Počet záznamů: 1  

Toxicity evaluation of monodisperse PEGylated magnetic nanoparticles for nanomedicine

  1. 1.
    SYSNO ASEP0506160
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevToxicity evaluation of monodisperse PEGylated magnetic nanoparticles for nanomedicine
    Tvůrce(i) Patsula, Vitalii (UMCH-V) RID, ORCID
    Tulinská, J. (SK)
    Trachtová, Š. (CZ)
    Kuricová, M. (SK)
    Lišková, A. (SK)
    Španová, A. (CZ)
    Čiampor, F. (SK)
    Vavra, I. (SK)
    Rittich, B. (CZ)
    Ursinyova, M. (SK)
    Dusinska, M. (NO)
    Ilavská, S. (SK)
    Horváthová, M. (SK)
    Masanova, V. (SK)
    Uhnakova, I. (SK)
    Horák, Daniel (UMCH-V) RID, ORCID
    Zdroj.dok.Nanotoxicology. - : Taylor & Francis - ISSN 1743-5390
    Roč. 13, č. 4 (2019), s. 510-526
    Poč.str.17 s.
    Jazyk dok.eng - angličtina
    Země vyd.GB - Velká Británie
    Klíč. slovairon oxide nanoparticles ; PCR inhibition ; cell interaction and uptake
    Vědní obor RIVCD - Makromolekulární chemie
    Obor OECDPolymer science
    CEPGA17-04918S GA ČR - Grantová agentura ČR
    LQ1604 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    ED1.1.00/02.0109 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Způsob publikováníOmezený přístup
    Institucionální podporaUMCH-V - RVO:61389013
    UT WOS000477976100006
    EID SCOPUS85060941650
    DOI10.1080/17435390.2018.1555624
    AnotaceInnovative nanotechnology aims to develop particles that are small, monodisperse, smart, and do not cause unintentional side effects. Uniform magnetic Fe3O4 nanoparticles (12 nm in size) were prepared by thermal decomposition of iron(III) oleate. To make them colloidally stable and dispersible in water and cell culture medium, they were modified with phosphonic acid- (PA) and hydroxamic acid (HA)-terminated poly(ethylene glycol) yielding PA-PEG@Fe3O4 and HA-PEG@Fe3O4 nanoparticles. Conventional gama-Fe2O3 particles were prepared as a control. Advanced techniques were used to evaluate the properties and safety of the particles. Completeness of the nanoparticle coating was tested by real-time polymerase chain reaction. Interaction of the particles with primary human peripheral blood cells, cellular uptake, cytotoxicity, and immunotoxicity were also investigated. Amount of internalized iron in peripheral blood mononuclear cells was 72, 38, and 25 pg Fe/cell for HA-PEG@Fe3O4,gama-Fe2O3, and PA-PEG@Fe3O4, respectively. Nanoparticles were localized within the cytoplasm and in the extracellular space. No cytotoxic effect of both PEGylated nanoparticles was observed (0.12–75 μg/cm2) after 24 and 72-h incubation. Moreover, no suppressive effect was found on the proliferative activity of T-lymphocytes and T-dependent B-cell response, phagocytic activity of monocytes and granulocytes, and respiratory burst of phagocytes. Similarly, no cytotoxic effect of gama-Fe2O3 particles was observed. However, they suppressed the proliferative activity of T-lymphocytes (75 μg/cm2, 72 h) and also decreased the phagocytic activity of monocytes (15 μg/cm2 24 h, 3–75 μg/cm2 72 h). We thus show that newly developed particles have great potential especially in cancer diagnostics and therapy.
    PracovištěÚstav makromolekulární chemie
    KontaktEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Rok sběru2020
    Elektronická adresahttps://www.tandfonline.com/doi/full/10.1080/17435390.2018.1555624
Počet záznamů: 1  

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