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通过原子力显微镜探测生物相容性团簇组装氧化钛表面的纳米级相互作用。

Probing nanoscale interactions on biocompatible cluster-assembled titanium oxide surfaces by atomic force microscopy.

作者信息

Vyas Varun, Podestà Alessandro, Milani Paolo

机构信息

C.I.Ma.I.Na and Dipartimento di Fisica, Università degli Studi di Milano, via Celoria 16, 20133 Milano, Italy.

出版信息

J Nanosci Nanotechnol. 2011 Jun;11(6):4739-48. doi: 10.1166/jnn.2011.4113.

DOI:10.1166/jnn.2011.4113
PMID:21770100
Abstract

We report on the investigation of the adhesive properties of cluster-assembled nanostructured TiO(x) (ns-TiO(x)) films against a Si3N4 AFM tip, in air and in water. The interacting AFM tip apex represents a model nanometer-sized probe, carrying both silanol (Si-OH) and silamine (Si2-NH) groups: it is therefore well suited to investigate biologically relevant molecular interactions with the biocompatible ns-TiO(x) surface. Coupling nanosphere lithography with supersonic cluster beam deposition we produced sub-micrometer patterns of ns-TiO(x) on a reference amorphous silica surface. These devices are ideal platforms for conducting comparative nanoscale investigations of molecular interactions between surfaces and specific groups. We have found that in the aqueous medium the adhesion is enhanced on ns-TiO(x) with respect to amorphous silica, opposed to the case of humid air. A comparative analysis of the different interactions channels (van der Waals, electrostatic, chemical bonding) led to the conclusion that the key for understanding this behavior can be the ability of incoming nucleophiles like nitrogen or oxygen on the Si3N4 tip to displace adsorbed molecules on ns-TiO(x) and link to Ti atoms via co-ordinate (dative covalent) bonding. This effect is likely enhanced on nanostructured TiO(x) with respect to crystalline or micro-porous TiO2, due to the greatly increased effective area and porosity. This study provides a clue for the understanding of interaction mechanisms of proteins with biocompatible ns-TiO(x), and in general with metal-oxide surfaces.

摘要

我们报告了在空气和水中对团簇组装的纳米结构TiO(x)(ns-TiO(x))薄膜与Si3N4原子力显微镜(AFM)探针之间粘附特性的研究。相互作用的AFM探针尖端代表一个模型纳米尺寸探针,带有硅醇(Si-OH)和硅胺(Si2-NH)基团:因此它非常适合研究与生物相容性ns-TiO(x)表面的生物相关分子相互作用。通过将纳米球光刻与超声团簇束沉积相结合,我们在参考非晶二氧化硅表面制备了ns-TiO(x)的亚微米图案。这些器件是用于进行表面与特定基团之间分子相互作用的比较纳米级研究的理想平台。我们发现,在水介质中,相对于非晶二氧化硅,ns-TiO(x)上的粘附力增强,这与潮湿空气的情况相反。对不同相互作用通道(范德华力、静电力、化学键合)的比较分析得出结论,理解这种行为的关键可能是Si3N4尖端上的氮或氧等亲核试剂取代ns-TiO(x)上吸附分子并通过配位(配位共价)键与Ti原子连接的能力。由于有效面积和孔隙率大大增加,相对于结晶或微孔TiO2,这种效应在纳米结构的TiO(x)上可能会增强。这项研究为理解蛋白质与生物相容性ns-TiO(x)以及一般与金属氧化物表面的相互作用机制提供了线索。

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