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      Effect of photofunctionalization on fluoride-treated nanofeatured titanium

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          Abstract

          The objective of this study was to evaluate the effect of ultraviolet light treatment, known as photofunctionalization, on the biological and osseointegration capability of nanofeatured titanium created by a combination of sandblasting and hydrofluoric acid treatment. Titanium samples in disk and cylinder forms were photofunctionalized by treatment with ultraviolet light for 15 min. The nanofeatured surface was converted from hydrophobic to superhydrophilic after photofunctionalization. The strength of osseointegration measured by a biomechanical push-in test in a rat model was stronger for photofunctionalized implants than for untreated implants by 2.2 and 2.3 times, respectively, at the early (week 2) and late (week 4) stages of healing, implying that photofunctionalization did not only accelerate but also increased the degree of osseointegration. Culture studies using bone marrow-derived osteoblasts showed that the attachment, spread, and functional phenotypes of osteogenic cells, such as alkaline phosphatase activity and mineralization, were remarkably increased on photofunctionalized titanium. In conclusion, photofunctionalization substantially increased biological and osseointegration capability of a nanofeatured titanium surface. In light with proven effectiveness on microfeatured surfaces in the literature, photofunctionalization may provide a novel and practical avenue to further improve osseointegration capability of implants in a wide range of surface morphology with micro-to-nano features.

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          Most cited references36

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          Vinculin controls focal adhesion formation by direct interactions with talin and actin

          Focal adhesions (FAs) regulate cell migration. Vinculin, with its many potential binding partners, can interconnect signals in FAs. Despite the well-characterized structure of vinculin, the molecular mechanisms underlying its action have remained unclear. Here, using vinculin mutants, we separate the vinculin head and tail regions into distinct functional domains. We show that the vinculin head regulates integrin dynamics and clustering and the tail regulates the link to the mechanotransduction force machinery. The expression of vinculin constructs with unmasked binding sites in the head and tail regions induces dramatic FA growth, which is mediated by their direct interaction with talin. This interaction leads to clustering of activated integrin and an increase in integrin residency time in FAs. Surprisingly, paxillin recruitment, induced by active vinculin constructs, occurs independently of its potential binding site in the vinculin tail. The vinculin tail, however, is responsible for the functional link of FAs to the actin cytoskeleton. We propose a new model that explains how vinculin orchestrates FAs.
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            Advancing dental implant surface technology--from micron- to nanotopography.

            Current trends in clinical dental implant therapy include use of endosseous dental implant surfaces embellished with nanoscale topographies. The goal of this review is to consider the role of nanoscale topographic modification of titanium substrates for the purpose of improving osseointegration. Nanotechnology offers engineers and biologists new ways of interacting with relevant biological processes. Moreover, nanotechnology has provided means of understanding and achieving cell specific functions. The various techniques that can impart nanoscale topographic features to titanium endosseous implants are described. Existing data supporting the role of nanotopography suggest that critical steps in osseointegration can be modulated by nanoscale modification of the implant surface. Important distinctions between nanoscale and micron-scale modification of the implant surface are presently considered. The advantages and disadvantages of nanoscale modification of the dental implant surface are discussed. Finally, available data concerning the current dental implant surfaces that utilize nanotopography in clinical dentistry are described. Nanoscale modification of titanium endosseous implant surfaces can alter cellular and tissue responses that may benefit osseointegration and dental implant therapy.
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              High surface energy enhances cell response to titanium substrate microstructure.

              Titanium (Ti) is used for implantable devices because of its biocompatible oxide surface layer. TiO2 surfaces that have a complex microtopography increase bone-to-implant contact and removal torque forces in vivo and induce osteoblast differentiation in vitro. Studies examining osteoblast response to controlled surface chemistries indicate that hydrophilic surfaces are osteogenic, but TiO2 surfaces produced until now exhibit low surface energy because of adsorbed hydrocarbons and carbonates from the ambient atmosphere or roughness induced hydrophobicity. Novel hydroxylated/hydrated Ti surfaces were used to retain high surface energy of TiO2. Osteoblasts grown on this modified surface exhibited a more differentiated phenotype characterized by increased alkaline phosphatase activity and osteocalcin and generated an osteogenic microenvironment through higher production of PGE2 and TGF-beta1. Moreover, 1alpha,25OH2D3 increased these effects in a manner that was synergistic with high surface energy. This suggests that increased bone formation observed on modified Ti surfaces in vivo is due in part to stimulatory effects of high surface energy on osteoblasts. (c) 2005 Wiley Periodicals, Inc.
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                Author and article information

                Journal
                Journal of Biomaterials Applications
                J Biomater Appl
                SAGE Publications
                0885-3282
                1530-8022
                July 31 2013
                August 28 2013
                : 28
                : 8
                : 1200-1212
                Article
                10.1177/0885328213501566
                23985537
                0cdee90d-5ef2-4a55-8bc0-fea26fe671c7
                © 2013
                History

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