Glycopolymer Polyelectrolyte Multilayers Composed of Heparin and Maltose-Modified Poly(ethylene imine) as a Strong/Weak Polyelectrolyte System for Future Drug Delivery Coatings: Influence of pH and Sugar Architecture on Growth of Multilayers and Multilayer Swelling and Stability

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Samaa Salem - , Leibniz Institute of Polymer Research Dresden, TUD Dresden University of Technology (Author)
  • Martin Mueller - , Leibniz Institute of Polymer Research Dresden (Author)
  • Bernhard Torger - , Chair of Organic Chemistry of Polymers, Technische Universität Dresden, Leibniz Institute of Polymer Research Dresden (Author)
  • Andreas Janke - , Leibniz Institute of Polymer Research Dresden (Author)
  • Klaus-Jochen Eichhorn - , Leibniz Institute of Polymer Research Dresden (Author)
  • Brigitte Voit - , Chair of Organic Chemistry of Polymers, Technische Universität Dresden, Leibniz Institute of Polymer Research Dresden (Author)
  • Dietmar Appelhans - , Leibniz Institute of Polymer Research Dresden (Author)

Abstract

Establishing highly sophisticated polymer films for delivery systems in a biological environment and bioanalytical tasks, the formation, thickness, swelling behavior, and (physiological) stability of highly biocompatible polyelectrolyte multilayers (PEMs) are described. These PEMs are composed of the very weak polycation maltose-modified hyperbranched poly(ethylene imine) (PEI-Mal) and the strong polyanion heparin sodium salt (HE-Na+) deposited on Si wafer substrates. Two different glyco architectures for PEI-Mal are used, characterized by two different degrees of maltose decoration on a PEI scaffold. Using two pH-dependent deposition approaches for optimizing the (physiological) PEM stability and swelling, PEMs are characterized by (in situ) ellipsometry, atomic force microscopy (AFM), and (in situ) attenuated total reflection-Fourier-transform infrared (ATR-FTIR). Thus, PEMs reveal significantly different thicknesses, growth mechanisms (linear versus exponential), and swelling behavior in dependence of both the polycation architectures and the deposition protocol. These PEMs will allow the study of their complexation and release properties as preswollen PEMs against anionic drug molecules, especially under physiological conditions in the future.

Details

Original languageEnglish
Pages (from-to)182-195
Number of pages14
JournalMacromolecular chemistry and physics : MCP
Volume216
Issue number2
Publication statusPublished - Jan 2015
Peer-reviewedYes

External IDs

Scopus 84920982591
ORCID /0000-0002-4531-691X/work/148607938

Keywords

Keywords

  • Dendritic glycopolymers, Drug delivery coatings, Heparin, Physiological stability, Polyelectrolyte multilayers