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...

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Veröffentlicht in:European journal of pharmaceutics and biopharmaceutics 2015-02, Vol.90, p.44-52
Hauptverfasser: Claeys, Bart, Vervaeck, Anouk, Hillewaere, Xander K.D., Possemiers, Sam, Hansen, Laurent, De Beer, Thomas, Remon, Jean Paul, Vervaet, Chris
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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
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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). 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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). 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dosage</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Polymers</subject><subject>Polyurethane</subject><subject>Polyurethanes - administration &amp; dosage</subject><subject>Polyurethanes - chemistry</subject><subject>Porosity</subject><subject>Tablets - administration &amp; 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 ; 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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>
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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
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