Thermoresponsive core–shell–corona micelles of poly(ethyleneglycol)- b-poly( N-isopropylacrylamide)- b-polystyrene
Core–shell–corona micelles with a thermoresponsive shell self-assembled by triblock copolymer of poly(ethyleneglycol)- b-poly( N-isopropylacrylamide)- b-polystyrene (PEG 45- b-PNIPAM 168- b-PS 46) are studied by 1H NMR, light scattering and atomic force microscopy. The thermoresponsive triblock copo...
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Veröffentlicht in: | Polymer (Guilford) 2006-11, Vol.47 (24), p.8203-8209 |
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container_title | Polymer (Guilford) |
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creator | Zhang, Wangqing Jiang, Xiaowei He, Zhenping Xiong, Dean Zheng, Peiwen An, Yingli Shi, Linqi |
description | Core–shell–corona micelles with a thermoresponsive shell self-assembled by triblock copolymer of poly(ethyleneglycol)-
b-poly(
N-isopropylacrylamide)-
b-polystyrene (PEG
45-
b-PNIPAM
168-
b-PS
46) are studied by
1H NMR, light scattering and atomic force microscopy. The thermoresponsive triblock copolymer, which has a relatively short hydrophobic PS block, can disperse in water at room temperature to form core–shell–corona micelles with the hydrophobic PS block as core, the thermoresponsive PNIPAM block as shell and the hydrophilic PEG block as corona. At temperature above lower critical solution temperature (LCST) of the PNIPAM block, the PNIPAM chains gradually collapse on the PS core to shrink the size and change the structure of the resultant core–shell–corona micelles with temperature increasing. It is found that there possibly exists an interface between the PNIPAM shell and PEG corona of the core–shell–corona micelles at temperature above LCST of the PNIPAM block. |
doi_str_mv | 10.1016/j.polymer.2006.09.053 |
format | Article |
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b-poly(
N-isopropylacrylamide)-
b-polystyrene (PEG
45-
b-PNIPAM
168-
b-PS
46) are studied by
1H NMR, light scattering and atomic force microscopy. The thermoresponsive triblock copolymer, which has a relatively short hydrophobic PS block, can disperse in water at room temperature to form core–shell–corona micelles with the hydrophobic PS block as core, the thermoresponsive PNIPAM block as shell and the hydrophilic PEG block as corona. At temperature above lower critical solution temperature (LCST) of the PNIPAM block, the PNIPAM chains gradually collapse on the PS core to shrink the size and change the structure of the resultant core–shell–corona micelles with temperature increasing. It is found that there possibly exists an interface between the PNIPAM shell and PEG corona of the core–shell–corona micelles at temperature above LCST of the PNIPAM block.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2006.09.053</identifier><identifier>CODEN: POLMAG</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Core–shell–corona micelles ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Polymers with particular properties ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; Self-assembly ; Thermoresponsive</subject><ispartof>Polymer (Guilford), 2006-11, Vol.47 (24), p.8203-8209</ispartof><rights>2006 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-5c6a026f799ee6aed3dc30d7267f034e0ef7a65e9e5ae1a801224462954384ae3</citedby><cites>FETCH-LOGICAL-c370t-5c6a026f799ee6aed3dc30d7267f034e0ef7a65e9e5ae1a801224462954384ae3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0032386106011153$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18267004$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Wangqing</creatorcontrib><creatorcontrib>Jiang, Xiaowei</creatorcontrib><creatorcontrib>He, Zhenping</creatorcontrib><creatorcontrib>Xiong, Dean</creatorcontrib><creatorcontrib>Zheng, Peiwen</creatorcontrib><creatorcontrib>An, Yingli</creatorcontrib><creatorcontrib>Shi, Linqi</creatorcontrib><title>Thermoresponsive core–shell–corona micelles of poly(ethyleneglycol)- b-poly( N-isopropylacrylamide)- b-polystyrene</title><title>Polymer (Guilford)</title><description>Core–shell–corona micelles with a thermoresponsive shell self-assembled by triblock copolymer of poly(ethyleneglycol)-
b-poly(
N-isopropylacrylamide)-
b-polystyrene (PEG
45-
b-PNIPAM
168-
b-PS
46) are studied by
1H NMR, light scattering and atomic force microscopy. The thermoresponsive triblock copolymer, which has a relatively short hydrophobic PS block, can disperse in water at room temperature to form core–shell–corona micelles with the hydrophobic PS block as core, the thermoresponsive PNIPAM block as shell and the hydrophilic PEG block as corona. At temperature above lower critical solution temperature (LCST) of the PNIPAM block, the PNIPAM chains gradually collapse on the PS core to shrink the size and change the structure of the resultant core–shell–corona micelles with temperature increasing. It is found that there possibly exists an interface between the PNIPAM shell and PEG corona of the core–shell–corona micelles at temperature above LCST of the PNIPAM block.</description><subject>Applied sciences</subject><subject>Core–shell–corona micelles</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polymers with particular properties</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>Self-assembly</subject><subject>Thermoresponsive</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFUMFO3DAQtVArsaV8AlIuIHpIOrYTJzlVFSptJUQv9GwZZ8J65cTBE1bKrf_QP-yX4GVX5cjFozd-b97MY-yMQ8GBq8-bYgp-GTAWAkAV0BZQySO24k0tcyFa_o6tAKTIZaP4MftAtAEAUYlyxbZ3a4xDiEhTGMltMbMJ_Pvzl9bofaoJhtFkg7MJI2Whz3ZulzivF48jPvjFBv8pz-7zl352mzsKUwzT4o2N6Rlch___aV5iUn1k73vjCU8P9YT9vv52d_Ujv_n1_efV15vcyhrmvLLKgFB93baIymAnOyuhq4Wqe5AlAva1URW2WBnkpgEuRFkq0ValbEqD8oRd7OemhR6fkGY9ONpdYkYMT6QTU4lSQSJWe6KNgShir6foBhMXzUHvUtYbfUhZ71LW0OqUctKdHwwMWeP7aEbr6FXcpFUBysT7sudhunbr0hSyDkeLnYtoZ90F94bTMxzZmmM</recordid><startdate>20061108</startdate><enddate>20061108</enddate><creator>Zhang, Wangqing</creator><creator>Jiang, Xiaowei</creator><creator>He, Zhenping</creator><creator>Xiong, Dean</creator><creator>Zheng, Peiwen</creator><creator>An, Yingli</creator><creator>Shi, Linqi</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope></search><sort><creationdate>20061108</creationdate><title>Thermoresponsive core–shell–corona micelles of poly(ethyleneglycol)- b-poly( N-isopropylacrylamide)- b-polystyrene</title><author>Zhang, Wangqing ; Jiang, Xiaowei ; He, Zhenping ; Xiong, Dean ; Zheng, Peiwen ; An, Yingli ; Shi, Linqi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-5c6a026f799ee6aed3dc30d7267f034e0ef7a65e9e5ae1a801224462954384ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Applied sciences</topic><topic>Core–shell–corona micelles</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polymers with particular properties</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>Self-assembly</topic><topic>Thermoresponsive</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Wangqing</creatorcontrib><creatorcontrib>Jiang, Xiaowei</creatorcontrib><creatorcontrib>He, Zhenping</creatorcontrib><creatorcontrib>Xiong, Dean</creatorcontrib><creatorcontrib>Zheng, Peiwen</creatorcontrib><creatorcontrib>An, Yingli</creatorcontrib><creatorcontrib>Shi, Linqi</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Wangqing</au><au>Jiang, Xiaowei</au><au>He, Zhenping</au><au>Xiong, Dean</au><au>Zheng, Peiwen</au><au>An, Yingli</au><au>Shi, Linqi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thermoresponsive core–shell–corona micelles of poly(ethyleneglycol)- b-poly( N-isopropylacrylamide)- b-polystyrene</atitle><jtitle>Polymer (Guilford)</jtitle><date>2006-11-08</date><risdate>2006</risdate><volume>47</volume><issue>24</issue><spage>8203</spage><epage>8209</epage><pages>8203-8209</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><coden>POLMAG</coden><abstract>Core–shell–corona micelles with a thermoresponsive shell self-assembled by triblock copolymer of poly(ethyleneglycol)-
b-poly(
N-isopropylacrylamide)-
b-polystyrene (PEG
45-
b-PNIPAM
168-
b-PS
46) are studied by
1H NMR, light scattering and atomic force microscopy. The thermoresponsive triblock copolymer, which has a relatively short hydrophobic PS block, can disperse in water at room temperature to form core–shell–corona micelles with the hydrophobic PS block as core, the thermoresponsive PNIPAM block as shell and the hydrophilic PEG block as corona. At temperature above lower critical solution temperature (LCST) of the PNIPAM block, the PNIPAM chains gradually collapse on the PS core to shrink the size and change the structure of the resultant core–shell–corona micelles with temperature increasing. It is found that there possibly exists an interface between the PNIPAM shell and PEG corona of the core–shell–corona micelles at temperature above LCST of the PNIPAM block.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2006.09.053</doi><tpages>7</tpages></addata></record> |
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source | Elsevier ScienceDirect Journals Complete |
subjects | Applied sciences Core–shell–corona micelles Exact sciences and technology Organic polymers Physicochemistry of polymers Polymers with particular properties Preparation, kinetics, thermodynamics, mechanism and catalysts Self-assembly Thermoresponsive |
title | Thermoresponsive core–shell–corona micelles of poly(ethyleneglycol)- b-poly( N-isopropylacrylamide)- b-polystyrene |
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