Hydrolytic Degradation of Polyisobutylene and Poly-L-Lactide-Based Multiblock Copolymers

被引:3
|
作者
Ojha, Umaprasana [1 ]
Kulkarni, Pallavi [1 ]
Cozzens, David [1 ]
Faust, Rudolf [1 ]
机构
[1] Univ Massachusetts, Dept Chem, Lowell, MA 01854 USA
关键词
block copolymers; biomaterials; hydrolytic stability; polyurethanes; IN-VITRO; THERMOPLASTIC ELASTOMERS; POLY(L-LACTIDE) SEGMENTS; BLOCK-COPOLYMERS; DRUG-RELEASE; END-GROUP; POLYLACTIDE; POLYURETHANES; BIOMATERIALS; BEHAVIOR;
D O I
10.1002/pola.24161
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The hydrolytic degradation of a series of poly-L-lactide (PLLA)-polyisobutylene (PIB) multiblock copolymers was studied in phosphate buffer solution (pH = 7.4) at 37 degrees C. The multiblock copolymers were synthesized by chain extension of PLLA-b-PIB-b-PLLA triblock copolymers, which were obtained by ring-opening polymerization of L-lactide initiated by hydroxyallyl telechelic PIB. The degradation strongly depended on the PLLA segment length. At constant PIB segment length, the multiblock copolymer with the shortest PLLA segment length (DPn = 10), showed significant weight loss after 8 weeks, whereas weight loss for DPn = 36 was only observed after 24 weeks. The gel-permeation chromatographic analysis showed a similar decrease in the number-average molecular weight (M-n) with time further supporting the weight loss data. Dynamic mechanical analysis showed a decrease in ultimate stress and modulus with time. The crystallinity of multiblock copolymers changed significantly with degradation time as indicated from differential scanning calorimetric analysis. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3767-3774, 2010
引用
收藏
页码:3767 / 3774
页数:8
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