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Biomedical subjects

I Eystein Ruyter

Publications and source records attributed to I Eystein Ruyter.

11 recordsLinked to original sources
PubMed2007

Evaluation of bond strength of soft relining materials to denture base polymers.

OBJECTIVES: To evaluate the initial bonding properties of recently and previously introduced soft relining materials to denture base polymers with different polymerization techniques and different water content. METHODS: The initial tensile bond strength of 10 soft liners (Mollosil Plus, Dentusil, Ufi gel Soft, GC Reline Soft, Silagum Comfort, Vertex Soft, Astron Soft, Molloplast B, Flexacryl Soft, Triad Resiline) to three denture base polymers (Paladon 65, Palapress Vario, Ivocap Plus) were assessed with a modified method. Paladon 65 specimens immersed in water for 3 months were also used to test the effect of water content of denture base polymer on bond strength results. After testing, a visual examination of the fracture surfaces and a SEM investigation of the interface structure were performed. Tensile strength of each soft liner material was also tested. Data were analyzed statistically by two-way ANOVA (alpha = 0.05). RESULTS: Significant differences were found among tensile bond strength results (P < 0.05). Vinyl poly(organosiloxane) soft liners (Mollosil Plus, Dentusil, Ufi gel Soft, GC Reline Soft, Silagum Comfort) and a plasticized PMMA soft liner (Vertex Soft) gave statistically similar bond strength results for different denture base polymers (P>0.05). For the other materials used (Astron Soft, Molloplast B, Flexacryl Soft, Triad Resiline), different denture base polymers caused significantly different results (P < 0.05). Poly(organosiloxane) based materials gave slightly higher bond strength results with water immersed specimens than with the dry specimens. SIGNIFICANCE: A wide variety of newly formulated soft liners used in this study gave comparable or better bond strength results compared to Molloplast B.

Adhesiveness↗
PubMed2006

Mechanical and physical properties of carbon-graphite fiber-reinforced polymers intended for implant suprastructures.

OBJECTIVES: Mechanical properties and quality of fiber/matrix adhesion of poly(methyl methacrylate) (PMMA)-based materials, reinforced with carbon-graphite (CG) fibers that are able to remain in a plastic state until polymerization, were examined. METHODS: Tubes of cleaned braided CG fibers were treated with a sizing resin. Two resin mixtures, resin A and resin B, stable in the fluid state and containing different cross-linking agents, were reinforced with CG fiber loadings of 24, 36, and 47 wt% (20, 29, and 38 vol.%). In addition, resin B was reinforced with 58 wt% (47 vol.%). After heat-polymerization, flexural strength and modulus were evaluated, both dry and after water storage. Coefficient of thermal expansion, longitudinally and in the transverse direction of the specimens, was determined. Adhesion between fibers and matrix was evaluated with scanning electron microscopy (SEM). RESULTS: Flexural properties and linear coefficient of thermal expansion were similar for both fiber composites. With increased fiber loading, flexural properties increased. For 47 wt% fibers in polymer A the flexural strength was 547.7 (28.12) MPa and for polymer B 563.3 (89.24) MPa when water saturated. Linear coefficient of thermal expansion was for 47 wt% CG fiber-reinforced polymers; -2.5 x 10(-6) degrees C-1 longitudinally and 62.4 x 10(-6) degrees C-1 in the transverse direction of the specimens. SEM revealed good adhesion between fibers and matrix. More porosity was observed with fiber loading of 58 wt%. CONCLUSIONS: The fiber treatment and the developed resin matrices resulted in good adhesion between CG fibers and matrix. The properties observed indicate a potential for implant-retained prostheses.

Carbon↗
PubMed2006

Effect of thermal cycling on composites reinforced with two differently sized silica-glass fibers.

OBJECTIVES: To evaluate the effects of thermal cycling on the flexural properties of composites reinforced with two differently sized fibers. METHODS: Acid-washed, woven, fused silica-glass fibers, were heat-treated at 500 degrees C, silanized and sized with one of two sizing resins (linear poly(butyl methacrylate)) (PBMA), cross-linked poly(methyl methacrylate) (PMMA). Subsequently the fibers were incorporated into a polymer matrix. Two test groups with fibers and one control group without fibers were prepared. The flexural properties of the composite reinforced with linear PBMA-sized fibers were evaluated by 3-point bend testing before thermal cycling. The specimens from all three groups were thermally cycled in water (12,000 cycles, 5/55 degrees C, dwell time 30 s), and afterwards tested by 3-point bending. SEM micrographs were taken of the fibers and of the fractured fiber reinforced composites (FRC). RESULTS: The reduction of ultimate flexural strength after thermal cycling was less than 20% of that prior to thermal cycling for composites reinforced with linear PBMA-sized silica-glass fibers. The flexural strength of the composite reinforced with cross-linked PMMA-sized fibers was reduced to less than half of the initial value. SIGNIFICANCE: This study demonstrated that thermal cycling differently influences the flexural properties of composites reinforced with different sized silica-glass fibers. The interfacial linear PBMA-sizing polymer acts as a stress-bearing component for the high interfacial stresses during thermal cycling due to the flexible structure of the linear PBMA above Tg. The cross-linked PMMA-sizing, however, acts as a rigid component and therefore causes adhesive fracture between the fibers and matrix after the fatigue process of thermal cycling and flexural fracture.

Composite Resins↗
PubMed2005

Evaluation of adhesion of chairside hard relining materials to denture base polymers.

STATEMENT OF PROBLEM: Removable denture bases are made of modified poly(methyl methacrylate) (PMMA), which has reliable bond strength with resins containing methyl methacrylate (MMA). However, some hard relining materials with different chemical compositions have been reported to have less than adequate bond strength to PMMA denture base polymers. PURPOSE: This in vitro study evaluated the initial bonding properties of chairside hard relining materials to different removable denture base polymers, as well as the structure of the interface. MATERIAL AND METHODS: The tensile strength (MPa) of adhesion of 8 chairside hard relining materials (Original Truliner, GC Reline Hard, Ufigel Hard, Triad Reline, New Truliner, Light Liner, Astron LC Hard, and Flexacryl Hard) was tested against 3 denture base polymers (Ivocap Plus, Paladon 65, and Palapress Vario). Dumbbell-shaped specimens with a 6-mm diameter of bonding surface were used for tensile testing of bond strength (n=5). An MMA containing hard relining material (Original Truliner) was used as a control. Tensile strength of the bond was calculated using the bonding area and maximum force under tension. Statistical analyses of data were conducted with 2-way analysis of variance (alpha=.05). The influence of the bonding agents and the relining materials on the PMMA denture base surface layer and its structure were investigated. The depths of the swollen layers were measured with a transmission light microscope. Fracture surfaces after testing were also visually evaluated. Chemical analyses of all materials prior to testing were performed using high-performance liquid chromatography. RESULTS: Significant differences were found among tensile bond strengths of chairside hard relining materials to PMMA denture base polymers forming 3 different groups (P<.001). No significant difference among different denture base polymers was found with regard to tensile strength of adhesion (P=.918), but the interaction term between hard relining material and denture base polymer was found to be significant (P<.001). The tensile bond strength of the relining materials and denture base polymers was found to range from 8% to 60% of the strength of the PMMA denture base polymers. CONCLUSION: The chemical composition of the bonding agents and the relining materials and their combinations affected the depth of the swollen layers of the denture base polymers and the tensile strength of adhesion.

Acrylic Resins↗
PubMed2005

Physicochemical evaluation of silica-glass fiber reinforced polymers for prosthodontic applications.

This investigation was designed to formulate silica-glass fiber reinforced polymeric materials. Fused silica-glass fibers were chosen for the study. They were heat-treated at various temperatures (500 degrees C, 800 degrees C and 1100 degrees C), silanized, sized and incorporated in two modified resin mixtures (A and B). The flexural properties in dry and wet conditions were tested and statistically analyzed, and the content of residual methyl methacrylate (MMA) monomer, dimensional changes with temperature, water sorption and solubility were determined. Woven fibers [36.9% (wt/wt)], heat-treated at 500 degrees C, gave the highest strength values for the polymeric composites (an ultimate transverse strength of 200 Mpa and a flexural modulus of 10 GPa) compared with the fibers heat-treated at other temperatures. There was no statistically significant difference in the measured flexural properties between resins A and B regarding fiber treatment and water storage time. These fiber composites had a small quantity of residual MMA content [0.37 +/- 0.007% (wt/wt)] and very low water solubility, indicating good biocompatibility. It was suggested that silica-glass fibers could be used for reinforcement as a result of their anticipated good qualities in aqueous environments, such as the oral environment.

Biocompatible Materials↗
PubMed2005

Evaluation of two matrix materials intended for fiber-reinforced polymers.

Two matrix resins for fiber composites that remain in a fluid state during storage and handling before polymerization were evaluated. The resin mixtures, based on methyl methacrylate (MMA), were produced with two different cross-linking agent systems: 1,4-butanediol dimethacrylate and ethylene glycol dimethacrylate or diethylene glycol dimethacrylate. Water sorption, water solubility, water uptake and residual MMA monomer were determined. Thermomechanical analysis was used to determine linear dimensional changes as a function of temperature. Flexural strength and modulus as well as fracture work and the maximum stress intensity factor were determined. The results revealed similar values for both matrix polymers regarding water sorption, water solubility, water uptake, residual MMA monomer (0.5 wt% (+/- 0.03)) and coefficient of linear thermal expansion. Flexural strength for polymer B was 68.7 MPa (+/- 9.8) compared to 56.0 MPa (+/- 13.3) for polymer A when tested dry and 64 MPa (+/- 6.1) compared to (54 MPa (+/- 3.3) when water-saturated. Fracture toughness tests showed higher maximum stress intensity factor values for polymer B (0.75 +/- 0.17) MPa x m1/2 than for polymer A (0.55 +/- 0.12) MPa x m1/2. The resin binders showed an appropriate consistency while remaining in a fluid state during storage and manipulation.

Absorption↗
PubMed2003

Resistance of medical gloves to permeation by methyl methacrylate (MMA), ethylene glycol dimethacrylate (EGDMA), and 1,4-butanediol dimethacrylate (1,4-BDMA).

Gloves afford hand protection by minimizing skin contact. The effectiveness of medical gloves to protect against permeation of the monomers, methyl methacrylate (MMA), ethylene glycol dimethacrylate (EGDMA), and 1,4-butanediol dimethacrylate (1,4-BDMA), was assessed focusing on permeation rates and degradation of glove materials caused by monomer contact. Fifteen different brands of gloves were tested using a European Standard procedure. Surface images of glove materials before and after exposure to the monomer mixture were obtained using a scanning electron microscope. The standard is not applicable as the only method for estimating the safety of gloves, but it is useful as guideline together with the cumulative permeation of acrylic monomers. Monomer contact on the outside resulted in substantial swelling of most glove materials, and structure changes of the inside surface.

Gloves, Surgical↗
PubMed2003

Adhesion of endodontic sealers: scanning electron microscopy and energy dispersive spectroscopy.

The microscopic details of the debonded interfaces between endodontic sealers and dentin or gutta-percha were assessed in this study. Dentin, conditioned with 37% H3PO4 for 30 s, 25% citric acid for 30 s, 17% EDTA for 5 min, or a rinse with 10 ml of distilled H2O (control), and gutta-percha surfaces were coated with freshly mixed sealer: Grossman's sealer, Apexit, Ketac-Endo, AH Plus, RoekoSeal Automix, or RoekoSeal Automix with an experimental primer. The surfaces were pressed together and the sealers were allowed to set. After tensile bond strength testing, the morphological aspects of the fractured surfaces were assessed by scanning electron microscopy and energy dispersive spectroscopy. The energy dispersive spectroscopy successfully traced sealer components to the debonded surfaces. Some of the sealers penetrated into the dentinal tubules when the dentin surface had been pretreated with acids. However, these sealer tags remained occluding the tubules after bond failure in some instances only (Grossman's sealer, RoekoSeal Automix with an experimental primer, AH Plus/EDTA). Penetration of the endodontic sealers into the dentinal tubules when the smear layer was removed was not associated with higher bond strength.

Acid Etching, Dental↗
PubMed2002

Permeability of medical gloves to mono- and dimethacrylate monomers in dental restorative materials.

Dental personnel manually handle methacrylate-based restorative materials, which can cause skin irritation and allergies. The protection given by different types of medical gloves is not well known. Breakthrough time (BTT, min) was used as a measure of protection according to a European standard, using 2 test mixtures consisting of respectively 3 and 5 monomers. Fourteen gloves representing natural rubber latex, synthetic rubber, and synthetic polymeric material were tested. The BTT ranged from some minutes to more than 2 hrs for the 4 monomers with a molecular mass less than 300. The longest protection was recorded for Nitra Touch (nitrile rubber), Tactylon (synthetic rubber), and Metin (PVC).

Dental Materials↗