Can drug release rate from implants be tailored using poly(urethane) mixtures?

[Display omitted] Hydrophobic and hydrophilic thermoplastic poly(urethane) (TPU) mixtures offer the opportunity to tune water swelling capacity and diffusion rate for drugs exhibiting broadly different properties. We sought to (1) assess the range of drug diffusion rates achieved by varying hydrophi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of pharmaceutics 2019-02, Vol.557, p.390-401
Hauptverfasser: Lowinger, Michael B., Su, Yongchao, Lu, Xingyu, Williams, Robert O., Zhang, Feng
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 401
container_issue
container_start_page 390
container_title International journal of pharmaceutics
container_volume 557
creator Lowinger, Michael B.
Su, Yongchao
Lu, Xingyu
Williams, Robert O.
Zhang, Feng
description [Display omitted] Hydrophobic and hydrophilic thermoplastic poly(urethane) (TPU) mixtures offer the opportunity to tune water swelling capacity and diffusion rate for drugs exhibiting broadly different properties. We sought to (1) assess the range of drug diffusion rates achieved by varying hydrophilic-to-hydrophobic TPU ratio relative to varying ethylene vinyl acetate (EVA) crystallinity; (2) investigate the effect of mixture ratio on permeability of emtricitabine; and (3) investigate the impact of the extrusion process on mixing of the two TPUs and the resulting impact on drug diffusion. The permeability of water-soluble emtricitabine exhibited a 736-fold range across the blends of TPU, but only a 3.4-fold range across the EVA grades investigated. Varying hydrophilic content of the TPU mixture from 0% to 25% (w/w) led to a negligible permeability change, while changing hydrophilic content from 55% to 100% resulted in a linear 3-fold increase in drug permeability. Interestingly, an 123-fold permeability change occurred between 50% and 55% hydrophilic polymer. Extrusion process parameters exhibited minimal impact on homogeneity and drug diffusion. These findings suggest that hydrophilic polymer domains form a continuous network at levels above 55% hydrophilic TPU, thus facilitating a water-filled porous network when exposed to water that provides a mechanism for accelerated drug diffusion.
doi_str_mv 10.1016/j.ijpharm.2018.11.067
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2155162504</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0378517318308949</els_id><sourcerecordid>2155162504</sourcerecordid><originalsourceid>FETCH-LOGICAL-c365t-2e636199cdd763c13f50f979f8ff5a2fcdf60d3679966ef716f76cb5b615b44a3</originalsourceid><addsrcrecordid>eNqFkE1v1DAQhi0EotvCTwD5WA4Jnng9Tk4VWpW2UgUXOFuOPW69yhd2UnX_Pal24drTaKTnnY-HsU8gShCAX_dl3E-PNvVlJaAuAUqB-g3bQK1lIbca37KNkLouFGh5xs5z3gshsAL5np1JoaoGVb1hP3Z24D4tDzxRRzYTT3YmHtLY89hPnR3mzFvis43dmMjzJcfhgU9jd7hcEs2PdqAvvI_P89rlqw_sXbBdpo-nesF-f7_-tbst7n_e3O2-3RdOopqLilAiNI3zXqN0IIMSodFNqENQtgrOBxReom4aRAoaMGh0rWoRVLvdWnnBLo9zpzT-WSjPpo_ZUbfeS-OSTQVKAVZKbFdUHVGXxpwTBTOl2Nt0MCDMi0qzNyeV5kWlATCryjX3-bRiaXvy_1P_3K3A1RGg9dGnSMlkF2lw5GMiNxs_xldW_AXik4fe</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2155162504</pqid></control><display><type>article</type><title>Can drug release rate from implants be tailored using poly(urethane) mixtures?</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Lowinger, Michael B. ; Su, Yongchao ; Lu, Xingyu ; Williams, Robert O. ; Zhang, Feng</creator><creatorcontrib>Lowinger, Michael B. ; Su, Yongchao ; Lu, Xingyu ; Williams, Robert O. ; Zhang, Feng</creatorcontrib><description>[Display omitted] Hydrophobic and hydrophilic thermoplastic poly(urethane) (TPU) mixtures offer the opportunity to tune water swelling capacity and diffusion rate for drugs exhibiting broadly different properties. We sought to (1) assess the range of drug diffusion rates achieved by varying hydrophilic-to-hydrophobic TPU ratio relative to varying ethylene vinyl acetate (EVA) crystallinity; (2) investigate the effect of mixture ratio on permeability of emtricitabine; and (3) investigate the impact of the extrusion process on mixing of the two TPUs and the resulting impact on drug diffusion. The permeability of water-soluble emtricitabine exhibited a 736-fold range across the blends of TPU, but only a 3.4-fold range across the EVA grades investigated. Varying hydrophilic content of the TPU mixture from 0% to 25% (w/w) led to a negligible permeability change, while changing hydrophilic content from 55% to 100% resulted in a linear 3-fold increase in drug permeability. Interestingly, an 123-fold permeability change occurred between 50% and 55% hydrophilic polymer. Extrusion process parameters exhibited minimal impact on homogeneity and drug diffusion. These findings suggest that hydrophilic polymer domains form a continuous network at levels above 55% hydrophilic TPU, thus facilitating a water-filled porous network when exposed to water that provides a mechanism for accelerated drug diffusion.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2018.11.067</identifier><identifier>PMID: 30529658</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Emtricitabine ; Implant ; Long-acting ; Polyurethane ; Sustained release ; TPU</subject><ispartof>International journal of pharmaceutics, 2019-02, Vol.557, p.390-401</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-2e636199cdd763c13f50f979f8ff5a2fcdf60d3679966ef716f76cb5b615b44a3</citedby><cites>FETCH-LOGICAL-c365t-2e636199cdd763c13f50f979f8ff5a2fcdf60d3679966ef716f76cb5b615b44a3</cites><orcidid>0000-0001-5063-3218 ; 0000-0002-5377-5841 ; 0000-0002-3084-6598 ; 0000-0003-4993-6427</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.2018.11.067$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30529658$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lowinger, Michael B.</creatorcontrib><creatorcontrib>Su, Yongchao</creatorcontrib><creatorcontrib>Lu, Xingyu</creatorcontrib><creatorcontrib>Williams, Robert O.</creatorcontrib><creatorcontrib>Zhang, Feng</creatorcontrib><title>Can drug release rate from implants be tailored using poly(urethane) mixtures?</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>[Display omitted] Hydrophobic and hydrophilic thermoplastic poly(urethane) (TPU) mixtures offer the opportunity to tune water swelling capacity and diffusion rate for drugs exhibiting broadly different properties. We sought to (1) assess the range of drug diffusion rates achieved by varying hydrophilic-to-hydrophobic TPU ratio relative to varying ethylene vinyl acetate (EVA) crystallinity; (2) investigate the effect of mixture ratio on permeability of emtricitabine; and (3) investigate the impact of the extrusion process on mixing of the two TPUs and the resulting impact on drug diffusion. The permeability of water-soluble emtricitabine exhibited a 736-fold range across the blends of TPU, but only a 3.4-fold range across the EVA grades investigated. Varying hydrophilic content of the TPU mixture from 0% to 25% (w/w) led to a negligible permeability change, while changing hydrophilic content from 55% to 100% resulted in a linear 3-fold increase in drug permeability. Interestingly, an 123-fold permeability change occurred between 50% and 55% hydrophilic polymer. Extrusion process parameters exhibited minimal impact on homogeneity and drug diffusion. These findings suggest that hydrophilic polymer domains form a continuous network at levels above 55% hydrophilic TPU, thus facilitating a water-filled porous network when exposed to water that provides a mechanism for accelerated drug diffusion.</description><subject>Emtricitabine</subject><subject>Implant</subject><subject>Long-acting</subject><subject>Polyurethane</subject><subject>Sustained release</subject><subject>TPU</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkE1v1DAQhi0EotvCTwD5WA4Jnng9Tk4VWpW2UgUXOFuOPW69yhd2UnX_Pal24drTaKTnnY-HsU8gShCAX_dl3E-PNvVlJaAuAUqB-g3bQK1lIbca37KNkLouFGh5xs5z3gshsAL5np1JoaoGVb1hP3Z24D4tDzxRRzYTT3YmHtLY89hPnR3mzFvis43dmMjzJcfhgU9jd7hcEs2PdqAvvI_P89rlqw_sXbBdpo-nesF-f7_-tbst7n_e3O2-3RdOopqLilAiNI3zXqN0IIMSodFNqENQtgrOBxReom4aRAoaMGh0rWoRVLvdWnnBLo9zpzT-WSjPpo_ZUbfeS-OSTQVKAVZKbFdUHVGXxpwTBTOl2Nt0MCDMi0qzNyeV5kWlATCryjX3-bRiaXvy_1P_3K3A1RGg9dGnSMlkF2lw5GMiNxs_xldW_AXik4fe</recordid><startdate>20190225</startdate><enddate>20190225</enddate><creator>Lowinger, Michael B.</creator><creator>Su, Yongchao</creator><creator>Lu, Xingyu</creator><creator>Williams, Robert O.</creator><creator>Zhang, Feng</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5063-3218</orcidid><orcidid>https://orcid.org/0000-0002-5377-5841</orcidid><orcidid>https://orcid.org/0000-0002-3084-6598</orcidid><orcidid>https://orcid.org/0000-0003-4993-6427</orcidid></search><sort><creationdate>20190225</creationdate><title>Can drug release rate from implants be tailored using poly(urethane) mixtures?</title><author>Lowinger, Michael B. ; Su, Yongchao ; Lu, Xingyu ; Williams, Robert O. ; Zhang, Feng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-2e636199cdd763c13f50f979f8ff5a2fcdf60d3679966ef716f76cb5b615b44a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Emtricitabine</topic><topic>Implant</topic><topic>Long-acting</topic><topic>Polyurethane</topic><topic>Sustained release</topic><topic>TPU</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lowinger, Michael B.</creatorcontrib><creatorcontrib>Su, Yongchao</creatorcontrib><creatorcontrib>Lu, Xingyu</creatorcontrib><creatorcontrib>Williams, Robert O.</creatorcontrib><creatorcontrib>Zhang, Feng</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>Lowinger, Michael B.</au><au>Su, Yongchao</au><au>Lu, Xingyu</au><au>Williams, Robert O.</au><au>Zhang, Feng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Can drug release rate from implants be tailored using poly(urethane) mixtures?</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2019-02-25</date><risdate>2019</risdate><volume>557</volume><spage>390</spage><epage>401</epage><pages>390-401</pages><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted] Hydrophobic and hydrophilic thermoplastic poly(urethane) (TPU) mixtures offer the opportunity to tune water swelling capacity and diffusion rate for drugs exhibiting broadly different properties. We sought to (1) assess the range of drug diffusion rates achieved by varying hydrophilic-to-hydrophobic TPU ratio relative to varying ethylene vinyl acetate (EVA) crystallinity; (2) investigate the effect of mixture ratio on permeability of emtricitabine; and (3) investigate the impact of the extrusion process on mixing of the two TPUs and the resulting impact on drug diffusion. The permeability of water-soluble emtricitabine exhibited a 736-fold range across the blends of TPU, but only a 3.4-fold range across the EVA grades investigated. Varying hydrophilic content of the TPU mixture from 0% to 25% (w/w) led to a negligible permeability change, while changing hydrophilic content from 55% to 100% resulted in a linear 3-fold increase in drug permeability. Interestingly, an 123-fold permeability change occurred between 50% and 55% hydrophilic polymer. Extrusion process parameters exhibited minimal impact on homogeneity and drug diffusion. These findings suggest that hydrophilic polymer domains form a continuous network at levels above 55% hydrophilic TPU, thus facilitating a water-filled porous network when exposed to water that provides a mechanism for accelerated drug diffusion.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30529658</pmid><doi>10.1016/j.ijpharm.2018.11.067</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-5063-3218</orcidid><orcidid>https://orcid.org/0000-0002-5377-5841</orcidid><orcidid>https://orcid.org/0000-0002-3084-6598</orcidid><orcidid>https://orcid.org/0000-0003-4993-6427</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0378-5173
ispartof International journal of pharmaceutics, 2019-02, Vol.557, p.390-401
issn 0378-5173
1873-3476
language eng
recordid cdi_proquest_miscellaneous_2155162504
source Elsevier ScienceDirect Journals Complete
subjects Emtricitabine
Implant
Long-acting
Polyurethane
Sustained release
TPU
title Can drug release rate from implants be tailored using poly(urethane) mixtures?
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T04%3A47%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=Can%20drug%20release%20rate%20from%20implants%20be%20tailored%20using%20poly(urethane)%20mixtures?&rft.jtitle=International%20journal%20of%20pharmaceutics&rft.au=Lowinger,%20Michael%20B.&rft.date=2019-02-25&rft.volume=557&rft.spage=390&rft.epage=401&rft.pages=390-401&rft.issn=0378-5173&rft.eissn=1873-3476&rft_id=info:doi/10.1016/j.ijpharm.2018.11.067&rft_dat=%3Cproquest_cross%3E2155162504%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=2155162504&rft_id=info:pmid/30529658&rft_els_id=S0378517318308949&rfr_iscdi=true