Electrospun nano- to microfiber fabrics made of biodegradable copolyesters: structural characteristics, mechanical properties and cell adhesion potential

被引:498
作者
Kwon, IK [1 ]
Kidoaki, S [1 ]
Matsuda, T [1 ]
机构
[1] Kyushu Univ, Grad Sch Med, Dept Biomed Engn, Fukuoka 8128582, Japan
关键词
electrospinning; nanofibers; microfibers; dielectric constant; human umbilical vein endothelial cell (HUVEC);
D O I
10.1016/j.biomaterials.2004.10.007
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Nano- to micro-structured biodegradable poly(L-lactide-co-epsilon-caprolactone) (PLCL) fabrics were prepared by electrospinning. Electrospun microfiber fabrics with different compositions of PLCL (mol% in feed; 70/30, 50150, and 30/70), poly(L-lactide) (PLL) and poly(c-caprolactone) (PCL) were obtained using methylene chloride (MC) as a solvent. The PLL microfiber exhibited a nanoscale-pore structure with a pore diameter of approximately 200-800 mn at the surface and subsurface regions, whereas such a surface structure was hardly observed in other polymers containing CL. The microfiber fabric made of PLCL 50/50 was elastomeric. Nanoscale-fiber fabrics with PLCL 50/50 (approx. 0.3 or 1.2 mum in diameter) were electrospun using 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) as a solvent. Mercury porosimetry showed that the decrease in the fiber diameter of the fabric decreased porosity, but increased fiber density and mechanical strength. Human umbilical vein endothelial cells (HUVECs) were adhered well and proliferated on the small-diameter-fiber fabrics (0.3 and 1.2 mum in diameter), both of which are dense fabrics, whereas markedly reduced cell adhesion, restricted cell spreading and no signs of proliferation were observed on the large-diameter-fiber fabric (7.0 mum in diameter), The potential biomedical application of electrospun PLCL 50/50 was discussed. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3929 / 3939
页数:11
相关论文
共 29 条
  • [1] Bognitzki M, 2001, ADV MATER, V13, P70, DOI 10.1002/1521-4095(200101)13:1<70::AID-ADMA70>3.0.CO
  • [2] 2-H
  • [3] Campbell C E, 1989, J Invest Surg, V2, P51, DOI 10.3109/08941938909016503
  • [4] Tissue engineering: the biophysical background
    Curtis, A
    Riehle, M
    [J]. PHYSICS IN MEDICINE AND BIOLOGY, 2001, 46 (04) : R47 - R65
  • [5] In vitro reaction of endothelial cells to polymer demixed nanotopography
    Dalby, MJ
    Riehle, MO
    Johnstone, H
    Affrossman, S
    Curtis, ASG
    [J]. BIOMATERIALS, 2002, 23 (14) : 2945 - 2954
  • [6] Meniscal tissue regeneration in porous 50/50 copoly(L-lactide/epsilon-caprolactone) implants
    deGroot, JH
    Zijlstra, FM
    Kuipers, HW
    Pennings, AJ
    Klompmaker, J
    Veth, RPH
    Jansen, HWB
    [J]. BIOMATERIALS, 1997, 18 (08) : 613 - 622
  • [7] Quantitative analysis of fibroblast morphology on microgrooved surfaces with various groove and ridge dimensions
    denBraber, ET
    deRuijter, JE
    Ginsel, LA
    vonRecum, AF
    Jansen, JA
    [J]. BIOMATERIALS, 1996, 17 (21) : 2037 - 2044
  • [8] BIOLOGICAL PERFORMANCE OF A DEGRADABLE POLY(LACTIC ACID-EPSILON-CAPROLACTONE) NERVE GUIDE - INFLUENCE OF TUBE DIMENSIONS
    DENDUNNEN, WFA
    VANDERLEI, B
    ROBINSON, PH
    HOLWERDA, A
    PENNINGS, AJ
    SCHAKENRAAD, JM
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1995, 29 (06): : 757 - 766
  • [9] COLLAGEN SUBSTRATA FOR STUDIES ON CELL BEHAVIOR
    ELSDALE, T
    BARD, J
    [J]. JOURNAL OF CELL BIOLOGY, 1972, 54 (03) : 626 - &
  • [10] Model of 1,1,1,3,3,3-hexafluoro-propan-2-ol for molecular dynamics simulations
    Fioroni, M
    Burger, K
    Mark, AE
    Roccatano, D
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (44) : 10967 - 10975