scholarly journals MC3T3-E1 Cells on Titanium Surfaces with Nanometer Smoothness and Fibronectin Immobilization

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Tohru Hayakawa ◽  
Eiji Yoshida ◽  
Yoshitaka Yoshimura ◽  
Motohiro Uo ◽  
Masao Yoshinari
Keyword(s):  
Cell Culture ◽  
Cell Viability ◽  
Total Protein ◽  
Mechanical Treatment ◽  
Titanium Surface ◽  
Activation Technique ◽  
Microscopy Observation ◽  
Biochemical Treatment ◽  
Titanium Surfaces ◽  
Scanning Electron

The present study was aimed to evaluate the viability and total protein contents of osteoblast-like cells on the titanium surface with different surface mechanical treatment, namely, nanometer smoothing (Ra: approximately 2.0 nm) and sandblasting (Ra: approximately 1.0 μm), and biochemical treatment, namely, with or without fibronectin immobilization. Fibronectin could be easily immobilized by tresyl chloride-activation technique. MC3T3-E1 cells were seeded on the different titanium surfaces. Cell viability was determined by MTT assay. At 1 day of cell culture, there were no significant differences in cell viability among four different titanium surfaces. At 11 days, sandblasted titanium surface with fibronectin immobilization showed the significantly highest cell viability than other titanium surface. No significant differences existed for total protein contents among four different titanium surfaces at 11 days of cell culture. Scanning electron microscopy observation revealed that smoothness of titanium surface produced more spread cell morphologies, but that fibronectin immobilization did not cause any changes of the morphologies of attached cells. Fibronectin immobilization provided greater amount of the number of attached cells and better arrangement of attached cells. In conclusion, the combination of sandblasting and fibronectin immobilization enhanced the cell viability and fibronectin immobilization providing better arrangements of attached cells.

Observation of Cells on a Simulated Titanium Surface with Transparency

2021 ◽  
pp. 002203452110002
Author(s):  
K. Teraoka ◽  
A. Watazu ◽  
T. Sonoda
Keyword(s):  
Cell Culture ◽  
Titanium Surface ◽  
Basal Layer ◽  
Time Lapse ◽  
Contact Angles ◽  
Titanium Implants ◽  
Active Movement ◽  
Titanium Layer ◽  
Inverted Microscope ◽  
Titanium Surfaces

The main driving force of osseointegration on titanium implants is believed to be the calcification caused by cellular activity. However, owing to the opacity of bulk titanium, live cells on titanium surfaces cannot be observed using an inverted microscope. To overcome this limitation, this study proposes a transparent titanium thin layer as a simulated titanium surface that allows live-cell observation from below. The titanium layer was fabricated on a polystyrene culture dish by magnetron DC sputtering using a pure Ti(JIS1) target. The titanium layer was characterized by transparency, composition, structure, and wettability. Osteoblast-like cells were cultured in the titanium-coated dishes. The cell culture was observed periodically using an inverted microscope, and the images were compiled into time-lapse videos. Cells on the titanium layer were characterized by movement speeds and doubling times. The titanium-coated dish was transparent gray, and its transmittance profile was consistent with that of the polystyrene dish. The titanium layer showed similarities to bulk titanium surfaces in terms of composition and structure; that is, it showed an oxidized titanium outermost layer and titanium metal basal layer. The wettability of the titanium layer was hydrophilic with mean contact angles of 67.52°. Osteoblast-like cells successfully adhered to the titanium layer and proliferated to confluence. The time-lapse videos demonstrated active movement of the cells on the titanium layer, which suggested the involvement of the titanium surface in cellular motility. The cell culture on the titanium layer can be considered cell culture on a titanium surface. In short, the titanium layer enabled the acquisition of information for living cells on titanium that has either been unknown or analogically understood based on cell culture on polystyrene dishes.

Studies on enhancement of biofilm formation and adherence due to mechanical treatment of titanium surfaces in cooling-water systems

Biofilms ◽  
2008 ◽  
pp. 1-7 ◽  
Author(s):  
R. P. George ◽  
J. Gopal ◽  
P. Muraleedharan ◽  
B. Anandkumar ◽  
R. Baskaran ◽  
...  
Keyword(s):  
Biofilm Formation ◽  
Power Plants ◽  
Mechanical Treatment ◽  
Titanium Surface ◽  
Sea Water ◽  
Long Term Effects ◽  
Wide Range ◽  
Titanium Surfaces ◽  
Mechanical Cleaning

ABSTRACTTitanium has proven to be the heat exchanger material of choice for sea-water-cooled power plants owing to its outstanding resistance to pitting and crevice corrosion in a wide range of aggressive media. However, the inertness of the titanium surface makes it highly susceptible to biofilm formation and subsequent biofouling. This can hinder the heat transfer properties and flow of water. Fouling control strategies in condensers include a combination of mechanical, chemical and thermal treatments. However, reports from various industrial situations suggest that mechanical treatment may not have long-term effects. This study aimed to find out whether mechanical cleaning eventually enhances biofilm formation and increases the adherence of biofilm. In our studies epifluorescence micrographs of biofilms on control and mechanically treated titanium surfaces clearly showed accelerated biofilm formation as well as increased adherence on the mechanically cleaned surface. Total counts of viable bacteria acquired by culturing technique, and biofilm thickness measurements made using microscopic techniques, confirmed this observation. Surface profilometry showed increased roughness of the titanium surface, facilitating adherence of biofilm. The number of microbial species was higher on mechanically cleaned and re-exposed surfaces than on fresh titanium. Thus we concluded that mechanical cleaning can increase biofilm formation and adherence of biofilm, thereby increasing the potential of biofouling in the long term.

scholarly journals Zinc, Zinc Transporters, and Cadmium Cytotoxicity in a Cell Culture Model of Human Urothelium

Toxics ◽  
2021 ◽  
Vol 9 (5) ◽  
pp. 94
Author(s):  
Soisungwan Satarug ◽  
Scott H. Garrett ◽  
Seema Somji ◽  
Mary Ann Sens ◽  
Donald A. Sens
Keyword(s):  
Dna Methylation ◽  
Cell Culture ◽  
Cell Viability ◽  
Zinc Transporters ◽  
Cell Culture Model ◽  
Induced Expression ◽  
Glutathione Biosynthesis ◽  
Culture Model ◽  
A Cell ◽  
Cd Exposure

We explored the potential role of zinc (Zn) and zinc transporters in protection against cytotoxicity of cadmium (Cd) in a cell culture model of human urothelium, named UROtsa. We used real-time qRT-PCR to quantify transcript levels of 19 Zn transporters of the Zrt-/Irt-like protein (ZIP) and ZnT gene families that were expressed in UROtsa cells and were altered by Cd exposure. Cd as low as 0.1 µM induced expression of ZnT1, known to mediate efflux of Zn and Cd. Loss of cell viability by 57% was seen 24 h after exposure to 2.5 µM Cd. Exposure to 2.5 µM Cd together with 10–50 µM Zn prevented loss of cell viability by 66%. Pretreatment of the UROtsa cells with an inhibitor of glutathione biosynthesis (buthionine sulfoximine) diminished ZnT1 induction by Cd with a resultant increase in sensitivity to Cd cytotoxicity. Conversely, pretreatment of UROtsa cells with an inhibitor of DNA methylation, 5-aza-2’-deoxycytidine (aza-dC) did not change the extent of ZnT1 induction by Cd. The induced expression of ZnT1 that remained impervious in cells treated with aza-dC coincided with resistance to Cd cytotoxicity. Therefore, expression of ZnT1 efflux transporter and Cd toxicity in UROtsa cells could be modulated, in part, by DNA methylation and glutathione biosynthesis. Induced expression of ZnT1 may be a viable mechanistic approach to mitigating cytotoxicity of Cd.

scholarly journals Long-lasting renewable antibacterial porous polymeric coatings enable titanium biomaterials to prevent and treat peri-implant infection

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Shuyi Wu ◽  
Jianmeng Xu ◽  
Leiyan Zou ◽  
Shulu Luo ◽  
Run Yao ◽  
...  
Keyword(s):  
Dental Implant ◽  
Pathogenic Bacteria ◽  
Titanium Surface ◽  
Polymeric Coating ◽  
Antibacterial Efficacy ◽  
Polymeric Coatings ◽  
Implant Infection ◽  
Titanium Surfaces

AbstractPeri-implant infection is one of the biggest threats to the success of dental implant. Existing coatings on titanium surfaces exhibit rapid decrease in antibacterial efficacy, which is difficult to promisingly prevent peri-implant infection. Herein, we report an N-halamine polymeric coating on titanium surface that simultaneously has long-lasting renewable antibacterial efficacy with good stability and biocompatibility. Our coating is powerfully biocidal against both main pathogenic bacteria of peri-implant infection and complex bacteria from peri-implantitis patients. More importantly, its antibacterial efficacy can persist for a long term (e.g., 12~16 weeks) in vitro, in animal model, and even in human oral cavity, which generally covers the whole formation process of osseointegrated interface. Furthermore, after consumption, it can regain its antibacterial ability by facile rechlorination, highlighting a valuable concept of renewable antibacterial coating in dental implant. These findings indicate an appealing application prospect for prevention and treatment of peri-implant infection.

Influence of chemical composition on cell viability on titanium surfaces: A systematic review

2020 ◽  
Author(s):  
Juliana Dias Corpa Tardelli ◽  
Mariana Lima da Costa Valente ◽  
Thaisa Theodoro de Oliveira ◽  
Andréa Cândido dos Reis
Keyword(s):  
Systematic Review ◽  
Chemical Composition ◽  
Cell Viability ◽  
Titanium Surfaces

scholarly journals Biological characterization of implant surfaces - in vitro study

2015 ◽  
Vol 44 (4) ◽  
pp. 195-199 ◽  
Author(s):  
Priscilla Barbosa Ferreira Soares ◽  
Camilla Christian Gomes Moura ◽  
Huberth Alexandre da Rocha Júnior ◽  
Paula Dechichi ◽  
Darceny Zanetta-Barbosa
Keyword(s):  
Alkaline Phosphatase ◽  
Cell Viability ◽  
Total Protein ◽  
Cell Attachment ◽  
Control Group ◽  
Mitochondrial Activity ◽  
Serum Total Protein ◽  
Trypan Blue Exclusion ◽  
Experimental Surface

<title>Abstract</title><sec><title>Objective</title><p>Evaluate the biological performance of titanium alloys grade IV under different surface treatments: sandblasting and double etching (Experimental surface 1; Exp1, NEODENT); surface with wettability increase (Experimental surface 2; Exp2, NEODENT) on response of preliminary differentiation and cell maturation.</p></sec><sec><title>Material and method</title><p>Immortalized osteoblast cells were plated on Exp1 and Exp2 titanium discs. The polystyrene plate surface without disc was used as control group (C). Cell viability was assessed by measuring mitochondrial activity (MTT) at 4 and 24 h (n = 5), cell attachment was performed using trypan blue exclusion within 4 hours (n = 5), serum total protein and alkaline phosphatase normalization was performed at 4, 7 and 14 days (n = 5). Data were analyzed using one-way ANOVA and Tukey test.</p></sec><sec><title>Result</title><p>The values of cell viability were: 4h: C– 0.32±0.01<sup>A</sup>; Exp1– 0.34±0.08<sup>A</sup>; Exp2– 0.29±0.03<sup>A</sup>. 24h: C– 0.43±0.02<sup>A</sup>; Exp1– 0.39±0.01<sup>A</sup>; Exp2– 0.37±0.03<sup>A</sup>. The cell adhesion counting was: C– 85±10<sup>A</sup>; Exp1- 35±5<sup>B</sup>; Exp2– 20±2<sup>B</sup>. The amounts of serum total protein were 4d: C– 40±2<sup>B</sup>; Exp1– 120±10<sup>A</sup>; Exp2– 130±20<sup>A</sup>. 7d: C– 38±2<sup>B</sup>; Exp1– 75±4<sup>A</sup>; Exp2– 70±6<sup>A</sup>. 14 d: C– 100±3<sup>A</sup>; Exp1– 130±5<sup>A</sup>; Exp2– 137±9<sup>A</sup>. The values of alkaline phosphatase normalization were: 4d: C– 2.0±0.1<sup>C</sup>; Exp1– 5.1±0.8<sup>B</sup>; Exp2– 9.8±2.0<sup>A</sup>. 7d: C– 1.0±0.01<sup>C</sup>; Exp1– 5.3±0.5<sup>A</sup>; Exp2– 3.0±0.3<sup>B</sup>. 14 d: C– 4.1±0.3<sup>A</sup>; Exp1– 4.4±0.8<sup>A</sup>; Exp2– 2.2±0.2<sup>B</sup>. Different letters related to statistical differences.</p></sec><sec><title>Conclusion</title><p>The surfaces tested exhibit different behavior at dosage of alkaline phosphatase normalization showing that the Exp2 is more associated with induction of cell differentiation process and that Exp1 is more related to the mineralization process.</p></sec>

scholarly journals Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophages

2014 ◽  
Vol 25 (2) ◽  
pp. 96-103 ◽  
Author(s):  
Camilla Christian Gomes Moura ◽  
Darceny Zanetta-Barbosa ◽  
Paula Dechichi ◽  
Valessa Florindo Carvalho ◽  
Priscilla Barbosa Ferreira Soares
Keyword(s):  
Cell Viability ◽  
Colorimetric Assay ◽  
Initial Period ◽  
Critical Role ◽  
Surface Characteristics ◽  
Th2 Cytokine ◽  
Titanium Surfaces ◽  
Control Surfaces ◽  
Immunoenzymatic Assays

Due to the critical role of monocytes/macrophages (Mϕ) in bone healing, this study evaluated the effects of bio-anodized, acid-etched, and machined titanium surfaces (Ti) on Mϕ behavior. Cells were separated from whole human blood from 10 patients, plated on Ti or polystyrene (control) surfaces, and cultured for 72 h. At 24, 48 and 72 h, cell viability, levels of IL1β, IL10, TNFα, TGFβ1 inflammatory mediators, and nitric oxide (NO) release were analyzed by mitochondrial colorimetric assay (MTT assay) and immunoenzymatic assays, respectively. Real-time PCR was used to verify the expression of TNFα and IL10 at 72 h. The data were subjected to a Kruskal-Wallis analysis. IL1β, TNFα and TGFβ1 release were not significantly different between the Ti surfaces (p>0.05). The presence of NO and IL10 was not detected in the samples. Cell viability did not differ between the samples cultivated on Ti and those cultivated on control surfaces, except at 24 h (p=0.0033). With respect to the mediators evaluated, the surface characteristics did not induce a typical Th1 or Th2 cytokine profile, although the cell morphology and topography were influenced by the Ti surface during the initial period.

scholarly journals Лазерно-индуцированные пространственно-периодические структуры на поверхности титана в среде н-гексана при различном давлении

2020 ◽  
Vol 46 (15) ◽  
pp. 51
Author(s):  
Д.А. Кочуев ◽  
К.С. Хорьков ◽  
А.С. Черников ◽  
Р.В. Чкалов ◽  
В.Г. Прокошев
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Laser Radiation ◽  
Pressure Range ◽  
Titanium Surface ◽  
Surface Structures ◽  
Femtosecond Laser Radiation ◽  
Periodic Surface ◽  
Laser Induced Plasma ◽  
Scanning Electron

The paper presents the results of processing titanium surface in n-hexane at various pressures by femtosecond laser radiation. The effect of laser-induced plasma on the nature of the formation of periodic surface structures in the pressure range from 6 mbar to 22 bar is considered. The study of the surface of the processed samples was carried out using scanning electron microscopy. The dependence of the period of obtained laser-induced periodic surface structures on the pressure in working vessel and the treatment regime is shown.

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