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dc.contributor.authorOusanee Issarachoten_US
dc.contributor.authorJiraphong Suksiriworapongen_US
dc.contributor.authorKittisak Sriphaen_US
dc.contributor.authorVaraporn Buraphacheep Junyapraserten_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-10-19T04:47:48Z-
dc.date.available2018-10-19T04:47:48Z-
dc.date.issued2013-07-15en_US
dc.identifier.citationJournal of Applied Polymer Science. Vol.129, No.2 (2013), 721-734en_US
dc.identifier.issn10974628en_US
dc.identifier.issn00218995en_US
dc.identifier.other2-s2.0-84876481195en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84876481195&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/31522-
dc.description.abstractRegarding polymer-drug conjugation, the reaction and drug characteristics are of important because they reflect the possibility of conjugation. Tri- and dicomponent azido-functionalized copolymers were initially synthesized. Tricomponent copolymers consisted of caproyl, azido-substituted caproyl, and ethylene glycol repeating units, whereas dicomponent ones contained solely the last two repeating units. In parallel, the terminal alkyne derivatives of methotrexate (MTX) and folic acid (FOL) were synthesized by coupling reaction using N,N-dicyclohexylcarbodiimide and 4-dimethylaminopyridine with an additional N-hydroxysuccinimide for FOL coupling. By click reaction, MTX and FOL were successfully conjugated with tri- and dicomponent copolymers, respectively, without polymer chain degradation. The grafting efficiencies of MTX and FOL were higher than 77 and 68% by using CuI/1,8-diazabicyclo[5.4.0] undec-7-ene and CuSO4.5H2O/sodium ascorbate, respectively. According to the differential scanning calorimetry thermograms, MTX did not change the semicrystalline property of copolymers except for high % molar grafting, whereas the presence of FOL affected thermal properties of copolymer except at 5 molar grafting. The resultant copolymers could be further used as polymer-drug conjugate delivery system for cancer therapy. Copyright © 2012 Wiley Periodicals, Inc.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84876481195&origin=inwarden_US
dc.subjectChemistryen_US
dc.subjectMaterials Scienceen_US
dc.titleModification of tricomponent and dicomponent poly(ε-caprolactone)-co- poly(ethylene glycol) with methotrexate and folic aciden_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1002/app.38781en_US
Appears in Collections:Scopus 2011-2015

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