All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Novel porphyrin conjugates with a potent photodynamic antitumor effect: differential efficacy of mono- and bis-b-cyclodextrin derivatives. In vitro and in vivo

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22340%2F06%3A00016680" target="_blank" >RIV/60461373:22340/06:00016680 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Novel porphyrin conjugates with a potent photodynamic antitumor effect: differential efficacy of mono- and bis-b-cyclodextrin derivatives. In vitro and in vivo

  • Original language description

    In the present study we investigated photosensitizing properties of two novel mono- and bis-cyclodextrin tetrakis(pentafluorophenyl) porphyrin derivatives in several tumor cell lines and in BALB/c mice bearing subcutaneously transplanted syngeneic mousemammary carcinoma, 4T1. Both studied sensitizers were localized mainly into lysosomes and were found to induce cells death by triggering apoptosis in human leukemic cells HL-60. In 4T1 and other cell lines both apoptotic and necrotic modes of cell deathoccurred dependently on drug and light doses. Mono-cyclodextrin porphyrin derivative, P(b-CD)1, exhibited stronger in vitro photodynamic efficacy than bis-cyclodextrin derivative, P(b-CD)2. However, when their efficacy was evaluated in vivo, P(b-CD)2 displayed faster tumor uptake with maximal accumulation 6 h after application leading to complete and prolonged elimination of subcutaneous tumors within 3 days after irradiation (100 J/cm2). In contrast P(b-CD)1 uptake was slower (48 h) and

  • Czech name

    Nové porfyrinové conjugaty s fotodynamickým protinádorovým efektem: účinnost mono- a bis-b-cyclodextrinových derivátů v in vivo a in vitro studiu

  • Czech description

    V představeném studiu byly sledované fotosensibilní vlastnosti dvou nových mono- a bis-cyclodextrin tetrakis(pentafluorofenyl) porfyrinových derivátů na kulturách nádorových buněk a na nádoru prsní žlázy 4T1 transplantovaného pod kůži BALB/c myši. Obě studované látky v experimentech in vitro prokázaly lokalizace v lysosomech buněčných kultur a indukovaly smrt buněk spouštěním apoptosy. Mono-cyclodextrin porfyrinový derivát, P(b-CD)1, projevoval silnější fotodynamický efekt in vitro než bis-cyclodextrinový derivat P(b-CD)2. Ale v experimentech in vivo P(b-CD)2 ukázal rychlejší lokalizace v nádorové tkáni s maximální obsahem už za 6 hodin po aplikace a silnější protinádorovou aktivitu na rozdíl od P(b-CD)1 z pomalejší lokalizace.

Classification

  • Type

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

  • CEP classification

    CB - Analytical chemistry, separation

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GA301%2F04%2F1315" target="_blank" >GA301/04/1315: Induction of apoptosis by macrocyclic compounds in cancer cells</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2006

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Photochemistry and Photobiology

  • ISSN

    0031-8655

  • e-ISSN

  • Volume of the periodical

    82

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    CA - CANADA

  • Number of pages

    7

  • Pages from-to

    432-438

  • UT code for WoS article

  • EID of the result in the Scopus database