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Biodegradable star HPMA polymer-drug conjugates: biodegradability, distribution and anti-tumor efficacy

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F11%3A00363631" target="_blank" >RIV/61389013:_____/11:00363631 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388971:_____/11:00363631

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.jconrel.2011.06.015" target="_blank" >http://dx.doi.org/10.1016/j.jconrel.2011.06.015</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jconrel.2011.06.015" target="_blank" >10.1016/j.jconrel.2011.06.015</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Biodegradable star HPMA polymer-drug conjugates: biodegradability, distribution and anti-tumor efficacy

  • Original language description

    New biodegradable star polymer?doxorubicin conjugates designed for passive tumor targeting were investigated, and their synthesis, physico-chemical characterization, drug release, biodegradation, biodistribution and in vivo anti-tumor efficacy are described. In the conjugates, the core formed by poly(amidoamine) (PAMAM) dendrimers was grafted with semitelechelic N-(2-hydroxypropyl)methacrylamide (HPMA) copolymers bearing doxorubicin (Dox) attached by hydrazone bonds, which enabled intracellular pH-controlled drug release. The described synthesis facilitated the preparation of biodegradable polymer conjugates in a broad range of molecular weights (200?1000 g/mol) while still maintaining low polydispersity ( 1.7). The polymer grafts were attached to thedendrimers through either stable amide bonds or enzymatically or reductively degradable spacers, which enabled intracellular degradation of the high-molecular-weight polymer carrier to excretable products.

  • 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 Controlled Release

  • ISSN

    0168-3659

  • e-ISSN

  • Volume of the periodical

    154

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    8

  • Pages from-to

    241-248

  • UT code for WoS article

    000295503300005

  • EID of the result in the Scopus database