Co-extrusion of biocompatible polymers for scaffolds with co-continuous morphology

被引:85
作者
Washburn, NR [1 ]
Simon, CG [1 ]
Tona, A [1 ]
Elgendy, HM [1 ]
Karim, A [1 ]
Amis, EJ [1 ]
机构
[1] Natl Inst Stand & Technol, Div Polymers, Gaithersburg, MD 20899 USA
来源
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH | 2002年 / 60卷 / 01期
关键词
polymers scaffolds; polymer processing; tissue; engineering; bone replacement materials; biocompatibility;
D O I
10.1002/jbm.10049
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A methodology for the preparation of porous scaffolds for tissue engineering using co-extrusion is presented. Poly (epsilon-caprolactone) is blended with poly(ethylene oxide) in a twin-screw extruder to form a two-phase material with micron-sized domains. Selective dissolution of the poly(ethylene oxide) with water results in a porous material. A range of blend volume fractions results in co-continuous networks of polymer and void spaces. Annealing studies demonstrate that the characteristic pore size may be increased to larger than 100 mum. The mechanical properties of the scaffolds are characterized by a compressive modulus on the order of 1 MPa at low strains but displaying a marked strain-dependence. The results of osteoblast seeding suggest it is possible to use co-extrusion to prepare polymer scaffolds without the introduction of toxic contaminants. Polymer co-extrusion is amenable to both laboratory- and industrial-scale production of scaffolds fur tissue engineering and only requires rheological characterization of the blend components. This method leads to scaffolds that have continuous void space and controlled characteristic length scales without the use of potentially toxic organic solvents. (C) 2002 John Wiley & Sons, Inc.* J Biomed Mater Res 60: 20-29, 2002.
引用
收藏
页码:20 / 29
页数:10
相关论文
共 47 条
[1]  
Agassant J., 1991, POLYM PROCESSING
[2]  
Alexander Harold, 1996, P37
[3]  
Altankov G, 1996, J BIOMED MATER RES, V30, P385, DOI 10.1002/(SICI)1097-4636(199603)30:3<385::AID-JBM13>3.0.CO
[4]  
2-J
[5]   In vitro bone biocompatibility of poly(anhydride-co-imides) containing pyromellitylimidoalanine [J].
Attawia, MA ;
Uhrich, KE ;
Botchwey, E ;
Langer, R ;
Laurencin, CT .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1996, 14 (03) :445-454
[6]   LOW-DENSITY, MICROCELLULAR POLYSTYRENE FOAMS [J].
AUBERT, JH ;
CLOUGH, RL .
POLYMER, 1985, 26 (13) :2047-2054
[7]   COMPARISON OF HEXAMETHYLDISILAZANE (HMDS), PELDRI-II, AND CRITICAL-POINT DRYING METHODS FOR SCANNING ELECTRON-MICROSCOPY OF BIOLOGICAL SPECIMENS [J].
BRAY, DF ;
BAGU, J ;
KOEGLER, P .
MICROSCOPY RESEARCH AND TECHNIQUE, 1993, 26 (06) :489-495
[8]  
Burg KJL, 2000, J BIOMED MATER RES, V51, P642, DOI 10.1002/1097-4636(20000915)51:4<642::AID-JBM12>3.0.CO
[9]  
2-L
[10]  
Calvert JW, 2000, J BIOMED MATER RES, V52, P279, DOI 10.1002/1097-4636(200011)52:2<279::AID-JBM6>3.0.CO