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”

Phosphonium carbosilane dendrimers for biomedical applications - synthesis, characterization and cytotoxicity evaluation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F44555601%3A13440%2F17%3A43892841" target="_blank" >RIV/44555601:13440/17:43892841 - isvavai.cz</a>

  • Alternative codes found

    RIV/67985858:_____/17:00473749

  • Result on the web

    <a href="http://pubs.rsc.org/en/content/articlepdf/2017/ra/c7ra01845b" target="_blank" >http://pubs.rsc.org/en/content/articlepdf/2017/ra/c7ra01845b</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c7ra01845b" target="_blank" >10.1039/c7ra01845b</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Phosphonium carbosilane dendrimers for biomedical applications - synthesis, characterization and cytotoxicity evaluation

  • Original language description

    We report the synthesis and cytotoxicity evaluation of a completely new class of cationic carbosilane dendrimers functionalized with several different phosphonium peripheral groups and an ammonium functionalised one as a reference. The carbosilane dendrimers with NMe3, PMe3, P(Et-2)(2)(CH2)(3)OH, PBu3, P(C6H4-OMe)(3) and P(Ph)(3) peripheral substituents were synthesized, thoroughly characterized and modelled by computer simulations. The cytotoxicities of the dendrimers were investigated in vitro on three model cell lines (B14, BRL and NRK cells) by MTT and CV assay methods. Generally, the cytotoxicities of PMe3 carbosilane dendrimers were similar or slightly lower when compared with NMe3 dendrimers. The substitution of methyl groups in PMe3 carbosilane dendrimers with more hydrophobic and bulky alkyl substituents (PBu3 and P(Et-2)(2)(CH2)(3)OH dendrimers) resulted in an increase of cytotoxicity. The P(C6H4-OMe)(3) dendrimer showed exceptionally low cytotoxicity across all cell lines or assay methods used. Generally, phosphonium carbosilane dendrimers could represent a valuable alternative to ammonium ones in gene therapy applications due to comparable or lower cytotoxicities, the presence of positive charge for nucleic acid electrostatic binding and in the cases of P(C6H4-OMe)(3) and P(Ph)(3) dendrimers high potential of mitochondrial targeting.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    20501 - Materials engineering

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)

Others

  • Publication year

    2017

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    RSC Advances

  • ISSN

    2046-2069

  • e-ISSN

  • Volume of the periodical

    2017

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    21

  • Pages from-to

    18724-18744

  • UT code for WoS article

    000399005500067

  • EID of the result in the Scopus database

    2-s2.0-85016408382