Please use this identifier to cite or link to this item: https://doi.org/10.1002/marc.200900876
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dc.titleFolate-conjugated polymer micelles with pH-triggered drug release properties
dc.contributor.authorZhao, H.
dc.contributor.authorDuong, H.H.P.
dc.contributor.authorYung, L.Y.L.
dc.date.accessioned2014-10-09T06:48:05Z
dc.date.available2014-10-09T06:48:05Z
dc.date.issued2010-07-01
dc.identifier.citationZhao, H., Duong, H.H.P., Yung, L.Y.L. (2010-07-01). Folate-conjugated polymer micelles with pH-triggered drug release properties. Macromolecular Rapid Communications 31 (13) : 1163-1169. ScholarBank@NUS Repository. https://doi.org/10.1002/marc.200900876
dc.identifier.issn10221336
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/88939
dc.description.abstractFolate has been applied as a targeting moiety for various anticancer drug-delivery agents to avoid non-specific attack of normal tissues as well as to increase cellular uptake at the target tumor cells. Polymer micelles made of poly[(D,L-lactide)-co-glycolide)]-poly(ethylene glycolfolate (PLGA-PEG-FOL) was fabricated as a tumor targeting carrier for encapsulating the anticancer drug doxorubicin. To accelerate the drug release in the endosóme after folatemediated cellular uptake, pH-sensitive poly(β-amino ester)-PEG-FOL (PAE-PEG-FOL) was added together with PLGA-PEG-FOL to form mixed micelles. The results showed that the drug release can be triggered at different pH due to the ionization of PAE. The IC50 of PLGA-PEG-FOL micelles is 0.46 × 10-6 M. With 20% PAE in the mixed micelles (20:80 mixed micelles), the IC50 decreases to 0.34 × 10-6 M, which is comparable to that of pure PAE-PEG-FOL micelles at pH 7.4. As a result of the pH sensitivity, the PAE-PEG-FOL micelles are not stable at pH 6.5 or lower, and the drug may be released from the micelles into the extracellular environment before uptake by the cells. The 20:80 mixed micelles are relatively stable at this condition. As a result, the micelles retain more drug in the micelles for a higher degree of cellular uptake by folate receptor-mediated endocytosis, and exhibit higher cytotoxicity. © 2010 WILEY-VCH Verlag GmbH & Co. KCaA, Weinheim.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/marc.200900876
dc.sourceScopus
dc.subjectBlock copolymers
dc.subjectDoxorubicin
dc.subjectFolate
dc.subjectMicelles
dc.subjectStimuli-sensitive polymers
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1002/marc.200900876
dc.description.sourcetitleMacromolecular Rapid Communications
dc.description.volume31
dc.description.issue13
dc.description.page1163-1169
dc.description.codenMRCOE
dc.identifier.isiut000280045400007
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