Regulating the gaps between folds on the surface of silk fibroin membranes via LBL deposition for improving their biomedical properties

Colloids Surf B Biointerfaces. 2017 Jun 1:154:228-238. doi: 10.1016/j.colsurfb.2017.02.038. Epub 2017 Mar 1.

Abstract

Silk fibroin (SF) has become a promising biomaterial in guided bone regeneration (GBR). In an attempt to modify the size of the gaps on the surface of SF barrier membrane and improve its antibacterial activity, biological and mechanical properties, positively charged Lysozyme (LY)-Collagen Type-I (COL) composites and negatively charged SF were introduced to the negatively charged surface of SF substrates utilizing the electrostatic layer-by-layer (LBL) self-assembly technique. The morphology, chemical structures and element content of the LBL structured membranes were investigated. The results suggested that LY and COL were successfully assembled and the gaps between the folds on the surface of the membranes became smaller gradually with the increase of coated film numbers. Besides, the content of β-sheets of the membranes increased after deposition, which indicated the improvement of their mechanical properties. Moreover, the results of the measurement of immobilized LY and antibacterial assay not only revealed that the enzymatic catalysis and antibacterial activity of the samples enhanced with the increase of coated bilayer numbers but also implied that LBL modified membranes had better antibacterial activity when LY-COL was on the outermost layer. Furthermore, CCK-8 assay certified both SF membrane and LBL structured membranes could facilitate cell growth and proliferation, and the introduction of COL could further promote this ability. Finally, cell attachment and morphology examination provided intuitional evidence that SF membrane and LBL modified membranes have excellent biocompatibility.

Keywords: Antibacterial activity; Cell migration properties; Gaps regulating; LBL deposition; Silk fibroin membrane.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / chemistry*
  • Anti-Bacterial Agents / pharmacology
  • Biocompatible Materials / chemistry*
  • Biocompatible Materials / pharmacology
  • Bone Regeneration / physiology
  • Cell Adhesion
  • Cell Line, Transformed
  • Cell Proliferation / drug effects
  • Collagen Type I / chemistry*
  • Collagen Type I / pharmacology
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial Cells / physiology
  • Escherichia coli / drug effects
  • Escherichia coli / growth & development
  • Fibroins / chemistry*
  • Fibroins / pharmacology
  • Humans
  • Mice
  • Microbial Sensitivity Tests
  • Muramidase / chemistry*
  • Muramidase / pharmacology
  • Osteoblasts / cytology
  • Osteoblasts / drug effects*
  • Osteoblasts / physiology
  • Protein Conformation, beta-Strand
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / growth & development
  • Static Electricity
  • Tissue Engineering / methods

Substances

  • Anti-Bacterial Agents
  • Biocompatible Materials
  • Collagen Type I
  • Fibroins
  • Muramidase