TY - JOUR A1 - Koshkina, Olga A1 - Westmeier, Dana A1 - Lang, Thomas A1 - Bantz, Christoph A1 - Hahlbrock, Angelina A1 - Würth, Christian A1 - Resch-Genger, Ute A1 - Braun, Ulrike A1 - Thiermann, Raphael A1 - Weise, Christoph A1 - Eravci, Murat A1 - Mohr, Benjamin A1 - Schlaad, Helmut A1 - Stauber, Roland H. A1 - Docter, Dominic A1 - Bertin, Annabelle A1 - Maskos, Michael T1 - Tuning the Surface of Nanoparticles: Impact of Poly(2-ethyl-2-oxazoline) on Protein Adsorption in Serum and Cellular Uptake JF - Macromolecular bioscience N2 - Due to the adsorption of biomolecules, the control of the biodistribution of nanoparticles is still one of the major challenges of nanomedicine. Poly(2-ethyl-2-oxazoline) (PEtOx) for surface modification of nanoparticles is applied and both protein adsorption and cellular uptake of PEtOxylated nanoparticles versus nanoparticles coated with poly(ethylene glycol) (PEG) and non-coated positively and negatively charged nanoparticles are compared. Therefore, fluorescent poly(organosiloxane) nanoparticles of 15 nm radius are synthesized, which are used as a scaffold for surface modification in a grafting onto approach. With multi-angle dynamic light scattering, asymmetrical flow field-flow fractionation, gel electrophoresis, and liquid chromatography-mass spectrometry, it is demonstrated that protein adsorption on PEtOxylated nanoparticles is extremely low, similar as on PEGylated nanoparticles. Moreover, quantitative microscopy reveals that PEtOxylation significantly reduces the non-specific cellular uptake, particularly by macrophage-like cells. Collectively, studies demonstrate that PEtOx is a very effective alternative to PEG for stealth modification of the surface of nanoparticles. KW - cellular uptake KW - nanoparticles KW - poly(2-ethyl-2oxazoline) KW - poly(ethylene glycol) KW - protein adsorption Y1 - 2016 U6 - https://doi.org/10.1002/mabi.201600074 SN - 1616-5187 SN - 1616-5195 VL - 16 SP - 1287 EP - 1300 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - de Jong, S. A1 - Kukreja, R. A1 - Trabant, C. A1 - Pontius, N. A1 - Chang, C. F. A1 - Kachel, T. A1 - Beye, Martin A1 - Sorgenfrei, Nomi A1 - Back, C. H. A1 - Braeuer, B. A1 - Schlotter, W. F. A1 - Turner, J. J. A1 - Krupin, O. A1 - Doehler, M. A1 - Zhu, D. A1 - Hossain, M. A. A1 - Scherz, A. O. A1 - Fausti, D. A1 - Novelli, F. A1 - Esposito, M. A1 - Lee, W. S. A1 - Chuang, Y. D. A1 - Lu, D. H. A1 - Moore, R. G. A1 - Yi, M. A1 - Trigo, M. A1 - Kirchmann, P. A1 - Pathey, L. A1 - Golden, M. S. A1 - Buchholz, Marcel A1 - Metcalf, P. A1 - Parmigiani, F. A1 - Wurth, W. A1 - Föhlisch, Alexander A1 - Schuessler-Langeheine, Christian A1 - Duerr, H. A. T1 - Speed limit of the insulator-metal transition in magnetite JF - Nature materials N2 - As the oldest known magnetic material, magnetite (Fe3O4) has fascinated mankind for millennia. As the first oxide in which a relationship between electrical conductivity and fluctuating/localized electronic order was shown(1), magnetite represents a model system for understanding correlated oxides in general. Nevertheless, the exact mechanism of the insulator-metal, or Verwey, transition has long remained inaccessible(2-8). Recently, three- Fe- site lattice distortions called trimeronswere identified as the characteristic building blocks of the low-temperature insulating electronically ordered phase(9). Here we investigate the Verwey transition with pump- probe X- ray diffraction and optical reflectivity techniques, and show how trimerons become mobile across the insulator-metal transition. We find this to be a two- step process. After an initial 300 fs destruction of individual trimerons, phase separation occurs on a 1.5 +/- 0.2 ps timescale to yield residual insulating and metallic regions. This work establishes the speed limit for switching in future oxide electronics(10). Y1 - 2013 U6 - https://doi.org/10.1038/NMAT3718 SN - 1476-1122 SN - 1476-4660 VL - 12 IS - 10 SP - 882 EP - 886 PB - Nature Publ. Group CY - London ER -