The influence of nanostructured features on bacterial adhesion and bone cell functions on severely shot peened 316L stainless steel

被引:202
作者
Bagherifard, Sara [1 ,2 ,3 ]
Hickey, Daniel J. [4 ]
de Luca, Alba C. [3 ]
Malheiro, Vera N. [3 ]
Markaki, Athina E. [3 ]
Guagliano, Mario [1 ]
Webster, Thomas J. [4 ,5 ]
机构
[1] Politecn Milan, Dept Mech Engn, I-20133 Milan, Italy
[2] MIT, Harvard MIT Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[3] Univ Cambridge, Dept Engn, Cambridge CB2 1PZ, England
[4] Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USA
[5] King Abdulaziz Univ, Ctr Excellence Adv Mat Res, Jeddah 21413, Saudi Arabia
基金
美国国家科学基金会; 欧洲研究理事会;
关键词
Surface nanocrystallization; Severe shot peening; Cell-substrate interaction; Bacteria adhesion; COMMERCIALLY PURE TITANIUM; SEVERE PLASTIC-DEFORMATION; HIGH-PRESSURE TORSION; FATIGUE BEHAVIOR; AUSTENITIC STAINLESS; SURFACE-ROUGHNESS; OSTEOBLAST; PROLIFERATION; REFINEMENT; METALS;
D O I
10.1016/j.biomaterials.2015.09.019
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Substrate grain structure and topography play major roles in mediating cell and bacteria activities. Severe plastic deformation techniques, known as efficient metal-forming and grain refining processes, provide the treated material with novel mechanical properties and can be adopted to modify nanoscale surface characteristics, possibly affecting interactions with the biological environment. This in vitro study evaluates the capability of severe shot peening, based on severe plastic deformation, to modulate the interactions of nanocrystallized metallic biomaterials with cells and bacteria. The treated 316L stainless steel surfaces were first investigated in terms of surface topography, grain size, hardness, wettability and residual stresses. The effects of the induced surface modifications were then separately studied in terms of cell morphology, adhesion and proliferation of primary human osteoblasts (bone forming cells) as well as the adhesion of multiple bacteria strains, specifically Staphylococcus aureus, Staphylococcus epidermidis, Pseudomonas aeruginosa, and ampicillin-resistant Escherichia coli. The results indicated a significant enhancement in surface work hardening and compressive residual stresses, maintenance of osteoblast adhesion and proliferation as well as a remarkable decrease in the adhesion and growth of gram-positive bacteria (S. aureus and S. epidermidis) compared to non-treated and conventionally shot peened samples. Impressively, the decrease in bacteria adhesion and growth was achieved without the use of antibiotics, for which bacteria can develop a resistance towards anyway. By slightly grinding the surface of severe shot peened samples to remove differences in nanoscale surface roughness, the effects of varying substrate grain size were separated from those of varying surface roughness. The expression of vinculin focal adhesions from osteoblasts was found to be singularly and inversely related to grain size, whereas the attachment of gram-positive bacteria (S. aureus and S. epidermidis) decreased with increasing nanoscale surface roughness, and was not affected by grain refinement. Ultimately, this study demonstrated the advantages of the proposed shot peening treatment to produce multifunctional 316L stainless steel materials for improved implant functions without necessitating the use of drugs. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:185 / 197
页数:13
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