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Träfflista för sökning "WFRF:(Cai Yanling) srt2:(2010-2014)"

Sökning: WFRF:(Cai Yanling) > (2010-2014)

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  • Cai, Yanling, et al. (författare)
  • Bacteria viability assessment after photocatalytic treatment
  • 2014
  • Ingår i: 3 Biotech. - : Springer. - 2190-5738 .- 2190-572X. ; 4:2, s. 149-157
  • Tidskriftsartikel (refereegranskat)abstract
    • The aim of the present work was to evaluate several methods for analyzing the viability of bacteria after antibacterial photocatalytic treatment. Colony-forming unit (CFU) counting, metabolic activity assays based on resazurin and phenol red and the Live/Dead® BacLight™ bacterial viability assay (Live/Dead staining) were employed to assess photocatalytically treated Staphylococcus epidermidis and Streptococcus mutans. The results showed conformity between CFU counting and the metabolic activity assays, while Live/Dead staining showed a significantly higher viability post-treatment. This indicates that the Live/Dead staining test may not be suitable for assessing bacterial viability after photocatalytic treatment and that, in general, care should be taken when selecting a method for determining the viability of bacteria subjected to photocatalysis. The present findings are expected to become valuable for the development and evaluation of photocatalytically based disinfection applications
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  • Cai, Yanling, et al. (författare)
  • Disinfection Kinetics and Contribution ofReactive Oxygen Species When EliminatingBacteria with TiO2 Induced Photocatalysis
  • 2014
  • Ingår i: Journal of Biomaterials and Nanobiotechnology. - : Scientific Research Publishing, Inc.. - 2158-7027 .- 2158-7043. ; 5:3, s. 200-209
  • Tidskriftsartikel (refereegranskat)abstract
    • Titania (TiO2) induced photocatalysis has been widely investigated and applied as a disinfectionstrategy in many industrial and clinical applications. Reactive oxygen species (ROS), including hydroxylradicals (•OH), superoxide radicals ( •−2 O ) and hydrogen peroxide (H2O2), generated in thephotocatalytic reaction process are considered to be the active components prompting the bactericidaleffect. In the present work, the kinetics of photocatalytic inactivation of Staphylococcus epidermidisand specific contributions of •OH, •−2 O and H2O2 to the bactericidal process were studiedusing two disinfection settings sutilizing photocatalytic resin-TiO2 nanocomposite surfacesand suspended TiO2 nanoparticles, respectively. In antibacterial tests against S. epidermidis with alayer of bacterial suspension on the resin-TiO2 surfaces, H2O2 was found to be the most efficientROS component contributing to the antibacterial effect. Disinfection kinetics showed a two-stepbehavior with an initial region having a lower disinfection rate followed by a higher rate regionafter 10 min of UV irradiation. By contrast, in antibacterial tests with suspended bacteria andphotocatalytic TiO2 nanoparticles, •OH and H2O2 showed equal significance in the bacterial inactivationhaving a typical Chick-Watson disinfection kinetics behavior with a steady disinfection rate.The results contribute to the understanding of the bactericidal mechanism and kinetics of photocatalyticdisinfection that are essential for designing specific antibacterial applications of photocatalyticmaterials.
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  • Cai, Yanling, et al. (författare)
  • Photocatalysis induces bioactivity of an organic polymer based material
  • 2014
  • Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 4:101, s. 57715-57723
  • Tidskriftsartikel (refereegranskat)abstract
    • Several materials, like bioglasses, sintered hydroxyapatite and Ti metals and alloys, have the ability to bond to living bone in vivo, which is a desirable property of biomaterials called bioactivity. In this work, we present a novel strategy to develop bioactivity on the non-bioactive surface of a resin-TiO2 nanocomposite through photocatalysis. The results show that UV irradiation (365 nm, 10 mW cm(-2)) for 8 to 16 h on the resin-TiO2 nanocomposite immersed in water induces bioactivity as indicated by hydroxyapatite growth following immersion of the samples in Dulbecco's phosphate buffered saline for 7 days at 37 degrees C. While a nonirradiated resin-TiO2 surface did not show any hydroxyapatite deposition, a surface after 16 h of UV irradiation was fully covered by hydroxyapatite. In vitro cell adhesion of osteoblast-like MG63 cells confirmed the biocompatibility and bioactivity of the resin-TiO2 surfaces with a hydroxyapatite deposition layer, while the non-irradiated resin-TiO2 surface showed no cell adhesion. Resin-TiO2 nanocomposites, with or without UV irradiation, proved to be nontoxic to two human cell lines, human dermal fibroblasts (hDF) and MG63 cells. It was also shown that an increased dose of UV irradiation decreased bacterial adhesion, which is an additional benefit of the UV treatment and a favourable property for biomedical applications. The combined benefits of biocompatibility, bioactivity, decreased bacterial adhesion and the highly efficient disinfection property of TiO2 photocatalysis under UV light make this resin-TiO2 material an interesting candidate for implant and biomedical device applications.
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  • Cai, Yanling, et al. (författare)
  • Photocatalytic Antibacterial Effects Are Maintained on Resin-Based TiO2 Nanocomposites after Cessation of UV Irradiation
  • 2013
  • Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 8:10, s. e75929-
  • Tidskriftsartikel (refereegranskat)abstract
    • Photocatalysis induced by TiO2 and UV light constitutes a decontamination and antibacterial strategy utilized in many applications including self-cleaning environmental surfaces, water and air treatment. The present work reveals that antibacterial effects induced by photocatalysis can be maintained even after the cessation of UV irradiation. We show that resin-based composites containing 20% TiO2 nanoparticles continue to provide a pronounced antibacterial effect against the pathogens Escherichia coli, Staphylococcus epidermidis, Streptococcus pyogenes, Streptococcus mutans and Enterococcus faecalis for up to two hours post UV. For biomaterials or implant coatings, where direct UV illumination is not feasible, a prolonged antibacterial effect after the cessation of the illumination would offer new unexplored treatment possibilities.
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  • Cai, Yanling, et al. (författare)
  • Photocatalytic inactivation of biofilms on bioactive dental adhesives
  • 2014
  • Ingår i: Journal of Biomedical Materials Research. Part B - Applied biomaterials. - : Wiley. - 1552-4973 .- 1552-4981. ; 102:1, s. 62-67
  • Tidskriftsartikel (refereegranskat)abstract
    • Biofilms are the most prevalent mode of microbial life in nature and are 10-1000 times more resistant to antibiotics than planktonic bacteria. Persistent biofilm growth associated at the margin of a dental restoration often leads to secondary caries, which remains a challenge in restorative dentistry. In this work, we present the first in vitro evaluation of on-demand photocatalytic inactivation of biofilm on a novel dental adhesive containing TiO2 nanoparticles. Streptococcus mutans biofilm was cultured on this photocatalytic surface for 16 h before photocatalytic treatment with ultraviolet-A (UV-A) light. UV-A doses ranging from 3 to 43 J/cm(2) were applied to the surface and the resulting viability of biofilms was evaluated with a metabolic activity assay incorporating phenol red that provided a quantitative measure of the reduction in viability due to the photocatalytic treatments. We show that an UV-A irradiation dose of 8.4 J/cm(2) leads to one order of magnitude reduction in the number of biofilm bacteria on the surface of the dental adhesives while as much as 5-6 orders of magnitude reduction in the corresponding number can be achieved with a dose of 43 J/cm(2). This material maintains its functional properties as an adhesive in restorative dentistry while offering the possibility of a novel dental procedure in the treatment or prevention of bacterial infections via on-demand UV-A irradiation. Similar materials could be developed for the treatment of additional indications such as peri-implantits.
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  • Cai, Yanling (författare)
  • Titanium Dioxide Photocatalysis in Biomaterials Applications
  • 2013
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Despite extensive preventative efforts, the problem of controlling infections associated with biomedical materials persists. Bacteria tend to colonize on biocompatible materials and form biofilms; thus, novel biomaterials with antibacterial properties are of great interest. In this thesis, titanium dioxide (TiO2)-associated photocatalysis under ultraviolet (UV) irradiation was investigated as a strategy for developing bioactivity and antibacterial properties on biomaterials. Although much of the work was specifically directed towards dental materials, the results presented are applicable to a wide range of biomaterial applications.Most of the experimental work in the thesis was based on a resin-TiO2 nanocomposite that was prepared by adding 20 wt% TiO2 nanoparticles to a resin-based polymer material. Tests showed that the addition of the nanoparticles endowed the adhesive material with photocatalytic activity without affecting the functional bonding strength. Subsequent studies indicated a number of additional beneficial properties associated with the nanocomposite that appear promising for biomaterial applications. For example, irradiation with UV light induced bioactivity on the otherwise non-bioactive nanocomposite; this was indicated by hydroxyapatite formation on the surface following soaking in Dulbecco’s phosphate-buffered saline. Under UV irradiation, the resin-TiO2 nanocomposite provided effective antibacterial action against both planktonic and biofilm bacteria. UV irradiation of the nanocomposite also provided a prolonged antibacterial effect that continued after removal of the UV light source. UV treatment also reduced bacterial adhesion to the resin-TiO2 surface.The mechanisms involved in the antibacterial effects of TiO2 photocatalysis were studied by investigating the specific contributions of the photocatalytic reaction products (the reactive oxygen species) and their disinfection kinetics. Methods of improving the viability analysis of bacteria subjected to photocatalysis were also developed. 
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  • Li, Cuiyan, et al. (författare)
  • Photocatalytic and antibacterial properties of Au-decorated Fe3O4@mTiO(2) core-shell microspheres
  • 2014
  • Ingår i: Applied Catalysis B. - : Elsevier BV. - 0926-3373 .- 1873-3883. ; 156, s. 314-322
  • Tidskriftsartikel (refereegranskat)abstract
    • A facile approach for the fabrication of Au-decorated mesoporous Fe3O4@TiO2 (Fe3O4@mTiO(2)) core-shell microspheres is demonstrated. The protocol involved the coating of a successive layer of TiO2 onto a magnetic Fe3O4 core via a sol-gel process, followed by TiO2 crystallization and mesopore-formation by a hydrothermal treatment, and then the deposition of Au nanoparticles onto Fe3O4@mTiO(2) microspheres through an in situ reduction of perchloric acid. The mesoporous microspheres (Fe3O4@mTiO(2)) showed stronger magnetic properties than the dense sample (Fe3O4@TiO2) before the hydrothermal treatment. The size and loading amount of Au nanoparticles were controlled by the reduction temperature and concentration of Au salt, respectively. Compared to unmodified Fe3O4@mTiO(2) microspheres, Fe3O4@mTiO(2)@Au microspheres showed higher photocatalytic activity for organic degradation and antibacterial action in water. These core-shell Fe3O4@mTiO(2)@Au microspheres can serve as efficient and recyclable photocatalysts, which have promising applications in environmental treatment.
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  • Li, Cuiyan, et al. (författare)
  • Polyacrylamide-metal nanocomposites : one-pot synthesis, antibacterial properties, and thermal stability
  • 2013
  • Ingår i: Journal of nanoparticle research. - : Springer Science and Business Media LLC. - 1388-0764 .- 1572-896X. ; 15:9, s. UNSP 1922-
  • Tidskriftsartikel (refereegranskat)abstract
    • The incorporation of inorganic nanoparticles into polymers is a hot research spot, since it endows the nanocomposites with new or improved properties by exploiting synergistic effects. Here we report a facile one-pot synthesis of polyacrylamide (PAM)-metal (M = Au, Ag, or Pd) nanocomposites in ethylene glycol (EG). The simultaneous polymerization of the acylamide (AM) monomer and formation of metal nanoparticles lead to a homogeneous distribution of metal nanoparticles in the PAM matrix. The sizes of Au, Ag, and Pd nanoparticles are 55.50 +/- 10.6, 14.15 +/- 2.57, and 7.74 +/- 1.82 nm, respectively. The reaction system only includes EG, AM monomer, and corresponding metal salt. EG acts as both the solvent and the reducing reagent. Also, no initiator for AM polymerization and no surfactant for stabilization of metal nanoparticles are used. Furthermore, this simple synthetic route does not rely on any special or expensive equipment, thus can be exploited to the synthesis of similar polymer-inorganic nanocomposites. Compared to PAM, the PAM-metal nanocomposites showed enhanced thermal stability and antibacterial properties.
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  • Olsson, Johan V., et al. (författare)
  • Reactive imidazole intermediates : simplified synthetic approach to functional aliphatic cyclic carbonates
  • 2014
  • Ingår i: Polymer Chemistry. - : Royal Society of Chemistry. - 1759-9954 .- 1759-9962. ; 5:23, s. 6651-6655
  • Tidskriftsartikel (refereegranskat)abstract
    • Reactive imidazole intermediates based on AB(2) and A(3) monomers, i.e. bis(methylol) propionic acid (bis-MPA) and trimethylolpropane (TMP) have successfully been synthesized and isolated on a 100 gram scale via a facile synthetic protocol using 1,1' -carbonyldiimidazole (CDI) as a key reagent. The robustness of the imidazole intermediates as bench stable precursors enabled the synthesis of a library of functional cyclic carbonates bearing relevant functionalities including hydrophilic PEGs, bioactive cholesterol and clickable groups. A number of functional polycarbonates were obtained by ring-opening polymerization, and their relevance in biomedical applications was highlighted by their low cytotoxicity on human dermal fibroblasts (hDF).
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  • Unosson, Erik, et al. (författare)
  • Antibacterial Properties of Dental Luting Agents : Potential to Hinder the Development of Secondary Caries
  • 2012
  • Ingår i: International Journal of Dentistry. - : Hindawi Publishing Corporation. - 1687-8736 .- 1687-8728. ; 2012, s. 529495-
  • Tidskriftsartikel (refereegranskat)abstract
    • A modified direct contact test was used to evaluate the antibacterial properties of four commercially available dental luting agents (RelyX Unicem, Ketac Cem, Ceramir Crown & Bridge and Harvard Cement) and two reference materials (glass-ionomer cement and calcium aluminate cement) compared to a negative-control material (PMMA). Streptococcus mutans bacteria were placed in direct contact with specimens that had been aged for 10 min, 1 day, and 7 days, in order to test the antibacterial properties of the materials. A metabolic assay containing resazurin was used to quantify the amount of viable bacteria remaining after the direct contact tests. The effects of pH and fluoride on bacteria proliferation were also evaluated. Strongest antibacterial properties were found for calcium aluminate cement, followed by Ceramir Crown & Bridge and RelyX Unicem. Ketac Cem, Harvard Cement, and the reference glass-ionomer cement showed bacteria content either higher than or not significantly different from the PMMA control in all instances. pH levels below 6.3 and above 9.0 were found to have negative effects on bacterial proliferation. No correlation between either acidic materials or fluoride release and antibacterial properties could be seen; rather, basic materials showed stronger antibacterial properties.
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  • Welch, Ken, et al. (författare)
  • Dental adhesives with bioactive and on-demand bactericidal properties
  • 2010
  • Ingår i: Dental Materials. - : Elsevier BV. - 0109-5641 .- 1879-0097. ; 26:5, s. 491-499
  • Tidskriftsartikel (refereegranskat)abstract
    • Objectives: The aim of the present work was to perform the first in vitro evaluation of a new interfacial bond-promoting material-and-method concept for on-demand long term bacteria inhibition in dental restoration procedures. Methods: The bioactivity, mechanical bonding strength and photocatalytic bactericidal properties, induced by low dose ultraviolet-A (UV-A) irradiation of dental adhesives containing crystalline titania nanoparticles (NPs), were analyzed. Results: Dental adhesives with a NP content of 20 wt% were shown to be bioactive in terms of spontaneous hydroxylapatite formation upon storage in simulated body fluid and the bioactivity was found to be promoted by chemical etching of the adhesives. The mechanical bonding strength between the adhesives and a HA tooth model was shown to be unaffected by the NPs up to a NP content of 30 wt%. Elimination of Staphylococcus epidermidis in contact with the adhesives was found to depend both on UV photocatalytic irradiation intensity and time. Efficient elimination of the bacteria could be achieved using a UV-A dose of 4.5 J/cm2 which is about 6 times below the safe maximum UV dose according to industry guidelines, and 20 times below the average UV-A dose received during an ordinary sun bed session. Significance: The combined features of bioactivity and on-demand bactericidal effect should open up the potential to create dental adhesives that reduce the incidence of secondary caries and promote closure of gaps forming at the interface towards the tooth via remineralization of adjacent tooth substance, as well as prevention of bacterial infections via on-demand UV-A irradiation.
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  • Xia, Wei, et al. (författare)
  • Mesoporous titanium dioxide coating for metallic implants
  • 2012
  • Ingår i: Journal of Biomedical Materials Research. Part B - Applied biomaterials. - : Wiley. - 1552-4973 .- 1552-4981. ; 100B:1, s. 82-93
  • Tidskriftsartikel (refereegranskat)abstract
    • A bioactive mesoporous titanium dioxide (MT) coating for surface drug delivery has been investigated to develop a multifunctional implant coating, offering quick bone bonding and biological stability. An evaporation induced self-assembly (EISA) method was used to prepare a mesoporous titanium dioxide coating of the anatase phase with BET surface area of 172 m2/g and average pore diameter of 4.3 nm. Adhesion tests using the scratch method and an in situ screw-in/screw-out technique confirm that the MT coating bonds tightly with the metallic substrate, even after removal from bone. Because of its high surface area, the bioactivity of the MT coating is much better than that of a dense TiO2 coating of the same composition. Quick formation of hydroxyapatite (HA) in vitro can be related to enhance bonding with bone. The uptake of antibiotics by the MT coating reached 13.4 mg/cm3 within a 24 h loading process. A sustained release behavior has been obtained with a weak initial burst. By using Cephalothin as a model drug, drug loaded MT coating exhibits a sufficient antibacterial effect on the material surface, and within millimeters from material surface, against E.coli. Additionally, the coated and drug loaded surfaces showed no cytotoxic effect on cell cultures of the osteoblastic cell line MG-63. In conclusion, this study describes a novel, biocompatiblemesoporous implant coating, which has the ability to induce HA formation and could be used as a surface drug-delivery system.
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