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Query: UMLS:C0001511 (Adhesion)
 5,955 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Adhesion durability between dentin pretreated with 10-3 and 4-META/MMA-TBB resin was studied. Reduction of etching periods with 10-3 was not so effective as expected. The weakening of bond strength during immersion in water at 37 degrees C to the dentin pretreated for 1 sec occurred faster than those for either 5 sec or 10 sec. The strength decreased from 12 MPa at 1 day to 9 MPa at 3 months, 3 MPa at 6 months and finally 2 MPa at 1 year in the case of 1 sec pretreated dentin. On the other hand, the strength became half after the storage in water for 1 year in the cases of 5 and 10 sec pretreated dentins. Combination of 10-3 pretreatment and subsequent glutaraldehyde treatment could stabilize the decrease but not completely. SEM and TEM examinations suggested that dentinal collagen exposed by the etching but not entangled and impregnated by poly (4-META-co-MMA) easily deteriorated by water during the longer immersion. Collagen modified with 10-3 and then with glutaraldehyde was also changed by the longer immersion.
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PMID:[Durability of bonding between 4-META/MMA-TBB resin to dentin pretreated with 10-3. The effect of 10-3 pretreating period and subsequent glutaraldehyde treatment]. 213 46

Adhesion between dentin and MMA resin was investigated using chemically activated initiator system consisting of 1,3,5-trimethyl-2-thiobarbituric acid, cupric salt, chloride ion, and tert.-butyl peroxymaleic acid (MA) with carboxyl group which usually has affinity to tooth. The adhesive strength of the MMA/PMMA resin to bovine dentin increased significantly to 8-10 MPa by addition of MA, while the adhesive strength was 4 MPa without MA. When the bonding broke at higher than 7 MPa, the adhesive resin layer usually fractured cohesively and the interfacial fracture did not occur. The bond strength obtained in this experiment was comparable to that obtained with MMA resin using TBBO and ferric ion initiator system which is known as the best initiator system for dentin available.
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PMID:[New low temperature initiator system for dental adhesive resins. Application of peroxyesters with carboxyl group]. 213 49

Adhesion of coagulase-negative staphylococci (CNS) was studied onto a homologous series of methacrylate polymers and copolymers. The materials varied in wettability (contact angles) and were either positively or negatively charged (zeta-potential). Bacterial adhesion experiments performed in a parallel-plate perfusion system showed that positively charged TMAEMA-Cl copolymers significantly promoted the adhesion of CNS as compared with all other methacrylate (co)polymers tested. The bacterial adhesion rates onto the positively charged surfaces are diffusion-controlled, whereas those onto the surfaces with a negative zeta-potential are more surface-reaction-controlled due to the presence of a potential energy barrier. The bacterial adhesion rates onto various poly (alkyl methacrylates) were similar. The number of adhering bacteria onto the negatively charged MMA/MAA copolymer did not differ from that onto pMMA, indicating that sufficient sites on the copolymer surface with the same potential energy barrier as that on pMMA, were available for adhesion. Decreasing rates of adhesion of CNS were observed onto MMA/HEMA copolymers with increasing HEMA content coinciding with increasing hydrophilicity. Low plateau values for the bacterial adhesion were observed on 50MMA/50HEMA, pHEMA, and 85HEMA/15MAA, indicating that the adhesion onto these materials was reversible. Four CNS strains with different surface characteristics all showed higher numbers of adhering bacteria onto 85MMA/15TMAEMA-Cl than onto 85MMA/15MAA and pMMA.
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PMID:Adhesion of coagulase-negative staphylococci to methacrylate polymers and copolymers. 370 Apr 46

Adhesion promoting monomers for dental metals, 5-(4-vinylbenzyl)-2-thiobarbituric acid (5VS), 6- (4-vinylbenzyl-n-propyl) amino-1,3,5-triazine-2,4-dithione (VBATDT) and 9,10-epithiodecyl methacrylate (EP8MA), were synthesized and surface treatment agents were prepared by dissolving each monomer in ethanol or acetone. Four non-precious and three precious metal adherends treated with each agent were butt-jointed together with MMA-PMMA resins. After 2,000 thermal cyclings in water, tensile bond strengths were measured and the percentage of area of cohesive failure after the tensile test was determined. The bond strengths to precious metal alloys generally increased in the order of 5VS<VBATDT<EP8MA. Bonding durability against water based on overall failure mode analysis was improved in the following order: for precious metal alloys; 5VS<VBATDT< or =EP 8MA, and for non-precious metal alloys; EP8MA, VBATDT<<5VS.
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PMID:Chemical structures of adhesion promoting monomers for precious metals and their bond strengths to dental metals. 1462 Oct

Adhesion promoting monomers -5-(4-vinylbenzyl)-2-thiobarbituric acid (5VS), 9,10-epithiodecyl methacrylate (EP8MA), 9,10-epithiodecyl 4-vinylbenzoate (EP8VB), and 3,4-epithiobutyl 2,2-bis(methacryloyloxymethyl)propionate (EP2BMA)--were added to the MMA liquid of a MMA-PMMA/TBBO resin. Three dental precious metal alloys were butt-jointed together with the MMA-PMMA/TBBO adhesive resin, and tensile bond strength was measured after 2,000 thermocycles in water. Polymerization kinetics of MMA by 2,2'-azobis (isobutyronitrile) at 70 degrees C in the presence of 5VS, EP8MA, EP8VB, or EP2BMA were examined quantitatively using a DSC to clarify the relationship between the adhesive properties of MMA-PMMA/TBBO adhesive resin and the kinetic polymerization behavior thereof. Obtained kinetic parameters indicated that 5VS was not suitable as an adhesive monomer for adhesive resin formulations and that EP2BMA possessed the latent potential as an adhesive monomer. Further, tensile test results revealed the applicability of EP8MA, EP8VB, and EP2BMA as an adhesive monomer component of adhesive resin formulations.
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PMID:Adhesive properties and kinetic polymerization behavior of resins containing adhesion promoting monomers for precious metals. 1627 23

Adhesion promoting monomers for precious metals, 2,3-epithiopropyl methacrylate (EP1MA), 4,5-epithiopentyl methacrylate (EP3MA), 9,10-epithiodecyl methacrylate (EP8MA), 10,11-epithioundecyl methacrylate (EP9MA), 9,10-epithiodecyl 4-vinylbenzoate (EP8VB), 2,3-epithiocyclohexyl methacrylate (EPCHMA), and 3,4-epithiobutyl 2,2-bis(methacryloyloxymethyl)-propionate (EP2BMA), were used as surface treatment agents for pure gold to improve the durability of resin bonds against water. Treated specimens were butt-jointed together with MMA-PMMA resins, and tensile bond strength was measured after 2,000 thermal cycles in water. Bond strength to precious metal alloys was also determined under the same condition to clarify the influence of metal composition. The adhesion performance of thiirane monomers to pure gold highly depended on their chemical structure. EP3MA, EP8MA, EP9MA, EP8VB, and EP2BMA showed excellent performance, while EP1MA exhibited a moderate one and EPCHMA a poor one. The comparison of pure gold with precious metal alloys revealed the usefulness of pure gold as a standard, common adherend for bond strength evaluations.
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PMID:Water durability of resin bond to pure gold treated with various adhesion promoting thiirane monomers. 1741 Aug 90