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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Journal of oral rehabilitation 30 (2003), S. 0 
    ISSN: 1365-2842
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: summary The purpose of this study was to determine changes in flexural properties of resin cement under simulated resin-bonded fixed partial denture (RBFPD) clinical conditions using aqueous ageing and cyclic loading. Panavia F flexural modulus and strength were measured by static loading to failure after 48-h and 60-day aqueous ageing at 37 °C with and without simulated cyclic occlusal loading. Panavia F sorption and solubility were also measured. Scanning electron microscopy (SEM) was used to characterize the morphology of the fractured surfaces. A two-factor anova (P ≤ 0·05) indicated that cyclic loading produced a significant increase in the flexural modulus with no significant effect on the flexural strength. Conversely, aqueous ageing time produced a significant decrease in flexural strength with no effect on the flexural modulus. The SEM fracture analysis indicated that resin matrix fracture occurred in static-aqueous specimens; while in the aqueous-cycled specimens, resin matrix fracture occurred in addition to an increasing proportion of filler/resin interface fracture. Collectively, these outcomes suggest that initial degradation under simulated resin cement clinical function may be related to breakdown of the filler/resin interface bond, which could contribute to in vivo RBFPD resin cement cohesive failure.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 10 (1972), S. 91-102 
    ISSN: 1432-0827
    Keywords: Hydroxyapatite ; Calcification ; Phases ; Growth ; Microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Description / Table of Contents: Résumé La croissance cristalline de l'hydroxyleapatite à 25° et à pH constant de 7.4 a été étudiée à l'aide du microscope électronique à balayage. La technique reproductible de croissance par ensemencement à partir de solutions stables sursaturées est utilisée efficacement pour produire des échantillons de minéral à divers stades distincts de croissance. Des changements de phase sont observés avec le progrès de la croissance; ils correspondent dans le temps avec les résultats cinétiques obtenus antérieurement. Un essai de rationalisation est tenté à la lumière des mécanismes proposés pour la formation d'hydroxyleapatite dans des conditionsin vivo.
    Abstract: Zusammenfassung Das Kristallwachstum von Hydroxyapatit bei 25° und einem konstanten pH von 7,4 wurde mit Hilfe eines Raster-Elektronenmikroskopes studiert. Die reproduzierbare Technik des Keimwachstums aus stabilen übersättigten Lösungen wurde mit Erfolg verwendet, um Mineralproben in verschiedenen bestimmten Stadien des Wachstums zu erhalten. Phasenveränderungen wurden beim fortschreitenden Wachstum beobachtet, und diese stimmten zeitlich gut überein mit kinetischen Resultaten, über welche früher berichtet wurde. Es wurde versucht, diese Beobachtungen zu erklären in Anbetracht von Mechanismen, welche für die Bildung von Hydroxyapatit unterin vivo-Bedingungen vorgeschlagen wurden.
    Notes: Abstract The crystal growth of hydroxyapatite at 25° and at a constant pH of 7.4 has been studied with the aid of a scanning electron microscope. The reproducible technique of seeded growth from stable supersaturated solutions was used effectively to produce samples of the mineral at various distinct stages of growth. Phase changes were observed as the growth proceeded and these corresponded favorably in time with kinetic results reported earlier. An attempt was made to rationalize the observations in light of mechanisms proposed for the formation of hydroxyapatite under conditions foundin vivo.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 1667-1673 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The design of spiroorthocarbonate monomers (SOCs) and related structures is discussed with the aim of maximizing monomer polymerizability in the absence of undesirable byproducts. The successful syntheses of N,S-analogs of aryl- and alkaryl-SOCs are reported; these are monomers of structure where P and Q are —O— and —OC(CH3)2-, mp 156-158°C; and P and Q are —OCH2— and —OCH2—, mp 148-150°C. As is indicated by infrared spectra, the polymerization of both monomers is initiated by boron trifluoride etherate. © 1993 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0887-6266
    Keywords: density change determination for polymerizations with minimal volume change ; spiro-orthocarbonates, expansion polymerization density change determination for ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Materials that polymerize without substantial volume contraction have numerous valuable applications in dentistry and other fields. Two new symmetrical aliphatic spiro-orthocar-bonates, formulated from cis- and trans-2-hydroxymethyl-cyclohexanol to give 2,3,8,9-di(tetramethylene)-1,5,7,11-tetraoxaspiro [5,5] undecanes, showed, by density determinations in dilute solution, that expansion occurs with polymerization. The cis / cis-spiroorthocarbonate racemic mixture showed a 3.9% expansion upon polymerization, and the trans/trans racemic mixture showed a 3.5% expansion. The densities were determined by pycnometry, with a precision reliable to at least four figures. This method is thus recommended for cases of soluble monomer/polymer pairs for which the density difference will be small and where the partial specific volumes are independent of concentration, thereby avoiding the complexities of variable physical states of monomer and/or polymer. © 1993 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 15 (1981), S. 565-575 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The A.D.A. acute systemic test for type II, class 11 materials defines compliance on the basis of fewer than 50% mortality at 2 weeks. Histopathologic criteria were developed from pilot study data to evaluate the effects of these materials. In this double blind study, the frequency of histopathological changes in lung, liver, small intestine, and kidney were rated at 2 and 5 weeks, for six dental crown and bridge alloys ranging from 44% to 97% (Au, Pt, and Pd). Two positive 360 mg/kg and 1 g/kg of cadmium and two negative, a blank capsule and untreated control groups were used. There was significant difference (chi square test, X2 = 0.95) between the positive and negative controls at 2 and 5 weeks. The lung, liver, kidney showed the highest level of histopathological changes. Significant changes occurred in the four tissues for all alloys at two and five weeks. At five weeks, alloys with a lower noble metal content (44-62%, Au, Pd, and Pt) elicited significant chronic changes, while higher noble metal content (78-97%) showed healing and no significant difference from the negative controls. Applying histopathologic criteria and statistical parameters independent examiners can examine experimental animals and arrive at conclusive and reproducible results.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 28 (1994), S. 59-63 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Current in vitro biocompatibility methods do not evaluate the degradation of biomaterials after contact with enzymes that might be present in the oral or systemic environment. In this study, two methods of in vitro enzyme degradation and a method for the separation of the degradative products by high performance thinlayer chromatography (HPTLC) are reported. In the first method two dental adhesives, Scotchbond and Scotchbond II, and two dental composites, Helimolar and P-50, were evaluated. These materials were incubated with four different enzymatic preparations for periods of up to 72 h. The enzymes were lipase, esterase, and liver enzyme extracts from both mouse and rat. Chloroform soluble products extracted from the aqueous phase were examined by HPTLC for decomposition products resulting from enzyme activity. The second method was similar, but analyzed the aqueous fraction directly without chloroform extraction. In this method five dental restorative materials, P-50, P-30, Scotochbond II, Silux, and Silux Plus, were incubated with a nonspecific porcine liver esterase. In addition to the polymerized biomaterials. Monomers containing methacrylic acid units were also hydrolyzed with esterase and analyzed by ion chromatography to establish the sensitivity of the enzyme simulator. Each biomaterial presented thin-layer zones not present before enzymatic action. These experiments provide support that aqueous enzymatic action may facilitate the hydrolytic weakening of polymeric biomaterials. © 1994 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 35 (1997), S. 191-197 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: When transmission electron microscopy (TEM) is used to evaluate resin-dentin interface specimens for completeness of hybridization, the epoxy resin embedding medium that normally facilitates ultrathin sectioning may produce a secondary or artifactual hybrid layer. This secondary hybrid layer, composed of epoxy resin rather than adhesive resin, may fill the pores that remain as evidence of incomplete resin infiltration, obscuring the fact that they ever existed. In this study, resin-dentin interfaces produced by two dentin adhesive systems, Optibond (OPTI, Kerr) and Scotch-bond Multi-Purpose (SBMP, 3M), were comparatively investigated by TEM in epoxy-embedded and nonembedded non-demineralized sections. The hypothesis advanced was that no difference in ultramorphology of the hybrid layer would result from either specimen preparation method. The two adhesive systems were applied to four mid-coronal dentin disks per manufacturer's instructions. One half of each sample was processed following common procedures for TEM sample preparation with epoxy embedding, whereas the other half was not embedded but instead immersed in hexamethyldisilazane (HMDS), dried and mounted so that it protruded from a base of cold-cure acrylic resin. Each sample was then sectioned using a diamond knife in an ultramicrotome. With either means of preparation, a hybrid layer with a relatively uniform electron density and a loose collagen fibril arrangement with electron lucent interfibrillar channels was formed by OPTI. At the base of the hybrid layer, collagen fibrils were anchored in the underlying unaffected dentin, and no microporosities or gaps were observed. Similarly, whether SBMP was embedded or nonembedded, it was found to have a hybrid layer of variable electron density and an electron dense phase localized at the surface of the hybrid layer. No porosities were evident at the base of the hybrid layer. Thus, with either of the two adhesive systems, no ultrastructural difference in hybrid layer formation was observed between epoxy-embedded and nonembedded sections, and no direct evidence of ineffective resin-infiltration of the demineralized collagen scaffold was found. © 1997 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 41 (1998), S. 237-243 
    ISSN: 0021-9304
    Keywords: solubility parameters ; dentin ; adhesives ; interpenetrating polymer networks ; bioadhesives ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The principal aim of this study was to investigate the relationships between the solubility parameters of etched dentin, and adhesive primer solutions and adhesive bond strength. Solubility parameters characterize the molecular interactions which determine physical properties such as wetting, and thus can serve as tools to aid development of polymeric adhesives and interpenetrating polymer networks. If an adhesive monomer has a solubility parameter close to that of a polymer substrate, then the monomer may act as a solvent for the polymer and penetrate below the surface. Subsequent polymerization of the monomer may then produce an interpenetrating network, thus adhering without necessarily forming primary chemical bonds to the substrate. The dentin substrate considered in this study was abraded dentin treated with ethylenediaminetetraacetic acid. Solubility parameters δp, δh, and δd calculated for the etched dentin substrate were 20.3, 23.6, and 16.0 (J/cm3)1/2, respectively. Solubility parameters of the primers were expressed using Hansen's three-dimensional scheme. The data indicate a correlation between the calculated solubility parameters of the etched dentin, and dentin primers and the resulting bond strengths. The results corroborate the significance of solubility parameter considerations for adhesive bonding to dentin. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 41, 237-243, 1998.
    Additional Material: 2 Ill.
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