<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>Moore, Thomas L.</dc:creator>
  <dc:creator>Urban, Dominic A.</dc:creator>
  <dc:creator>Rodriguez-Lorenzo, Laura</dc:creator>
  <dc:creator>Milosevic, Ana</dc:creator>
  <dc:creator>Crippa, Federica</dc:creator>
  <dc:creator>Spuch-Calvar, Miguel</dc:creator>
  <dc:creator>Balog, Sandor</dc:creator>
  <dc:creator>Rothen-Rutishauser, Barbara</dc:creator>
  <dc:creator>Lattuada, Marco</dc:creator>
  <dc:creator>Petri-Fink, Alke</dc:creator>
  <dc:date>2019-01-29</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">As a highly interdisciplinary field, working with nanoparticles in a biomedical context  requires a robust understanding of soft matter physics, colloidal behaviors, nano- characterization methods, biology, and bio-nano interactions. When reporting results,  it can be easy to overlook simple, seemingly trivial experimental details. In this  context, we set out to understand how in vitro technique, specifically the way we  administer particles in 2D culture, can influence experimental outcomes. Gold  nanoparticles coated with poly(vinylpyrrolidone) were added to J774A.1 mouse  monocyte/macrophage cultures as either a concentrated bolus, a bolus then mixed via  aspiration, or pre-mixed in cell culture media. Particle-cell interaction was monitored  via inductively coupled plasma-optical emission spectroscopy and we found that  particles administered in a concentrated dose interacted more with cells compared to  the pre-mixed administration method. Spectroscopy studies reveal that the initial  formation of the protein corona upon introduction to cell culture media may be  responsible for the differences in particle-cell interaction. Modeling of particle  deposition using the in vitro sedimentation, diffusion and dosimetry model helped to  clarify what particle phenomena may be occurring at the cellular interface. We found  that particle administration method in vitro has an effect on particle-cell interactions  (i.e. cellular adsorption and uptake). Initial introduction of particles in to complex  biological media has a lasting effect on the formation of the protein corona, which in  turn mediates particle-cell interaction. It is of note that a minor detail, the way in which  we administer particles in cell culture, can have a significant effect on what we  observe regarding particle interactions in vitro.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307512</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307512/files/lat_nam.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307512/files/lat_nam_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1038/s41598-018-36954-4</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Scientific Reports. - 2019, vol. 9, no. 1, p. 900</dc:source>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Nanoparticle administration method in cell culture alters particle-cell interaction</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
