During the past decade, important advances have been made in the understanding of the hydrolytic degradation characteristics of aliphatic polyesters derived from lactic acid (LA) and glycolic acid (GA). Degradation of large poly(LAGA) (PLAGA) polymers is autocatalyzed by carboxyl end groups initiall
Hydrolytic Degradation of Aliphatic Polyesters Copolymerized with Poly(ethylene glycol)s
β Scribed by Nagata, Minoru; Kiyotsukuri, Tsuyoshi; Takeuchi, Shigeki; Tsutsumi, Naoto; Sakai, Wataru
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 276 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0959-8103
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β¦ Synopsis
Poly(1,4-butanediol succinate) copolymers were prepared by melt polycondensation of succinic acid and 1,4-butanediol with 10Γ50 mol% (in feed) of poly(ethylene glycol) (PEG), where molecular weight (MW) of PEG is 200Γ 2000. The reduced speciΓc viscosity of the copolymers increased with incorporation of the PEG component, but a higher PEG content in the copolymers reduced it. The temperature of melting and crystallinity decreased with (T m ) increasing PEG content. depression of the copolymers followed approx-T m imately FloryΓs equation, suggesting that these are random type copolymers. Tensile strength and elongation decreased with increasing MW and content of PEG. The weight loss of copolymer Γlms in a bu β er solution with or without lipase at 37Β‘C, as well as water absorption, increased with increasing PEG content, implying that higher water absorption contributes to hydrolytic degradation of the Γlms. However, the weight loss of copolymers with PEG of lower MW increased greatly in spite of lower water absorption, demonstrating that hydrolytic degradation is inΓuenced by the concentration of degradable ester linkages between succinic acid and PEG segments rather than water absorption.
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