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Photocurable Biodegradable Liquid Copolymers: Synthesis of Acrylate-End-Capped Trimethylene Carbonate-Based Prepolymers,Photocuring,and Hydrolysis

机译:可光固化的可生物降解液体共聚物:丙烯酸酯封端的碳酸三亚甲基酯基预聚物的合成,光固化和水解

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摘要

Various photocurable liquid biodegradable trimethylene carbonate (TMC)-based (co)oligomers were prepared by ring-opening (co)polymerization of TMC with or without L-lactide (LL) using low molecular weight polyethylene glycol) (PEG) (mol wt 200,600,or 1000) or trimethylolpropane (IMP) as an initiator.Resultant (co)oligomers were pastes,viscous liquids,or liquids at room temperature,depending on the monomer composition and monomer/initiator ratio.Liquid (co)oligomers were subsequently end-capped with acrylate groups.Upon visible-light irradiation in the presence of camphorquinone as a radical generator,rapid liquid-to-solid transformation occurred to produce photocured solid.The photocuring yield increased with photoirradiation time,photointensity,and camphorquinone concentration.The photocured polymers derived from low molecular weight PEG (PEG200) and TMP exhibited much reduced hydrolysis potential compared with PEGl000-derived polymers in terms of weight loss,water uptake,and swelling depth.Force-distance curve measurements by nanoindentation using atomic force microscopy clearly showed that Young's moduli of the photocured polymer films decreased with increasing hydrolysis time.Their potential biomedical applications are discussed.
机译:各种光可固化的可生物降解的碳酸亚丙三酯(TMC)的低聚物(co)低聚物是通过使用低分子量聚乙二醇(PEG)(摩尔重量200,600)在有或没有L-丙交酯(LL)的情况下将TMC开环(共)聚合来制备的(或1000)或三羟甲基丙烷(IMP)作为引发剂。生成的(共)低聚物是糊状物,粘稠液体或室温下的液体,具体取决于单体组成和单体/引发剂的比例。在存在樟脑醌作为自由基产生剂的情况下,在可见光照射下发生液-固快速转变,生成光固化固体。光固化产率随光照射时间,光强度和樟脑醌浓度的增加而增加。与低分子量PEG(PEG200)和TMP衍生的聚合物相比,在重量减轻,吸水率和溶胀方面,与PEG1000衍生的聚合物相比,水解潜力大大降低。使用原子力显微镜通过纳米压痕法测得的力距曲线清楚地表明,光固化的聚合物薄膜的杨氏模量随水解时间的延长而降低,讨论了其潜在的生物医学应用。

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