Degradation of cross-linked aliphatic polyester composed of poly(ε-caprolactone-co-D,L-lactide) depending on the thermal properties

被引:21
|
作者
Muroya, Takanari [1 ]
Yamamoto, Kazuya [1 ]
Aoyagi, Takao [1 ]
机构
[1] Kagoshima Univ, Grad Sch Sci & Engn, Dept Nanostruct & Adv Mat, Kagoshima 8900065, Japan
关键词
Aliphatic polyester; Caprolactone; Lactide; Cross-link; Degradation; Enzyme; porous structure; IN-VITRO HYDROLYSIS; EPSILON-CAPROLACTONE; BIODEGRADABLE POLYESTERS; ENZYMATIC DEGRADATION; POLY(L-LACTIDE); BIOCOMPATIBILITY; MORPHOLOGY; POLYMERIZATION; POLYLACTIDE; RELEASE;
D O I
10.1016/j.polymdegradstab.2008.12.014
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study, we prepared cross-linked aliphatic polyester derived from branched poly(c-caprolactone (abbreviated as CL)-co-D,L-lactide (abbreviated as LA)) macromonomers with different CL and LA compositions and investigated the effect of thermal properties on their degradation. According to the degradation study, the weight loss became larger with increasing LA composition in poly(CL-co-LA). The introduction of LA units that can degrade easily disturbed the crystallinity of the PCL segments; as result, the hydrolysis became accelerated. Also, we studied the temperature dependency of degradation of a series of cross-linked poly(CL-co-LA) materials with different melting points. We found that the degradation of these materials related closely to the crystallinity, which could be controlled by the composition of CL and LA. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:285 / 290
页数:6
相关论文
共 50 条
  • [1] Blends as a strategy towards tailored hydrolytic degradation of poly(ε-caprolactone-co-D,L-lactide)-poly(ethylene glycol)-poly(ε-caprolactone-co-D,L-lactide) co-polymers
    Bramfeldt, Hanna
    Sarazin, Pierre
    Vermette, Patrick
    POLYMER DEGRADATION AND STABILITY, 2008, 93 (04) : 877 - 882
  • [2] Cross-linked poly(ε-caprolactone/D,L-lactide) copolymers with elastic properties
    Helminen, AO
    Korhonen, H
    Seppälä, JV
    MACROMOLECULAR CHEMISTRY AND PHYSICS, 2002, 203 (18) : 2630 - 2639
  • [3] Thermogelling hydrogels of poly(ε-caprolactone-CO-D,L-lactide)-poly(ethylene glycol)-poly(ε-caprolactone-CO-D,L-lactide) and poly(ε-caprolactone-CO-L-lactide)poly(ethylene glycol)-poly(ε-caprolactone-CO-L-lactide) aqueous solutions
    Jiang, Zhiqiang
    Deng, Xianmo
    Hao, Jianyuan
    JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2007, 45 (17) : 4091 - 4099
  • [4] In vivo degradation behavior of photo-cross-linked star-poly(ε-caprolactone-co-D,L-lactide) elastomers
    Amsden, BG
    Tse, MY
    Turner, ND
    Knight, DK
    Pang, SC
    BIOMACROMOLECULES, 2006, 7 (01) : 365 - 372
  • [5] In Vivo Degradation and Tissue Response to Poly(5-ethylene ketal ε-caprolactone-co-D,L-lactide)
    Babasola, Iyabo Oladunni
    Bianco, Juares
    Amsden, Brian G.
    BIOMACROMOLECULES, 2012, 13 (07) : 2211 - 2217
  • [6] Release of ibuprofen from poly(Ε-caprolactone-co-D,L-lactide) and simulation of the release
    Seppälä, J. (seppala@polte.hut.fi), 1600, John Wiley and Sons Inc. (88):
  • [7] Release of ibuprofen from poly(ε-caprolactone-co-D,L-lactide) and simulation of the release
    Ahola, N
    Rich, J
    Karjalainen, T
    Seppälä, J
    JOURNAL OF APPLIED POLYMER SCIENCE, 2003, 88 (05) : 1279 - 1288
  • [8] Preparation and characterization of blends of star-poly(ε-caprolactone-co-D,L-lactide) and oligo(ε-caprolactone)
    Tomkins, A
    Kontopoulou, M
    Amsden, B
    JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2005, 16 (08) : 1009 - 1021
  • [9] Crystallization Studies on the Stereocomplexation of Poly(L-lactide)/4-Armed Poly(ε-caprolactone-co-D,L-lactide)- block-poly(D-lactide) Blends
    Jin, Tingting
    Dai, Suyang
    Wang, Xiangyu
    Jiang, Ni
    Ning, Zhenbo
    Gan, Zhihua
    CHEMISTRYSELECT, 2023, 8 (30):
  • [10] Enzymatic and thermal degradation of poly(ε-caprolactone), poly(D,L-lactide), and their blends
    Sivalingam, G
    Vijayalakshmi, SP
    Madras, G
    INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2004, 43 (24) : 7702 - 7709