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Fullerene as a transporter for doxorubicin investigated by analytical methods and in vivo imaging

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62156489%3A43210%2F14%3A00225111" target="_blank" >RIV/62156489:43210/14:00225111 - isvavai.cz</a>

  • Alternative codes found

    RIV/62157124:16270/14:43872966 RIV/00216305:26620/14:PU109895

  • Result on the web

    <a href="http://dx.doi.org/10.1002/elps.201300393" target="_blank" >http://dx.doi.org/10.1002/elps.201300393</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/elps.201300393" target="_blank" >10.1002/elps.201300393</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Fullerene as a transporter for doxorubicin investigated by analytical methods and in vivo imaging

  • Original language description

    Carbon nanomaterials, including fullerenes, exhibit not only unique structure and electronic properties but also a significant potential to serve as radical scavengers and/or anti-oxidants. Their conjugation with anticancer drugs such as doxorubicin (DOX) may help to balance severe negative side effects of these cytostatics and also improve the delivery of the drug taking advantage of the enhanced cellular uptake, selectivity to cancer cells, and pH regulated release. In this study, the fullerene (C60)surface was oxidized by concentrated nitric acid, which enabled simple DOX--fullerene conjugation based on pi-pi stacking and hydrophilic interactions with carboxylic groups. The strength of this noncovalent binding is pH dependent. At a low pH, the amino group of DOX is protonated, however at a higher pH, the amino group is deprotonated, resulting in stronger hydrophobic interactions with the fullerene walls. CE and HPLC were employed for characterization of resulting complexes. The cel

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CE - Biochemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/ED1.1.00%2F02.0068" target="_blank" >ED1.1.00/02.0068: Central european institute of technology</a><br>

  • Continuities

    O - Projekt operacniho programu

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Electrophoresis

  • ISSN

    0173-0835

  • e-ISSN

  • Volume of the periodical

    35

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    10

  • Pages from-to

    1040-1049

  • UT code for WoS article

    333644600016

  • EID of the result in the Scopus database