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Magnetic poly(N-propargylacrylamide) microspheres: preparation by precipitation polymerization and use in model click reactions

  1. 1.
    SYSNO ASEP0365161
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleMagnetic poly(N-propargylacrylamide) microspheres: preparation by precipitation polymerization and use in model click reactions
    Author(s) Macková, Hana (UMCH-V) RID
    Proks, Vladimír (UMCH-V) RID, ORCID
    Horák, Daniel (UMCH-V) RID, ORCID
    Kučka, Jan (UMCH-V) RID, ORCID
    Trchová, Miroslava (UMCH-V) RID, ORCID
    Source TitleJournal of Polymer Science. Part A - Polymer Chemistry. - : WILEY-BLACKWELL - ISSN 0887-624X
    Roč. 49, č. 22 (2011), s. 4820-4829
    Number of pages10 s.
    Languageeng - English
    CountryUS - United States
    Keywordsclick chemistry ; magnetic ; microspheres
    Subject RIVCD - Macromolecular Chemistry
    R&D ProjectsKJB400500904 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    KAN401220801 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    GAP503/10/0664 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z40500505 - UMCH-V (2005-2011)
    UT WOS000296255900013
    DOI10.1002/pola.24930
    AnnotationMagnetic poly(N-propargylacrylamide) (PPRAAm) microspheres were prepared by the precipitation polymerization of N-propargylacrylamide in a toluene/propan-2-ol medium in the presence of magnetic nanoparticles. The effects of polymerization parameters, including the polarity of the medium, polymerization temperature, the concentration of monomer, and the amount of magnetite in the polymerization feed, were examined. The microspheres were characterized in terms of their morphology, size, distribution, and iron content using TEM, SEM and AAS. As expected, Oleic acid-coated Fe3O4 nanoparticles contributed to the stabilization of the magnetic microspheres. Alkyne groups in magnetic PPRAAm microspheres were detected by IR. Microspheres were used as the anchor to enable a ‘‘click’’ reaction with an azido-end-functionalized model peptide (radiolabeled azidopentanoyl-GGGRGDSGGGY(125I)-NH2) and 4-azidophenylalanine using a Cu(I)-catalyzed 1,3-dipolar azide-alkyne cycloaddition reaction in water.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2012
Number of the records: 1  

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