Biodegradable elastomeric polyurethane membranes as chondrocyte carriers for cartilage repair

被引:39
作者
Chia, Shi-Lu
Gorna, Katarzyna
Gogolewski, Sylwester
Alini, Mauro
机构
[1] AO Res Inst, Dept Biochem & Cell Biol, CH-7270 Davos, Switzerland
[2] AO Res Inst, Dept Polymer Res, CH-7270 Davos, Switzerland
[3] Singapore Gen Hosp, Dept Orthoped Surg, Singapore 0316, Singapore
来源
TISSUE ENGINEERING | 2006年 / 12卷 / 07期
关键词
D O I
10.1089/ten.2006.12.1945
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Autologous chondrocyte implantation in combination with an autologous periosteal patch has become a clinically accepted procedure for the treatment of articular cartilage defects. The use of periosteum has, however, several drawbacks. We have been able to fabricate thin elastomeric biodegradable polyurethane (PU) membranes that may possibly have an application as a tissue-engineered substitute for the periosteal patch. Three types of membranes varying in pore size and surface texture were used as substrates for bovine chondrocytes in culture. The membranes, marked as P-I, P-II, and P-R, had average pore sizes of 10 to 20 mu m, 40 to 60 mu m, and less than 5 mu m, respectively. A poly(L/DL-lactide) 80/20% micro-porous membrane (PLA) with an average pore size in the range of 10 to 70 mu m was used as a control. There was no difference in the cell proliferation profile among the 4 membranes. In terms of proteoglycan and collagen production, P-I, P-R, and PLA performed similarly to one another. The rate of matrix production appears to be greater in the PU membranes than in the PLA membrane in the first 10 days, although by day 30, the PLA membrane had caught up. In all comparisons, the performance of P-II lagged behind those of the other materials. In conclusion, this preliminary study supports the potential use of this novel group of PUs as a periosteal flap substitute or perhaps as a chondrocyte carrier for matrix-assisted chondrocyte implantation and related techniques. Further studies will be necessary to better define their role in clinical applications for cartilage repair.
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页码:1945 / 1953
页数:9
相关论文
共 71 条
[1]  
[Anonymous], 1996, DESK REFERENCE FUNCT
[2]  
Bhardwaj T, 2001, J BIOMED MATER RES, V57, P190, DOI 10.1002/1097-4636(200111)57:2<190::AID-JBM1158>3.3.CO
[3]  
2-A
[4]   TREATMENT OF DEEP CARTILAGE DEFECTS IN THE KNEE WITH AUTOLOGOUS CHONDROCYTE TRANSPLANTATION [J].
BRITTBERG, M ;
LINDAHL, A ;
NILSSON, A ;
OHLSSON, C ;
ISAKSSON, O ;
PETERSON, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (14) :889-895
[5]  
BRUIN P, 1988, MAKROMOL CHEM-RAPID, V9, P589
[6]   Articular cartilage injuries [J].
Buckwalter, JA .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2002, (402) :21-37
[7]  
COUTTS RD, 2001, CLIN ORTHOP S, V391, P271
[8]   Use of porous polyurethanes for meniscal reconstruction and meniscal prostheses [J].
deGroot, JH ;
deVrijer, R ;
Pennings, AJ ;
Klompmaker, J ;
Veth, RPH ;
Jansen, HWB .
BIOMATERIALS, 1996, 17 (02) :163-173
[9]   Meniscal tissue regeneration in porous 50/50 copoly(L-lactide/epsilon-caprolactone) implants [J].
deGroot, JH ;
Zijlstra, FM ;
Kuipers, HW ;
Pennings, AJ ;
Klompmaker, J ;
Veth, RPH ;
Jansen, HWB .
BIOMATERIALS, 1997, 18 (08) :613-622
[10]   IMPROVED QUANTITATION AND DISCRIMINATION OF SULFATED GLYCOSAMINOGLYCANS BY USE OF DIMETHYLMETHYLENE BLUE [J].
FARNDALE, RW ;
BUTTLE, DJ ;
BARRETT, AJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 883 (02) :173-177