材料科学
生物相容性
聚合物
烯类反应
3D打印
脆性
丙烯酸酯
生物材料
橡胶弹性
复合材料
纳米技术
高分子化学
共聚物
有机化学
化学
冶金
作者
Quinten Thijssen,Astrid Quaak,Joseph Toombs,Elly De Vlieghere,Laurens Parmentier,Hayden Taylor,Sandra Van Vlierberghe
标识
DOI:10.1002/adma.202210136
摘要
Abstract Current thoroughly described biodegradable and cross‐linkable polymers mainly rely on acrylate cross‐linking. However, despite the swift cross‐linking kinetics of acrylates, the concomitant brittleness of the resulting materials limits their applicability. Here, photo‐cross‐linkable poly(ε‐caprolactone) networks through orthogonal thiol‐ene chemistry are introduced. The step‐growth polymerized networks are tunable, predictable by means of the rubber elasticity theory and it is shown that their mechanical properties are significantly improved over their acrylate cross‐linked counterparts. Tunability is introduced to the materials, by altering M c (or the molar mass between cross‐links), and its effect on the thermal properties, mechanical strength and degradability of the materials is evaluated. Moreover, excellent volumetric printability is illustrated and the smallest features obtained via volumetric 3D‐printing to date are reported, for thiol‐ene systems. Finally, by means of in vitro and in vivo characterization of 3D‐printed constructs, it is illustrated that the volumetrically 3D‐printed materials are biocompatible. This combination of mechanical stability, tunability, biocompatibility, and rapid fabrication by volumetric 3D‐printing charts a new path toward bedside manufacturing of biodegradable patient‐specific implants.
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