Liquid photocurable biodegradable copolymers:: In vivo degradation of photocured poly(ε-caprolactone-co-trimethylene carbonate)

被引:26
作者
Mizutani, M [1 ]
Matsuda, T [1 ]
机构
[1] Natl Cardiovasc Ctr, Res Inst, Dept Bioengn, Osaka 5658565, Japan
来源
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH | 2002年 / 61卷 / 01期
关键词
biodegradation; epsilon-caprolactone; trimethylene carbonate; photocured film; in vivo degradation;
D O I
10.1002/jbm.10166
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Liquid photoreactive poly(epsilon-caprolactone-co-trimethylene carbonate)s endcapped with a coumarin group [coumarinated poly(CL/TMC)s] were prepared using tetra-functional hydroxylated substances such as pentaerythritol or four-branched poly(ethylene glycol), b-PEG. These coumarinated copolymers are tetra-branched and exist as a viscous liquid (MW 5 x 10(3)-7 x 10(3)). They were photocured by ultraviolet (UV) light irradiation to obtain a swelling or non-swelling solid under water, depending on the type of initiator used. The resultant films were implanted into the subcutaneous tissues of rats for up to 5 months. The photocured b-PEG-based copolymer was completely degraded and sorbed within a I month. On the other hand, surface-eroding degradation of pentaerythritol-based, coumarinated poly(CL/TMC) progressed with implantation time, and minimal recruitment of neutrophils, macrophages, and multinucleated giant cells was observed over the implantation period. Among the pentaerythritol-based copolymers, the fastest surface erosion was observed for the copolymer with the highest epsilon-caprolactone content. Microfabricated films with microarrays in which photoconstructs were stereolithographically prepared, using three different coumarinated copolymers at different regions, showed that upon implantation there was regionally differentiated biodegradation of microarrays, and the degree of region-specific biodegradation depended on the type of photocured copolymer. The observed tendency for biodegradation was in good agreement with that observed during implantation of individual films in vivo. This study also demonstrates that the use of multi-material-arrayed films enables the determination of different responses in vivo using only one sample. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:53 / 60
页数:8
相关论文
共 15 条
[1]   DEGRADABLE POLYMERS FOR THE FUTURE [J].
ALBERTSSON, AC ;
KARLSSON, S .
ACTA POLYMERICA, 1995, 46 (02) :114-123
[2]   SYNTHESIS OF COPOLYMERS OF 1,3-DIOXAN-2-ONE AND OXEPAN-2-ONE USING COORDINATION CATALYSTS [J].
ALBERTSSON, AC ;
EKLUND, M .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1994, 32 (02) :265-279
[3]  
BEZWADA RS, 1995, Patent No. 5653992
[4]  
Han DK, 1998, J BIOMAT SCI-POLYM E, V9, P667
[5]   Kinetic studies of a new photoinitiator hybrid system based on camphorquinone-N-phenylglicyne derivatives for laser polymerization of dental restorative and stereolithographic (3D) formulations [J].
Kucybala, Z ;
Pietrzak, M ;
Paczkowski, J ;
Linden, LA ;
Rabek, JF .
POLYMER, 1996, 37 (20) :4585-4591
[6]   Molecular design of photocurable liquid biodegradable copolymers. 1. Synthesis and photocuring characteristics [J].
Matsuda, T ;
Mizutani, M ;
Arnold, SC .
MACROMOLECULES, 2000, 33 (03) :795-800
[7]   Molecular design of photocurable liquid biodegradable copolymers. 2. Synthesis of coumarin-derivatized oligo(methacrylate)s and photocuring [J].
Matsuda, T ;
Mizutani, M .
MACROMOLECULES, 2000, 33 (03) :791-794
[8]  
MIZUTANI M, IN PRESS BIOMACROMOL
[9]  
Palser R, 1990, Can Assoc Radiol J, V41, P339
[10]  
Piskin E., 1994, J BIOMAT SCI-POLYM E, V6, P775