1SzCYDWpr3dFhSXctezhie0OKHgXQgeB7V6M2t_VJypvQc1qb0HtfegOFephxS6evFv3Yz9a-T_4RNwcwIwbfls0KsABhfA3vh0EtU785b_H-0Qnhc</recordid><startdate>20150201</startdate><enddate>20150201</enddate><creator>Claeys, Bart</creator><creator>Vervaeck, Anouk</creator><creator>Hillewaere, Xander K.D.</creator><creator>Possemiers, Sam</creator><creator>Hansen, Laurent</creator><creator>De Beer, Thomas</creator><creator>Remon, Jean Paul</creator><creator>Vervaet, Chris</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>20150201</creationdate><title>Thermoplastic polyurethanes for the manufacturing of highly dosed oral sustained release matrices via hot melt extrusion and injection molding</title><author>Claeys, Bart ; Vervaeck, Anouk ; Hillewaere, Xander K.D. ; Possemiers, Sam ; Hansen, Laurent ; De Beer, Thomas ; Remon, Jean Paul ; Vervaet, Chris</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-b6f894205c94c61c6c877cb7bb3695cfce0c5b03ccfec873e2ca7e45c92cd6e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Administration, Oral</topic><topic>Chemistry, Pharmaceutical - methods</topic><topic>Controlled release</topic><topic>Delayed-Action Preparations - administration & dosage</topic><topic>Delayed-Action Preparations - chemistry</topic><topic>Dosage Forms</topic><topic>Drug Carriers - administration & dosage</topic><topic>Drug Carriers - chemistry</topic><topic>Drug Compounding - methods</topic><topic>Drug delivery systems</topic><topic>Dyphylline - administration & dosage</topic><topic>Dyphylline - chemistry</topic><topic>Excipients - chemistry</topic><topic>Extrusion</topic><topic>Hot Temperature</topic><topic>Humans</topic><topic>Injection molding</topic><topic>Metoprolol - administration & dosage</topic><topic>Metoprolol - chemistry</topic><topic>Polyethylene Glycols - administration & dosage</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Polymers</topic><topic>Polyurethane</topic><topic>Polyurethanes - administration & dosage</topic><topic>Polyurethanes - chemistry</topic><topic>Porosity</topic><topic>Tablets - administration & dosage</topic><topic>Tablets - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Claeys, Bart</creatorcontrib><creatorcontrib>Vervaeck, Anouk</creatorcontrib><creatorcontrib>Hillewaere, Xander K.D.</creatorcontrib><creatorcontrib>Possemiers, Sam</creatorcontrib><creatorcontrib>Hansen, Laurent</creatorcontrib><creatorcontrib>De Beer, Thomas</creatorcontrib><creatorcontrib>Remon, Jean Paul</creatorcontrib><creatorcontrib>Vervaet, Chris</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>European journal of pharmaceutics and biopharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Claeys, Bart</au><au>Vervaeck, Anouk</au><au>Hillewaere, Xander K.D.</au><au>Possemiers, Sam</au><au>Hansen, Laurent</au><au>De Beer, Thomas</au><au>Remon, Jean Paul</au><au>Vervaet, Chris</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thermoplastic polyurethanes for the manufacturing of highly dosed oral sustained release matrices via hot melt extrusion and injection molding</atitle><jtitle>European journal of pharmaceutics and biopharmaceutics</jtitle><addtitle>Eur J Pharm Biopharm</addtitle><date>2015-02-01</date><risdate>2015</risdate><volume>90</volume><spage>44</spage><epage>52</epage><pages>44-52</pages><issn>0939-6411</issn><eissn>1873-3441</eissn><abstract>[Display omitted]
•Thermoplastic polyurethanes (TPUR) were evaluated as matrix excipients to produce high drug load solid dosage forms.•A high drug load (65wt.%) was achieved in combination with an in vitro and in vivo controlled release capacity.•Oral administration of TPUR did not affect the GI ecosystem.
This study evaluated thermoplastic polyurethanes (TPUR) as matrix excipients for the production of oral solid dosage forms via hot melt extrusion (HME) in combination with injection molding (IM). We demonstrated that TPURs enable the production of solid dispersions – crystalline API in a crystalline carrier – at an extrusion temperature below the drug melting temperature (Tm) with a drug content up to 65% (wt.%). The release of metoprolol tartrate was controlled over 24h, whereas a complete release of diprophylline was only possible in combination with a drug release modifier: polyethylene glycol 4000 (PEG 4000) or Tween 80. No burst release nor a change in tablet size and geometry was detected for any of the formulations after dissolution testing. The total matrix porosity increased gradually upon drug release. Oral administration of TPUR did not affect the GI ecosystem (pH, bacterial count, short chain fatty acids), monitored via the Simulator of the Human Intestinal Microbial Ecosystem (SHIME). The high drug load (65wt.%) in combination with (in vitro and in vivo) controlled release capacity of the formulations, is noteworthy in the field of formulations produced via HME/IM.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25448075</pmid><doi>10.1016/j.ejpb.2014.11.003</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0939-6411 |
ispartof | European journal of pharmaceutics and biopharmaceutics, 2015-02, Vol.90, p.44-52 |
issn | 0939-6411 1873-3441 |
language | eng |
recordid | cdi_proquest_miscellaneous_1664205081 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Administration, Oral Chemistry, Pharmaceutical - methods Controlled release Delayed-Action Preparations - administration & dosage Delayed-Action Preparations - chemistry Dosage Forms Drug Carriers - administration & dosage Drug Carriers - chemistry Drug Compounding - methods Drug delivery systems Dyphylline - administration & dosage Dyphylline - chemistry Excipients - chemistry Extrusion Hot Temperature Humans Injection molding Metoprolol - administration & dosage Metoprolol - chemistry Polyethylene Glycols - administration & dosage Polyethylene Glycols - chemistry Polymers Polyurethane Polyurethanes - administration & dosage Polyurethanes - chemistry Porosity Tablets - administration & dosage Tablets - chemistry |
title | Thermoplastic polyurethanes for the manufacturing of highly dosed oral sustained release matrices via hot melt extrusion and injection molding |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T10%3A39%3A28IST&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=Thermoplastic%20polyurethanes%20for%20the%20manufacturing%20of%20highly%20dosed%20oral%20sustained%20release%20matrices%20via%20hot%20melt%20extrusion%20and%20injection%20molding&rft.jtitle=European%20journal%20of%20pharmaceutics%20and%20biopharmaceutics&rft.au=Claeys,%20Bart&rft.date=2015-02-01&rft.volume=90&rft.spage=44&rft.epage=52&rft.pages=44-52&rft.issn=0939-6411&rft.eissn=1873-3441&rft_id=info:doi/10.1016/j.ejpb.2014.11.003&rft_dat=%3Cproquest_cross%3E1664205081%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=1664205081&rft_id=info:pmid/25448075&rft_els_id=S0939641114003208&rfr_iscdi=true |