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1.
Sci Rep ; 6: 22444, 2016 Mar 01.
Article in English | MEDLINE | ID: mdl-26925553

ABSTRACT

Many dental implants fail due to the infection and inflammation that walk hand in hand with poor healing and soft tissue integration. Titanium surfaces were nanocoated with quercitrin, a natural flavonoid, with the aim to improve soft tissue integration and increase dental implants success. Streptococcus mutans attachment and biofilm formation was analysed. Then, the anti-inflammatory properties and the potential of quercitrin-nanocoated surfaces to boost soft tissue regeneration were tested using human gingival fibroblasts. An inflammatory situation was mimicked using interleulin-1-beta. We found that quercitrin-nanocoated surfaces decreased initial bacterial adhesion while increasing human gingival fibroblasts attachment. Furthermore, quercitrin-nanocoated Ti increased collagen mRNA levels and decreased matrix metalloproteinase-1/tissue inhibitor of metalloproteinanse-1 mRNA ratio, which is related to a reduced metalloproteinase-mediated collagen degradation, while also decreasing the pro-inflammatory prostaglandin E2 release under basal and inflammatory conditions. These results suggest that quercitrin-nanocoated surfaces could enhance the soft tissue integration and increase dental implants success.


Subject(s)
Anti-Bacterial Agents/pharmacology , Anti-Inflammatory Agents/pharmacology , Bacterial Adhesion/drug effects , Biofilms/drug effects , Cell Adhesion/drug effects , Dental Implants/microbiology , Gingiva/microbiology , Quercetin/analogs & derivatives , Streptococcus mutans/metabolism , Adult , Biofilms/growth & development , Cells, Cultured , Dinoprostone/metabolism , Female , Gingiva/cytology , Humans , Inflammation/prevention & control , Male , Matrix Metalloproteinase 1/metabolism , Middle Aged , Quercetin/pharmacology , Tissue Inhibitor of Metalloproteinase-1/metabolism , Titanium , Young Adult
2.
J Biomed Mater Res A ; 104(4): 866-78, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26662548

ABSTRACT

In this work, we investigated a new approach to incorporate Mg particles within a PDLLA matrix using a solvent-free commercially available process. PDLLA/Mg composites were manufactured by injection moulding and the effects of Mg incorporated into PDLLA on MSC and macrophage responses were evaluated. Small amounts of Mg particles (≤ 1 wt %) do not cause thermal degradation of PDLLA, which retains its mechanical properties. PDLLA/Mg composites release hydrogen, alkaline products and Mg(2+) ions without changing pH of culture media. Mg-containing materials provide a noncytotoxic environment that enhances MSC viability. Concentration of Mg(2+) ions in extracts of MSCs increases with the increment of Mg content in the composites. Incorporation of Mg particles into PDLLA stimulates FN production, ALP activity, and VEGF secretion in MSCs, an effect mediated by degradation products dissolved from the composites. Degradation products of PDLLA induce an increase in MCP-1, RANTES, and MIP-1α secretion in macrophages while products of composites have minimal effect on these chemokines. Regulation of MSC behavior at the biomaterial's interface and macrophage-mediated inflammatory response to the degradation products is related to the incorporation of Mg in the composites. These findings suggest that including small amounts of Mg particles into polymeric devices can be a valuable strategy to promote osseointegration and reduce host inflammatory response.


Subject(s)
Biocompatible Materials/metabolism , Macrophages/cytology , Magnesium/metabolism , Mesenchymal Stem Cells/cytology , Polyesters/metabolism , Alkaline Phosphatase/metabolism , Biocompatible Materials/chemistry , Cell Line , Cell Survival , Cells, Cultured , Chemokine CCL2/metabolism , Chemokine CCL3/metabolism , Chemokine CCL5/metabolism , Humans , Macrophages/metabolism , Magnesium/chemistry , Mesenchymal Stem Cells/metabolism , Polyesters/chemistry , Vascular Endothelial Growth Factor A/metabolism
3.
Biomaterials ; 28(30): 4343-54, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17624424

ABSTRACT

We have investigated a novel ultrafine grained (UFG) Zr obtained by severe plastic deformation (SPD) which resulted in a refinement of the grain size by several orders of magnitude. Compared to conventional Zr, higher hardness values were measured on UFG Zr. Polished surfaces having similar topographical features from both materials were prepared, as assessed by atomic force microscopy (AFM). Surface hydrophobicity of Zr, evaluated by measuring water contact angles, was unaffected by grain size reduction. In vitro biocompatibility was addressed on conventional and UFG Zr surfaces and, for comparative purposes, a polished Ti6Al4V alloy was also investigated. Cell attachment and spreading, actin and beta-tubulin cytoskeleton reorganisation, fibronectin secretion and cellular distribution as well as cell viability were evaluated by culturing human osteoblastic Saos-2 cells on the surfaces. The osteoblastic response to conventional Zr was found to be essentially identical to Ti6Al4V and was not affected by grain size reduction. In order to evaluate the ability of the surfaces to promote osteogenic maturation and bone matrix mineralisation, human mesenchymal cells from bone marrow were switched to the osteoblastic phenotype by incubation in osteogenic induction media. Compared to undifferentiated mesenchymal cells, alkaline phosphatase activity and formation of mineralisation nodules were enhanced to the same extent on both Zr surfaces and Ti6Al4V alloy after induction of osteoblastic differentiation. In summary, improved mechanical properties together with excellent in vitro biocompatibility make UFG Zr a promising biomaterial for surgical implants.


Subject(s)
Biocompatible Materials/chemistry , Zirconium/chemistry , Zirconium/pharmacology , Actins/metabolism , Alkaline Phosphatase/analysis , Alloys/chemistry , Calcification, Physiologic , Cell Adhesion/drug effects , Cell Line, Tumor , Cell Survival/drug effects , Cells, Cultured , Cytoskeleton/metabolism , Fibronectins/metabolism , Humans , Hydrophobic and Hydrophilic Interactions , In Vitro Techniques , Materials Testing , Mesenchymal Stem Cells/cytology , Mesenchymal Stem Cells/drug effects , Mesenchymal Stem Cells/metabolism , Microscopy, Electron, Scanning , Osteoblasts/cytology , Osteoblasts/drug effects , Osteoblasts/metabolism , Osteoblasts/ultrastructure , Osteogenesis , Particle Size , Surface Properties , Titanium/chemistry , Tubulin/metabolism
4.
Antonie Van Leeuwenhoek ; 89(3-4): 495-509, 2006.
Article in English | MEDLINE | ID: mdl-16779641

ABSTRACT

Scanning force microscopy has been used to probe the surface of the emerging pathogenic yeast Candida parapsilosis, in order to get insight into its surface structure and properties at submicrometer scales. AFM friction images eventually show patches with a very strong contrast, showing high lateral interaction with the tip. Adhesion force measurement also reveals a high normal interaction with the tip, and patches show extraordinarily high pull off values. The tip eventually sticks completely at the center of the patches. While an extraordinarily high interaction is measured by the tip at those zones, topographic images show extraordinarily flat topography over those zones, both of which characteristics are consistent with a liquid-like area. High resolution friction images show those zones to be surrounded by microfibrillar structures, concentrically oriented, of a mean width of about 25 nm, structures that become progressively less defined as we move away from the center of the patches. No structure can be appreciated inside the zones of maximum contrast. Also some helical or ribbon-like structure can be resolved from friction images. There is not only an ordered disposition of the microfibrillar structures, but also the adhesion force increases radially in the direction towards the center of the patches. These structures responsible for the high adhesion are thought to be incipient-emerging budding zones. Microfibrillar structures are thought to represent the first steps of chitin biosynthesis and cell wall digestion, with chitin polymers being biosynthesized, associated with other macromolecules of the yeast cell wall. They can be also beta glucan helical structures, made visible in the zone of yeast division due to the action of autolysins. The observed gradient in surface adhesion and elastic properties correlates well with that expected from a biochemical point of view. The higher adhesion force measured could be either due to the different macromolecular nature of the patches, or to a mechanical adhesion effect due to the different plasticity of that zone. This work reveals the importance of taking into account the dynamic nature of the cell wall physico-chemical properties. Processes related to the normal cell-cycle, as division, can strongly alter the surface morphology and physico-chemical properties and cause important heterogeneities that might have a profound impact on the adhesion behavior of a single cell, which could not be detected by more macroscopic methods.


Subject(s)
Candida/ultrastructure , Candida/chemistry , Candida/physiology , Cell Wall/chemistry , Cell Wall/physiology , Cell Wall/ultrastructure , Microscopy, Atomic Force/instrumentation , Microscopy, Atomic Force/methods , Surface Properties , Tissue Adhesions
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