<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Pavic, Aleksandar</dc:creator>
  <dc:creator>Savić, Nada D.</dc:creator>
  <dc:creator>Glišić, Biljana Đ.</dc:creator>
  <dc:creator>Crochet, Aurélien</dc:creator>
  <dc:creator>Vojnovic, Sandra</dc:creator>
  <dc:creator>Kurutos, Atanas</dc:creator>
  <dc:creator>Stanković, Dalibor M.</dc:creator>
  <dc:creator>Fromm, Katharina M.</dc:creator>
  <dc:creator>Nikodinovic-Runic, Jasmina</dc:creator>
  <dc:creator>Djuran, Miloš I.</dc:creator>
  <dc:date>2019-06-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Five novel silver(I) complexes with 4,7-phenanthroline (4,7-phen), [Ag(NO3-O)(4,7- phen-μ-N4,N7)]n (1), [Ag(ClO4-О)(4,7-phen-μ-N4,N7)]n (2), [Ag(CF3COO-O)(4,7- phen-μ-N4,N7)]n (3), [Ag2(H2O)0.58(4,7-phen)3](SbF6)2 (4) and {[Ag2(H2O)(4,7- phen-μ-N4,N7)2](BF4)2}n (5) were synthesized, structurally elucidated and  biologically evaluated. These complexes showed selectivity towards Candida spp. in  comparison to the tested bacteria and effectively inhibited the growth of four different  Candida species, particularly of C. albicans strains, with minimal inhibitory  concentrations (MICs) in the range of 2.0–10.0 μM. In order to evaluate the  therapeutic potential of 1–5, in vivo toxicity studies were conducted in the zebrafish  model. Based on the favorable therapeutic profiles, complexes 1, 3 and 5 were  selected for the evaluation of their antifungal efficacy in vivo using the zebrafish model  of lethal disseminated candidiasis. Complexes 1 and 3 efficiently controlled and  prevented fungal filamentation even at sub-MIC doses, while drastically increased the  survival of the infected embryos. Moreover, at the MIC doses, both complexes totally  prevented C. albicans filamentation and rescued almost all infected fish of the fatal  infection outcome. On the other side, complex 5, which demonstrated the highest  antifungal activity in vitro, affected the neutrophils occurrence of the infected host,  failed to inhibit the C. albicans cells filamentation and showed a poor potential to cure  candidal infection, highlighting the importance of the in vivo activity evaluation early in  the therapeutic design and development process. The mechanism of action of the  investigated silver(I) complexes was related to the induction of reactive oxygen  species (ROS) response in C. albicans, with DNA being one of the possible target  biomolecules.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307991</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307991/files/fro_scw.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307991/files/fro_scw_sm.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307991/files/fro_scw_sm2.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jinorgbio.2019.03.017</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Journal of Inorganic Biochemistry. - 2019, vol. 195, p. 149–163</dc:source>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Silver(I) complexes with 4,7-phenanthroline efficient in rescuing the zebrafish embryos of lethal Candida albicans infection</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
