Temperature-sensitive releases from liposomes containing hydrophobically modified poly(N-isopropylacrylamide)

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dc.contributor.authorKim, J.-C.ko
dc.contributor.authorKim, M.-S.ko
dc.contributor.authorKim, Jong-Dukko
dc.date.accessioned2013-03-02T21:11:02Z-
dc.date.available2013-03-02T21:11:02Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1999-
dc.identifier.citationKOREAN JOURNAL OF CHEMICAL ENGINEERING, v.16, no.1, pp.28 - 33-
dc.identifier.issn0256-1115-
dc.identifier.urihttp://hdl.handle.net/10203/75531-
dc.description.abstractNovel temperature-sensitive liposomes containing hydrophobically modified poly(N-isopropylacrylamide) (HPNIPAM) and their release behaviors were investigated using calcein as a fluorescence probe. Above the lower critical solution temperature (LCST) of the polymer (e.g., 40 degrees C), the degree of calcein release in 280 sec from reverse-phase evaporation vesicles (REVs) of egg phosphatidylcholine (egg PC) was 43 %, while egg PC MLVs was 16 %. Such a large difference of release may be attributed to the lamellarity of liposomes. The incorporation of dioleoylphosphatidylethanolamine (DOPE) into the PC bilayer enhanced the release by 10-13 % at 40 degrees C, probably due to the increased instability of mixture bilayers. Meanwhile, a temperature-sensitive device of DOPE liposomes was prepared by using HPNIPAM as a stabilizer. The optimal ratio of HPNIPAM to lipid to stabilize the bilayer was 0.1. Above the LCST (e.g., 40 degrees C), the release percentage was about 80 % of the entrapped calcein. DOPE liposomes were the most temperature-sensitive among liposomes tested. This is probably because DOPE liposomes disintegrate into a non-liposomal phase, such as hexagonal (H-Pi), by a thermal contraction of HPNIPAM.-
dc.languageEnglish-
dc.publisherKOREAN INST CHEM ENGINEERS-
dc.subjectPHOSPHATIDYLETHANOLAMINE-
dc.subjectCARRIERS-
dc.subjectDELIVERY-
dc.subjectDRUGS-
dc.titleTemperature-sensitive releases from liposomes containing hydrophobically modified poly(N-isopropylacrylamide)-
dc.typeArticle-
dc.identifier.wosid000078558500004-
dc.identifier.scopusid2-s2.0-0033434910-
dc.type.rimsART-
dc.citation.volume16-
dc.citation.issue1-
dc.citation.beginningpage28-
dc.citation.endingpage33-
dc.citation.publicationnameKOREAN JOURNAL OF CHEMICAL ENGINEERING-
dc.identifier.doi10.1007/BF02699001-
dc.contributor.localauthorKim, Jong-Duk-
dc.contributor.nonIdAuthorKim, J.-C.-
dc.contributor.nonIdAuthorKim, M.-S.-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorliposomes-
dc.subject.keywordAuthorpoly(N-isopropylacrylamide)-
dc.subject.keywordAuthortemperature-sensitivity-
dc.subject.keywordAuthordioleoylphosphatidylethanolamine-
dc.subject.keywordAuthorreverse-phase evaporation vesicles-
dc.subject.keywordPlusPHOSPHATIDYLETHANOLAMINE-
dc.subject.keywordPlusCARRIERS-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusDRUGS-
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