@article{WischkeBaehrRachevaetal.2018,
  author    = {Wischke, Christian and Baehr, Elen and Racheva, Miroslava and Heuchel, Matthias and Weigel, Thomas and Lendlein, Andreas},
  title     = {Surface immobilization strategies for tyrosinase as biocatalyst applicable to polymer network synthesis},
  series = {MRS Advances},
  volume    = {3},
  journal   = {MRS Advances},
  number    = {63},
  publisher = {Cambridge Univ. Press},
  address   = {New York},
  issn      = {2059-8521},
  doi       = {10.1557/adv.2018.630},
  pages     = {3875 -- 3881},
  year      = {2018},
  abstract  = {Enzymes have recently attracted increasing attention in material research based on their capacity to catalyze the conversion of polymer-bound moieties for synthesizing polymer networks, particularly bulk hydrogels. hi this study. the surface immobilization of a relevant enzyme. mushroom tyrosinase, should be explored using glass as model surface. In a first step. the glass support was functionalized with silanes to introduce either amine or carboxyl groups, as confirmed e.g. by X-ray photoelectron spectroscopy. By applying glutaraldehyde and EDC/NHS chemistry, respectively, surfaces have been activated for subsequent successful coupling of tyrosinase. Via protein hydrolysis and amino acid characterization by HPLC, the quantity of bound tyrosinase was shown to correspond to a full surface coverage. Based on the visualized enzymatic conversion of a test substrate at the glass support. the functionalized surfaces may be explored for surface-associated material synthesis in the future.},
  language  = {en}
}
@article{DalBiancoWischkeZhouetal.2017,
  author    = {Dal Bianco, Andrea and Wischke, Christian and Zhou, Shuo and Lendlein, Andreas},
  title     = {Controlling surface properties and permeability of polyglycerol network films},
  series = {Polymers for advanced technologies},
  volume    = {28},
  journal   = {Polymers for advanced technologies},
  publisher = {Wiley},
  address   = {Hoboken},
  issn      = {1042-7147},
  doi       = {10.1002/pat.3917},
  pages     = {1263 -- 1268},
  year      = {2017},
  abstract  = {While branched polyglycerol (PG)-based molecules are well established as hydrophilic particles, the capacity of utilizing PG in bulk materials and opportunities arising by their further surface functionalization have only recently been considered. Here we investigated how the mold used in PG network synthesis may affect surface composition and how the permeability of substances through PG can be controlled by altering network structure, i.e. introducing 20mol\% oligoethylene glycol (OEG) bifunctional spacer molecules. Overall, PG-based bulk network materials were shown to be tailorable, hydrophilic, low swelling and relatively stiff polyether-based materials, with low impact of salt onto material properties. Based on these features, but also on the principal capacity of free hydroxyl groups to be used for functionalization reactions, these materials may be an interesting platform for medical and technical applications, e.g. as diffusion-rate controlling membrane in aqueous environment. Copyright (c) 2016 John Wiley \& Sons, Ltd.},
  language  = {en}
}
@inproceedings{FriessLendleinWischke2013,
  author    = {Friess, Fabian and Lendlein, Andreas and Wischke, Christian},
  title     = {Investigating side-reactions during UV-induced preparation of oligo(epsilon-caprolactone) based shape-memory polymer networks},
  series = {Abstracts of papers : joint conference / The Chemical Institute of Cananda, CIC, American Chemical Society, ACS},
  volume    = {245},
  booktitle = {Abstracts of papers : joint conference / The Chemical Institute of Cananda, CIC, American Chemical Society, ACS},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {0065-7727},
  pages     = {1},
  year      = {2013},
  language  = {en}
}