Fonner John M, Forciniti Leandro, Nguyen Hieu, Byrne James D, Kou Yann-Fuu, Syeda-Nawaz Jeja, Schmidt Christine E
Department of Biomedical Engineering, The University of Texas at Austin, Austin, Texas, 1 University Station, MC C0800, Austin, TX 78712, USA.
Biomed Mater. 2008 Sep;3(3):034124. doi: 10.1088/1748-6041/3/3/034124. Epub 2008 Sep 3.
Polypyrrole (PPy) is an inherently conducting polymer that has shown great promise for biomedical applications within the nervous system. However, to effectively use PPy as a biomaterial implant, it is important to understand and reproducibly control the electrical properties, physical topography and surface chemistry of the polymer. Although there is much research published on the use of PPy in various applications, there is no systematic study linking the methodologies used for PPy synthesis to PPy's basic polymeric properties (e.g., hydrophilicity, surface roughness), and to the biological effects these properties have on cells. Electrochemically synthesized PPy films differ greatly in their characteristics depending on synthesis parameters such as dopant, substrate and thickness, among other parameters. In these studies, we have used three dopants (chloride (Cl), tosylate (ToS), polystyrene sulfonate (PSS)), two substrates (gold and indium tin oxide-coated glass), and a range of thicknesses, to measure and compare the biomedically important characteristics of surface roughness, contact angle, conductivity, dopant stability and cell adhesion (using PC-12 cells and Schwann cells). As predicted, we discovered large differences in roughness depending on the dopant used and the thickness of the film, while substrate choice had little effect. From contact angle measurements, PSS was found to yield the most hydrophilic material, most likely because of free charges from the long PSS chains exposed on the surface of the PPy. ToS-doped PPy films were tenfold more conductive than Cl- or PSS-doped films. X-ray photoelectron spectroscopy studies were used to evaluate dopant concentrations of PPy films stored in water and phosphate buffered saline over 14 days, and conductance studies over the same timeframe measured electrical stability. PSS proved to be the most stable dopant, though all films experienced significant decay in conductivity and dopant concentration. Cell adhesion studies demonstrated the dependence of cell outcome on film thickness and dopant choice. The strengths and weaknesses of different synthesis parameters, as demonstrated by these experiments, are critical design factors that must be leveraged when designing biomedical implants. The results of these studies should provide practical insight to researchers working with conducting polymers, and particularly PPy, on the relationships between synthesis parameters, polymeric properties and biological compatibility.
聚吡咯(PPy)是一种本征导电聚合物,在神经系统的生物医学应用中显示出巨大潜力。然而,要有效地将PPy用作生物材料植入物,了解并可重复控制该聚合物的电学性质、物理形貌和表面化学性质非常重要。尽管有许多关于PPy在各种应用中的研究发表,但尚无系统研究将用于PPy合成的方法与PPy的基本聚合物性质(如亲水性、表面粗糙度)以及这些性质对细胞的生物学效应联系起来。电化学合成的PPy薄膜,其特性会因掺杂剂、基底和厚度等合成参数以及其他参数而有很大差异。在这些研究中,我们使用了三种掺杂剂(氯离子(Cl)、对甲苯磺酸根(ToS)、聚苯乙烯磺酸根(PSS))、两种基底(金和氧化铟锡涂层玻璃)以及一系列厚度,来测量和比较表面粗糙度、接触角、电导率、掺杂剂稳定性和细胞黏附(使用PC - 12细胞和雪旺细胞)等对生物医学重要的特性。正如预期的那样,我们发现粗糙度因所用掺杂剂和薄膜厚度的不同而有很大差异,而基底的选择影响较小。通过接触角测量发现,PSS产生的材料亲水性最强,这很可能是由于PPy表面暴露的长PSS链上的自由电荷所致。ToS掺杂的PPy薄膜的导电性比Cl或PSS掺杂的薄膜高十倍。利用X射线光电子能谱研究评估了在水和磷酸盐缓冲盐水中储存14天的PPy薄膜的掺杂剂浓度,并在相同时间范围内进行的电导率研究测量了电稳定性。结果表明,PSS是最稳定的掺杂剂,不过所有薄膜的电导率和掺杂剂浓度都经历了显著下降。细胞黏附研究表明细胞结果取决于薄膜厚度和掺杂剂选择。这些实验所展示的不同合成参数的优缺点,是设计生物医学植入物时必须利用的关键设计因素。这些研究结果应为从事导电聚合物特别是PPy研究的人员提供关于合成参数、聚合物性质和生物相容性之间关系的实际见解。