Chemical activation and changes in surface morphology of poly(ε-caprolactone) modulate VEGF responsiveness of human

Thilo Storm1, Katharina Wulf, Michael Teske

  • 1Institute for Biomedical Engineering, Rostock University Medical Center, Friedrich-Barnewitz-Str. 4, 18119, Rostock, Germany, thilostorm@gmail.com.

Insights

Improving cardiovascular implants requires better endothelialization. Plasma-activated poly(ε-caprolactone) (PCL) with VEGF stimulation significantly enhances endothelial cell adhesion and proliferation, crucial for healing after stenting.

Area of Science:

  • Biomaterials Science
  • Cardiovascular Engineering
  • Cell Biology

Background:

  • Coronary heart disease patients undergoing percutaneous transluminal coronary angioplasty (PTCA) with stenting face post-operative complications like restenosis and thrombosis.
  • Effective re-endothelialization is critical for wound healing after cardiovascular implant surgery.
  • There is a need for advanced biomaterials that promote endothelial cell adhesion and functional recovery post-stenting.

Purpose of the Study:

  • To systematically evaluate chemical polymer modifications for improved endothelialization.
  • To investigate poly(ε-caprolactone) (PCL) and its activated forms, surface morphology, and matrix protein precoating effects on endothelialization.
  • To assess the impact of Vascular Endothelial Growth Factor (VEGF) on endothelial cell proliferation on modified PCL surfaces.

Main Methods:

  • Chemical modification and plasma activation of poly(ε-caprolactone) (PCL) surfaces.
  • In vitro characterization of endothelial cell responses using human umbilical vein endothelial cells (HUVECs) for viability and adhesion assays.
  • Application of VEGF as a stimulus to promote endothelial cell proliferation on polymer surfaces.

Main Results:

  • Plasma chemical activation of PCL surfaces significantly impacts endothelial cell adhesion and viability.
  • Surface morphology and precoating with matrix proteins influence endothelialization.
  • VEGF stimulation effectively boosts endothelial cell proliferation on modified PCL, particularly on plasma-activated surfaces.

Conclusions:

  • Plasma chemical activation of PCL, combined with VEGF stimulation, represents a promising strategy to enhance in vitro endothelialization.
  • This study contributes novel insights into optimizing polymer surface properties for improved cardiovascular implant performance.
  • The findings support the development of advanced biomaterials for better post-stenting healing and reduced complications.