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PubMed1984

The sensitizing potential of di-(meth)acrylates based on bisphenol A or epoxy resin in the guinea pig.

Most composite materials in dentistry used today, contain resins based on dimethacrylates. BIS-GMA [2,2-bis-(4-(2-hydroxy-3-methacryloxypropoxy)phenyl)propane], the addition reaction product of bisphenol A and glycidyl methacrylate or an epoxy resin and methacrylic acid, is used most extensively. More recently, dimethacrylates based on bisphenol A, with various chain lengths have appeared on the market as a substitute for or in addition to BIS-GMA. Such compounds are BIS-MA [2,2-bis-(4-(methacryloxy)phenyl)propane], BIS-EMA [2,2-bis-(4-(2-methacryloxyethoxy)phenyl)propane] and BIS-PMA [2,2-bis-(4-(3-methacryloxypropoxy)phenyl)propane]. Increasing interest in the radiaton cure of coatings and printing inks have focused attention on these substances and on epoxy diacrylates as radiation-curable resins. The sensitizing capacity of the different acrylates based on bisphenol A or epoxy resin have been investigated with the guinea pig maximization test. The pattern of simultaneous reactivity of the compounds was also studied. Epoxy diacrylate [2,2-bis-(4-(2-hydroxy-3-acryloxy-propoxy)phenyl)propane], BIS-EMA and BIS-MA are shown to be strong sensitizers, while the linear fraction of BIS-GMA and its isomers and BIS-PMA have none or a low sensitizing capacity. The impurities in the BIS-GMA and BIS-MA batches seem to have high allergenic potential. These results stress the importance of a pure substance when discussing allergenicity and cross reactions.

Acrylates↗

PubMed2000

Two-year clinical evaluation of a high-density posterior restorative material.

The purpose of this study was to clinically evaluate SureFil high-density posterior composite for Class 2 restorations of permanent first and second molars. All teeth were restored in occlusion with the natural dentition. After cavity preparation, the enamel was etched for 15 seconds with 34% phosphoric acid. No liner/base material was used for the dentin. Prime & Bond 2.1 (two applications) was applied for adhesion to the exposed dentin and etched enamel. The first coat of adhesive was cured for 20 seconds with a curing light and the next coat was only spread thin with a gentle jet of air. The cavity was restored in 3-mm to 5-mm increments. Clinical evaluation (US Public Health Service method) and wear analysis (indirect cast comparison method) were conducted immediately after placement (baseline) and at 3 months, 6 months, 9 months, 1 year, and 2 years. A total of 25 restorations were inserted. At baseline and after 3, 6, and 9 months (n = 24), all restorations were graded Alfa in all categories. At the 1-year recall, 3 restorations (n = 22) were graded Bravo for surface staining. At the 2-year recall, an additional 3 restorations (n = 22) were graded Bravo for surface staining. No restoration was graded Charlie in any category at any time. Wear analysis revealed an average of 13.8 microns of wear at the 2-year recall (n = 22). No evidence of recurrent caries was observed. In conclusion, after 2 years, this high-density composite material demonstrated clinical acceptability and excellent wear characteristics in all categories, making it suitable for posterior restorations.

Acetone↗

PubMed2003

Optimization of methacrylic acid ester copolymers blends as controlled release coatings using response surface methodology.

The aim of this study was to statistically optimize the use of blends of methacrylic acid ester copolymers with different permeability properties as controlled-release coating systems for tablets to produce predictable predesigned release profiles. A full factorial design was used to study and optimize the use of methacrylic acid ester copolymers Eudragit RS 30D and Eudragit RL 30D as coating materials for controlled release. Directly compressed theophylline tablets were coated with aqueous dispersions containing different proportions of the two copolymers using a side-vented coating pan (Accela Cota). The effect of polymer loading level at 5, 7.5, and 10% weight gain and curing time at 50 degrees C for 12 and 24 hours were also evaluated. Coated tablets were tested for their drug release in water using a United States Pharmacopeia (USP) dissolution apparatus #2. The results showed that increasing the content of the lower permeability copolymer Eudragit RS 30D, increasing the polymer load, and increasing curing time at 50 degrees C resulted in slower drug release. A statistical model that describes and predicts the drug release properties of the coated tablets as a function of the copolymers ratio in the coating dispersion, polymer load, and curing time at 50 degrees C was developed. The most significant factor affecting drug release was found to be the ratio of the two copolymers in the coating dispersion followed by the curing time at 50 degrees C and the polymer loading level. Good correlations were observed between the model fitted values andthe experimental values. An optimized formula prepared by superimposing two-dimensional contour plots was prepared; its release profile was found to be in agreement with the prediction obtained from the model.

Delayed-Action Preparations↗

PubMed2001

How wet should dentin be? Comparison of methods to remove excess water during moist bonding.

PURPOSE: The aim of this study was to evaluate the shear bond strength of two adhesive systems when applied on dentin surfaces with different degrees of wetness. MATERIALS AND METHODS: Two-hundred ten dentin specimens were used. After conditioning with 35% phosphoric acid gel and washing, seven methods of drying dentin were used: 30 s air spray (groups 1 and 2), 5 s air spray (groups 3 and 4), dry cotton pellets (groups 7 and 8), wet cotton pellets (groups 9 and 10), microbrush (groups 11 and 12), absorbent paper (groups 13 and 14). The last group was not dried; the dentin surfaces were left overwet (groups 5 and 6). Prime & Bond 2.1 adhesive was applied on the odd-numbered groups and Scotchbond Multi Purpose on the even-numbered groups. Z100 composite cylinders were bonded to the adhesive and the specimens were subjected to a shear bond test. RESULTS: The Least-Squares Means test was used to compare the following results, where different letters indicate significantly different mean values: Group 9 (G9) = 23.2 MPa (a), G3 = 21.3 MPa (ab), G2 = 19.5 MPa (bc), G10 = 18.6 MPa (bc), G14 = 16.3 MPa (cd), G8 = 16.1 MPa (cd), G4 = 14.6 MPa (de), G13 = 14.0 MPa (de), G11 = 13.9 MPa (de), G7 = 13.5 MPa (de), G12 = 12.1 MPa (e), G1 = 8.2 MPa (f), G5 = 2.7 MPa (g), G6 = 2.4 MPa (g). CONCLUSION: The adhesion values were affected both by the degree of dentin wetness and by the adhesive systems.

Acetone↗

PubMed2004

Endothelial cell adhesion on RGD-containing methacrylate terpolymers.

Hexyl methacrylate (HMA), methyl methacrylate (MMA), and methacrylic acid (MAA) were used as comonomers to produce a low glass transition temperature material, potentially useful in fabricating a small diameter vascular graft. Because it has been shown that grafts seeded with endothelial cells have better resistance to thrombosis, RGD-based peptide sequences were incorporated into the terpolymer. The two methods used for incorporating peptide sequences were a chain transfer reaction during polymerization, and a coupling reaction between the amine terminus of the peptide and the carboxyl groups of the MAA. Polymers were synthesized using the chain transfer reaction with peptide concentrations ranging from 1.7 to 7.0 micromol/g. Weight-average molecular weights decreased with increasing peptide concentration from 310,000 g/mol for the terpolymer without peptide, to 110,000 g/mol for a peptide concentration of 7.0 micromol/g. As a result, Young's modulus decreased with increasing peptide concentration. Terpolymers with peptides attached through a coupling reaction showed no decrease in molecular weight or mechanical properties. Confocal microscopy showed cells seeded on the RGD surfaces adhered and spread, while terpolymers with RGE sequences showed cells that were rounded and not spreading. Cell density on RGD surfaces increased with increasing peptide concentration up to a bulk peptide concentration of approximately 5 micromol/g and reached a plateau, which indicated the minimum peptide concentration necessary for maximum cell adhesion.

Biocompatible Materials↗

PubMed2000

In vitro studies of the interaction of poly(NIPAm/MAA) nanoparticles with proteins and cells.

The pH- and temperature-responsive poly(N-isopropylacrylamide-co-methacrylic acid) (PNIPAm/MAA) nanoparticles are of potential application in targeted drug delivery. Their responsive properties in the presence of human serum albumin were investigated using dynamic light scattering (DLS), protein assay, and electron spin resonance (ESR) spectroscopy. Their interaction with human monocytes and polymorphonuclear leukocytes (PMNLs) was studied using scanning electron microscopy (SEM) and oxygen consumption method. The nanoparticles exhibited a volume phase transition at 35-40 degrees C in Hanks balanced salt solution (HBSS) and in phosphate buffer solution (PBS) of pH 7.4. The diameter of the nanoparticles decreased slightly in the presence of HSA at 25 degrees C at neutral pH, whereas an increase in the diameter in pH 6 PBS at 40 degrees C was revealed. The amount of albumin adsorbed onto the nanoparticles decreased with increasing temperature. The ESR spectra of spin labeled HSA indicated a more restricted environment in the nanoparticles at elevated temperatures. The stimulation of PMNL oxygen consumption by PNIPAm based nanoparticles, an indication of phagocytosis of the particles, was not observed regardless whether the nanoparticles were incubated in plasma or serum. In contrast, the more hydrophobic polystyrene (PSt) particles induced a significant increase in the rate of oxygen consumption after the incubation. PNIPAm/MAA-grafted-PSt particles behaved similarly to the PNIPAm/MAA nanoparticles, suggesting that surface properties dictate the recognition of colloids by PMNLs.

Acrylamides↗

PubMed2003

Strengthening effect of aluminum fluoride added to resin composites based on polyacid-containing polymer.

OBJECTIVES: The study investigates the possible strengthening effect of aluminum ions liberated during long-time water storage of experimental resin composites containing a polymer with carboxylic acid groups. METHODS: The organic part of the resin composites was formed by photopolymerization of methacrylate monomers. The monomer mixture was composed of UEDMA, HEMA or TEGDMA, and 0-40 mol% HEMAN (the adduct of HEMA and maleic anhydride). The filler part of the resin composites consisted of a conventional silanated glass filler and 1 or 5 wt% of AlF3 x 3H2O. The rupture strength and bending modulus were measured without water storage and after 1 month, 1 year, and 3 years of water storage at 37 degrees C of the resin composite. RESULTS: The experimental composites that had been stored in water had lower rupture strength and modulus than the composites that were tested without water storage. Specimens containing 30 or 40 mol% HEMAN increased in strength, and specimens containing 20, 30, or 40 mol% HEMAN increased in modulus during the period of water storage. Depending on composition, values for strength and modulus obtained after 3 years of water storage was up to 50% higher than the values obtained after 1 month. SIGNIFICANCE: The strengthening effect of aluminum fluoride may be interpreted as the result of increased crosslinking by aluminum ions and carboxylate groups. The results may serve as a basis for the improvement of the mechanical properties of polyacid-modified resin composites.

Aluminum Compounds↗

PubMed2006

In vitro release and in vivo absorption in beagle dogs of meloxicam from Eudragit FS 30 D-coated pellets.

The objective of this study was to develop meloxicam-loaded colon-specific pellets coated with Eudragit FS 30 D and further evaluate their in vitro release and in vivo absorption in beagle dogs. Meloxicam-loaded cores (drug loading, 4.8%, w/w) were prepared by layering drug-binder (HPMC)-solubilizer (beta-cyclodextrin) solution onto nonpareils (710-850 microm) and then coated with a copolymer of methyl acrylate, methyl methacrylate and methacrylic acid (Eudragit FS 30 D). The obtained pellets with 15% (w/w) coating level had a spherical form and a smooth surface with coating thickness approximately 28 microm. The in vitro drug release from the pellets was pH-dependent with sufficient gastric resistance (pH 1.2: no release; pH 6.8: 6%; pH 7.0: 52%; pH 7.2: 100%; pH 7.4: 100%, after 3 h incubation). In vivo study was carried out using pentagastrin-pretreated beagle dogs. The onset of meloxicam absorption from the coated pellets with 15% (w/w) Eudragit FS 30 D (3.0+/-0.8 h) was significantly delayed (p<0.05) compared to that from the uncoated drug-layered cores (0.6+/-0.3 h). The area under the meloxicam plasma concentration-time curve (AUC(0-->96)(h) was not significantly different between the two preparations (p>0.05), although AUC(0-->96)(h) obtained after oral administration of coated pellets (142.5+/-59.6 microg h/ml) was lower than that obtained after administration of uncoated drug-layered cores (180.8+/-61.9 microg h/ml). These results suggested that meloxicam could be delivered to the colon with 15% (w/w) coating level of Eudragit FS 30 D and this polymer coating had no significant influence on the relative bioavailability of meloxicam of the pellets.

Animals↗

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

Scanning electron microscopy examination of 3 different adhesive systems.

OBJECTIVES: The aim of this study was to compare the interaction of dentin with 2 different self-etch resin bonding systems, as well as with a total-etch resin bonding system. METHOD AND MATERIALS: Nine recently extracted, unerupted third molars, roots, and occlusal thirds were used. A standardized smear layer was produced on the occlusal dentin surface exposed. The specimens were split into 3 groups of 3 specimens each, 1 group for each bonding agent: Clearfil Liner Bond 2, Prime & Bond 2.1, and Scotchbond Multipurpose (control group). After the tooth was briefly sprayed with an air/water mixture, 1 of the experimental adhesive systems was applied on the dentin surface. A 2-mm layer of composite was applied over the adhesive system layer. After 7 days in distilled water at 37 degrees C, the specimens were cross-sectioned perpendicular to the resin-dentin interface. The crosssections were mounted on aluminum stubs, etched with 2% hydrochloridric acid, and studied using scanning electron microscopy. A descriptive analysis of the images of the interdiffusion zone characteristics was done first. Afterwards, statistical analyses of the measurements of the interdiffusion zone structures-hybrid layer thickness, resin tags penetration, and adhesive layer thickness using analysis of variance, followed by "post hoc" test-were carried out to compare the bonding systems' interactions. RESULTS: The descriptive analysis of the self-etch bonding systems studied showed a good interlocking of Clearfil Liner Bond 2 with dentin, similar to Scotchbond Multipurpose and better than Prime & Bond 2.1. The analysis of variance, followed by the "post hoc" test, identified statistical differences just for the adhesive layer thickness that was thicker for Scotchbond than for Prime & Bond (P = .020). The "post hoc" test also showed a strong tendency to identify differences between the Scotchbond and the Prime & Bond groups (P = .062), and the Clearfil and the Prime & Bond groups (P = .069). CONCLUSION: Within the limitations of this study, Clearfil Liner Bond 2 produced the thickest hybrid layer with deepest tag formation and good interlocking with dentin, similar to the control. Statistical differences among the interdiffusion zone of the 3 bonding systems studied were identified just for the adhesive layer thickness, which was thicker for Scotchbond than for Prime & Bond.

Acetone↗

PubMed2005

Removal and pre-concentration of phenolic species onto beta-cyclodextrin modified poly(hydroxyethylmethacrylate-ethyleneglycoldimethacrylate) microbeads.

Poly(Hydroxyethylmethacrylate-Ethyleneglycoldimethacrylate), poly(HEMA-EGDMA), microbeads with 150-200 microm in size, was prepared by suspension polymerization. Beta-cyclodextrin was modified onto the polymeric microbeads using glutaraldahyde activation in an acidic medium at pH=2.5. FT-IR and TGA were used for the characterization of modified polymers and the determination of the nature of the interaction between phenolic compounds and the modified polymeric microbeads. Plain and beta-cyclodextrin modified microbeads were used in adsorption-desorption studies of phenolic species in single solution. Adsorption capacities of the phenolic species onto the plain microbeads were found to be 28.2, 17.0, 14.3, 9.8, and 1.92 mg/g polymer for o-chloro phenol, p-nitro phenol, p-chloro phenol, o-nitro phenol, and phenol, respectively. However, for beta-cyclodextrin modified microbeads, adsorption capacity of phenolic species was determined as 274, 365, 128, 182, and 87 mg/g for phenol, o-nitro phenol, p-nitro phenol, o-chloro phenol, and p-chloro phenol, respectively. Desorption ratio for the phenolic species was more than 90%, except for o-nitro phenol. Detection limits of the phenolic species were improved at least 500-fold for UV-Vis spectrophotometric detection, after the pre-concentration of all phenolic species used in this study. Adsorption time for the phenolic species onto beta-cyclodextrin-modified poly(HEMA-EGDMA) microbeads was found to be reasonable short (10-60 min) and suitable for the applications. Also, synthesized microbeads were useful for the repeated use for the removal and pre-concentration of phenolic species.

Adsorption↗

PubMed2000

A pH-dependent colon-targeted oral drug delivery system using methacrylic acid copolymers. II. Manipulation of drug release using Eudragit L100 and Eudragit S100 combinations.

Tablets containing mesalazine as a model drug were coated using various combinations of two methacrylic acid copolymers, (Eudragit L100 and Eudragit S100) by spraying from aqueous systems. The Eudragit L100-Eudragit S100 (w/w) combinations studied were 1:0, 4:1, 3:2, 1:1, 2:3, 1:4, 1:5, and 0:1. The coated tablets were tested in vitro for their suitability for pH-dependent colon-targeted oral drug delivery. The dissolution profiles of the drug obtained from the studied tablets demonstrate that the release of the drug could be manipulated by changing the Eudragit L100-Eudragit S100 ratios in the combinations within the pH range between 6.0 and 7.0 in which the individual polymers are soluble, and a coating formulation consisting of a combination of the two polymers can overcome the issue of high gastrointestinal (GI) pH variability among individuals. The results also demonstrate the feasibility of using aqueous dispersions of Eudragit L100-Eudragit S100 combinations for coating tablets for colon-targeted delivery of drugs, and that the formulation can be adjusted to deliver drug(s) at any other desirable site of the intestinal region of the GI tract in which pH of the fluid is within the range 6.0 to 7.0. For colon-targeted delivery of drugs, the proposed combination system is superior to tablets coated with either Eudragit L100 or Eudragit S100 alone.

Administration, Oral↗

PubMed2001

Effects of adhesive composition on microtensile bond strength to human dentin.

PURPOSE: To evaluate the role of adhesive composition (solvent and filler content) on microtensile bond strength (muTBS) to human dentin. MATERIALS AND METHODS: 15 third molars were ground to expose superficial dentin, which was polished to 600-grit. The dentin was etched for 15 s with 37.5% phosphoric acid, rinsed, and blotted with tissue paper. The surface remained visibly moist for all specimens. The following adhesives were applied to the etched dentin according to manufacturers' directions: Single Bond (SB), experimental Single Bond (with filler) (ExpSB), Prime & Bond NT (NT), experimental Prime & Bond NT (without nanofiller) (ExpNT), and One Coat Bond (with filler) (OC). Each adhesive was applied to three teeth, and a cylinder of resin-based composite was built up on the occlusal surface. After 24-hour water storage, each tooth was vertically sectioned with a low-speed saw to produce a series of 0.7 mm slabs. Each slab was then sectioned to obtain "sticks" with a cross-sectional area ranging from 0.35 to 0.45 mm2. muTBS were determined using an Instron universal testing machine. Data were analyzed using one-way ANOVA, and Duncan's test. RESULTS: For filled adhesives, mean bond strengths ranged from 57.9 MPa for ExpSB to 48.2 MPa for NT. The unfilled adhesives SB and ExpNT had mean bond strengths of 75.9 MPa and 38.7 MPa, respectively. Unfilled SB had a significantly higher mean bond strength than the experimental filled version. The ethanol-based adhesive SB had a significantly higher mean bond strength than either the nonvolatile solvent-based OC or the acetone-based NT.

Acetone↗

PubMed1998

Immortalized mouse odontoblast cell line MO6-G3 application for in vitro biocompatibility testing.

PURPOSE: This study was designed to determine the usefulness of an established stable immortalized mouse odontoblast cell line (MO6-G3) for dental material biocompatibility testing. Using a standard toxicity assay based on cell respiratory activity, the response to MO6-G3 cells was compared to the mouse fibroblastic cell line, L929, presently used for dental materials testing. The dental resin monomer TEGDMA was used as the dental material for the assay. MATERIALS AND METHODS: Cell lines (1 x 10(3)/well) were plated in 96 well culture plates and grown in DMEM supplemented with 10% FCS, 100 units/ml each of penicillin and streptomycin, and 50 micrograms/ml ascorbic acid in an atmosphere of 95% air and 5% CO2. Cells were exposed to TEGDMA resin monomer covering a dose range of 1 x 10(-6) to 0.5 x 10(-3) M. Unexposed control cells, as well as cells exposed to the DMSO vehicle in which the TEGDMA was dissolved, were included in all assays. Cytotoxicity was evaluated by determining cell respiratory activity spectrophotometrically using the tetrazolium compound WST-1. RESULTS: Statistical analysis by ANOVA using Tukey's method for pair wise comparisons as the post hoc test indicated toxic effects of TEGDMA at 1 x 10(-5) M in the odontoblast cell line MO6-G3. By contrast, the monomer produced no toxic effects on the L929 fibroblast cell line after 24 hours of exposure, over the entire concentration range tested. Furthermore, MO6-G3 cells exposed to a concentration of 0.5 x 10(-3) M were unable to recover from the effects of the exposure 48 hours after removal of the resin. MO6-G3 cells exposed to 1 x 10(-4) and 0.5 x 10(-4) TEGDMA recovered 40-50% and 75-80% of control respiratory activity respectively, 48 hours after removal of the resin. Respiratory activity by L929 cells exposed to all TEGDMA concentrations tested was not different from the vehicle control 48 hours after removal of the resin.

Analysis of Variance↗

PubMed1992

Effect of loading on swelling-controlled drug release from hydrophobic polyelectrolyte gel beads.

The effect of oxprenolol HCl loading on the kinetics of polymer swelling and drug release from suspension-polymerized poly(methyl methacrylate-co-methacrylic acid) (PMMA/MAA) beads has been studied in detail. Within the range of variables studied, the polymer swelling rate increases with buffer pH and concentration. And an ionization-controlled swelling mechanism (analogous to the relaxation-controlled mechanism) mechanism) seems to become more rate-limiting at higher buffer concentrations. At oxprenolol HCL loading levels below 17.8%, the drug release and associated dimensional changes (in pH 7.4) exhibit an extended quasi-linear region despite the inherent limitation of spherical geometry. At higher loading levels, the drug release becomes faster and first-order in nature. This is apparently a result of the transition from a dissolved to a dispersed system above a percolation threshold (15-18% loading in the present study). As a result of competition from processes such as the reduction of bead dimension due to drug release and the dimensional increase due to polymer swelling and osmotic contributions from the drug, the transient bead diameter increases monotonically during drug release at loading levels up to 25.6%, whereas upon further increasing the drug loading, the bead diameter goes through a maximum during the early drug release, which eventually increases again as a result of the slow but continuous increase in polymer swelling due to further ionization. In all cases, both the drug release and the dimensional changes approach completion as the penetrating ionization fronts meet at the center, indicating a true swelling-controlled behavior.

Buffers↗

PubMed1998

Effect of polymerization mode on bond strengths of resin adhesive/cement systems.

PURPOSE: The purpose of this study was to examine the effect of resin adhesive/cement system primer and cement polymerization mode (auto- vs dual-polymerized) on the shear bond strength to dentin. MATERIALS AND METHODS: Dentin surfaces of 90 bovine teeth were polished to 600 grit. The dentin was etched for 15 seconds with phosphoric acid, rinsed, and blotted. Three adhesive systems, All-Bond 2, Prime & Bond 2.1 Dual-Cure, or Scotchbond Multi-Purpose Plus, were applied. Three primer polymerization methods were used with each system: dual-polymerized, autopolymerized, or strictly following manufacturers' recommendations. Resin cements, which were also either auto- or dual-polymerized, were applied to dentin using gelatin capsules. Shear bond strengths were determined using an Instron universal testing machine. RESULTS: The greatest bond strength, 15.4 MPa, was found with the Scotchbond system when the primer was dual-polymerized and the cement was autopolymerized. The lowest bond strength, 7.5 MPa, was found with All-Bond 2/Duo-Link, when the primer and cement were dual-polymerized. The autopolymerization mode produced the highest mean bond strength for All-Bond 2, while dual-polymerization of primer and cement resulted in the highest mean bond strength for Prime & Bond 2.1. Scotchbond Multi-Purpose Plus was least affected by the polymerization method. Two-way ANOVA showed that the interaction between the type of adhesive system and the method of polymerization significantly influenced bond strength (p = .0001). CONCLUSIONS: The effect of the primer polymerization method on ultimate bond strength was different for each adhesive system evaluated. More research is needed to elucidate the interaction between adhesive system and method of polymerization on bonding of resin cements to dentin.

Animals↗

PubMed1993

Mechanism of cytoplasmic calcium changes in platelets in contact with polystyrene and poly(acrylamide-co-methacrylic acid) surfaces.

Changes in cytoplasmic free calcium levels ([Ca2+]i) in platelets in contact with polystyrene (PSt) and poly(acrylamide-co-methacrylic acid) (PAAmMAc) particles were evaluated and results were compared with those from two representative biological calcium agonists; thrombin and calcium ionophore A23187. PSt particles stimulated a steep increase in cytoplasmic calcium levels in platelets as much as thrombin and A23187. Serratia protease-treated platelets showed a steep increase in [Ca2+]i by PSt particles, suggesting that PSt surfaces can initiate platelet activation independent of a glycoprotein Ib (GPIb)-mediated pathway. By contrast, dibucaine-treated platelets showed little increase in [Ca2+]i by PSt particles, indicating that microfilament assembly, including binding of GPIb with actin binding protein, should be required for platelet activation in contact with PSt surfaces. PAAmMAc particles induced little increase in cytoplasmic calcium levels in platelets. However, PAAmMAc particle-treated platelets demonstrated little response to thrombin in terms of an increase in [Ca2+]i and ATP release, suggesting the possibility that PAAmMAc surfaces may regulate [Ca2+]i by influencing platelet metabolism. Furthermore, sodium azide-treated platelets showed an increase in [Ca2+]i in platelets when contacting PAAmMAc particles, supporting the suggestion that PAAmMAc surfaces could regulate platelet functions. Fluorescence polarization measurements using 1,6-diphenyl-1,3,5-hexatriene-loaded platelets revealed that PAAmMAc particles increased membrane fluidity in platelets, which may be due to physicochemical interaction with PAAmMAc surfaces.

Acrylic Resins↗

PubMed2000

Shear bond strengths of one-bottle adhesives to oil-contaminated enamel.

PURPOSE: To evaluate resin bond strength to enamel contaminated with handpiece oil. MATERIALS AND METHODS: Bovine teeth were randomly assigned to six groups of 20 teeth each for treatment with one of six different bonding systems (five one-bottle and one multibottle). For each system, 10 enamel specimens were contaminated with handpiece oil before acid-etching and 10 were contaminated after acid-etching. The enamel was etched for 15 seconds using 35% phosphoric acid. Following adhesive application, composite resin was bonded using a gelatin capsule technique. Shear bond strengths from the two contaminated groups were compared to bond strengths to uncontaminated enamel obtained from a previous study that was performed by the same group of investigators, using the same facility, materials, and methods. RESULTS: Two-way analysis of variance (ANOVA) showed that the factor "surface contamination" did not have a significant effect on bond strength (p > .542). The type of adhesive and the interaction of adhesive and surface contamination were significant (p < .0001 and p < .003, respectively). When oil was applied before etching, mean bond strengths ranged from 18.0 +/- 4.8 MPa for OptiBond SOLO (Kerr Corp., Orange, California) to 25.3 +/- 5.6 MPa for Tenure Quik with Fluoride (Den-Mat Corp., Santa Maria, California). With oil applied after etching, bond strengths ranged from 18.4 +/- 8.0 MPa for Tenure Quik with Fluoride to 27.4 +/- 5.4 MPa for Single Bond (3M Dental Products, St. Paul, Minnesota). For the same adhesive, comparing uncontaminated and "oil-before-etch" contaminated groups, the only statistically significant difference in bond strengths was for OptiBond SOLO: 21.8 +/- 4.0 MPa (uncontaminated) versus 18.0 +/- 4.8 MPa (oil before etch). Comparing uncontaminated and "oil-after-etch" groups, the only statistically significant difference was for Tenure: 24.5 +/- 5.7 MPa (uncontaminated) and 18.4 +/- 8.0 MPa (oil after etch).

Analysis of Variance↗