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Novel star HPMA-based polymer conjugates for passive targeting to solid tumors

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F11%3A00367005" target="_blank" >RIV/61389013:_____/11:00367005 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388971:_____/11:00367005

  • Result on the web

    <a href="http://dx.doi.org/10.3109/1061186X.2011.622402" target="_blank" >http://dx.doi.org/10.3109/1061186X.2011.622402</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3109/1061186X.2011.622402" target="_blank" >10.3109/1061186X.2011.622402</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Novel star HPMA-based polymer conjugates for passive targeting to solid tumors

  • Original language description

    Novel star polymer-doxorubicin conjugates designed for passive tumor targeting have been developed and their potential for treatment of cancer has been investigated. In the present study the synthesis, physico-chemical characterization, drug release, bio-distribution and preliminary data of in vivo efficacy of the conjugates are described. In the water-soluble conjugates the core of a molecule formed by poly(amido amine) dendrimers was grafted with semitelechelic N-(2-hydroxypropyl)methacrylamide copolymers bearing doxorubicin attached by hydrazone bonds enabling intracellular pH-controlled hydrolytic drug release, or by GFLG sequence susceptible to enzymatic degradation. The controlled synthesis utilizing semitelechelic copolymer precursors facilitated preparation of polymer conjugates in a broad range of molecular weights. The star polymer-Dox conjugates showed significantly higher anti-tumor activity in vivo than Dox HCl or its linear or graft polymer conjugates.

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CD - Macromolecular chemistry

  • OECD FORD branch

Result continuities

  • Project

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

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2011

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Drug Targeting

  • ISSN

    1061-186X

  • e-ISSN

  • Volume of the periodical

    19

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    16

  • Pages from-to

    874-889

  • UT code for WoS article

    000297057100003

  • EID of the result in the Scopus database