Synthesis and biological evaluation of a polysialic acid-based hydrogel as enzymatically degradable scaffold material for tissue engineering

Biomacromolecules. 2008 Sep;9(9):2353-9. doi: 10.1021/bm800327s. Epub 2008 Aug 9.

Abstract

Restorative medicine has a constant need for improved scaffold materials. Degradable biopolymers often suffer from uncontrolled chemical or enzymatic hydrolysis by the host. The need for a second surgery on the other hand is a major drawback for nondegradable scaffold materials. In this paper we report the design and synthesis of a novel polysialic acid-based hydrogel with promising properties. Hydrogel synthesis was optimized and enzymatic degradation was studied using a phage-born endosialidase. After addition of endosialidase, hydrogels readily degraded depending on the amount of initially used cross-linker within 2 to 11 days. This polysialic acid hydrogel is not cytotoxic, completely stable under physiological conditions, and could be evaluated as growth support for PC12 cells. Here, additional coating with collagen I, poly-L-lysine or matrigel is mandatory to improve the properties of the material.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion / drug effects
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Cells, Cultured
  • Collagen / chemistry
  • Collagen Type I / chemistry
  • Drug Combinations
  • Electrophoresis, Polyacrylamide Gel
  • Hydrogels / chemical synthesis*
  • Hydrogels / chemistry
  • Hydrogels / metabolism*
  • Hydrolysis
  • Laminin / chemistry
  • Molecular Conformation
  • Neuraminidase / metabolism*
  • PC12 Cells
  • Polylysine / chemistry
  • Proteoglycans / chemistry
  • Rats
  • Sialic Acids / metabolism*
  • Tissue Engineering / methods*

Substances

  • Collagen Type I
  • Drug Combinations
  • Hydrogels
  • Laminin
  • Proteoglycans
  • Sialic Acids
  • polysialic acid
  • matrigel
  • Polylysine
  • Collagen
  • endo-N-acetylneuraminidase
  • Neuraminidase