Hierro-Oliva Margarita, Gallardo-Moreno Amparo M, González-Martín María Luisa
Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), 06006 Badajoz, Spain.
Department of Applied Physics, Faculty of Science, University of Extremadura, 06006 Badajoz, Spain.
Materials (Basel). 2021 Dec 3;14(23):7416. doi: 10.3390/ma14237416.
Adpsortion of protein layers on biomaterials plays an important role in the interactions between implants and the bio-environment. In this context, human serum albumin (HSA) layers have been deposited on modified Ti6Al4V surfaces at different ultraviolet (UV-C) irradiation times to observe possible changes in the adsorbed protein layer. Protein adsorption was done from solutions at concentraions lower than the serum protein concentration, to follow the surface modifications at the beginning of the albumin adhesion process. For this purpose, the surface of the protein-coated samples has been characterized by time of flight secondary ion mass spectrometry (ToF-SIMS), contact angle and zeta potential measurements. The results obtained show a reduction in the total surface tension and zeta potential of samples treated with UV-C light when coated with a protein layer. Furthermore, the UV-C light treatment applied to titanium alloy surfaces is able to modify the conformation, orientation and packing of the proteins arranged in the adsorbed layer. Low irradiation time generates an unstable surface with the lowest protein adsorption and the highest hydrophobic/hydrophilic protein ratio, indicating a possible denaturalization of the protein on these surfaces. However, surface changes are stabilized after 15 h or UV-C irradiation, favoring the protein adsorption through electrical interactions.
蛋白质层在生物材料上的吸附在植入物与生物环境之间的相互作用中起着重要作用。在此背景下,已在不同紫外线(UV-C)照射时间下将人血清白蛋白(HSA)层沉积在改性Ti6Al4V表面上,以观察吸附蛋白层中可能发生的变化。蛋白质吸附是从浓度低于血清蛋白浓度的溶液中进行的,以便在白蛋白粘附过程开始时跟踪表面改性情况。为此,已通过飞行时间二次离子质谱(ToF-SIMS)、接触角和zeta电位测量对蛋白质涂层样品的表面进行了表征。获得的结果表明,涂有蛋白质层的UV-C光处理样品的总表面张力和zeta电位降低。此外,应用于钛合金表面的UV-C光处理能够改变吸附层中蛋白质的构象、取向和堆积。低照射时间会产生一个不稳定的表面,蛋白质吸附最少,疏水/亲水蛋白质比例最高,表明这些表面上的蛋白质可能发生了变性。然而,在UV-C照射15小时后表面变化趋于稳定,有利于通过电相互作用进行蛋白质吸附。