Department of Biomedical and Chemical Engineering, BioInspired Syracuse, Syracuse University, Syracuse, NY, USA.
Department of Chemistry, State University of New York ESF, Syracuse, NY, USA.
J Mater Chem B. 2024 Jan 31;12(5):1217-1231. doi: 10.1039/d3tb02472e.
Biostable shape memory polymers that remain stable in physiological conditions are beneficial for user-defined shape recovery in response to a specific stimulus. For potential commercialization and biocompatibility considerations, biomaterial synthesis must be simple and scalable. Hence, a library of biostable and cytocompatible shape memory polymers with tunable thermomechanical properties based on hard segment content was synthesized using a solvent-free method. Polymer surface chemistry, thermomechanical and shape memory properties, and biostability were assessed. We also investigated the effects of processing methods on thermomechanical and shape memory properties. All polymers showed high glass transition temperatures (>50 °C), which indicates that their temporary shape could be preserved after implantation. Polymers also demonstrate high shape fixity (73-80%) and shape recovery (93-95%). Minimal mass loss (<5%) was observed in accelerated oxidative (20% HO) and hydrolytic (0.1 M NaOH) media. Additionally, minimal shape recovery (∼0%) occurred in programmed samples with higher hard segment content that were stored in degradation media. After 40 days of storage in media, programmed samples recovered their primary shapes upon heating to temperatures above their transition temperature. Annealing to above the polymer melting point and solvent casting of polymers improved shape memory and thermal properties. To enable their potential use as biomaterial scaffolds, fiber formation of synthesized polyurethanes was compared with those of samples synthesized using a previously reported solvent-based method. The new method provided polymers that can form fibrous scaffolds with improved mechanical and shape memory properties, which is attributed to the higher molecular weight and crystalline content of polymers synthesized using the new, solvent-free approach. These biostable segmented polyurethanes could be coupled with a range of components that respond to specific stimuli, such as enzymes, magnetic field, pH, or light, to enable a specific shape change response, which could be coupled with drug and/or bioactive material delivery in future work.
具有生物稳定性的形状记忆聚合物在生理条件下保持稳定,有利于针对特定刺激进行用户定义的形状恢复。出于潜在的商业化和生物相容性考虑,生物材料的合成必须简单且可扩展。因此,使用无溶剂法合成了具有可调温机械性能的基于硬段含量的生物稳定且细胞相容的形状记忆聚合物库。评估了聚合物的表面化学、热机械和形状记忆性能以及生物稳定性。我们还研究了加工方法对热机械和形状记忆性能的影响。所有聚合物均表现出较高的玻璃化转变温度(>50°C),这表明其临时形状在植入后可以保留。聚合物还表现出较高的形状固定率(73-80%)和形状恢复率(93-95%)。在加速氧化(20% HO)和水解(0.1 M NaOH)介质中观察到的质量损失最小(<5%)。此外,在存储在降解介质中的具有较高硬段含量的程控样品中,仅发生最小程度的形状恢复(约 0%)。在介质中储存 40 天后,程控样品在加热至高于其转变温度的温度时恢复其原始形状。高于聚合物熔点的退火和聚合物的溶剂浇铸改善了形状记忆和热性能。为了使它们能够用作生物材料支架,比较了合成的聚氨基甲酸酯与使用先前报道的基于溶剂的方法合成的样品的纤维形成。新方法提供了能够形成具有改善的机械和形状记忆性能的纤维状支架的聚合物,这归因于使用新的无溶剂方法合成的聚合物具有较高的分子量和结晶含量。这些生物稳定的嵌段型聚氨基甲酸酯可以与一系列对特定刺激(如酶、磁场、pH 值或光)做出响应的组件结合,以实现特定的形状变化响应,这可以与药物和/或生物活性材料的输送相结合,这是未来的工作重点。