Počet záznamů: 1  

Metastatic spread inhibition of cancer cells through stimuli-sensitive HPMA copolymer-bound actinonin nanomedicines

  1. 1.
    0559474 - ÚMCH 2023 RIV US eng J - Článek v odborném periodiku
    Kousalová, Jana - Šírová, Milada - Kostka, Libor - Šubr, Vladimír - Kovářová, Jiřina - Běhalová, Kateřina - Studenovský, Martin - Kovář, Marek - Etrych, Tomáš
    Metastatic spread inhibition of cancer cells through stimuli-sensitive HPMA copolymer-bound actinonin nanomedicines.
    Nanomedicine: Nanotechnology, Biology and Medicine. Roč. 44, August (2022), č. článku 102578. ISSN 1549-9634. E-ISSN 1549-9642
    Grant CEP: GA MŠMT(CZ) LTAUSA18083
    Grant ostatní: AV ČR(CZ) JSPS-22-01
    Program: Bilaterální spolupráce
    Institucionální podpora: RVO:61389013 ; RVO:61388971
    Klíčová slova: matrix metalloproteinases * metastases * actinonin
    Obor OECD: Polymer science; Oncology (MBU-M)
    Impakt faktor: 5.4, rok: 2022
    Způsob publikování: Omezený přístup
    https://www.sciencedirect.com/science/article/pii/S1549963422000648?via%3Dihub

    The unresolved task of modern medicine is to prevent metastatic spread during and after the treatment of primary tumors. Here, the design, controlled synthesis, in-depth physicochemical and biological characteristics of a novel panel of well-defined water-soluble copolymer conjugates bearing actinonin intended for advanced drug delivery and inhibition of metastatic spread are described. Three different synthetic approaches were employed to covalently attach actinonin to the N-(2-hydroxypropyl)methacrylamide copolymers to control the release of actinonin to its pharmacologically active form. Actinonin was attached to the polymers via hydroxamate group suppressing its activity during the delivery, with the activity restored after its release in the primary tumors or metastatic foci. Importantly, developed nanosystems with favorable drug release kinetics inhibited the metastatic spread of cancer cells from primary 4T1 tumors into the lungs as well as invasion of B16F10 melanoma cells from circulation into the lungs at the dosage without any sign of toxicity.
    Trvalý link: https://hdl.handle.net/11104/0332758

     
     
Počet záznamů: 1  

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