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dc.contributor.authorCuong, Nguyen-Vanen_US
dc.contributor.authorHsieh, Ming-Faen_US
dc.contributor.authorChen, Yung-Tsungen_US
dc.contributor.authorLiau, Ianen_US
dc.date.accessioned2014-12-08T15:48:17Z-
dc.date.available2014-12-08T15:48:17Z-
dc.date.issued2010-09-15en_US
dc.identifier.issn0021-8995en_US
dc.identifier.urihttp://dx.doi.org/10.1002/app.32266en_US
dc.identifier.urihttp://hdl.handle.net/11536/32188-
dc.description.abstractTriblock copolymers of monomethoxy poly(ethylene glycol) (mPEG) and epsilon-caprolactone (CL) were prepared with varying lengths of poly(E-caprolactone) (PCL) compositions and a fixed length of mPEG segment. The molecular characteristics of triblock copolymers were characterized by NMR, gel permeation chromatography (GPC), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). These amphiphilic linear copolymers based on PCL hydrophobic chain and hydrophilic mPEG ending, which can self-assemble into nanoscopic micelles with their hydrophobic cores, encapsulated doxorubicin (DOX) in an aqueous solution. The particle size of prepared micelles was around 40-92 nm. The DOX loading content and DOX loading efficiency were from 3.7-7.4% to 26-49%, respectively. DOX-released profile was pH-dependent and faster at pH 5.4 than pH 7.4. Additionally, the cytotoxicity of DOX-loaded micelles was found to be similar with free DOX in drug-resistant cells (MCF-7/adr). The great amounts of DOX and fast uptake accumulated into the MCF-7/adr cells from DOX-loaded micelles suggest a potential application in cancer chemotherapy. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 117: 3694-3703, 2010en_US
dc.language.isoen_USen_US
dc.subjectnanoparticlesen_US
dc.subjectmicellesen_US
dc.subjectdrug delivery systemsen_US
dc.subjectmultidrug resistanceen_US
dc.subjectmonomethoxy poly(ethylene glycol)en_US
dc.subjectpoly(epsilon-caprolactone)en_US
dc.titleSynthesis and Characterization of PEG-PCL-PEG Triblock Copolymers as Carriers of Doxorubicin for the Treatment of Breast Canceren_US
dc.typeArticleen_US
dc.identifier.doi10.1002/app.32266en_US
dc.identifier.journalJOURNAL OF APPLIED POLYMER SCIENCEen_US
dc.citation.volume117en_US
dc.citation.issue6en_US
dc.citation.spage3694en_US
dc.citation.epage3703en_US
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000279958200077-
dc.citation.woscount11-
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