Lee J H, Khang G, Lee J W, Lee H B
Department of Macromolecular Science, Hannam University, Taejon, Korea.
J Biomed Mater Res. 1998 May;40(2):180-6. doi: 10.1002/(sici)1097-4636(199805)40:2<180::aid-jbm2>3.0.co;2-h.
Functional group gradients were prepared on low-density polyethylene (PE) sheets. The surface density of grafted functional groups was gradually changed along the sample length by way of corona discharge treatment with gradually increasing power following graft copolymerization of acrylic acid (AA), sodium p-styrene sulfonate (NaSS), or N,N-dimethyl aminopropyl acrylamide (DMAPAA). AA and NaSS are negatively chargeable and DMAPAA is positively chargeable in phosphate-buffered saline or plasma solution at pH 7.3-7.4. The prepared functional group gradient surfaces were characterized by measurement of the water contact angle, by electron spectroscopy for chemical analysis, and by Fourier transform infrared spectroscopy in the attenuated total reflectance mode. All these measurements indicated that the functional groups were grafted onto the PE surfaces with gradually increasing density. The platelets adhered to the functional group gradient surfaces along the sample length were counted and observed by scanning electron microscopy. It was observed that the platelet adhesion to the gradient surfaces decreased gradually with the increasing surface density of functional groups. This may be related to the hydrophilicity of the surfaces. The DMAPAA-grafted surface showed a large amount of platelet adhesion, probably due to its positive charge character, while the AA-grafted surface, which is charged negatively, showed poor platelet adhesion. However, the NaSS-grafted surface, which is also charged negatively, showed a relatively large amount of platelet adhesion. This may be associated with the existence of an aromatic ring close to the ionizable group in NaSS. It seems that surface functional groups and their charge character, as well as wettability, play important roles for platelet adhesion.
在低密度聚乙烯(PE)片材上制备了官能团梯度。通过在丙烯酸(AA)、对苯乙烯磺酸钠(NaSS)或N,N - 二甲基氨基丙基丙烯酰胺(DMAPAA)接枝共聚后,以逐渐增加的功率进行电晕放电处理,使接枝官能团的表面密度沿样品长度逐渐变化。在pH 7.3 - 7.4的磷酸盐缓冲盐水或血浆溶液中,AA和NaSS可带负电荷,DMAPAA可带正电荷。通过测量水接触角、化学分析电子能谱以及衰减全反射模式下的傅里叶变换红外光谱对制备的官能团梯度表面进行表征。所有这些测量表明,官能团以逐渐增加的密度接枝到PE表面。通过扫描电子显微镜对接枝官能团梯度表面沿样品长度粘附的血小板进行计数和观察。观察到随着官能团表面密度的增加,血小板在梯度表面的粘附逐渐减少。这可能与表面的亲水性有关。DMAPAA接枝表面显示出大量的血小板粘附,可能是由于其正电荷特性,而带负电荷的AA接枝表面显示出血小板粘附性较差。然而,同样带负电荷的NaSS接枝表面显示出相对大量的血小板粘附。这可能与NaSS中靠近可电离基团的芳环的存在有关。表面官能团及其电荷特性以及润湿性似乎对血小板粘附起着重要作用。