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Tuning polymer-blood and polymer-cytoplasm membrane interactions by manipulating the architecture of poly(2-oxazoline) triblock copolymers

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    SYSNO ASEP0575786
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleTuning polymer-blood and polymer-cytoplasm membrane interactions by manipulating the architecture of poly(2-oxazoline) triblock copolymers
    Author(s) Lobaz, Volodymyr (UMCH-V) RID, ORCID
    Liščáková, Veronika (UOCHB-X) ORCID
    Sedlák, František (UOCHB-X) RID, ORCID
    Musil, Dominik (UOCHB-X)
    Lukáš Petrova, Svetlana (UMCH-V) ORCID, RID
    Šeděnková, Ivana (UMCH-V) RID
    Pánek, Jiří (UMCH-V) RID, ORCID
    Kučka, Jan (UMCH-V) RID, ORCID
    Konefal, Rafal (UMCH-V) RID, ORCID
    Tihlaříková, Eva (UPT-D) RID, ORCID, SAI
    Neděla, Vilém (UPT-D) RID, ORCID, SAI
    Pankrác, J. (CZ)
    Šefc, L. (CZ)
    Hrubý, Martin (UMCH-V) RID, ORCID
    Šácha, Pavel (UOCHB-X) RID, ORCID
    Štěpánek, Petr (UMCH-V) RID, ORCID
    Article number113564
    Source TitleColloids and Surfaces B-Biointerfaces. - : Elsevier - ISSN 0927-7765
    Roč. 231, November (2023)
    Number of pages9 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsamphiphilic triblock polyoxazoline ; drug delivery ; blood proteins
    OECD categoryPolymer science
    Subject RIV - cooperationInstitute of Macromolecular Chemistry - Macromolecular Chemistry
    Institute of Organic Chemistry and Biochemistry - Biochemistry
    Institute of Scientific Instruments - Electronics ; Optoelectronics, Electrical Engineering
    R&D ProjectsNU22-03-00318 GA MZd - Ministry of Health (MZ)
    GA21-04166S GA ČR - Czech Science Foundation (CSF)
    GA22-25799S GA ČR - Czech Science Foundation (CSF)
    LX22NPO5102 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    LM2023053 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportUMCH-V - RVO:61389013 ; UOCHB-X - RVO:61388963 ; UPT-D - RVO:68081731
    UT WOS001082347700001
    EID SCOPUS85171621348
    DOI10.1016/j.colsurfb.2023.113564
    AnnotationBioactive moieties designed to bind to cell membrane receptors benefit from coupling with polymeric carriers that have enhanced affinity to the cell membrane. When bound to the cell surface, such carriers create a “2D solution” of a ligand with a significantly increased concentration near a membrane-bound receptor compared to a freely water-soluble ligand. Bifunctional polymeric carriers based on amphiphilic triblock copolymers were synthesized from 2-pent-4-ynyl oxazoline, 2-nonyl oxazoline and 2-ethyl oxazoline. Their self-assembly and interactions with plasma proteins and HEK 293 cells were studied in detail. The affinity of these triblock copolymers to HEK 293 cell membranes and organ tissues was tunable by the overall hydrophobicity of the polymer molecule, which is determined by the length of the hydrophobic and hydrophilic blocks. The circulation time and biodistribution of three representative triblock copolymers were monitored after intravenous administration to C57BL/6 albino mice. A prolonged circulation time was observed for polymers with longer hydrophobic blocks, despite their molecular weight being below the renal threshold.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2024
    Electronic addresshttps://www.sciencedirect.com/science/article/pii/S0927776523004423?via%3Dihub
Number of the records: 1  

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