S-nitroso-N-acetylpenicillamine (SNAP) derivatization of peptide primary amines to create inducible nitric oxide donor biomaterials

ACS Appl Mater Interfaces. 2013 Sep 11;5(17):8430-9. doi: 10.1021/am4017945. Epub 2013 Aug 21.

Abstract

An S-nitroso-N-acetylpenicillamine (SNAP) derivatization approach was used to modify existing free primary amines found in fibrin (a natural protein-based biomaterial) to generate a controlled nitric oxide (NO) releasing scaffold material. The duration of the derivatization reaction affects the NO release kinetics, the induction of controlled NO-release, hydrophobicity, swelling behavior, elastic moduli, rheometric character, and degradation behavior. These properties were quantified to determine changes in fibrin hydrogels following covalent attachment of SNAP. NO-releasing materials exhibited minimal cytotoxicity when cultured with fibroblasts or osteoblasts. Cells maintained viability and proliferative character on derivatized materials as demonstrated by Live/Dead cell staining and counting. In addition, SNAP-derivatized hydrogels exhibited an antimicrobial character indicative of NO-releasing materials. SNAP derivatization of natural polymeric biomaterials containing free primary amines offers a means to generate inducible NO-releasing biomaterials for use as an antimicrobial and regenerative support for tissue engineering.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • 3T3 Cells
  • Amines / chemistry*
  • Animals
  • Biocompatible Materials / chemistry*
  • Biocompatible Materials / toxicity
  • Cell Line
  • Cell Survival / drug effects
  • Fibrin / chemistry*
  • Hydrogels / chemistry
  • Hydrogels / toxicity
  • Hydrophobic and Hydrophilic Interactions
  • Mice
  • Nitric Oxide Donors / chemistry*
  • S-Nitroso-N-Acetylpenicillamine / chemistry*
  • Tissue Engineering

Substances

  • Amines
  • Biocompatible Materials
  • Hydrogels
  • Nitric Oxide Donors
  • S-Nitroso-N-Acetylpenicillamine
  • Fibrin