PubMed Health⌕ Search

PubMed · 1805028

Clinical correlations of dentin structure and function.

Abstract

Dentin, a porous, fluid-filled mineralized tissue, may provide critical mechanical support to overlying enamel. Once the enamel or cementum surface seals are lost by disease or trauma, the same organization that provided critical mechanical support then becomes a liability, offering millions of fluid-filled diffusion channels from the periphery directly to the pulp. If restorative materials placed in cavities do not seal the dentin, there is a fluid-filled continuum from the cavosurface margins, around gaps between the restorative material and the tooth, to dentin surfaces, then through dentin via its tubules to the pulp. Under most conditions these channels permit bidirectional diffusion of exogenous and endogenous substances across dentin. Occasionally, hydrodynamic stimuli will produce transient, rapid movement of dentinal fluid that will induce pain. The tubules are sometimes so close together in deep dentin that their intrinsic wetness interferes with the bonding of adhesive resins. This permits the formation of gaps, microleakage, dentin sensitivity, and, occasionally, pulpal irritation. Many clinical problems such as poor dentin bonding, microleakage, dentin sensitivity, and pulpal irritation have a common denominator in the structure and function of dentin.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

D H Pashley. 1991. Clinical correlations of dentin structure and function.. https://doi.org/10.1016/0022-3913(91)90414-r

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Interphase effects in dental nanocomposites investigated by small-angle neutron scattering.

Small-angle and ultrasmall-angle neutron scattering (SANS and USANS) were used to characterize silica nanoparticle dispersion morphologies and the interphase in thermoset dimethacrylate polymer nanocomposites. Silica nanoparticle fillers were silanized with varying mass ratios of 3-methacryloxypropyltrimethoxysilane (MPTMS), a silane that interacts with the matrix through covalent and H-bonding, and n-octyltrimethoxysilane (OTMS), a silane that interacts through weak dispersion forces. Interphases with high OTMS mass fractions were found to be fractally rough with fractal dimensions, D(s), between 2.19 and 2.49. This roughness was associated with poor interfacial adhesion and inferior mechanical properties. Mean interparticle distances calculated for composites containing 10 mass % and 25 mass % silica suggest that the nanoparticles treated with more MPTMS than OTMS may be better dispersed than OTMS-rich nanoparticles. The results indicate that the covalent bonding and H-bonding of MPTMS-rich nanoparticles with the matrix are necessary for preparing well-dispersed nanocomposites. In addition, interphases containing equal masses of MPTMS and OTMS may yield composites with overall optimal properties. Finally, the combined SANS/USANS data could distinguish the differences, as a function of silane chemistry, in the nanoparticle/silane and silane/matrix interfaces that affect the overall mechanical properties of the composites.

Dental Materials↗

Size control of silica nanoparticles and their surface treatment for fabrication of dental nanocomposites.

Nearly monodispersed silica nanoparticles having a controlled size from 5 to 450 nm were synthesized via a sol-gel process, and then the optimum conditions for the surface treatment of the synthesized silica nanoparticles with a silane coupling agent (i.e., 3-methacryloxypropyltrimethoxysilane (gamma-MPS)) were explored to produce dental composites exhibiting enhanced adhesion and dispersion of silica nanoparticles in the resin matrix. The particle size was increased by increasing amounts of the catalyst (NH4OH) and silica precursor (tetraethylorthosilicate, TEOS) and by decreasing the amount of water in the reaction mixtures regardless of solvents used for the synthesis. The particle size prepared by using ethanol as a solvent was significantly larger than that prepared by using methanol as a solvent when the composition of the reaction mixture was fixed. The nanosized particles in the 5-25 nm range were aggregated. The amount of grafted gamma-MPS on the surface of the synthesized silica nanoparticles was dependent on the composition of the reaction mixture when an excess amount of gamma-MPS was used. When surface treatment was performed at optimum conditions found here, the amount of the grafted gamma-MPS per unit surface area of the silica nanoparticles was nearly the same regardless of the particle size. Dispersion of the silica particles in the resin matrix and interfacial adhesion between silica particles and resin matrix were enhanced when surface treated silica nanoparticles were used for preparing dental nanocomposites.

Dental Materials↗