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迈向调控具有双连续微相分离的聚氨酯共聚物各阶段的生物降解。

Toward regulating biodegradation in stages of polyurethane copolymers with bicontinuous microphase separation.

作者信息

Wang Man, Liu Hong-Ying, Ke Neng-Wen, Wu Gang, Chen Si-Chong, Wang Yu-Zhong

机构信息

The Collaborative Innovation Center for Eco-Friendly and Fire-Safety Polymeric Materials (MoE), National Engineering Laboratory of Eco-Friendly Polymeric Materials (Sichuan), College of Chemistry, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu 610064, China.

Department of Pancreatic Surgery, West China Hospital, Sichuan University/West China School of Nursing, Sichuan University, China.

出版信息

J Mater Chem B. 2023 Apr 5;11(14):3164-3175. doi: 10.1039/d3tb00011g.

Abstract

For typical biodegradable polymers, their overall performance almost declines exponentially to the degradation degree, which inevitably leads to a dilemma between the requirements of service life and retention time in the environment (both and ). It is a great challenge to develop a biodegradable polymeric device with relatively stable performance in service while rapidly degrading out of service. Herein, we demonstrate an effective strategy to control degradation of biodegradable polymers in stages by constructing separated bicontinuous microphases with very different microphase degradation rates. First, polyurethane copolymers (PCL-b-CrP-U) containing two blocks, , semicrystalline poly(ε-caprolactone) (PCL) blocks and amorphous random copolymer blocks (CrP) based on ε-CL and -dioxanone (PDO), were synthesized. The microscopic morphology of PCL-b-CrP-U is investigated by an alkali-accelerated degradation experiment, which also demonstrates that the chain cleavage-induced crystallization during degradation resulted in a self-reinforcement by forming degradation residues with a scaffold-like morphology. The tensile test shows that PCL-b-CrP-U has excellent mechanical properties (1500% of elongation at break, a tensile strength of about 7.5 MPa, and an elastic modulus of 40.0 MPa). The degradation experiments with artificial pancreatic juice as a working medium reveal that PCL-b-CrP-U samples containing relatively high PDO units exhibit a three-stage degradation, an induction stage, a steady degradation stage and an accelerated degradation stage. The CrP phase preferentially hydrolyzes to form some microchannels due to its amorphous nature and relatively high hydrophilicity, effectively accelerating the entry of water and enzymes into the inner parts of the sample. Meanwhile, at this stage, those originally amorphous PCL segments gradually crystalize owing to their enhanced chain mobility induced by the chain cleavage, forming a "scaffold"-like structure, which effectively reinforces the sample to resist the damage from external force and therefore guarantees a relatively stable mechanical performance of PCL--CrP-U during service. With the further depletion of the CrP phase, the intermediate "scaffold"-like structure is also very beneficial to accelerate the degradation of residues owing to its large specific surface area, which is expected to be beneficial for preventing long-term retention of the implantation devices.

摘要

对于典型的可生物降解聚合物,它们的整体性能几乎随降解程度呈指数下降,这不可避免地导致了使用寿命要求与在环境中的保留时间之间的两难困境(两者都有要求)。开发一种在使用中具有相对稳定性能而在停用后能快速降解的可生物降解聚合物装置是一项巨大挑战。在此,我们展示了一种通过构建具有非常不同微相降解速率的分离双连续微相来分阶段控制可生物降解聚合物降解的有效策略。首先,合成了包含两个嵌段的聚氨酯共聚物(PCL-b-CrP-U),即半结晶聚(ε-己内酯)(PCL)嵌段和基于ε-己内酯和对二氧环己酮(PDO)的无规共聚物嵌段(CrP)。通过碱加速降解实验研究了PCL-b-CrP-U的微观形态,该实验还表明降解过程中链断裂诱导的结晶通过形成具有支架状形态的降解残余物导致了自增强。拉伸试验表明PCL-b-CrP-U具有优异的力学性能(断裂伸长率为1500%,拉伸强度约为7.5 MPa,弹性模量为40.0 MPa)。以人工胰液为工作介质的降解实验表明,含有相对较高PDO单元的PCL-b-CrP-U样品呈现三阶段降解,即诱导阶段、稳定降解阶段和加速降解阶段。由于其无定形性质和相对较高的亲水性,CrP相优先水解形成一些微通道,有效地加速了水和酶进入样品内部。同时,在此阶段,那些原本无定形的PCL链段由于链断裂诱导的链迁移率增强而逐渐结晶,形成“支架”状结构,这有效地增强了样品以抵抗外力的破坏,因此保证了PCL-b-CrP-U在使用过程中相对稳定的力学性能。随着CrP相的进一步消耗,中间的“支架”状结构由于其大的比表面积也非常有利于加速残余物的降解,这有望有利于防止植入装置的长期留存。

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