In vitro and in vivo characteristics of PCL scaffolds with pore size gradient fabricated by a centrifugation method

被引:587
作者
Oh, Se Heang
Park, Il Kyu
Kim, Jin Man
Lee, Jin Ho
机构
[1] Hannam Univ, Dept Adv Mat, Taejon 306791, South Korea
[2] Chungnam Natl Univ, Dept Pathol, Taejon 301131, South Korea
基金
新加坡国家研究基金会;
关键词
pore size; scaffold; porosity; polycaprolactone (PCL); cell adhesion; bone regeneration;
D O I
10.1016/j.biomaterials.2006.11.024
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Polycaprolactone (PCL) cylindrical scaffolds with gradually increasing pore size along the longitudinal direction were fabricated by a novel centrifugation method to investigate pore size effect on cell and tissue interactions. The scaffold was fabricated by the centrifugation of a cylindrical mold containing fibril-like PCL and the following fibril bonding by heat treatment. The scaffold showed gradually increasing pore size (from similar to 88 to similar to 405 mu m) and porosity (from similar to 80% to similar to 94%) along the cylindrical axis by applying the centrifugal speed, 3000 mu m. The scaffold sections were examined for their in vitro cell interactions using different kinds of cells (chondrocytes, osteoblasts, and fibroblasts) and in vivo tissue interactions using a rabbit model (skull bone defects) in terms of scaffold pore sizes. It was observed that different kinds of cells and bone tissue were shown to have different pore size ranges in the scaffold for effective cell growth and tissue regeneration. The scaffold section with 380-405 mu m pore size showed better cell growth for chondrocytes and osteoblasts, while the scaffold section with 186-200 mu m pore size was better for fibroblasts growth. Also the scaffold section with 290-310 mu m pore size showed faster new bone formation than those of other pore sizes. The pore size gradient scaffolds fabricated by the centrifugation method can be a good tool for the systematic studies of the interactions between cells or tissues and scaffolds with different pore size. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1664 / 1671
页数:8
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