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Stimuli Responsive Polymers for Enhanced Drug Release Applications

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dc.creator Tam, Michael K. C.
dc.date 2003-12-16T14:29:04Z
dc.date 2003-12-16T14:29:04Z
dc.date 2004-01
dc.date.accessioned 2013-10-09T02:33:18Z
dc.date.available 2013-10-09T02:33:18Z
dc.date.issued 2013-10-09
dc.identifier http://hdl.handle.net/1721.1/3951
dc.identifier.uri http://koha.mediu.edu.my:8181/xmlui/handle/1721
dc.description This 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.description Singapore-MIT Alliance (SMA)
dc.format 12331 bytes
dc.format application/pdf
dc.language en_US
dc.relation Molecular Engineering of Biological and Chemical Systems (MEBCS);
dc.subject drug and gene delivery applications
dc.subject stimuli responsive polymers
dc.title Stimuli Responsive Polymers for Enhanced Drug Release Applications
dc.type Article


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