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      <dc:title>Cytokine adsorption/release on uniform magnetic nanoparticles for localized drug delivery</dc:title>
      <dc:creator>Mejías, Raquel</dc:creator>
      <dc:creator>Costo, Rocío</dc:creator>
      <dc:creator>Roca, Alejandro G.</dc:creator>
      <dc:creator>Fernández Arias, Cristina</dc:creator>
      <dc:creator>Veintemillas-Verdaguer, S.</dc:creator>
      <dc:creator>González-Carreño, T.</dc:creator>
      <dc:creator>Puerto Morales, M. del</dc:creator>
      <dc:creator>Serna, C.J.</dc:creator>
      <dc:creator>Mañes, S.</dc:creator>
      <dc:creator>Barber, D.F.</dc:creator>
      <dc:description>Attachment of cytokines to magnetic nanoparticles has been developed as a system for controlled local drug release in cancer therapy. We studied the adsorption/release of murine interferon gamma (IFN-gamma) on negatively charged magnetic nanoparticles prepared by three different methods, including coprecipitation, decomposition in organic media, and laser pyrolysis. To facilitate IFN-gamma adsorption, magnetic nanoparticles were surface modified by distinct molecules to achieve high negative charge at pH 7, maintaining small aggregate size and stability in biological media. We analyzed carboxylate-based coatings and studied the colloidal properties of the resulting dispersions. Finally, we incubated the magnetic dispersions with IFN-gamma and determined optimal conditions for protein adsorption onto the particles, as well as the release capacity at different pH and as a function of time. Particles prepared by decomposition in organic media and further modified with dimercaptosuccinic acid showed the most efficient adsorption/release capacity. IFN-gamma adsorbed on these nanoparticles would allow concentration of this protein or other biomolecules at specific sites for treatment of cancer or other diseases.</dc:description>
      <dc:date>2024-01-30T12:16:59Z</dc:date>
      <dc:date>2024-01-30T12:16:59Z</dc:date>
      <dc:date>2008-09-10</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>0168-3659</dc:identifier>
      <dc:identifier>10.1016/j.jconrel.2008.05.028</dc:identifier>
      <dc:identifier>https://hdl.handle.net/20.500.14352/96469</dc:identifier>
      <dc:identifier>1873-4995</dc:identifier>
      <dc:identifier>https://www.sciencedirect.com/science/article/abs/pii/S0168365908003301?via%3Dihub</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>restricted access</dc:rights>
      <dc:publisher>Elsevier</dc:publisher>
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