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Evaluation of linear versus star-like polymer anti-cancer nanomedicines in mouse models

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    SYSNO ASEP0565337
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleEvaluation of linear versus star-like polymer anti-cancer nanomedicines in mouse models
    Author(s) Kostka, Libor (UMCH-V) RID, ORCID
    Kotrchová, Lenka (UMCH-V) RID, ORCID
    Randárová, Eva (UMCH-V) RID
    Ferreira, C. A. (US)
    Malátová, Iva (MBU-M)
    Lee, H. J. (US)
    Olson, A. P. (US)
    Engle, J. W. (US)
    Kovář, Marek (MBU-M) RID, ORCID
    Cai, W. (US)
    Šírová, Milada (MBU-M) RID, ORCID
    Etrych, Tomáš (UMCH-V) RID, ORCID
    Source TitleJournal of Controlled Release. - : Elsevier - ISSN 0168-3659
    Roč. 353, January (2023), s. 549-562
    Number of pages14 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsdrug delivery ; cancer ; polymeric carriers
    Subject RIVCD - Macromolecular Chemistry
    OECD categoryPolymer science
    Subject RIV - cooperationInstitute of Microbiology - Pharmacology ; Medidal Chemistry
    R&D ProjectsLX22NPO5102 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    LTAUSA18083 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportUMCH-V - RVO:61389013 ; MBU-M - RVO:61388971
    UT WOS000992308100001
    EID SCOPUS85143725488
    DOI10.1016/j.jconrel.2022.11.060
    AnnotationNanomedicines are considered next generation therapeutics with advanced therapeutic properties and reduced side effects. Herein, we introduce tailored linear and star-like water-soluble nanosystems as stimuli-sensitive nanomedicines for the treatment of solid tumors or hematological malignancies. The polymer carrier and drug pharmacokinetics were independently evaluated to elucidate the relationship between the nanosystem structure and its distribution in the body. Positron emission tomography and optical imaging demonstrated enhanced tumor accumulation of the polymer carriers in 4T1-bearing mice with increased tumor-to-blood and tumor-to-muscle ratios. Additionally, there was a significant accumulation of doxorubicin bound to various polymer carriers in EL4 tumors, as well as excellent in vivo therapeutic activity in EL4 lymphoma and moderate efficacy in 4T1 breast carcinoma. The linear nanomedicine showed at least comparable pharmacologic properties to the star-like nanomedicines regarding doxorubicin transport. Therefore, if multiple parameters are considered such as its optimized structure and simple and reproducible synthesis, this polymer carrier system is the most promising for further preclinical and clinical investigations.
    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/S0168365922008148?via%3Dihub
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