Biodegradability and biocompatibility of copoly(butylene sebacate-co-terephthalate)s

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• 作者：Nina Heidarzadeh^a ; Mehdi Rafizadeh^a ; ^{mehdi@aut.ac.ir} ; Faramarz Afshar Taromi^a ; Luí ; s J. del Valle^b ; Lourdes Franco^b ; Jordi Puiggalí ; ^b ; ^{Jordi.Puiggali@upc.edu}
• 关键词：Poly(butylene terephthalate) ; poly(butylene sebacate) ; Copolyesters ; Biocompatibility ; Hydrolytic degradation ; Enzymatic degradation
• 刊名：Polymer Degradation and Stability
• 出版年：2017
• 出版时间：January 2017
• 年：2017
• 卷：135
• 期：Complete
• 页码：18-30
• 全文大小：3518 K
• 卷排序：135

文摘

In the present study poly (butylene sebacate-co-terephthalate)s having different compositions were synthesized with a high yield and a random distribution by thermal transesterification of poly (butylene sebacate) and poly (butylene terephthalate) homopolymers. The copolymer with the highest comonomer ratio was the least crystalline sample, although the melting peaks corresponding to both, sebacate and terephthalate-rich phases were still observable in calorimetric heating runs. This copolymer was associated with interesting thermal and mechanical properties, as the maximum melting point was higher than 100 °C and the storage modulus was also high (i.e. 1.1 × 109 N/m2 and 1.7 108 N/m2 were determined just before and after the main glass transition temperature of −12 °C).As all studied samples were thermally stable up to temperatures clearly higher than the fusion temperature, they could be easily processed. Increasing the terephthalate content of the copolymers resulted in higher hydrophobicity, which had a minor influence on cell adhesion and proliferation of both fibroblast-like and epithelial-like cells. Hydrolytic and enzymatic degradability were assessed and the effect of composition and crystallinity on the degradation rate was investigated. Molecular weight measurements during exposure to a hydrolytic media indicated a first order kinetic mechanism during the initial stages of degradation before reaching a limiting molecular size, which was indicative of solubilization. The most amorphous sample appears as a highly promising biodegradable material since it showed a significant weight loss during exposure to all selected degradation media, but also exhibited good performance and properties that were comparable to those characteristic of polyethylene.