Liu Xiaolong, Xia Yiran, Liu Lulu, Zhang Dongmei, Hou Zhaosheng
1 College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan, China.
2 Shandong Academy of Pharmaceutical Sciences, Shandong Provincial Key Laboratory of Biomedical Polymer, Jinan, China.
J Biomater Appl. 2018 May;32(10):1329-1342. doi: 10.1177/0885328218763912. Epub 2018 Mar 16.
The purpose of this study is to offer a novel kind of polyurethane with improved surface blood compatibility for long-term implant biomaterials. In this work, the aliphatic poly(ester-urethane) (PEU) with uniform-size hard segments was prepared and the PEU surface was grafted with hydrophilic poly(ethylene glycol) (PEG). The PEU was obtained by chain-extension of poly(ɛ-caprolactone) (PCL) with isocyanate-terminated urethane triblock. Free amino groups were introduced onto the surface of PEU film via aminolysis with hexamethylenediamine, and then the NH-grafted PEU surfaces (PEU-NH) were reacted with isocyanate-terminated monomethoxyl PEG (MPEG-NCO) to obtain the PEG-grafted PEU surfaces (PEU-PEG). Analysis by nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy, and gel permeation chromatography were performed to confirm the chemical structures of the chain extender, PCL, PEU, and PEU-PEG. Additionally, the influence of aminolysis on the physical-mechanical properties of PEU films was investigated. Two glass transition temperatures and a broad endothermic peak were observed in the differential scanning calorimetry curves of PEU, which demonstrated a microphase-separated and semicrystalline structure, respectively. The PEU-PEG film exhibited excellent mechanical properties with an ultimate stress of ∼39 MPa and an elongation at break of ∼1190%, which was slightly lower than that of PEU, indicating that the aminolysis has little influence on the tensile properties. Evaluation of the blood compatibility of the films by bovine serum albumin adsorption and the platelet adhesion test revealed that the PEG-grafted surface had improved resistance to protein adsorption and excellent resistance to platelet adhesion. In vitro degradation tests showed that the PEU-PEG film could maintain its mechanical properties for more than six months and only lost ∼25% weight after 18 months. Due to the excellent mechanical properties, good blood compatibility and slow degradability, this novel kind of polyurethane hold significant promise for long-term implant biomaterials, especially soft tissue augmentation and regeneration.
本研究的目的是提供一种新型聚氨酯,用于长期植入生物材料,其具有改善的表面血液相容性。在这项工作中,制备了具有尺寸均匀硬段的脂肪族聚(酯 - 聚氨酯)(PEU),并在PEU表面接枝了亲水性聚(乙二醇)(PEG)。通过用异氰酸酯封端的聚氨酯三嵌段对聚(ε - 己内酯)(PCL)进行扩链反应得到PEU。通过用六亚甲基二胺进行氨解反应,将游离氨基引入到PEU膜表面,然后使接枝NH的PEU表面(PEU - NH)与异氰酸酯封端的单甲氧基PEG(MPEG - NCO)反应,以获得接枝PEG的PEU表面(PEU - PEG)。通过核磁共振光谱、傅里叶变换红外光谱和凝胶渗透色谱分析来确认扩链剂、PCL、PEU和PEU - PEG的化学结构。此外,研究了氨解对PEU膜物理机械性能的影响。在PEU的差示扫描量热曲线中观察到两个玻璃化转变温度和一个宽吸热峰,分别表明其具有微相分离和半结晶结构。PEU - PEG膜表现出优异的机械性能,极限应力约为39 MPa,断裂伸长率约为1190%,略低于PEU,表明氨解对拉伸性能影响较小。通过牛血清白蛋白吸附和血小板粘附试验对膜的血液相容性进行评估,结果表明接枝PEG的表面具有改善的抗蛋白质吸附性能和优异的抗血小板粘附性能。体外降解试验表明,PEU - PEG膜在六个月以上可保持其机械性能,18个月后仅失重约25%。由于其优异的机械性能、良好的血液相容性和缓慢的降解性,这种新型聚氨酯在长期植入生物材料方面具有巨大潜力,特别是在软组织增强和再生方面。