Enhanced biocompatibility and osteogenic potential of mesoporous magnesium silicate/polycaprolactone/wheat protein composite scaffolds

Int J Nanomedicine. 2018 Feb 26:13:1107-1117. doi: 10.2147/IJN.S157921. eCollection 2018.

Abstract

Background: Successful bone tissue engineering using scaffolds is primarily dependent on the properties of the scaffold, including biocompatibility, highly interconnected porosity, and mechanical integrity.

Methods: In this study, we propose new composite scaffolds consisting of mesoporous magnesium silicate (m_MS), polycaprolactone (PCL), and wheat protein (WP) manufactured by a rapid prototyping technique to provide a micro/macro porous structure. Experimental groups were set based on the component ratio: (1) WP0% (m_MS:PCL:WP =30:70:0 weight per weight; w/w); (2) WP15% (m_MS:PCL:WP =30:55:15 w/w); (3) WP30% (m_MS:PCL:WP =30:40:30 w/w).

Results: Evaluation of the properties of fabricated scaffolds indicated that increasing the amount of WP improved the surface hydrophilicity and biodegradability of m_MS/PCL/WP composites, while reducing the mechanical strength. Moreover, experiments were performed to confirm the biocompatibility and osteogenic differentiation of human mesenchymal stem cells (MSCs) according to the component ratio of the scaffold. The results confirmed that the content of WP affects proliferation and osteogenic differentiation of MSCs. Based on the last day of the experiment, ie, the 14th day, the proliferation based on the amount of DNA was the best in the WP30% group, but all of the markers measured by PCR were the most expressed in the WP15% group.

Conclusion: These results suggest that the m_MS/PCL/WP composite is a promising candidate for use as a scaffold in cell-based bone regeneration.

Keywords: bone tissue engineering; mesoporous magnesium silicate; osteogenic differentiation; scaffold; wheat protein.

MeSH terms

  • Absorption, Physicochemical
  • Alkaline Phosphatase / metabolism
  • Animals
  • Biocompatible Materials / pharmacology*
  • Cell Death / drug effects
  • Cell Differentiation / drug effects
  • Cell Differentiation / genetics
  • Cell Line
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Cells, Cultured
  • Compressive Strength
  • DNA / metabolism
  • Gene Expression Regulation / drug effects
  • Humans
  • Magnesium Silicates / chemistry
  • Magnesium Silicates / pharmacology*
  • Mice
  • Osteogenesis* / drug effects
  • Osteogenesis* / genetics
  • Plant Proteins / pharmacology*
  • Polyesters / pharmacology*
  • Porosity
  • Tissue Scaffolds / chemistry*
  • Triticum / chemistry*

Substances

  • Biocompatible Materials
  • Magnesium Silicates
  • Plant Proteins
  • Polyesters
  • polycaprolactone
  • DNA
  • Alkaline Phosphatase