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Synthetic Mimics of Antimicrobial Peptides (SMAMPs) in Layer‐by‐Layer Architectures: Possibilities and Limitations
Authors:Franziska Dorner  Alicia Malek‐Luz  Julia S. Saar  Sebastian Bonaus  Ali Al‐Ahmad  Karen Lienkamp
Affiliation:1. Bioactive Polymer Synthesis and Surface Engineering Group, Department of Microsystems Engineering (IMTEK) and Freiburg Centre for Interactive Materials and Bioinspired Technologies (FIT), Freiburg, Germany;2. Department of Operative Dentistry and Periodontology, Center for Dental Medicine of the Albert‐Ludwigs‐Universit?t, Freiburg, Germany
Abstract:Polymer‐based synthetic mimics of antimicrobial peptides (SMAMPs) show promising antimicrobial activity in solution and as surface‐attached networks. In this paper, their potential as active ingredients in layer‐by‐layer (LbL) assemblies is evaluated. These consist of the weak, anionic polyelectrolyte poly(acrylic acid), and either the hydrophobic butyl SMAMP or the hydrophilic diamine SMAMP (both of which are cationic, weak polyelectrolytes). In situ surface plasmon resonance spectroscopy is used to optimize the LbL assembly conditions. An “overshooting” is observed when depositing the SMAMP layer. Zeta potential measurements show that the layer charge inversion is reduced at each build‐up step due to layer interpenetration. Thus, the positive charge of LbL assemblies with SMAMPs as the top layer is low; a significant part is consumed to maintain layer stability. This leads to reduced antimicrobial activity. Fine‐tuning of the assembly and post‐treatment conditions leads to SMAMP‐PAA LbL systems with optimized antimicrobial activity and stability.
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Keywords:antimicrobial polymer surfaces  layer‐by‐layer method  structure–  property relations  surface plasmon resonance spectroscopy  zeta potential
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