Ketabchi Amirhossein, Komm Kristopher, Miles-Rossouw Malaika, Cassani Davide A D, Variola Fabio
Department of Mechanical Engineering, University of Ottawa, Ottawa, Canada.
Department of Mechanical Engineering, University of Ottawa, Ottawa, Canada; Department of Chemical and Biological Engineering, University of Ottawa, Ottawa, Canada.
PLoS One. 2014 Mar 14;9(3):e92080. doi: 10.1371/journal.pone.0092080. eCollection 2014.
Current medically relevant metals for prosthetic reconstructions enjoy a relatively good success rate, but their performance drops significantly in patients with compromised health status, and post-surgical infections still remain an important challenge. To address these problems, different nanotechnology-based strategies have been exploited to create implantable metals with an enhanced bioactivity and antibacterial capacities. Among these, oxidative nanopatterning has emerged as a very effective approach to engender nanoporous surfaces that stimulate and guide the activity of adhering cells. The resulting nanoporosity is also attractive because it offers nanoconfined volumes that can be exploited to load bioactive compounds and modulate their release over time. Such extended elution is needed since a single exposure to growth factors and/or antibiotics, for instance, may not be adequate to further sustain bone regeneration and/or to counteract bacterial colonization. In this article, we assessed the capacities of nanoporous titanium surfaces generated by oxidative nanopatterning to provide controlled and sustained elution of proteins and antibiotic molecules. To this end, we have selected bovine serum albumin (BSA) and vancomycin to reflect commonly used compounds, and investigated their adsorption and elution by Fourier-transform infrared (FT-IR) and ultraviolet-visible (UV-VIS) spectroscopy. Our results demonstrate that while the elution of albumin is not significantly affected by the nanoporosity, in the case of vancomycin, nanoporous surfaces provided an extended release. These findings were successively correlated to the establishment of interactions with the surface and physical-entrapment effects exerted by the nanopores, ultimately highlighting their synergistic contribution to the release profiles and thus their importance in the design of nanostructured eluting platforms for applications in medicine.
目前用于假体重建的具有医学相关性的金属具有相对较高的成功率,但在健康状况不佳的患者中其性能会显著下降,并且术后感染仍然是一个重大挑战。为了解决这些问题,人们采用了不同的基于纳米技术的策略来制造具有增强生物活性和抗菌能力的可植入金属。其中,氧化纳米图案化已成为一种非常有效的方法,可产生能刺激和引导黏附细胞活性的纳米多孔表面。所形成的纳米孔隙率也很有吸引力,因为它提供了纳米受限体积,可用于负载生物活性化合物并调节其随时间的释放。由于单次接触生长因子和/或抗生素可能不足以进一步维持骨再生和/或抵抗细菌定植,因此需要这种延长的洗脱。在本文中,我们评估了通过氧化纳米图案化产生的纳米多孔钛表面提供蛋白质和抗生素分子的可控和持续洗脱的能力。为此,我们选择了牛血清白蛋白(BSA)和万古霉素来代表常用化合物,并通过傅里叶变换红外(FT-IR)和紫外可见(UV-VIS)光谱研究了它们的吸附和洗脱。我们的结果表明,虽然白蛋白的洗脱不受纳米孔隙率的显著影响,但对于万古霉素,纳米多孔表面提供了延长释放。这些发现相继与表面相互作用的建立以及纳米孔施加的物理截留效应相关,最终突出了它们对释放曲线的协同贡献,从而突出了它们在设计用于医学应用的纳米结构洗脱平台中的重要性。