Enzymatic degradation of poly(ether urethane) and poly(carbonate urethane) by cholesterol esterase

被引:123
作者
Christenson, EM
Patel, S
Anderson, JM
Hiltner, A [1 ]
机构
[1] Case Western Reserve Univ, Ctr Appl Polymer Res, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Macromol Sci, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
关键词
poly(carbonate urethane); poly(ether urethane); biodegradation; cholesterol esterase; in vivo; in vitro;
D O I
10.1016/j.biomaterials.2006.03.012
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
This study examined the effect of cholesterol esterase (CE) on the degradation of commercial poly(ether urethane) (PEU) and poly(carbonate urethane) (PCU). Unstrained PEU and PCU films were incubated in 400 U/mL CE solution or a buffer control for 36 days. The study used a concentration of cholesterol esterase that was considerably higher than the estimated physiological level in order to accelerate degradation. However, characterization of treated polyurethane films with SEM, attenuated total reflectance Fourier transform infrared (ATR-FTIR) and GPC analysis revealed only a small loss in surface soft segment content. Comparison with implanted PEU and PCU films led to the conclusion that any effect of enzymatic hydrolysis was confined to the immediate surface, and the magnitude of the effect was too small to contribute significantly to in vivo degradation. The study confirmed that oxidation, rather than enzymatic hydrolysis, is the primary mechanism responsible for the observed biodegradation of PEU and PCU. The oxidative H2O2/CoCl2 treatment continues to accurately predict the long-term biostability of polyurethanes. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3920 / 3926
页数:7
相关论文
共 37 条
[1]
ANDERSON JM, 1996, BIOMATERIALS SCI, P451
[2]
Antioxidant inhibition of poly(carbonate urethane) in vivo biodegradation [J].
Christenson, EM ;
Anderson, JM ;
Hiltner, A .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2006, 76A (03) :480-490
[3]
Biostability and macrophage-mediated foreign body reaction of silicone-modified polyurethanes [J].
Christenson, EM ;
Dadsetan, M ;
Anderson, JM ;
Hiltner, A .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2005, 74A (02) :141-155
[4]
Oxidative mechanisms of poly(carbonate urethane) and poly(ether urethane) biodegradation:: In vivo and in vitro correlations [J].
Christenson, EM ;
Anderson, JM ;
Hiltner, A .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 70A (02) :245-255
[5]
Poly(carbonate urethane) and poly(ether urethane) biodegradation:: In vivo studies [J].
Christenson, EM ;
Dadsetan, M ;
Wiggins, M ;
Anderson, JM ;
Hiltner, A .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 69A (03) :407-416
[6]
In vivo biostability of polyether polyurethanes with polyethylene oxide surface-modifying end groups;: resistance to biologic oxidation and stress cracking [J].
Ebert, M ;
Ward, B ;
Anderson, J ;
McVenes, R ;
Stokes, K .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2005, 75A (01) :175-184
[7]
Faré S, 1999, J BIOMED MATER RES, V45, P62, DOI 10.1002/(SICI)1097-4636(199904)45:1<62::AID-JBM9>3.0.CO
[8]
2-F
[9]
Biostability of polyether-urethane scaffolds: A comparison of two novel processing methods and the effect of higher gamma-irradiation dose [J].
Haugen, H ;
Gerhardt, LC ;
Will, J ;
Wintermantel, E .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2005, 73B (02) :229-237
[10]
MACROPHAGES FORM CIRCULAR ZONES OF VERY CLOSE APPOSITION TO IGG-COATED SURFACES [J].
HEIPLE, JM ;
WRIGHT, SD ;
ALLEN, NS ;
SILVERSTEIN, SC .
CELL MOTILITY AND THE CYTOSKELETON, 1990, 15 (04) :260-270