• Valeriya Kudryavtseva
  • Ksenia Stankevich
  • Alexandu Gudima
  • Elina Kibler
  • Yuri Zhukov
  • Evgeniy Bolbasov
  • Anna Malashicheva
  • Mikhail Zhuravlev
  • Vladimir Riabov
  • Tengfei Liu
  • Victor Filimonov
  • Gennady Remnev
  • Harald Klüter
  • Julia Kzhyshkowska
  • Sergei Tverdokhlebov

Bioactive polylactic acid based (PLA) scaffolds with hyaluronic acid immobilized on their surface by atmospheric pressure plasma assisted modification method were developed. By using X-ray photoelectron spectroscopy and wettability measurements it was shown that atmospheric pressure plasma treatment leads to the changes in surface chemical composition of the PLA-based scaffolds that resulted in an increased long-term hydrophilicity of the scaffolds surface. Scanning electron microscopy and mechanical studies revealed that the use of plasma for surface activation allows for the non-destructive immobilization of bioactive compounds like hyaluronic acid. The modified PLA-based scaffolds effect on the release of cytokines and matrix metalloproteinases by primary human monocyte-derived macrophages was investigated. The macrophages reaction to the scaffolds was donor-specific, however, the two best materials from immunological point of view were identified - plasma treated PLA-based scaffold and PLA-based scaffold with the least amount of immobilized hyaluronic acid. Both hyaluronic acid attachment and atmospheric pressure plasma treatment enhance PLA-based scaffolds biocompatibility. It was found that supernatants collected after the macrophages coculture with modified PLA-based scaffolds stimulate HUVECs' tube formation. The modified PLA-based scaffolds possess pro-angiogenic activity. Thus, our research offers a high-performing method for the creation of polymer-based tissue engineering scaffolds with modified bioactive surface.

Original languageEnglish
Pages (from-to)261-271
Number of pages11
JournalMaterials and Design
Volume127
DOIs
StatePublished - 5 Aug 2017

    Research areas

  • Polylactic acid (PLA), Hyaluronic acid (HA), Tissue engineering scaffold (TES), Plasma, Macrophages, Cytokines, DIELECTRIC BARRIER DISCHARGE, RAY PHOTOELECTRON-SPECTROSCOPY, SURFACE MODIFICATION, POLYLACTIC ACID, MATRIX METALLOPROTEINASES, BIOMATERIALS, ADHESION, CELLS, PTFE, DBD

    Scopus subject areas

  • Materials Science(all)
  • Mechanics of Materials
  • Mechanical Engineering

ID: 35806787