<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>Drasler, Barbara</dc:creator>
  <dc:creator>Kucki, Melanie</dc:creator>
  <dc:creator>Delhaes, Flavien</dc:creator>
  <dc:creator>Buerki-Thurnherr, Tina</dc:creator>
  <dc:creator>Vanhecke, Dimitri</dc:creator>
  <dc:creator>Korejwo, Daria</dc:creator>
  <dc:creator>Chortare, Savvina</dc:creator>
  <dc:creator>Barosova, Hana</dc:creator>
  <dc:creator>Hirsch, Cordula</dc:creator>
  <dc:creator>Petri-Fink, Alke</dc:creator>
  <dc:creator>Rothen-Rutishauser, Barbara</dc:creator>
  <dc:creator>Wick, Peter</dc:creator>
  <dc:date>2018-10-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The increased mass production of graphene related materials (GRM), intended for a  broad spectrum of applications, demands a thorough assessment of their potential  hazard to humans and the environment. Particularly, the paramount concern has been  expressed in regard to their interaction with the respiratory system in occupational  exposure settings. It has been shown that GRM are easily respirable and can interact  with lung cells resulting in the induction of oxidative stress or pulmonary inflammation.  However, a comprehensive assessment of potential biological effects induced by  GRM is currently hardly feasible to accomplish due to the lack of well-defined GRM  materials and realistic exposure data. Herein, a 3D human lung model was combined  with a commercial aerosolization system to study potential side effects of GRM. Two  representative types of GRM were aerosolized onto the lung epithelial tissue surface.  After 24 h post exposure, selected biological endpoints were evaluated, such as cell  viability, morphology, barrier integrity, induction of (pro-)inflammation and oxidative  stress reactions and compared with the reference material carbon black. Single  exposure to all tested GRM at the two different exposure concentrations (∼300 and  1000 ng/cm2) did not initiate an observable adverse effect to the 3D lung model under  acute exposure scenarios.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307323</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307323/files/fin_sea.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307323/files/fin_sea_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.carbon.2018.05.012</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Carbon. - 2018, vol. 137, p. 125–135</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Single exposure to aerosolized graphene oxide and graphene nanoplatelets did not initiate an acute biological response in a 3D human lung model</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
