Solvent/non-solvent sintering: A novel route to create porous microsphere scaffolds for tissue regeneration

被引:79
作者
Brown, Justin L. [1 ]
Nair, Lakshmi S. [2 ]
Laurencin, Cato T. [1 ,2 ,3 ]
机构
[1] Univ Virginia, Dept Biomed Engn, Charlottesville, VA 22903 USA
[2] Univ Virginia, Dept Orthopaed Surg, Charlottesville, VA 22903 USA
[3] Univ Virginia, Dept Chem Engn, Charlottesville, VA 22903 USA
关键词
polyphosphazene; sintered microspheres; poly(lactide-co-glycolide); scaffolds; tissue engineering;
D O I
10.1002/jbm.b.31033
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Solvent/non-solvent sintering creates porous polymeric microsphere scaffolds suitable for tissue engineering purposes with control over the resulting porosity, average pore diameter, and mechanical properties. Five different biodegradable biocompatible polyphosphazenes exhibiting glass transition temperatures from -8 to 41 degrees C and poly (lactide-co-glycolide), (PLAGA) a degradable polymer used in a number of biomedical settings, were examined to study the versatility of the process and benchmark the process to heat sintering. Parameters such as: solvent/non-solvent sintering solution composition and submersion time effect the sintering process. PLAGA microsphere scaffolds fabricated with solvent/non-solvent sintering exhibited an interconnected porosity and pore size of 31.9% and 179.1 mu m, respectively which was analogous to that of conventional heat sintered PLAGA microsphere scaffolds. Biodegradable polyphosphazene microsphere scaffolds exhibited a maximum interconnected porosity of 37.6% and a maximum compressive modulus of 94.3 MPa. Solvent/non-solvent sintering is an effective strategy for sintering polymeric microspheres, with a broad spectrum of glass transition temperatures, under ambient conditions making it an excellent fabrication route for developing tissue engineering scaffolds and drug delivery vehicles. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:396 / 406
页数:11
相关论文
共 25 条
[1]
Microcellular polyHIPE polymer supports osteoblast growth and bone formation in vitro [J].
Akay, G ;
Birch, MA ;
Bokhari, MA .
BIOMATERIALS, 2004, 25 (18) :3991-4000
[2]
Allcock H. R., 2003, CHEM APPL POLYPHOSPH
[3]
POLY[(AMINO-ACID-ESTER)PHOSPHAZENES] - SYNTHESIS, CRYSTALLINITY, AND HYDROLYTIC SENSITIVITY IN SOLUTION AND THE SOLID-STATE [J].
ALLCOCK, HR ;
PUCHER, SR ;
SCOPELIANOS, AG .
MACROMOLECULES, 1994, 27 (05) :1071-1075
[4]
An experimental study and model assessment of polymer sintering [J].
Bellehumeur, CT ;
Bisaria, MK ;
Vlachopoulos, J .
POLYMER ENGINEERING AND SCIENCE, 1996, 36 (17) :2198-2207
[5]
Tissue-engineered bone formation in vivo using a novel sintered polymeric microsphere matrix [J].
Borden, M ;
Attawia, M ;
Khan, Y ;
El-Amin, SE ;
Laurencin, CT .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2004, 86B (08) :1200-1208
[6]
Structural and human cellular assessment of a novel microsphere-based tissue engineered scaffold for bone repair [J].
Borden, M ;
El-Amin, SF ;
Attawia, M ;
Laurencin, CT .
BIOMATERIALS, 2003, 24 (04) :597-609
[7]
The sintered microsphere matrix for bone tissue engineering:: In vitro osteoconductivity studies [J].
Borden, M ;
Attawia, M ;
Laurencin, CT .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 61 (03) :421-429
[8]
Tissue engineered microsphere-based matrices for bone repair: design and evaluation [J].
Borden, M ;
Attawia, M ;
Khan, Y ;
Laurencin, CT .
BIOMATERIALS, 2002, 23 (02) :551-559
[9]
EBEWELE RO, 1998, POLYM SCI TECHNOL, V544, P316
[10]
Bone cells and matrices in orthopedic tissue engineering [J].
Fleming, JE ;
Cornell, CN ;
Muschler, GE .
ORTHOPEDIC CLINICS OF NORTH AMERICA, 2000, 31 (03) :357-+