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Nanocarriers for Anticancer Drugs - New Trends in Nanomedicine

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F13%3A10209664" target="_blank" >RIV/00216208:11130/13:10209664 - isvavai.cz</a>

  • Alternative codes found

    RIV/62156489:43210/13:00212804 RIV/00216305:26620/13:PU95529 RIV/00064203:_____/13:10209664

  • Result on the web

    <a href="http://www.ncbi.nlm.nih.gov/pubmed/23687925" target="_blank" >http://www.ncbi.nlm.nih.gov/pubmed/23687925</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Nanocarriers for Anticancer Drugs - New Trends in Nanomedicine

  • Original language description

    This review provides a brief overview of the variety of carriers employed for targeted drug delivery used in cancer therapy and summarizes advantages and disadvantages of each approach. Particularly, the attention was paid to polymeric nanocarriers, liposomes, micelles, polyethylene glycol, poly(lactic-co-glycolic acid), dendrimers, gold and magnetic nanoparticles, quantum dots, silica nanoparticles, and carbon nanotubes. Further, this paper briefly focuses on several anticancer agents (paclitaxel, docetaxel, camptothecin, doxorubicin, daunorubicin, cisplatin, curcumin, and geldanamycin) and on the influence of their combination with nanoparticulate transporters to their properties such as cytotoxicity, short life time and/or solubility.

  • 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

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Current Drug Metabolism

  • ISSN

    1389-2002

  • e-ISSN

  • Volume of the periodical

    14

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    AE - UNITED ARAB EMIRATES

  • Number of pages

    18

  • Pages from-to

    547-564

  • UT code for WoS article

    000320161000005

  • EID of the result in the Scopus database