Počet záznamů: 1  

Evaluation of Toxicological and Teratogenic Effects of Carbosilane Glucose Glycodendrimers in Zebrafish Embryos and Model Rodent Cell Lines.

  1. 1.
    SYSNO ASEP0496563
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevEvaluation of Toxicological and Teratogenic Effects of Carbosilane Glucose Glycodendrimers in Zebrafish Embryos and Model Rodent Cell Lines.
    Tvůrce(i) Liegertová, M. (CZ)
    Wróbel, D. (CZ)
    Herma, R. (CZ)
    Müllerová, Monika (UCHP-M) RID, ORCID, SAI
    Červenková Šťastná, Lucie (UCHP-M) RID, ORCID, SAI
    Cuřínová, Petra (UCHP-M) RID, SAI, ORCID
    Strašák, Tomáš (UCHP-M) RID, ORCID, SAI
    Malý, M. (CZ)
    Čermák, Jan (UCHP-M) RID, ORCID, SAI
    Smejkal, J. (CZ)
    Štofik, M. (CZ)
    Malý, J. (CZ)
    Zdroj.dok.Nanotoxicology. - : Taylor & Francis - ISSN 1743-5390
    Roč. 12, č. 8 (2018), s. 797-818
    Poč.str.22 s.
    Jazyk dok.eng - angličtina
    Země vyd.GB - Velká Británie
    Klíč. slovacarbosilane dendrimers ; glycodendrimers ; zebrafish
    Vědní obor RIVCE - Biochemie
    Obor OECDToxicology
    CEPGA15-05903S GA ČR - Grantová agentura ČR
    Institucionální podporaUCHP-M - RVO:67985858
    UT WOS000452281100001
    EID SCOPUS85053272451
    DOI10.1080/17435390.2018.1475582
    AnotaceGlycodendrimers (Glyco-DDMs) represent a rapidly growing class of nanoparticles with promising properties for biomedical applications but concerns regarding the impact on human health and environment are still justified. Here we report, for the first time, the comparative study of in vivo developmental toxicity of carbosilane Glyco-DDMs and their cytotoxicity in vitro. Carbosilane Glyco-DDMs (generation 1-3) containing 4, 8, and 16 beta-d-glucopyranosyl units at the periphery (DDM1Glu, DDM2Glu, and DDM3Glu) were synthesized and characterized by 1H, 13C and 29Si NMR, mass spectrometry, dynamic light scattering, atomic force microscopy (AFM), and computer modeling. In vitro cytotoxicity assay (MTT) of DDM1-3Glu was performed on three different rodent cell lines (Cricetulus griseus) - B14 (ATCC, CCL-14.1), BRL 3A (ATCC, CRL-1442), and NRK 52E (ATCC, CRL-1571). Overall, very low cytotoxicity was observed with calculated IC50 in mM range with slight difference between each cell line and DDM generation investigated. Modified fish embryo test (FET) was further used for DDM3Glu developmental toxicity testing on zebrafish (Danio rerio) embryos. While seemingly harmless to intact embryos, adverse effects of DDMs on the embryonic development become evident after chorion removal (LD50=2.78M at 96hpe). We summarized that the modified FET test showed a two to three orders of magnitude difference between the in vitro cytotoxicity and in vivo developmental toxicity of DDM3Glu. While, in general, the Glyco-DDMs show great promises as efficient vectors in targeted drug delivery or as therapeutic molecules itself, we suggest that their developmental toxicity should be thoroughly investigated to exclude safety risks associated with their potential biomedical use.
    PracovištěÚstav chemických procesů
    KontaktEva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227
    Rok sběru2019
Počet záznamů: 1  

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