Surface activation with oxygen plasma promotes osteogenesis with enhanced extracellular matrix formation in three-dimensional microporous scaffolds

J Biomed Mater Res A. 2021 Sep;109(9):1560-1574. doi: 10.1002/jbm.a.37151. Epub 2021 Mar 5.

Abstract

Various types of synthetic polyesters have been developed as biomaterials for tissue engineering. These materials commonly possess biodegradability, biocompatibility, and formability, which are preferable properties for bone regeneration. The major challenge of using synthetic polyesters is the result of low cell affinity due to their hydrophobic nature, which hinders efficient cell seeding and active cell dynamics. To improve wettability, plasma treatment is widely used in industry. Here, we performed surface activation with oxygen plasma to hydrophobic copolymers, poly(l-lactide-co-trimethylene carbonate), which were shaped in 2D films and 3D microporous scaffolds, and then we evaluated the resulting surface properties and the cellular responses of rat bone marrow stem cells (rBMSC) to the material. Using scanning electron microscopy and Fourier-transform infrared spectroscopy, we demonstrated that short-term plasma treatment increased nanotopographical surface roughness and wettability with minimal change in surface chemistry. On treated surfaces, initial cell adhesion and elongation were significantly promoted, and seeding efficiency was improved. In an osteoinductive environment, rBMSC on plasma-treated scaffolds exhibited accelerated osteogenic differentiation with osteogenic markers including RUNX2, osterix, bone sialoprotein, and osteocalcin upregulated, and a greater amount of collagen matrix and mineral deposition were found. This study shows the utility of plasma surface activation for polymeric scaffolds in bone tissue engineering.

Keywords: biomaterials; bone tissue engineering; lactide-TMC; mesenchymal stem cells; osteogenic differentiation; plasma activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Animals
  • Calcification, Physiologic / drug effects
  • Cell Adhesion / drug effects
  • Cell Adhesion / genetics
  • Cell Differentiation / drug effects
  • Cell Differentiation / genetics
  • Cell Proliferation / drug effects
  • Cell Proliferation / genetics
  • Collagen / metabolism
  • Dioxanes / pharmacology
  • Extracellular Matrix / drug effects
  • Extracellular Matrix / metabolism*
  • Hydrophobic and Hydrophilic Interactions
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / drug effects
  • Nanoparticles / chemistry
  • Nanoparticles / ultrastructure
  • Osteogenesis* / drug effects
  • Osteogenesis* / genetics
  • Oxygen / pharmacology*
  • Plasma Gases / pharmacology*
  • Porosity
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred Lew
  • Surface Properties
  • Tissue Scaffolds / chemistry*

Substances

  • Dioxanes
  • Plasma Gases
  • RNA, Messenger
  • trimethylene carbonate
  • Collagen
  • dilactide
  • Alkaline Phosphatase
  • Oxygen