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Glass Surface (glass + surface)
Selected AbstractsA New Heterobifunctional Reagent for Immobilization of Biomolecules on Glass SurfaceCHEMINFORM, Issue 25 2004P. Kumar Abstract For Abstract see ChemInform Abstract in Full Text. [source] Elastic Indentation Response of Float Glass SurfacesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2010Andrea M. Muller Instrumented Hertzian indentation was used to evaluate the reduced elastic modulus and cone-crack initiation forces for the as-received surfaces of commercial float glasses. Custom-built indentation equipment with the capability of acoustic emission detection was used to monitor continuously the load and depth of penetration at the microscopic scale for forces up to 1 kN. Equipment verification was performed using a reference material, GE 124. The air and tin surfaces of commercial soda,lime,silica and borosilicate float glasses were tested to determine any difference in indentation response for the elastic and fracture behavior of as-received surfaces. Information obtained from the analysis of the load,displacement curves and from the visual inspection of the indentation sites was used to determine the elastic modulus, and the conditions for the onset of cone cracking as a function of surface roughness. The reduced modulus results were verified using additional equipment that allowed the in situ observation of the contact area during loading and unloading. The results showed that there was no difference in the reduced modulus data for the air and tin surfaces for the range of surface displacements studied. The same conclusions were found for cone-cracking loads on as-received surfaces but tests on abraded surfaces showed that the tin surfaces had slightly more resistance to cone cracking than the air surfaces. [source] Functionalization of Gold and Glass Surfaces with Magnetic Nanoparticles Using Biomolecular InteractionsBIOTECHNOLOGY PROGRESS, Issue 1 2006Bala G. Nidumolu Advances in nanotechnology have enabled the production and characterization of magnetic particles with nanometer-sized features that can be functionalized with biological recognition elements for numerous applications in biotechnology. In the present study, the synthesis of and interactions between self-assembled monolayers (SAMs) on gold and glass surfaces and functionalized magnetic nanoparticles have been characterized. Immobilization of 10,15 nm streptavidin-functionalized nanoparticles to biotinylated gold and glass surfaces was achieved by the strong interactions between biotin and streptavidin. Fluorescent streptavidin-functionalized nanoparticles, biotinylated surfaces, and combinations of the two were characterized by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and electron and fluorescent microscopy to confirm that little or no functionalization occurred in nonbiotinylated regions of the gold and glass surfaces compared to the biotinylated sites. Together these techniques have potential use in studying the modification and behavior of functionalized nanoparticles on surfaces in biosensing and other applications. [source] Laser-induced crystal growth of nonlinear optical Ba3Ti3O6(BO3)2 on glass surfaceCRYSTAL RESEARCH AND TECHNOLOGY, Issue 12 2008T. Oikawa Abstract Nonlinear optical Ba3Ti3O6(BO3)2 crystals were patterned on the surface of CuO (1 mol%)-doped 40BaO-40TiO2 -20B2O3 glass by irradiations of continuous-wave Nd:YAG (wavelength: ,=1064 nm) and Yb:YVO4 (,=1080 nm) lasers. Laser energies absorbed by Cu2+ ions were transferred to the lattice system through a nonradiative relaxation process, consequently heating the glass and inducing local crystallizations. For the lines patterned by Yb:YVO4 laser irradiations with a power of 1 W and a scanning speed of 20 ,m/s, a c -axis orientation of Ba3Ti3O6(BO3)2 crystals along the laser scanning direction is proposed from measurements of X-ray diffraction analyses, polarized optical photographs, polarized micro-Raman scattering spectra, and azimuthal dependence of second harmonic generations. The laser-induced crystallization technique is found to be applied successfully for the spatially selective patterning of nonlinear optical Ba3Ti3O6(BO3)2 crystals in glass. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Ca2+ -dependent in vitro contractility of a precipitate isolated from an extract of the heliozoon Actinophrys solCYTOSKELETON, Issue 2 2006Mikihiko Arikawa Abstract Contraction of axopodia in actinophrid heliozoons (protozoa) is induced by a unique contractile structure, the "contractile tubules structure (CTS)". We have previously shown that a cell homogenate of the heliozoon Actinophrys sol yields a precipitate on addition of Ca2+ that is mainly composed of filamentous structures morphologically identical to the CTS. In this study, to further characterize the nature of the CTS in vitro, biochemical and physiological properties of the precipitate were examined. SDS-PAGE analysis showed that the Ca2+ -induced precipitate was composed of many proteins, and that no proteins in the precipitate showed any detectable changes in electrophoretic mobility on addition of Ca2+. Addition of extraneous proteins such as bovine serum albumin to the cell homogenate resulted in cosedimentation of the proteins with the Ca2+ -induced precipitate, suggesting that the CTS has a high affinity for other proteins that are not related to precipitate formation. Appearance and disappearance of the precipitate were repeatedly induced by alternating addition of Ca2+ and EGTA, and its protein composition remained unchanged even after repeated cycles. When adhered to a glass surface, the precipitate showed Ca2+ -dependent contractility with a threshold of 10,100 nM, and this contractility was not inhibited by colchicine or cytochalasin B. The precipitate repeatedly contracted and relaxed with successive addition and removal of Ca2+, indicating that the contraction was controlled by Ca2+ alone with no need for any other energy supply. From our characterization of the precipitate, we concluded that its Ca2+ -dependent formation and contraction are associated with the unique contractile organelle, the "contractile tubules structure". Cell Motil. Cytoskeleton 2006. © 2005 Wiley-Liss, Inc. [source] Larval pupation site preference on fruit in different species of DrosophilaENTOMOLOGICAL RESEARCH, Issue 3 2008Nakul B. VANDAL Abstract Larval pupation site preference (PSP) of different species of Drosophila was analyzed on fruit in the laboratory. The larvae of D. melanogaster, D. ananassae, D. virilis, D. novamexicana and D. hydei pupated on the surface of glass vials; D. simulans, D. yakuba, D. mauritiana and D. malerkotliana pupated in/on fruit; and D. rajasekari pupated on cotton plugs in all experiments. D. bipectinata larvae changed their preference from fruit in the control to glass surface for all of the fruits tested. The statistical analysis of PSP (glass and fruit) found a significant result in that compared to other species, D. mauritiana and D. ananassae preferred to pupate on cotton compared to the control. [source] Genotoxicity of inorganic lead salts and disturbance of microtubule functionENVIRONMENTAL AND MOLECULAR MUTAGENESIS, Issue 4 2005Daniela Bonacker Abstract Lead compounds are known genotoxicants, principally affecting the integrity of chromosomes. Lead chloride and lead acetate induced concentration-dependent increases in micronucleus frequency in V79 cells, starting at 1.1 ,M lead chloride and 0.05 ,M lead acetate. The difference between the lead salts, which was expected based on their relative abilities to form complex acetato-cations, was confirmed in an independent experiment. CREST analyses of the micronuclei verified that lead chloride and acetate were predominantly aneugenic (CREST-positive response), which was consistent with the morphology of the micronuclei (larger micronuclei, compared with micronuclei induced by a clastogenic mechanism). The effects of high concentrations of lead salts on the microtubule network of V79 cells were also examined using immunofluorescence staining. The dose effects of these responses were consistent with the cytotoxicity of lead(II), as visualized in the neutral-red uptake assay. In a cell-free system, 20,60 ,M lead salts inhibited tubulin assembly dose-dependently. The no-observed-effect concentration of lead(II) in this assay was 10 ,M. This inhibitory effect was interpreted as a shift of the assembly/disassembly steady-state toward disassembly, e.g., by reducing the concentration of assembly-competent tubulin dimers. The effects of lead salts on microtubule-associated motor-protein functions were studied using a kinesin-gliding assay that mimics intracellular transport processes in vitro by quantifying the movement of paclitaxel-stabilized microtubules across a kinesin-coated glass surface. There was a dose-dependent effect of lead nitrate on microtubule motility. Lead nitrate affected the gliding velocities of microtubules starting at concentrations above 10 ,M and reached half-maximal inhibition of motility at about 50 ,M. The processes reported here point to relevant interactions of lead with tubulin and kinesin at low dose levels. Environ. Mol. Mutagen., 2005. © 2005 Wiley-Liss, Inc. [source] Microstructure of fat crystallizing on a collagenous surfaceEUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY, Issue 9 2005Michael A. Rogers Abstract The effect of surface quality on fat crystallization was examined for glass and gelatin surfaces using three-dimensional polarized light microscopy in an attempt to develop a model system for how fat may crystallize in arteries. A mixture of the high-melting fraction of milk fat and triolein was crystallized from 60,°C to 30,°C at a rate of 0.5,°C/min on both glass and gelatin surfaces. Crystallization of fat on the gelatin surface led to an increase in the amount of nucleation and resulted in a more even distribution of crystal mass than crystallization on the glass surface. No evidence of crystal precipitation or glass surface crystallization was evident. We postulate that the gelatin acted as a template for nucleation. Similar trends were identified using fractal analysis. Fat crystallized on gelatin had a higher fractal dimension than fat crystallized on glass. [source] Hydroxyapatite/Bioactive Glass Films Produced by a Sol,Gel Method: In Vitro BehaviorADVANCED ENGINEERING MATERIALS, Issue 11 2009Nihat C. Köseo Abstract Hydroxyapatite (HA) and HA/bioactive glass (49S) films were deposited on Si(100) substrates by a sol,gel dip-coating method. The microstructure and in vitro bioactivity of the films were investigated by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). Polycrystalline HA and amorphous bioactive glass films were obtained after annealing at 600 and 400,°C, respectively. The crystallization temperature of HA was determined to be around 568,°C. The surfaces of the HA films were covered with an apatite layer consists of spherulites formed by nanosized needle-like aggregates after the soaking in simulated body fluid (SBF) for 10 days, while amorphous HA/bioactive glass surface was covered with larger spherical crystallites. Both XPS and EDS results obtained from HA/bioactive glass film, after soaking in SBF, showed increasing P amounts on the surface at the expense of Si. The higher density of the newly formed layer on HA/bioactive glass surface than that of the HA surface after 10 days of soaking was evidence of increased reaction rate and apatite forming ability when bioactive glass layer is present on the HA films. [source] Self-assembled pearling structure of long duplex DNA with histone H1FEBS JOURNAL, Issue 9 2001Yuko Yoshikawa We report that complexes of giant DNA molecules with histone H1 proteins form a pearl necklace-like structure when the complexes are prepared by natural dilution from a high-salt solution (2 m NaCl) to a low-salt solution (0.2 m and 50 mm NaCl). We performed real-time observations on the conformational changes of individual T4 phage DNA (166 kb) molecules in bulk solution by fluorescence microscopy. To identify H1-binding regions on individual DNA molecules, we also performed immunofluorescence microscopic observations on the DNA,H1 complex spread on a glass surface. It was found that histone H1 binds DNA in a highly co-operative manner and is accompanied by local folding of the DNA. On the basis of the experimental observations and a theoretical simulation, we propose a self-assembling mechanism for the pearling structure. [source] Conjugated Polyelectrolyte,Metal Nanoparticle Platforms for Optically Amplified DNA DetectionADVANCED MATERIALS, Issue 5 2010Yusong Wang A conjugated polyelectrolyte (CPE)-silver nanoparticle platform for DNA-sensing applications is fabricated (see figure), which provides over 17-fold enhancement of dye emission intensity, as compared to the intrinsic dye emission observed atop a conventional glass surface. Examination of the distance-dependence amplification process reveals that the role of the silver nanoparticles is to increase the effective field experienced by the light-harvesting CPE, and the metal enhanced fluorescence of the CPE could be translated into higher dye signal intensities for the detection platform. [source] Determination of haplotypes from single DNA molecules: a method for single-molecule barcoding,,HUMAN MUTATION, Issue 9 2007Ming Xiao Abstract Determining the haplotypes in a diploid individual is a major technical challenge in genetic studies of human complex traits. Here we report a method of molecular haplotyping by directly imaging multiple polymorphic sites on individual DNA molecules simultaneously. DNA fragments amplified by long-range PCR were labeled with fluorescent dyes at each polymorphic site using a modified gap-filled padlock probe ligation approach. The labeled DNA molecules were then stretched into linear form on a functionalized glass surface and imaged with multicolor total internal reflection fluorescence (TIRF) microscopy. By determining the colors and positions of the fluorescent labels with respect to the backbone at polymorphic sites, the haplotype can be inferred accurately, in a manner similar to reading a barcode, even when the DNA fragments are not fully labeled. The feasibility of this technology is demonstrated by the determination of the haplotype of a 9.3-kbp DNA fragment containing four SNPs. Hum Mutat 28(9), 913,921, 2007. Published 2007 Wiley-Liss, Inc. [source] Metal Corrosion and its Impact on Glass Tempering Furnace DesignINTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 5 2010Peter Tiernan A reliable well-designed tempering furnace is considered to be the cornerstone of any modern glass-processing facility. This paper addresses a series of engineering anomalies encountered during the commissioning of such a glass-processing furnace. Following the installation of a furnace in a European facility, small black deposits were noticed on both the silica-fused rollers used to transport the glass through the hearth of the furnace and on the processed glass surface itself. EDAX and scanning electron microscopy investigations indicated conclusively that the deposits were primarily constituted of sodium sulfate and trace elements consistent with stainless steel (chromium, iron, and nickel). Traditionally, high-density glass fiber was used to insulate the roof walls and side walls of tempering furnaces; however, it was noticed in this particular case that rolled stainless steel sheeting (SS316) was used. Chemical and X-ray diffraction analyses were used to pinpoint the origin of the deposits. It was determined that poor material selection choices taken during the design stage of the furnace in question were at fault. The combination of stainless steel and sulfur dioxide (SO2 is used as a lubricant to prevent scuffing) at elevated temperatures (>650°C) generated droplets of sodium sulfate, which condensed due to the convectional flow of the heat currents within the oven. These droplets scorched the glass surface and destroyed the fused silica rollers. As a recommendation, the usage of stainless steel and other nonrefractory metals should be avoided in the design of any future glass tempering furnaces. [source] Homeotropic Alignment of Columnar Liquid Crystals in Open Films by Means of Surface Nanopatterning,ADVANCED MATERIALS, Issue 6 2007I. Gearba Columnar liquid crystals (LCs) are reported to align spontaneously homeotropically,that is, orthogonally to the surface (see figure and inside cover),on a glass surface covered with a layer of poly(tetrafluoroethylene) transferred by friction (rubbing). This strategy for producing macroscopic monodomains of homeotropically aligned LCs may find important applications in the fabrication of LC-based organic solar cells. [source] A microwave-assisted process for coating polymer and glass surfaces with semiconducting ZnO submicron particlesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2009Alexander Irzh Abstract A new method for coating glass slides with ZnO particles with an average size of 200 nm is proposed in the current article. The coating was performed under microwave radiation. Two main morphologies are found for the ZnO crystals that are deposited on glass slides. The first morphology is that of a very dense coating of ZnO hexagonal rods growing perpendicular to the glass surface. The second is the growth of ZnO flower-like particles. In addition to coating the glass by ZnO particles, we also report on coating other polymers [poly(methyl methacrylate) plate, polycarbonate beads, Nylon 6,6 beads, and polypropylene beads) by ZnO. The morphology obtained for ZnO coated on polymers is different from that detected for coating ZnO on glass. The unorganized coating of ZnO rods on polymers has been observed. The coated glass slides were characterized by X-ray diffraction, volumetric titration, EDS, scanning electron microscope, and optical measurements (DRS and transmittance spectroscopy). © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Preparation and applications of novel fluoroalkyl end-capped sulfonic acid oligomers,silica gel polymer hybridsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007Kazuo Sasazawa Abstract Fluoroalkyl end-capped 2-methacryloxyethanesulfonic acid homo-oligomer [RF,(MES)n,RF] and 2-methacryloxyethanesulfonic acid,N,N -dimethylacrylamide co-oligomers [RF,(MES)x,(DMAA)y,RF] reacted with tetraethoxysilane (TEOS) under acidic conditions to afford RF,(MES)n,RF homo-oligomer,SiO2 polymer hybrid and RF,(MES)x,(DMAA)y,RF co-oligomer,SiO2 polymer hybrid, respectively. Thermogravimetric,mass spectra showed that the thermal stability of RF,(MES)n,RF homo-oligomer,SiO2 polymer hybrid was superior to that of traditionally well-known perfluorinated ion exchange polymers such as Nafion 112 (TR). The sol solutions of the fluorinated co-oligomer,SiO2 polymer hybrid were applied to the surface modification of glass to exhibit not only a strong oleophobicity imparted by fluorine but also a good hydrophilicity on the glass surface. On the other hand, RF,(MES)x,(DMAA)y,RF co-oligomer reacted with TEOS in the presence of a variety of silica nanoparticles (mean diameters: 11,95 nm) under alkaline conditions to afford fluoroalkyl end-capped oligomers,silica nanoparticles (mean diameters: 32,173 nm) with a good dispersibility and stability in methanol. Similarly, a variety of fluorinated oligomers containing sulfo groups,silica nanoparticles were prepared by the homo- and co-oligomerizations of fluoroalkanoyl peroxides with 2-methacryloxyethane sulfonic acid (MES) and comonomers such as N,N -dimethylacrylamide (DMAA) and acryloylmorpholine (ACMO) in the presence of silica nanoparticles. Interestingly, these isolated fluorinated particle powders were found to afford nanometer size-controlled colloidal particles with a good redispersibility and stability in aqueous and organic media such as methanol. These fluorinated nanoparticles containing sulfo groups were also applied to an excellent heterogeneous catalyst for Bronsted acid-catalyzed transformations. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 110,117, 2007 [source] Effect of enamel matrix proteins (Emdogain®) on healing after re-implantation of "periodontally compromised" rootsJOURNAL OF CLINICAL PERIODONTOLOGY, Issue 10 2003An experimental study in the dog Abstract Objective: The present experiment was performed to assess whether Emdogain® applied on the root surface of extracted teeth or teeth previously exposed to root planning can protect the tooth from ankylosis following re-implantation. Material and Methods: The experiment included two groups of dogs, including five animals each. The root canals of all mandibular third premolars (3 P 3) were reamed and filled with gutta-percha. A crestal incision was placed from the area of the second to the fourth premolar. Buccal and lingual full thickness flaps were elevated. With the use of a fissure bur, the crown and furcation area of 3 P 3 were severed in an apico-coronal cut. The distal and mesial tooth segments were luxated with an elevator and extracted with forceps. Group A: The mesial and distal segments of 3 P 3 were air dried on a glass surface for 60 min. The roots from the right side were conditioned and exposed to Emdogain® application. The roots from the left side received the same treatment with the exception of Emdogain® application. The mesial and distal tooth segments were re-implanted and the crown portions were severed with a horizontal cut and removed. The buccal and lingual flaps were mobilized and sutured to obtain complete coverage of the submerged roots. Group B: A notch was prepared in each root, 4,5 mm apical of the cemento-enamel junction. The area of the root that was located coronal to the notch was scaled and planned. The roots in the right side of the mandible were treated with Emdogain®, while the roots in the left side served as controls. After 6 months of healing, the dogs were killed and blocks containing one root with surrounding tissues were harvested, and prepared for histological examination, which also included morphometric assessments. Thus, the proportions of the roots that exhibited signs of (i) replacement (ii) inflammatory and (iii) surface resorption were calculated. Results and Conclusion: It was demonstrated that healing of a re-implanted root that had been extracted and deprived of vital cementoblasts was characterized by processes that included root resorption, ankylosis and new attachment formation. It was also demonstrated that Emdogain® treatment, i.e. conditioning with EDTA and placement of enamel matrix proteins on the detached root surface, failed to interfere with the healing process. Zusammenfassung Zielsetzung: Untersuchung, ob Emdogain®, wenn es auf die Wurzeloberfläche extrahierter Zähne oder von Zähnen, die zuvor eine Wurzelglättung bekommen haben, appliziert wird, die Zähne nach Reimplantation vor Ankylose schützen kann. Material und Methoden: Die Studie wurde bei 2 Gruppen von Hunden durchgeführt, die je 5 Tiere umfasste. Die Wurzelkanäle aller 3. Prämolaren des Unterkiefers (3 P 3) wurden aufbereitet und mit Guttapercha gefüllt. Ein Schnitt auf dem Limbus alveolaris wurde vom 2. zum 4 Prämolaren geführt. Bukkal und lingual wurde ein Vollschichtlappen mobilisiert. Mit einem Fissurenbohrer wurden die 3 P 3 mit einem Schnitt in koronoapikaler Richtung im Bereich der Krone und der Furkation geteilt. Die distalen und mesialen Zahnsegmente wurden mit einem Elevator luxiert und mit einer Zange extrahiert. Gruppe A: Die mesialen und distalen Segmente von 3 P 3 wurden auf einer Glasoberfläche 60 min lang luftgetrocknet. Die Wurzeln der rechten Seite wurden konditioniert und mit Emdogain® beschickt. Die Wurzeln der linken Seite erhielten die gleiche Behandlung mit der Ausnahme, dass keine Applikation von Emdogain® erfolgte. Die mesialen und distalen Wurzeln wurden reimplantiert und die Kronenanteile durch einen horizontalen Schnitt getrennt und entfernt. Die bukkalen und lingualen Lappen wurden mobilisiert und durch Naht ein vollständiger Verschluss der reimplantierten Wurzeln erreicht. Gruppe B: In jede Wurzel wurde 4,5 mm apikal der Schmelz-Zement-Grenze eine Kerbe präpariert. Der Bereich der Wurzel, der koronal dieser Kerbe lag, wurde gescalt und wurzelgeglättet. Die Wurzeln der rechten Unterkieferseite wurden mit Emdogain® behandelt, während die Wurzeln der linken Seite als Kontrolle dienten. Nach einer Heilung von 6 Monaten wurden die Hunde getötet und Blöcke, die eine Wurzel und das umgebende Gewebe enthielten, gewonnen und für die histologische Untersuchung präpariert, die auch morphometrische Befunde einschloss. Es wurden also die Anteile der Wurzeln berechnet, die Zeichen von (i) Ersatz- (ii) entzündlicher und (iii) Oberflächenresorption zeigten. Ergebnisse und Schlussfolgerungen: Es wurde gezeigt, dass die Heilung von reimplantierten Wurzeln, die extrahiert und von vitalen Zementoblasten befreit worden waren, durch Prozesse charakterisiert war, die Wurzelresorption, Ankylose und die Bildung neuen Attachments umfassten. Es wurde gezeigt, dass die Behandlung mit Emdogain®, d.h. Konditionierung mit EDTA und Applikation des Schmelz-Matrix-Proteins auf die freie Wurzeloberfläche diesen Heilungsprozess nicht beeinflussen konnte. Résumé Objectif: Cette expérimentation fut réalisée pour déterminer si Emdogain® appliqué sur la surface radiculaire de dents extraites ou de dents préalablement soumises à un surfaçage radiculaire pouvait protéger la dent de l'ankylose après réimplantation. Matériel et Méthodes: L'expérience comprenait 2 groupes de 5 chiens. Les canaux radiculaires de toutes les troisièmes premolaires mandibulaires (3 P 3) furent alésés et bouchés à la gutta-percha. Une incision crestale de la deuxième à la quatrième prémolaire permit de soulever un lambeau de pleine épaisseur vestibulaire et lingual. La couronne et la zone de furcation de 3 P 3 furent découpées à l'aide d'une fraise fissure d'apical en coronaire. Les segments distaux et mésiaux furent luxés avec un élévateur et extraits avec un davier. Groupe A: Les segments mésiaux et distaux de 3 P 3 furent séchés à l'air sur une plaque de verre pendant 60 min. Les racines du coté droit furent préparées et imprégnées d' Emdogain®. Les racines gauches reçurent le même traitement sans application d'Emdogain ®. Les segments mésiaux et distaux furent alors réimplantés et les couronnes découpées par un trait horizontal et éliminées. Les lambeaux vestibulaires et linguaux furent déplacés et suturés pour obtenir un recouvrement complet des racines enfouies. Groupe B: Une entaille a été préparée sur chaque racine, à 4,5 mm en apical de la jonction amélo-cémentaire. La surface de racine située coronairement à cette entaille fut alors détartrée et surfacée. Les racines du coté droit furent traitées par Emdogain® alors que les racines du coté gauche firent office de contrôle. Après 6 mois de cicatrisation, les chiens furent sacrifiés et des blocs contenant une racine et les tissus environnant furent prélevés pour un examen histologique et morphométrique. Ainsi, les proportions de racine présentant des signes de (i) remplacement (ii) d'inflammation et (iii) de résorption furent calculées. Résultats et conclusion: Nous avons démontré que la cicatrisation de racine réimplantées après extraction et élimination des cémentoblastes se caractérisait par un processus qui comprenait résorption radiculaire, ankylose et formation d'une nouvelle attache. Nous avons aussi démontré que le traitement par Emdogain®, c'est à dire conditionnement à l'EDTA et mise en place de protéines de la matrice améllaire sur la surface radiculaire, ne pouvait pas interférer avec le processus de cicatrisation. [source] Application of a Service Climbing Robot with Motion Planning and Visual SensingJOURNAL OF FIELD ROBOTICS (FORMERLY JOURNAL OF ROBOTIC SYSTEMS), Issue 4 2003Jian Zhu This paper describes an application of a service climbing robot aimed to clean the glass wall of high-rise buildings. The robot utilizes suction cups to adhere to the glass and moves with a translational mechanism to follow a predetermined path in cleaning the whole glass surface. By a flexible waist, the robot can adjust its posture. The robot has the ability to cross the window frame to clean different sections of the glass wall. A visual sensing system, composed of an omnidirectional CCD camera and two laser diodes, enables the robot to measure its orientation and the distance between the robot and the window frame. The real-time applications and some experimental results demonstrate the effectiveness of the developed system. © 2003 Wiley Periodicals, Inc. [source] Visual gene diagnosis of HBV and HCV based on nanoparticle probe amplification and silver staining enhancementJOURNAL OF MEDICAL VIROLOGY, Issue 2 2003Ye-Fu Wang Abstract A visual gene-detecting technique using nanoparticle-supported gene probes is described. With the aid of gold nanoparticle-supported 3,-end,mercapto-derivatized oligonucleotide serving as detection probe, and 5,-end ,amino-derivatized oligonucleotide immobilized on glass surface acting as capturing probe, target DNA was detected visually by sandwich hybridization based on highly sensitive "nano-amplification" and silver staining. Different genotypes of Hepatitis B and C viruses in the serum samples from infected patients were detected using home-made HBV, HCV, and HBV/HCV gene chips by the gold/silver nanoparticle staining amplification method. The present visual gene-detecting technique may avoid limitations with the reported methods, for its high sensitivity, good specificity, simplicity, speed, and cheapness. This technique has potential applications in many fields, especially in multi-gene detection gene chips coupled with the detection will find applications in clinic. Additionally, resonance Rayleigh light scattering (RLS) spectroscopy is used, for the first time, to judge and monitor the immobilization of gene probes on gold nanoparticle surfaces. J. Med. Virol. 70: 205,211, 2003. © 2003 Wiley-Liss, Inc. [source] Nanometre localization of single ReAsH moleculesJOURNAL OF MICROSCOPY, Issue 3 2004H. PARK Summary ReAsH is a red-emitting dye that binds to the unique sequence Cys-Cys-Xaa-Xaa-Cys-Cys (where Xaa is a noncysteine amino acid) in the protein. We attached a single ReAsH to a calmodulin with an inserted tetracysteine motif and immobilized individual calmodulins to a glass surface at low density. Total internal reflection fluorescence microscopy was used to image individual ReAsH molecules. We determined the centre of the distribution of photons in the image of a single molecule in order to determine the position of the dye within 5 nm precision and with an image integration time of 0.5 s. The photostability of ReAsH was also characterized and observation times ranging from several seconds to over a minute were observed. We found that 2-mercaptoethanesulphonic acid increased the number of collected photons from ReAsH molecules by a factor of two. Individual ReAsH molecules were then moved via a nanometric stage in 25 or 40 nm steps, either at a constant rate or at a Poisson-distributed rate. Individual steps were clearly seen, indicating that the observation of translational motion on this scale, which is relevant for many biomolecular motors, is possible with ReAsH. [source] Versatile ,-end group functionalization of RAFT polymers using functional methane thiosulfonatesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 12 2009Peter J. Roth Abstract Five different polymers, poly[methyl methacrylate] (PMMA), poly[lauryl methacrylate] (PLMA), poly[diethylene glycol methacrylate] (PDEGMA), poly[N -isopropylacrylamide] (PNIPA), and poly[styrene] (PS) prepared by the RAFT process and thus terminated with dithioesters were aminolyzed in the presence of S -3-butynyl methane thiosulfonate (MTS), which was synthesized in two steps. Analysis of the polymers by 2D NMR, UV,vis absorbance, and gel permeation chromatography revealed them to quantitatively carry acetylene end groups connected with disulfide bridges, indicating that functional MTS reagents can be employed for end group functionalization of RAFT polymers. This versatile method is of advantage compared with conjugations with functional maleimides, where isolation of terminal thiols is often required but inexpedient for poly[(meth)acrylates] because their terminal thiols may undergo backbiting and thus avoid conjugation. The acetylene-terminated polymers were bound to an azide functionalized glass surface in a Cu(I) catalyzed cycloaddition. The modified surfaces exhibited water contact angles corresponding to the polarity of the attached polymers. In the case of the stimulus responsive polymers PNIPA and PDEGMA, the surfaces showed temperature-dependent contact angles. The disulfide bond connecting the polymers to the surface could be selectively cleaved and resulted in all surfaces having the same contact angle, independent of the nature of the polymer prior attached to the surface. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3118,3130, 2009 [source] Morphological and Physical Properties of Triblock Copolymers of Methyl Methacrylate and 2-Ethylhexyl MethacrylateMACROMOLECULAR MATERIALS & ENGINEERING, Issue 9 2006Hormoz Eslami Abstract Summary: Triblock copolymers of methyl methacrylate (MMA) and 2-ethylhexyl methacrylate (EHMA) [that is, poly(MMA,EHMA,MMA)] were prepared by an emulsion atom-transfer radical polymerization. The relationships of their structural, morphological, and physical properties were investigated. The latex particles had core-shell morphologies and the block copolymers experienced phase separation. Small latex particles with a low number of cores could deform and wet silicon-wafer surfaces, but the deformation of large latex particles was restricted by the internal two-phase morphology of the particles. Latex casting produced continuous pinhole-free films, in which hard poly(MMA) (PMMA) cores of different latex particles merged and provided interparticle connections. The morphology of solution-cast films depended on block composition, solvent type, and film thickness. For all the prepared polymer samples, thick films cast in toluene had poly(EHMA) (PEHMA) materials at air surface, whereas those cast in tetrahydrofuran had a sponge-like PMMA surface structure. Thin toluene-cast films from P(MMA,EHMA,MMA) with the block degrees of polymerization () 200,930,200 showed spherical PMMA domains and those from 380,930,380 yielded a protruded worm-like PMMA structure. The copolymer materials were coated on a glass surface for peeling tests. The films gave good hot-melt adhesion properties when the of the PEHMA block was over 600. The peeling strength depended on the lengths of both PEHMA and PMMA blocks. The P(MMA,EHMA,MMA) sample with of 310,930,310 yielded the highest peeling strength of 7.4 kgf,·,inch,1. The developed material is demonstrated to be a good candidate for a solvent-free, hot-melt, pressure-sensitive adhesives for special-purpose applications such as medical tapes and labels. [source] Product decomposition of measured Mueller matrices from the FLC based NIR Mueller Matrix EllipsometerPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 5 2008F. Stabo-Eeg Abstract This paper reports on the application of the first near-infrared spectroscopic Mueller Matrix Ellipsometer (MME) based on Ferro-electric Liquid Crystal retarders (FLC) and fixed waveplates. Operation of the instrument is demonstrated by transmission Mueller matrix measurements, and product decomposition of an imperfect dichroic polarizer and a depolarizing rough glass surface. The decomposition of the measured matrices is qualtitatively discussed in terms of retardance, diattenuation, depolarization, and azimuthal orientation. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Light source inner surface changes depending on treatmentPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 4 2008A. Skudra Abstract Our work is connected with the preparation of different type of electrodeless discharge lamps. In this work we investigate the influence of the SiO2 glass wall treatment procedures on the inner surface of the electrodeless lamps. Three different treatment procedures were applied: vacuum cleaning, vacuum-thermal cleaning and training in the high frequency discharge. The surface modification has been investigated by means of atomic force microscopy. Substantial changes of the SiO2 glass surface have been observed. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Antibiotic glass slide coated with silver nanoparticles and its antimicrobial capabilitiesPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 11 2008Yaohui Lv Abstract Silver nanoparticles were covalently coated on a glass surface by overnight exposure of the glass substrate to nanoparticle solutions, using 3-aminopropyltriethoxysilane (APTES) as a coupling agent. Washing and air-drying yield a uniformly coated glass substrate, which can be used as a material capable of killing harmful microorganisms in food industry. Nanoparticles are stable on the glass surface and are not washed away by water; they even remain on the glass surface under short-term ultrasonic irradiation. The morphology of silver nanoparticles on the glass substrate was characterized by scanning electron microscope (SEM). The existence of Ag nanoparticles on the substrate was also confirmed by ultraviolet-visible (UV,Vis) spectroscopy. Fourier transform infrared (FT-IR) measurement shows that the connection is based on covalent bonds between silver nanoparticle surface/APTES molecules. Combining the effects of low cost and effectiveness in prohibiting the growth of Escherichia coli, such materials are expected to be used as antibacterial coatings, which may have large potential applications in food industry. Copyright © 2008 John Wiley & Sons, Ltd. [source] Inhibition of Vorticetta microstoma Stalk Formation by Wheat Germ AgglutininTHE JOURNAL OF EUKARYOTIC MICROBIOLOGY, Issue 4 2004MICHAEL G. BRAMUCCI ABSTRACT Fluorescently labeled conjugates of wheat germ agglutinin and concanavalin A stained the contractile stalk but not the cell body of Vorticetta microstoma trophonts. Binding of the fluorescent conjugants did not noticeably alter the activity of the trophonts. However, unconjugated wheat germ agglutinin prevented free swimming telotrochs from adhering to a glass surface and deploying a contractile stalk during differentiation into trophonts. These observations indicated that the stalk, the material that binds the stalk to surfaces, and the precursors for these components have saccharide residues in common. [source] In Vitro and In Vivo Evaluation of Albumin Synthesis Rate of Porcine Hepatocytes in a Flat-Plate BioreactorARTIFICIAL ORGANS, Issue 7 2001Masaya Shito Abstract: Several configurations of extracorporeal bioartificial liver devices have been developed for the potential treatment of fulminant hepatic failure or as a bridge to liver transplantation. Recently, we developed a microchannel flat-plate bioreactor with an internal membrane oxygenator in which porcine hepatocytes are cultured as a monolayer on the bottom glass surface. In the present study, we investigated synthetic function of porcine hepatocytes in the bioreactor in both in vitro and in vivo flow circuit models. In vitro, albumin synthesis was stable in the bioreactor for up to 4 days of perfusion. In vivo, with the extracorporeal connection of the bioreactor to rat vasculature, porcine albumin was detectable for 24 h in the rat plasma. We also developed a simple mathematical model to predict the in vivo porcine albumin concentration in rat plasma. These results indicate that this configuration of a microchannel flat-plate bioreactor has potential as a liver support device and warrants further investigation. [source] Surface-directed assembly of cell-laden microgels,,BIOTECHNOLOGY & BIOENGINEERING, Issue 3 2010Yanan Du Abstract Cell-laden microscale hydrogels (microgels) can be used as tissue building blocks and assembled to create 3D tissue constructs with well-defined microarchitecture. In this article, we present a bottom-up approach to achieve microgel assembly on a patterned surface. Driven by surface tension, the hydrophilic microgels can be assembled into well-defined shapes on a glass surface patterned with hydrophobic and hydrophilic regions. We found that the cuboidic microgels (,100,200,µm in width) could self-assemble into defined shapes with high fidelity to the surface patterns. The microgel assembly process was improved by increasing the hydrophilicity of the microgels and reducing the surface tension of the surrounding solution. The assembled microgels were stabilized by a secondary crosslinking step. Assembled microgels containing cells stained with different dyes were fabricated to demonstrate the application of this approach for engineering microscale tissue constructs containing multiple cell types. This bottom-up approach enables rapid fabrication of cell-laden microgel assemblies with pre-defined geometrical and biological features, which is easily scalable and can be potentially used in microscale tissue engineering applications. Biotechnol. Bioeng. 2010; 105: 655,662. © 2009 Wiley Periodicals, Inc. [source] Multienzyme catalysis in microfluidic biochipsBIOTECHNOLOGY & BIOENGINEERING, Issue 1 2003Moo-Yeal Lee Abstract The attachment of enzymes to glass microfluidic channels has been achieved using a highly reactive poly(maleic anhydride- alt -,-olefin) (PMA)-based coating that is supplied to the microchannel in a toluene solution. The PMA reacts with 3-aminopropyltriethoxysilane groups linked to the glass surface to form a matrix that enables additional maleic anhydride groups to react with free amino groups on enzymes to give a mixed covalent,noncovalent immobilization support. Using a simple T-channel microfluidic design, with reaction channel dimensions of 200 ,m wide (at the center), 15 ,m deep, and 30 mm long giving a reaction volume of 90 nL, soybean peroxidase (SBP) was attached at an amount up to 0.6 ,g/channel. SBP-catalyzed oxidation of p -cresol was performed in aqueous buffer (with 20% [v/v], dimethylformamide) containing H2O2, with microfluidic transport enabled by electroosmotic flow (EOF). Michaelis,Menten kinetics were obtained with Km and Vmax values of 0.98 mM and 0.21 ,mol H2O2 converted/mg SBP per minute, respectively. These values are nearly identical to nonimmobilized SBP kinetics in aqueous,DMF solutions in 20-,L volumes in 384-well plates and 5-mL reaction volumes in 20-mL scintillation vials. These results indicate that SBP displays intrinsically native activity even in the immobilized form at the microscale, and further attests to the mild immobilization conditions afforded by PMA. Bienzymic and trienzymic reactions were also performed in the microfluidic biochip. Specifically, a combined Candida antarctica lipase B,SBP bienzymic system was used to convert tolyl acetate into poly(p -cresol), and an invertase,glucose oxidase SBP trienzymic system was used to take sucrose and generate H2O2 for SBP-catalyzed synthesis of poly(p -cresol). © 2003 Wiley Periodicals, Inc. Biotechnol Bioeng 83: 20,28, 2003. [source] Chemical strategies for immobilization of oligonucleotidesBIOTECHNOLOGY JOURNAL, Issue 11 2009Dalip Sethi Abstract The development of oligonucleotide-based microarrays (biochips) is a major thrust area in the rapidly growing biotechnology industry, which encompasses a diverse range of research areas including genomics, proteomics, computational biology, and pharmaceuticals, among other activities. Microarray experiments have proved to be unique in offering cost-effective and efficient analysis at the genomic level. In the last few years, biochips have gained increasing acceptance in the study of genetic and cellular processes. As the increase in experimental throughput has posed many challenges to the research community, considerable progress has been made in the advancement of microarray technology. In this review, chemical strategies for immobilization of oligonucleotides have been highlighted with special emphasis on post-synthetic immobilization of oligonucleotides on glass surface. The major objective of this article is to make the researchers acquainted with some most recent advances in this area. [source] | ||||||||||||||||||||||||||||||||||||||||