Enhanced biodegradable copolymers: Synthesis and characterization of high molecular weight poly(L‐lactide‐ r ‐ε‐caprolactone)

结晶度 共聚物 材料科学 丙交酯 己内酯 延伸率 高分子化学 开环聚合 极限抗拉强度 可生物降解聚合物 单体 玻璃化转变 生物相容性 聚合 质子核磁共振 微观结构 聚合物 立体化学 复合材料 化学 冶金
作者
Liu Dongyang,Xia Qi,Wuyou Ye,Zhang Shinuo,Wenjie Yu,Zhou Zhengzhe,Zhongyong Fan
出处
期刊:Polymer Engineering and Science [Wiley]
卷期号:65 (3): 1242-1254
标识
DOI:10.1002/pen.27072
摘要

Abstract Semi‐crystalline poly(L‐lactide‐ r ‐ε‐caprolactone) (P(LLA‐ r ‐ε‐CL)) as an important biodegradable material applied in biomedical devices has attracted much attention from researchers. A series of high molecular weight P(LLA‐ r ‐ε‐CL) semi‐crystalline copolymers attached with various monomer molar ratio of L‐lactide (LLA) and ε‐caprolactone (ε‐CL) with up to 2.9 × 10 5 g/mol were synthesized first time by ring‐opening copolymerization under high vacuum condition. The chemical composition, chain sequence microstructure and their relationship of P(LLA‐ r ‐ε‐CL) were characterized by 1 H NMR and 13 C NMR. Spectra results shown that as the ε‐CL content increased from 3 mol% to 15 mol%, the average LLA sequence length decreased from 80.4 to 19.6 units. With decrease of LLA sequence length, the glass transition temperature ( T g ), melting temperature( T m ) and the crystallinity ( χ c ) of copolymers had a reduction. Meantime, it resulted in a high degradation rate of samples in enzyme‐catalyzed condition. With loss of rigid crystal and plasticization from soft ε‐CL segment, P(LLA‐ r ‐ε‐CL) had an improved toughness as the elongation at break reaching 195.5%, while still had a considerable tensile strength of 49.2 MPa. Further data analysis exhibited an exponential relationship between LLA sequence length and mechanical performance. Additionally, biocompatibility assessments through CCK‐8 and Live/Dead cell assays confirmed the good cytocompatibility of the enhanced biomedical materials.
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