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At least 721 records · Page 40Linked to original sources
PubMed2004

Effect of LED curing on microleakage and microhardness of Class V resin-based composite restorations.

BACKGROUND: Polymerisation shrinkage is a critical limitation of dental composites and may contribute to microleakage, postoperative pain, tooth fracture, and secondary caries. It has been shown that curing methods play a significant role in polymerisation shrinkage of light-cured dental resins. The purpose of this study was to investigate the effect of a LED curing light on microleakage as well as microhardness of a dental composite. METHOD: For the microleakage test 32 Class V cavities were prepared in human premolars, conditioned with 35% phosphoric acid and treated with the bonding agent Prime & Bond NT. They were then incrementally filled with the composite Esthet-X and randomly divided into two groups of 16 each. The first group was cured by means of a Spectrum 800 set at 500 mW/cm2 for 40 seconds and the second group with the GC E-Light in standard mode. The specimens were thermo-cycled in a 0.5% basic fuchsin solution, sectioned and evaluated for dye penetration. For the microhardness test two groups of 6 specimens each were exposed using either the LED- or the Halogen curing unit. Vickers microhardness tests were performed immediately after curing as well as 24 hours later, on the top, and at the bottom surface. RESULTS: At the dentine/cementum interface, significantly less microleakage (p=0.004) was found when the restorations were cured with the LED-unit. At the enamel interface no significant difference (p=0.340) in microleakage was found between curing methods. Immediately after exposure significantly harder surfaces were found at the top (p<0.001) as well as at the bottom (p<0.001), using the halogen unit (p<0.05). CONCLUSION: Although a reduction in microleakage could be demonstrated exposing the composite restoration to an LED LCU, an effective microhardness ratio was not achieved.

Bicuspid↗
PubMed2005

Elastic deformation of mineralized collagen fibrils: an equivalent inclusion based composite model.

Mineralized collagen fibrils are the basic building blocks of bone tissue at the supramolecular level. Several disease states, manipulation of the expression of specific proteins involved in biomineralization, and treatment with different agents alter the extent of mineralization as well as the morphology of mineral crystals which in turn affect the mechanical function of bone tissue. An experimental assessment of mineralized fibers' mechanical properties is challenged by their small size, leaving analytical and computational models as a viable alternative for investigation of the fibril-level mechanical properties. In the current study the variation of the elastic stiffness tensor of mineralized collagen fibrils with changing mineral volume fraction and mineral aspect ratios was predicted via a micromechanical model. The partitioning of applied stresses between mineral and collagen phases is also predicted for normal and shear loading of fibrils. Model predictions resulted in transversely isotropic collagen fibrils in which the modulus along the longer axis of the fibril was the greatest. All the elastic moduli increased with increasing mineral volume fraction whereas Poisson's ratios decreased with the exception of v12 (=v21). The partitioning of applied stresses were such that the stresses acting on mineral crystals were about 1.5, 15, and 3 times greater than collagen stresses when fibrils were loaded transversely, longitudinally, and in shear, respectively. In the overall the predictions were such that: (a) greatest modulus along longer axis; (b) the greatest mineral/collagen stress ratio along the longer axis of collagen fibers (i.e., greatest relief of stresses acting on collagen); and (c) minimal lateral contraction when fibers are loaded along the longer axis. Overall, the pattern of mineralization as put forth in this model predicts a superior mechanical function along the longer axis of collagen fibers, the direction which is more likely to experience greater stresses.

Animals↗
PubMed1975

Deoxyribonucleic acid base composition and biochemical properties of certain coagulase-negative enterotoxigenic cocci.

Eight coagulase-negative, enterotoxigenic strains of cocci and one weakly coagulase-positive strain isolated from a number of different sources, including cases of food poisoning incidents, were evaluated for their relationship to Staphylococcus aureus on the basis of deoxyribonucleic acid (DNA) buoyant density and physiological studies. One strain of cocci produced enterotoxins A and C, two strains produced types B and C, four strains produced only type C, and one strain only type D. The enterotoxin produced by one strain of cocci was serologically untypable. None of the test organisms produced detectable amounts of enterotoxin in broth cultures. The test strains of cocci exhibited the following profile: all produced catalase; all grew anaerobically and fermented glucse; five were sensitive to lysostaphin; the percentage of guanine plus cytosine content of their DNA varied from 32.7 to 37.6; five produced acid from mannitol both aerobically and anaerobically; two formed delta-hemolysin; five produced phosphatase and acetoin; and all produced heat-stable nuclease. None of the organisms exhibited typical characteristics of S. aureus, S. epidermidis, or S. saprophyticus. On the basis of the present data and data reported elsewhere, these organisms should be considered as variants or mutants of S. aureus.

Aerobiosis↗