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Träfflista för sökning "WAKA:ref ;pers:(Inganäs Olle);srt2:(2005-2009);pers:(Wigenius Jens)"

Search: WAKA:ref > Inganäs Olle > (2005-2009) > Wigenius Jens

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1.
  • Björk, Per, et al. (author)
  • Oligothiophene Assemblies Defined by DNA Interaction : From Single Chains to Disordered Clusters
  • 2009
  • In: SMALL. - : Wiley. - 1613-6810 .- 1613-6829. ; 5:1, s. 96-103
  • Journal article (peer-reviewed)abstract
    • The organization of conjugated polyelectrolytes (CPEs) interacting with biomolecules sets conditions for the biodetection of biological processes and identity, through the use of optical emission from the CPE. Herein, a well-defined CPE and its binding to DNA is studied. By using dynamic light scattering and circular dichroism spectroscopy, it is shown that the CPE forms a multimolecule ensemble in aqueous solution that is more than doubled it? size when interacting with a small DNA chain, while single chains are evident in ethanol. The related changes in the fluorescence spectra upon polymer aggregation are assigned to oscillator strength redistribution between vibronic transitions in weakly coupled H-aggregates. An enhanced single-molecule spectroscopy technique that allows full control of excitation and emission light polarization is applied to combed and decorated;,DNA chains. It is found that the organization of combed CPE-lambda DNA complexes (when dry on the surface) allows considerable variation of CPE distances and direction relative to the DNA chain. By analysis of the polarization data. energy transfer between the polymer chains in individual complexes is confirmed and their sizes estimated.
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2.
  • Karlsson, Roger, et al. (author)
  • Iron-Catalyzed Polymerization of Alkoxysulfonate-Functionalized 3,4-Ethylenedioxythiophene Gives Water-Soluble Poly(3,4-ethylenedioxythiophene) of High Conductivity
  • 2009
  • In: Chemistry of Materials. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 21:9, s. 1815-1821
  • Journal article (peer-reviewed)abstract
    • Chemical polymerization of a 3,4-ethylenedioxythiophene derivative bearing a sulfonate group (EDOTS) is reported. The polymer, PEDOT-S, is fully water-soluble and has been produced by polymerizing EDOT-S in water, using Na2S2O8 and a catalytic amount of FeCl 3. Elemental analysis and XPS measurements indicate that PEDOT-S is a material with a substantial degree of self-doping, but also contains free sulfate ions as charge-balancing counterions of the oxidized polymer. Apart from selfdoping PEDOT-S, the side chains enable full water solubility of the material; DLS studies show an average cluster size of only 2 nm. Importantly, the solvation properties of the PEDOT-S are reflected in spin-coated films, which show a surface roughness of 1.2 nm and good conductivity (12 S/cm) in ambient conditions. The electro-optical properties of this material are shown with cyclic voltammetry and spectroelectrochemical experiment reveals an electrochromic contrast (̃48% at λmax ) 606 nm).
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3.
  • Teixeira, A.I., et al. (author)
  • The promotion of neuronal maturation on soft substrates
  • 2009
  • In: Biomaterials. - : Elsevier BV. - 0142-9612 .- 1878-5905. ; 30:27, s. 4567-4572
  • Journal article (peer-reviewed)abstract
    • Microenvironmental mechanical properties of stem cell niches vary across tissues and developmental stages. Accumulating evidence suggests that matching substrate elasticity with in vivo tissue elasticity facilitates stem cell differentiation. However, it has not been established whether substrate elasticity can control the maturation stage of cells generated by stem cell differentiation. Here we show that soft substrates with elasticities commensurable to the elasticity of the brain promote the maturation of neural stem cell-derived neurons. In the absence of added growth factors, neurons differentiated on soft substrates displayed long neurites and presynaptic terminals, contrasting with the bipolar immature morphology of neurons differentiated on stiff substrates. Further, soft substrates supported an increase in astrocytic differentiation. However, stiffness cues could not override the dependency of astrocytic differentiation on Notch signaling. These results demonstrate that substrate elasticity per se can drive neuronal maturation thus defining a crucial parameter in neuronal differentiation of stem cells.
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4.
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5.
  • Wigenius, Jens, 1975-, et al. (author)
  • Limits to Nanopatterning of Fluids on Surfaces in Soft Lithography
  • 2008
  • In: Advanced Functional Materials. - : Wiley. - 1616-301X .- 1616-3028. ; 18:17, s. 2563-2571
  • Journal article (peer-reviewed)abstract
    • Soft lithographic microcontact printing using the residual polydimethylsiloxane (PDMS) found in elastomeric PDMS stamps is demonstrated to lead to unstable prints with sub-micrometer dimensions. The statics and dynamics of the process have been followed with time-resolved atomic force microscopy, imaging ellipsometry, water contact angle measurement, and optical diffraction. It is proposed that this instability places a fundamental limitation on patterning by macromolecular fluids, which is of general relevance to soft lithography and nanoimprint lithography with low viscosity polymers.
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6.
  • Wigenius, Jens, et al. (author)
  • Protein biochips patterned by microcontact printing or by adsorption-soft lithography in two modes
  • 2008
  • In: Biointerphases. - : American Vacuum Society. - 1934-8630 .- 1559-4106. ; 3:3, s. 75-82
  • Journal article (peer-reviewed)abstract
    • Patterning of proteins is critical to protein biochips. Printing of layers of proteins is well established, as is adsorption of proteins to surfaces properly modified with surface chemical functionalities. The authors show that simple methods based on soft lithography stamps can be used to prepare functional antibody chips through both these routes. Both methods incorporate transfer of the stamp material poly(dimethylsiloxane) (PDMS) to the biochip, whether intended or not intended. The results indicate that microcontact printing of proteins always includes PDMS transfer, thereby creating a possibility of unspecific adsorption to a hydrophobic domain. © 2008 American Vacuum Society.
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  • Result 1-6 of 6

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