Electrospun chitosan-graft-poly (ε -caprolactone)/poly (ε-caprolactone) cationic nanofibrous mats as potential scaffolds for skin tissue engineering

Int J Biol Macromol. 2011 Jan 1;48(1):13-9. doi: 10.1016/j.ijbiomac.2010.09.019. Epub 2010 Oct 8.

Abstract

This research is aimed to develop cationic nanofibrous mats with improved cellular adhesion profiles and stability of three-dimensional fibrous structure as potential scaffolds for skin tissue engineering. Firstly, amino-remained chitosan-graft-poly (ɛ-caprolactone) (CS-g-PCL) was synthesized with a facile one-step manner by grafting ɛ-caprolactone oligomers onto the hydroxyl groups of CS via ring-opening polymerization by using methanesulfonic acid as solvent and catalyst. And then, CS-g-PCL/PCL nanofibrous mats were obtained by electrospinning of CS-g-PCL/PCL mixed solution. Scanning electron microscopy (SEM) images showed that the morphologies and diameters of the nanofibers were mainly affected by the weight ratio of CS-g-PCL to PCL. The enrichment of amino groups on the nanofiber surface was confirmed by X-ray photoelectron spectroscopy (XPS). With the increase of CS-g-PCL in CS-g-PCL/PCL nanofiber, the content of amino groups on the nanofiber surface increased, which resulted in the increase of zeta-potential of nanofibers. Studies on cell-scaffold interaction were carried out by culturing mouse fibroblast cells (L929) on CS-g-PCL/PCL nanofibrous mats with various contents of CS-g-PCL by assessing the growth, proliferation and morphologies of cells. The results of MTS assay and SEM observation showed that CS-g-PCL/PCL (2/8) mats with a moderate surface zeta-potential (ζ=3mV) were the best in promoting the cell attachment and proliferation. Toluidine blue staining further confirmed that L929 cells grew well and exhibited a normal morphology on the CS-g-PCL/PCL (2/8) mats. These results suggested the potential utilization of CS-g-PCL/PCL (2/8) nanofibrous mats for skin tissue engineering.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caproates / pharmacology*
  • Cations
  • Cell Proliferation / drug effects
  • Cell Shape / drug effects
  • Chitosan / pharmacology*
  • Elements
  • Hydrophobic and Hydrophilic Interactions / drug effects
  • Lactones / pharmacology*
  • Magnetic Resonance Spectroscopy
  • Mice
  • Nanofibers / chemistry*
  • Nanofibers / ultrastructure
  • Particle Size
  • Polyesters / pharmacology*
  • Porosity / drug effects
  • Skin / drug effects*
  • Spectroscopy, Fourier Transform Infrared
  • Staining and Labeling
  • Static Electricity
  • Surface Properties / drug effects
  • Tissue Engineering / methods*
  • Tissue Scaffolds / chemistry*

Substances

  • Caproates
  • Cations
  • Elements
  • Lactones
  • Polyesters
  • polycaprolactone
  • caprolactone
  • Chitosan