<?xml version="1.0" encoding="utf-8"?>
<export-example>
  <doc>
    <id>44563</id>
    <completedYear/>
    <publishedYear>2018</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>255</pageFirst>
    <pageLast>266</pageLast>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume>113</volume>
    <type>article</type>
    <publisherName>Elsevier</publisherName>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Comparative proteomic analysis of hepatic effects induced by nanosilver, silver ions and nanoparticle coating in rats</title>
    <abstract language="eng">The presence of nano-scaled particles in food and food-related products has drawn attention to the oral uptake of nanoparticles and their interactions with biological systems. In the present study, we used a toxicoproteomics approach to allow for the untargeted experimental identification and comparative analysis of cellular Responses in rat liver after repeated-dose treatment with silver nanoparticles, ions, and the coating matrix used for particle stabilization.&#13;
The proteomic analysis revealed treatment-related effects caused by exposure to silver in particulate and ionic form. Both silver species induced similar patterns of signaling and metabolic alterations. Silver-induced cellular alterations comprised, amongst others, proteins involved in metal homeostasis, oxidative stress response, and energy metabolism. However, we discovered that secondary nano-scaled structures were formed from ionic silver. Furthermore, also the coating matrix alone gave rise to the formation of nano-scaled particles.&#13;
The present data confirm, complement, and extend previous knowledge on silver toxicity in rodent liver by providing a comprehensive proteomic data set. The observation of secondary particle formation from nonparticle controls underlines the difficulties in separating particle-, ion-, and matrix coating-related effects in biological systems. Awareness of this issue will support proper evaluation of nanotoxicology-related data in the future.</abstract>
    <parentTitle language="eng">Food and Chemical Toxicology</parentTitle>
    <identifier type="doi">10.1016/j.fct.2018.01.056</identifier>
    <identifier type="issn">0278-6915</identifier>
    <identifier type="issn">1873-6351</identifier>
    <enrichment key="date_peer_review">19.04.2018</enrichment>
    <author>S. Juling</author>
    <author>L. Böhmert</author>
    <author>D. Lichtenstein</author>
    <author>A. Oberemm</author>
    <author>O. Creutzenberg</author>
    <author>Andreas Thünemann</author>
    <author>A. Braeuning</author>
    <author>A. Lampen</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Silver nanoparticles</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Small-angle X-ray scattering</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>SAXS</value>
    </subject>
    <collection role="ddc" number="620">Ingenieurwissenschaften und zugeordnete Tätigkeiten</collection>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Datei im Netzwerk der BAM verfügbar ("Closed Access")</collection>
  </doc>
</export-example>
