TY - JOUR
T1 - Simultaneous enhancement of the strength and elongation of polycaprolactone
T2 - The role of Chitosan-graft-Polycaprolactone
AU - Zhou, Ziyan
AU - Huang, Haitao
AU - Xu, Peihu
AU - Fan, Lihong
AU - Yu, Jiahui
AU - Huang, Jin
PY - 2009/4/15
Y1 - 2009/4/15
N2 - Polycaprolactone (PCL) is a basic substance for biomedical materials and especially for scaffolds in tissue engineering. To improve the performance of PCL-based materials, we filled a PCL matrix with a biocompatible poly-saccharide-grafted PCL, chitosan-g-polycaprolactone (CS-g-PCL). The results showed that the strength, elongation, and Young's modulus of the resultant composites were simultaneously enhanced in contrast with those of neat PCL. The structures of the PCL/CS-g-PCL blends were investigated with Fourier transform infrared, X-ray diffraction, differential scanning calorimetry, dynamic mechanical analysis, and scanning electron microscopy, and the effects of the chitosan (CS) content in CS-g-PCL and the CS-g-PCL content in the blends on the mechanical properties and structures of the blends were examined. The rigidity of CS chains and the increasing crystallinity induced by the nucleation of CS-g-PCL contributed to the enhancement of the strength, whereas the cocontinuous interfacial structure and improved misci-bility between CS and PCL matrix mediated with grafted PCL chains greatly enhanced the elongation of the composite materials. This work presents a strategy for enhancing the mechanical performance of PCL as a biomaterial.
AB - Polycaprolactone (PCL) is a basic substance for biomedical materials and especially for scaffolds in tissue engineering. To improve the performance of PCL-based materials, we filled a PCL matrix with a biocompatible poly-saccharide-grafted PCL, chitosan-g-polycaprolactone (CS-g-PCL). The results showed that the strength, elongation, and Young's modulus of the resultant composites were simultaneously enhanced in contrast with those of neat PCL. The structures of the PCL/CS-g-PCL blends were investigated with Fourier transform infrared, X-ray diffraction, differential scanning calorimetry, dynamic mechanical analysis, and scanning electron microscopy, and the effects of the chitosan (CS) content in CS-g-PCL and the CS-g-PCL content in the blends on the mechanical properties and structures of the blends were examined. The rigidity of CS chains and the increasing crystallinity induced by the nucleation of CS-g-PCL contributed to the enhancement of the strength, whereas the cocontinuous interfacial structure and improved misci-bility between CS and PCL matrix mediated with grafted PCL chains greatly enhanced the elongation of the composite materials. This work presents a strategy for enhancing the mechanical performance of PCL as a biomaterial.
KW - Blends
KW - Graft copolymers
KW - Mechanical properties
UR - https://www.scopus.com/pages/publications/64249120742
U2 - 10.1002/app.29432
DO - 10.1002/app.29432
M3 - 文章
AN - SCOPUS:64249120742
SN - 0021-8995
VL - 112
SP - 692
EP - 699
JO - Journal of Applied Polymer Science
JF - Journal of Applied Polymer Science
IS - 2
ER -