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Synthesis and characterization of a conductive, biodegradable polyurethane elastomer

机译:导电,可生物降解的聚氨酯弹性体的合成与表征

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Introduction: Biodegradable conductive materials have promises to be applied for myocardium, nerve, muscle and bone tissue repair. The conductive hydrogel promoted growth and maturation of cardiac cells, and enhanced the electrical and mechanical coupling and contractile properties. The conductive material also improved neurite outgrowths from the nerve cells by integrating biochemical and electrical stimulations. However, biodegradable conductive elastomer was rarely reported. To address this limitation, we will utilize polyurethane chemistry to design a biodegradable polymer with elasticity and conductivity. Here, we combined polycaprolactone diol (PCL) as a soft segment, 1,6-hexamethylene diisocyante (HDI) as a hard segment and aniline trimer as a chain extender to achieve a biodegradable polyurethane with electrical and electrochemical properties. The electrical and electrochemical properties, morphologies, mechanical properties, degradation behavior, electrical stability and cytocompatibility of the conductive polyurethane were evaluated. Materials and Methods: The conductive polyurethane (CPU) was synthesized by a two-step process (Fig. 1) and then fabricated into films doped with (1S)-(+)-10-camphorsulfonic acid (CSA) by solvent casting. The chemical structures of oxidized aniline trimer and CPU films were confirmed by ~1H NMR, ~(13)C NMR and FTIR, respectively. The morphologies of CPU films were observed on a scanning electron microscope (SEM). The electrical conductivities of CPU films at dry and wet states were measured by four-probe technique. The electroactivities of CPU films were characterized by UV-vis and cyclic voltammogram measurements. Mechanical properties of CPU films were measured on a MTS workstation with a head crossing rate of 10 mm/min. Cyclic stretching of CPU films at a maximum strain of 30% was tested at a constant rate of 10 mm/min for 10 cycles. The electrical stability of doped CPU films was carried out in cell culture medium under a constant DC voltage of 100±2 mV for 150 h. In vitro degradation of CPU films was detected in phosphate buffer solution (PBS) and lipase/PBS solutions. The electrical conductivity changes of CPU films were measured after degradation in 100 U/mL lipase/PBS solution for 3 and 7 d at 37 °C. The cytocompatibility of CPU films was evaluated using 3T3 fibroblasts. Results and Discussion: All CPU films showed good elasticity within 30% strain range, and their initial moduli increased with increasing CSA content. The roughness of CPU films increased with increasing CSA amount. The electrical conductivity of CPU films also enhanced with increasing CSA dopant amount, ranging from 2.7±0.9×10~(-10) to 4.4±0.6×10~(-7) S/cm at dry state and 4.2±0.5×10~(-8) to 7.3±1.5×10~(-5) S/cm at wet state. These values (wet) were in the semiconductive region. The redox peaks (0.17 V and 0.82 V) of CPU1.5 film (molar ratio of CSA:aniline trimer was 1.5:1) in cyclic voltammogram indicated its good electroactivity. The doped CPU film exhibited excellent electrical stability (91 % of initial conductivity after 150 h charge) in cell culture medium. The degradation of CPU films became faster with increasing CSA dopant amount in either PBS or lipase/PBS solutions. After 7 d of enzymatic degradation, all CSA doped CPU films lost their conductivity. Their conductivities were similar to that of the undoped CPU film, which may attribute to the dopant leaching during degradation. The 3T3 fibroblasts proliferated and spread on all CPU films. There was no significantly difference on cell proliferation between CPU films and the tissue culture polystyrene, except for the CPU1.5 film. The CPU 1.5 film having the highest dopant content showed less cell viability within 5 d incubation, which may be resulted from the rough surface and leached dopant. Conclusions: A biodegradable conductive polyurethane containing aniline trimer was synthesized. They had good elasticity conductive stability and biocompatibility, which are closely relevant with dopant amount. This biodegradable conductive polyurethane would find opportunities to be applied as tissue engineered scaffolds and smart drug release carriers.
机译:简介:可生物降解的导电材料有望用于心肌,神经,肌肉和骨骼组织的修复。导电水凝胶促进心肌细胞的生长和成熟,并增强了电气和机械耦合以及收缩性能。导电材料还通过整合生化和电刺激改善了神经细胞中神经突的生长。然而,很少报道可生物降解的导电弹性体。为了解决这一局限性,我们将利用聚氨酯化学技术来设计具有弹性和导电性的可生物降解的聚合物。在这里,我们结合使用聚己内酯二醇(PCL)作为软链段,1,6-六亚甲基二异氰酸酯(HDI)作为硬链段和苯胺三聚体作为扩链剂,以实现具有电和电化学特性的可生物降解的聚氨酯。评价了导电聚氨酯的电和电化学性质,形态,机械性质,降解行为,电稳定性和细胞相容性。材料和方法:导电聚氨酯(CPU)是通过两步过程合成的(图1),然后通过溶剂浇铸将其制成掺杂有(1S)-(+)-10-樟脑磺酸(CSA)的薄膜。分别通过〜1H NMR,〜(13)C NMR和FTIR确认氧化的苯胺三聚体和CPU膜的化学结构。在扫描电子显微镜(SEM)上观察到CPU膜的形貌。通过四探针技术测量CPU膜在干态和湿态下的电导率。通过紫外可见和循环伏安法测量来表征CPU膜的电活性。在MTS工作站上以10 mm / min的头部交叉速度测量CPU膜的机械性能。以10 mm / min的恒定速率测试CPU膜在最大应变为30%时的循环拉伸10个循环。在细胞培养基中在100±2 mV的恒定DC电压下进行150 h掺杂的CPU膜的电稳定性。在磷酸盐缓冲溶液(PBS)和脂肪酶/ PBS溶液中检测到CPU膜的体外降解。在37°C下在100 U / mL脂肪酶/ PBS溶液中降解3天和7天后,测量CPU膜的电导率变化。使用3T3成纤维细胞评估了CPU膜的细胞相容性。结果与讨论:所有CPU膜在30%的应变范围内均显示出良好的弹性,并且其初始模量随CSA含量的增加而增加。 CPU膜的粗糙度随着CSA量的增加而增加。随着CSA掺杂量的增加,CPU薄膜的电导率也随之提高,在干燥状态下为2.7±0.9×10〜(-10)至4.4±0.6×10〜(-7)S / cm,在4.2±0.5×10〜湿态为(-8)至7.3±1.5×10〜(-5)S / cm。这些值(湿)在半导体区域中。循环伏安图中CPU1.5膜(CSA:苯胺三聚体的摩尔比为1.5:1)的氧化还原峰(0.17 V和0.82 V)表明其良好的电活性。掺杂的CPU膜在细胞培养基中表现出出色的电稳定性(150 h充电后初始电导率的91%)。随着PBS或脂肪酶/ PBS溶液中CSA掺杂量的增加,CPU膜的降解变得更快。酶降解7天后,所有CSA掺杂的CPU膜都失去了导电性。它们的电导率与未掺杂的CPU膜的电导率相似,这可能归因于在降解过程中掺杂剂的浸出。 3T3成纤维细胞在所有CPU膜上增殖并扩散。除了CPU1.5膜外,CPU膜与组织培养聚苯乙烯之间的细胞增殖没有显着差异。具有最高掺杂剂含量的CPU 1.5膜在5 d的孵育时间内显示出较低的细胞活力,这可能是由于表面粗糙和浸出的掺杂剂引起的。结论:合成了一种可生物降解的含苯胺三聚体的导电聚氨酯。它们具有良好的弹性导电稳定性和生物相容性,这与掺杂量密切相关。这种可生物降解的导电聚氨酯将找到机会用作组织工程支架和智能药物释放载体。

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