Molecular architectures of glycosylated dendronized bottle brushes in action: Biocompatibility and anti-amyloidogenic activity of pseudo-glycodendrimers

  • Mater Today Bio. 2025 May 10:32:101771. doi: 10.1016/j.mtbio.2025.101771.
Tom Kösterke  1  2 Radika Thakore  3  4  5 Silvia Moreno  6 Jan Skov Pedersen  7 Brigitte Voit  1  2 Oxana Klementieva  3  4  5 Dietmar Appelhans  1
Affiliations
  • 1. Leibniz-Institut für Polymerforschung Dresden e.V., Hohe Straße 6, 01069, Dresden, Germany.
  • 2. Organic Chemistry of Polymers, TUD Dresden University of Technology, 01062, Dresden, Germany.
  • 3. Medical Microspectroscopy, Department of Experimental Medical Science, Lund University, 22180, Lund, Sweden.
  • 4. NanoLund, Lund University, 22180, Lund, Sweden.
  • 5. Multipark, Lund University, 22180, Lund, Sweden.
  • 6. Department of Organic and Inorganic Chemistry, University of Alcalá, 28805, Madrid, Spain.
  • 7. Department of Chemistry and Interdisciplinary Nanoscience Center (iNANO), Aarhus University, Gustav Wieds Vej 14, Aarhus C, DK-8000, Denmark.
Abstract

Glycopolymers are versatile Materials for biomedical and healthcare applications, e.g., as carrier and polymeric therapeutics. Especially, the topology and surface composition of such Materials play a key role in being promising Materials in the anti-amyloidogenic interventions. Herein, 2nd and 3rd generation of pseudo-glycodendrimers (PGDs), based on hyperbranched polyester core with different sugar decorations, are synthesized, characterized, and used to investigate their anti-amyloidogenic properties toward Aβ (1-40) and (1-42), key players in Alzheimerś disease. The findings reveal that PGDs have a dendronized bottle brush architecture, as determined by SAXS analysis. PGDs are capable of interfering with the aggregation process of Amyloid-β peptides due to the high degree of sugar functionalization on the outer surface and the specific molecular shape. Additionally, cell viability studies indicate that PGDs exhibit concentration-dependent biocompatibility. Importantly, it is demonstrated that PGDs can be multi-functionalized by various sugar molecules, dyes, and/or peptides in a final one-pot approach. These findings suggest that PGDs may offer new avenues for therapeutic research in neurodegenerative diseases. Finally, it should be noted that this kind of highly branched glycopolymers possesses a molecular shape of dendronized bottle brushes and not a globular perfectly branched structure like glycodendrimers, as originally postulated.

Keywords
Anti-amyloidogenic agent; Biocompatibility; Dendronized bottle brushes; Post-modification; Pseudo-glycodendrimers.
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