@article{LaschewskyKirstenSkrabaniaetal.2006,
  author    = {Laschewsky, Andr{\´e} and Kirsten, Juliane and Skrabania, Katja and Storsberg, Joachim},
  title     = {Designing functional macrosurfactants via triblock tercopolymers},
  issn      = {0065-7727},
  year      = {2006},
  language  = {en}
}
@article{LaroqueReifarthSperlingetal.2020,
  author    = {Laroque, Sophie and Reifarth, Martin and Sperling, Marcel and Kersting, Sebastian and Kloepzig, Stefanie and Budach, Patrick and Hartlieb, Matthias and Storsberg, Joachim},
  title     = {Impact of multivalence and self-assembly in the design of polymeric antimicrobial peptide mimics},
  series = {ACS applied materials \& interfaces},
  volume    = {12},
  journal   = {ACS applied materials \& interfaces},
  number    = {27},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {1944-8244},
  doi       = {10.1021/acsami.0c05944},
  pages     = {30052 -- 30065},
  year      = {2020},
  abstract  = {Antimicrobial resistance is an increasingly serious challenge for public health and could result in dramatic negative consequences for the health care sector during the next decades. To solve this problem, antibacterial materials that are unsusceptible toward the development of bacterial resistance are a promising branch of research. In this work, a new type of polymeric antimicrobial peptide mimic featuring a bottlebrush architecture is developed, using a combination of reversible addition-fragmentation chain transfer (RAFT) polymerization and ring-opening metathesis polymerization (ROMP). This approach enables multivalent presentation of antimicrobial subunits resulting in improved bioactivity and an increased hemocompatibility, boosting the selectivity of these materials for bacterial cells. Direct probing of membrane integrity of treated bacteria revealed highly potent membrane disruption caused by bottlebrush copolymers. Multivalent bottlebrush copolymers clearly outperformed their linear equivalents regarding bioactivity and selectivity. The effect of segmentation of cationic and hydrophobic subunits within bottle brushes was probed using heterograft copolymers. These materials were found to self-assemble under physiological conditions, which reduced their antibacterial activity, highlighting the importance of precise structural control for such applications. To the best of our knowledge, this is the first example to demonstrate the positive impact of multivalence, generated by a bottlebrush topology in polymeric antimicrobial peptide mimics, making these polymers a highly promising material platform for the design of new bactericidal systems.},
  language  = {en}
}
@article{BaussardHabibJiwanLaschewskyetal.2004,
  author    = {Baussard, Jean-Francois and Habib-Jiwan, Jean-Louis and Laschewsky, Andr{\´e} and Mertoglu, Murat and Storsberg, Joachim},
  title     = {New chain transfer agents for reversible addition-fragmentation chain transfer (RAFT) polymerisation in aqueous media : 1. Synthesis and stability in water},
  year      = {2004},
  abstract  = {New chain transfer agents for free radical polymerisation via reversible addition-fragmentation chain transfer (RAFT) were synthesised that are particularly suited for aqueous solution polymerisation. The new compounds bear dithioester and trithiocarbonate moieties as well as permanently ionic groups to confer solubility in water. Their stability against hydrolysis was studied, and compared with the one of a frequently employed water-soluble RAFT agent, using UV-Vis-spectroscopy and H-1-NMR measurements. An improved resistance to hydrolysis was found for the new RAFT agents compared to the reference one, providing good stabilities in the pH range between 1 and 8, and up to temperatures of 70 degreesC. (C) 2004 Elsevier Ltd. All rights reserved},
  language  = {en}
}