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Dendrimeric based microbicides against sexual transmitted infections associated to heparan sulfate

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F44555601%3A13440%2F16%3A43893542" target="_blank" >RIV/44555601:13440/16:43893542 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1039/c6ra06969j" target="_blank" >http://dx.doi.org/10.1039/c6ra06969j</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c6ra06969j" target="_blank" >10.1039/c6ra06969j</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Dendrimeric based microbicides against sexual transmitted infections associated to heparan sulfate

  • Original language description

    Cell surface heparan sulfate (HS) represents a common link that many sexually transmitted infections (STIs) require for infection. The role of HS is associated with several viral STIs, which include those caused by herpes simplex virus (HVS), human immunodeficiency virus (HIV), human papillomavirus (HPV) and hepatitis C virus (HCV). Nowadays, no cure has been found for any of the STIs associated with viral pathogens. In this review, we evaluate dendrimers such as peptide derivatized-dendrimers, carbosilane dendrimers, polysulfated galactose functionalized glycodendrimers and PAMAM dendrimers, among others, as potential candidates for the development of topical microbicides against viral STIs associated with HS. Subsequently, we propose the mechanism of action of these dendrimers and how it might be associated with the relevance of HS in several STIs. HS in just an ancillary factor in the case of HIV-1 infection and it plays a major role in the case of HCV, HSV-2 and HPV viruses. However, the mechanism of action presented by these dendrimers is common in all pathologies, acting at the level of viral entry into the target cell, either directly blocking the viral particles that are meant to bind to the HS or binding to cellular co-receptors.

  • 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

    30107 - Medicinal chemistry

Result continuities

  • Project

    <a href="/en/project/GA15-05903S" target="_blank" >GA15-05903S: Novel carbosilane dendrimers for biomedical applications - interactions with biomolecules and biomembranes</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2016

  • 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

    2016

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    46755-46764

  • UT code for WoS article

    000377254800078

  • EID of the result in the Scopus database