Please use this identifier to cite or link to this item: http://dspace.mediu.edu.my:8181/xmlui/handle/1721.1/3951
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dc.creatorTam, Michael K. C.-
dc.date2003-12-16T14:29:04Z-
dc.date2003-12-16T14:29:04Z-
dc.date2004-01-
dc.date.accessioned2013-10-09T02:33:18Z-
dc.date.available2013-10-09T02:33:18Z-
dc.date.issued2013-10-09-
dc.identifierhttp://hdl.handle.net/1721.1/3951-
dc.identifier.urihttp://koha.mediu.edu.my:8181/xmlui/handle/1721-
dc.descriptionThis talk will focus on the development of polymeric nano-structured systems for drug and gene delivery applications. Two major classes of polymer systems will be considered; namely poly(ethylene-oxide-b-propylene-oxide-b-ethylene-oxide) (Pluronics) tri-block copolymers (FDA approved) and methacrylic acid (MAA) block and random copolymers. These polymers were functionalised with biodegradable or stimuli-sensitive functional groups to produce stimuli-sensitive nano-structure for efficient delivery of drugs and DNAs. The atom transfer radical polymerisation (ATRP) was adopted to synthesize a range of mono-dispersed block copolymers (e.g. PEO-b-MAA, MMA-b-MAA). Ring opening polymerization method was used to functionalize Pulronics with degradable functional groups, such as lactide (LA), and caprolactone (CL). Other stimuli-sensitive functional groups such as methacrylic acid was used to impart pH sensitivity to the polymers. Various types of methacrylic acid block and random cross-linked copolymers and other novel systems, such as fullerene based block copolymers were synthesized. Detailed mechanism and physics that control the micellization, microstructure and drug/polymer interactions will be discussed.-
dc.descriptionSingapore-MIT Alliance (SMA)-
dc.format12331 bytes-
dc.formatapplication/pdf-
dc.languageen_US-
dc.relationMolecular Engineering of Biological and Chemical Systems (MEBCS);-
dc.subjectdrug and gene delivery applications-
dc.subjectstimuli responsive polymers-
dc.titleStimuli Responsive Polymers for Enhanced Drug Release Applications-
dc.typeArticle-
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