Preparation of α-Cyclodextrin-Terminated Polyrotaxane Consisting of β-Cyclodextrins and Pluronic as a Building Block of a Biodegradable Network
A β‐CD‐based biodegradable polyrotaxane was prepared by capping both terminals of polypseudorotaxane consisting of hydrazide‐terminated PEG‐block‐PPG‐block‐PEG (Pluronic P‐105®) and β‐CD‐succinates with mono‐aldehyde α‐CDs. By decreasing pH, the fluorescent intensity of TNS was increased with time,...
Gespeichert in:
Veröffentlicht in: | Macromolecular bioscience 2005-05, Vol.5 (5), p.379-383 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 383 |
---|---|
container_issue | 5 |
container_start_page | 379 |
container_title | Macromolecular bioscience |
container_volume | 5 |
creator | Ooya, Tooru Ito, Akihiro Yui, Nobuhiko |
description | A β‐CD‐based biodegradable polyrotaxane was prepared by capping both terminals of polypseudorotaxane consisting of hydrazide‐terminated PEG‐block‐PPG‐block‐PEG (Pluronic P‐105®) and β‐CD‐succinates with mono‐aldehyde α‐CDs. By decreasing pH, the fluorescent intensity of TNS was increased with time, indicating cleavage of the terminal hydrazone bonds followed by β‐CD‐succinate release. The terminal α‐CD moieties of the polyrotaxane are useful for self‐assembled formation with some guest molecules. |
doi_str_mv | 10.1002/mabi.200400216 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_20866891</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20866891</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4426-7fa86a88a05ae9507293149148ea86b391f44383c27953283217b0ae4241631a3</originalsourceid><addsrcrecordid>eNqFkcty0zAUhj0MDC2FLUvGG9g56GZZWjaZNpQJpYsyXWqObbkjIktBsqfJY_Ao8CA8EzLJpLBipdv3nSPpz7LXGM0wQuR9D7WZEYRYWmD-JDvFHPOixLJ8epyL6iR7EeNXhHAlJHmeneBSyJJV5Wn2_SboDQQYjHe57_JfP4rFrrG-1dshGFfc6tAbB4Nu8xtvd8EPsAWn84V30cTBuPs_1s9_rJiDS7wdg3emySGt8_lobDvhc-ub9SSlPZOM-wAt1Fbn13p48GH9MnvWgY361WE8y75cXtwuPhSrz8urxfmqaBgjvKg6EByEAFSCliWqiKSYScyETgc1lbhjjArakEqWlAhKcFUj0IwwzCkGepa929fdBP9t1HFQvYmNtjY9z49RESQ4FxIncLYHm-BjDLpTm2B6CDuFkZpCUFMI6hhCEt4cKo91r9tH_PDrCXh7ACA2YLsArjHxkeMCcUKmznLPPRird_9pqz6dz6_-vkSxd1NKent0IawVr2hVqrvrpVperpZY3FH1kf4GsrCxfQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20866891</pqid></control><display><type>article</type><title>Preparation of α-Cyclodextrin-Terminated Polyrotaxane Consisting of β-Cyclodextrins and Pluronic as a Building Block of a Biodegradable Network</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Ooya, Tooru ; Ito, Akihiro ; Yui, Nobuhiko</creator><creatorcontrib>Ooya, Tooru ; Ito, Akihiro ; Yui, Nobuhiko</creatorcontrib><description>A β‐CD‐based biodegradable polyrotaxane was prepared by capping both terminals of polypseudorotaxane consisting of hydrazide‐terminated PEG‐block‐PPG‐block‐PEG (Pluronic P‐105®) and β‐CD‐succinates with mono‐aldehyde α‐CDs. By decreasing pH, the fluorescent intensity of TNS was increased with time, indicating cleavage of the terminal hydrazone bonds followed by β‐CD‐succinate release. The terminal α‐CD moieties of the polyrotaxane are useful for self‐assembled formation with some guest molecules.</description><identifier>ISSN: 1616-5187</identifier><identifier>EISSN: 1616-5195</identifier><identifier>DOI: 10.1002/mabi.200400216</identifier><identifier>PMID: 15895475</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>alpha-Cyclodextrins - chemistry ; Applied sciences ; association ; beta-Cyclodextrins - chemistry ; biodegradable ; Biodegradation, Environmental ; Chemical modifications ; Chemical reactions and properties ; Exact sciences and technology ; fluorescence ; Hydrogen-Ion Concentration ; Optical Rotation ; Organic polymers ; Physicochemistry of polymers ; Poloxamer - chemistry ; Polyethylene Glycols ; Polymers ; polyrotaxanes ; Propylene Glycols ; Rotaxanes - chemical synthesis ; Rotaxanes - chemistry ; supramolecular structures</subject><ispartof>Macromolecular bioscience, 2005-05, Vol.5 (5), p.379-383</ispartof><rights>Copyright © 2005 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4426-7fa86a88a05ae9507293149148ea86b391f44383c27953283217b0ae4241631a3</citedby><cites>FETCH-LOGICAL-c4426-7fa86a88a05ae9507293149148ea86b391f44383c27953283217b0ae4241631a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmabi.200400216$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmabi.200400216$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16806221$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15895475$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ooya, Tooru</creatorcontrib><creatorcontrib>Ito, Akihiro</creatorcontrib><creatorcontrib>Yui, Nobuhiko</creatorcontrib><title>Preparation of α-Cyclodextrin-Terminated Polyrotaxane Consisting of β-Cyclodextrins and Pluronic as a Building Block of a Biodegradable Network</title><title>Macromolecular bioscience</title><addtitle>Macromol. Biosci</addtitle><description>A β‐CD‐based biodegradable polyrotaxane was prepared by capping both terminals of polypseudorotaxane consisting of hydrazide‐terminated PEG‐block‐PPG‐block‐PEG (Pluronic P‐105®) and β‐CD‐succinates with mono‐aldehyde α‐CDs. By decreasing pH, the fluorescent intensity of TNS was increased with time, indicating cleavage of the terminal hydrazone bonds followed by β‐CD‐succinate release. The terminal α‐CD moieties of the polyrotaxane are useful for self‐assembled formation with some guest molecules.</description><subject>alpha-Cyclodextrins - chemistry</subject><subject>Applied sciences</subject><subject>association</subject><subject>beta-Cyclodextrins - chemistry</subject><subject>biodegradable</subject><subject>Biodegradation, Environmental</subject><subject>Chemical modifications</subject><subject>Chemical reactions and properties</subject><subject>Exact sciences and technology</subject><subject>fluorescence</subject><subject>Hydrogen-Ion Concentration</subject><subject>Optical Rotation</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Poloxamer - chemistry</subject><subject>Polyethylene Glycols</subject><subject>Polymers</subject><subject>polyrotaxanes</subject><subject>Propylene Glycols</subject><subject>Rotaxanes - chemical synthesis</subject><subject>Rotaxanes - chemistry</subject><subject>supramolecular structures</subject><issn>1616-5187</issn><issn>1616-5195</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcty0zAUhj0MDC2FLUvGG9g56GZZWjaZNpQJpYsyXWqObbkjIktBsqfJY_Ao8CA8EzLJpLBipdv3nSPpz7LXGM0wQuR9D7WZEYRYWmD-JDvFHPOixLJ8epyL6iR7EeNXhHAlJHmeneBSyJJV5Wn2_SboDQQYjHe57_JfP4rFrrG-1dshGFfc6tAbB4Nu8xtvd8EPsAWn84V30cTBuPs_1s9_rJiDS7wdg3emySGt8_lobDvhc-ub9SSlPZOM-wAt1Fbn13p48GH9MnvWgY361WE8y75cXtwuPhSrz8urxfmqaBgjvKg6EByEAFSCliWqiKSYScyETgc1lbhjjArakEqWlAhKcFUj0IwwzCkGepa929fdBP9t1HFQvYmNtjY9z49RESQ4FxIncLYHm-BjDLpTm2B6CDuFkZpCUFMI6hhCEt4cKo91r9tH_PDrCXh7ACA2YLsArjHxkeMCcUKmznLPPRird_9pqz6dz6_-vkSxd1NKent0IawVr2hVqrvrpVperpZY3FH1kf4GsrCxfQ</recordid><startdate>20050523</startdate><enddate>20050523</enddate><creator>Ooya, Tooru</creator><creator>Ito, Akihiro</creator><creator>Yui, Nobuhiko</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley-VCH</general><scope>BSCLL</scope><scope>IQODW</scope><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20050523</creationdate><title>Preparation of α-Cyclodextrin-Terminated Polyrotaxane Consisting of β-Cyclodextrins and Pluronic as a Building Block of a Biodegradable Network</title><author>Ooya, Tooru ; Ito, Akihiro ; Yui, Nobuhiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4426-7fa86a88a05ae9507293149148ea86b391f44383c27953283217b0ae4241631a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>alpha-Cyclodextrins - chemistry</topic><topic>Applied sciences</topic><topic>association</topic><topic>beta-Cyclodextrins - chemistry</topic><topic>biodegradable</topic><topic>Biodegradation, Environmental</topic><topic>Chemical modifications</topic><topic>Chemical reactions and properties</topic><topic>Exact sciences and technology</topic><topic>fluorescence</topic><topic>Hydrogen-Ion Concentration</topic><topic>Optical Rotation</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Poloxamer - chemistry</topic><topic>Polyethylene Glycols</topic><topic>Polymers</topic><topic>polyrotaxanes</topic><topic>Propylene Glycols</topic><topic>Rotaxanes - chemical synthesis</topic><topic>Rotaxanes - chemistry</topic><topic>supramolecular structures</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ooya, Tooru</creatorcontrib><creatorcontrib>Ito, Akihiro</creatorcontrib><creatorcontrib>Yui, Nobuhiko</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Macromolecular bioscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ooya, Tooru</au><au>Ito, Akihiro</au><au>Yui, Nobuhiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of α-Cyclodextrin-Terminated Polyrotaxane Consisting of β-Cyclodextrins and Pluronic as a Building Block of a Biodegradable Network</atitle><jtitle>Macromolecular bioscience</jtitle><addtitle>Macromol. Biosci</addtitle><date>2005-05-23</date><risdate>2005</risdate><volume>5</volume><issue>5</issue><spage>379</spage><epage>383</epage><pages>379-383</pages><issn>1616-5187</issn><eissn>1616-5195</eissn><abstract>A β‐CD‐based biodegradable polyrotaxane was prepared by capping both terminals of polypseudorotaxane consisting of hydrazide‐terminated PEG‐block‐PPG‐block‐PEG (Pluronic P‐105®) and β‐CD‐succinates with mono‐aldehyde α‐CDs. By decreasing pH, the fluorescent intensity of TNS was increased with time, indicating cleavage of the terminal hydrazone bonds followed by β‐CD‐succinate release. The terminal α‐CD moieties of the polyrotaxane are useful for self‐assembled formation with some guest molecules.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>15895475</pmid><doi>10.1002/mabi.200400216</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1616-5187 |
ispartof | Macromolecular bioscience, 2005-05, Vol.5 (5), p.379-383 |
issn | 1616-5187 1616-5195 |
language | eng |
recordid | cdi_proquest_miscellaneous_20866891 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | alpha-Cyclodextrins - chemistry Applied sciences association beta-Cyclodextrins - chemistry biodegradable Biodegradation, Environmental Chemical modifications Chemical reactions and properties Exact sciences and technology fluorescence Hydrogen-Ion Concentration Optical Rotation Organic polymers Physicochemistry of polymers Poloxamer - chemistry Polyethylene Glycols Polymers polyrotaxanes Propylene Glycols Rotaxanes - chemical synthesis Rotaxanes - chemistry supramolecular structures |
title | Preparation of α-Cyclodextrin-Terminated Polyrotaxane Consisting of β-Cyclodextrins and Pluronic as a Building Block of a Biodegradable Network |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T23%3A50%3A55IST&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=Preparation%20of%20%CE%B1-Cyclodextrin-Terminated%20Polyrotaxane%20Consisting%20of%20%CE%B2-Cyclodextrins%20and%20Pluronic%20as%20a%20Building%20Block%20of%20a%20Biodegradable%20Network&rft.jtitle=Macromolecular%20bioscience&rft.au=Ooya,%20Tooru&rft.date=2005-05-23&rft.volume=5&rft.issue=5&rft.spage=379&rft.epage=383&rft.pages=379-383&rft.issn=1616-5187&rft.eissn=1616-5195&rft_id=info:doi/10.1002/mabi.200400216&rft_dat=%3Cproquest_cross%3E20866891%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=20866891&rft_id=info:pmid/15895475&rfr_iscdi=true |