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Biomedical subjects

G C Paffenbarger

Publications and source records attributed to G C Paffenbarger.

At least 19 recordsLinked to original sources

Discoloration of dental cements and composites in a sulfide solution.

In an early study the discoloration of certain hardened silicate cements, after exposure to an atmosphere of hydrogen sulfide (H2S) for 24 h at room temperature, was ascribed to the formation of dark-colored sulfides of base metal impurities (Paffenbarger et al. JADA 25,32,1938). A recent study noted that, in general, silicate and glass ionomer cements were more prone to color shifts than composites after exposure to H2S for 9 weeks (Sugawara, Ph. D. Thesis, Nihon Univ.). The aim of the present study was to devise a simple, aqueous sulfide exposure test for esthetic restorative materials. The general procedure was to expose specimen disks to a 0.1% (w/v) sodium sulfide solution, adjusted to pH 9, for 1-7 days at 37 degrees or 55 degrees C. The 55 degrees C-Na2S exposure was designed as an accelerated test. Materials studied included: 1 silicate and 2 silicophosphate cements of known lead content, a glass ionomer cement (FIIF), several commercial composites and an experimental, hydrophilic composite. Known amounts of base metal contaminants in the form of appropriate salt solutions were added to the liquid components of FIIF and the composites. Specimens exposed to distilled water under the same conditions served as controls. Exposure to the aqueous sulfide medium resulted in the following ranking in order of decreasing discoloration: Glass ionomer cement greater than silicophosphate cement greater than silicate cement greater than hydrophilic composite greater than hydrophobic composite. Generally, the results of the aq. Na2S test paralleled those obtained with H2S. The degree of discoloration is dependent on a number of factors: the nature, concentration and leachability of the metal impurities, and the hydrophilicity and permeability to sulfide of the esthetic restoratives.

Chlorides↗

Detection of lead in human teeth by exposure to aqueous sulfide solutions.

A recent study has shown that the presence of lead (Pb) as well as other base metals in esthetic restorative materials, especially dental cements, is detectable by color shifts induced by exposure of hardened specimens to a 0.1% (w/v) aqueous solution of sodium sulfide, Na2S. The present study was initiated to determine the applicability of this simple exposure test to the detection of Pb in human teeth. Extracted whole teeth as well as sectioned, thin specimens were exposed first to either a 0.01% or a 0.001% (w/v) aqueous solution of lead nitrate, Pb (NO3)2, at 37 degrees C for 24 h. After rinsing with distilled H2O and a subsequent 24 h exposure to the 0.1% Na2S solution at 37 degrees C, the tooth specimens were examined visually and by a dental color analyzer for color changes. The latter color measurements were evaluated by the Lab system of Hunter, and the color difference, delta E, was determined. Neither control specimens exposed to distilled H2O only or to 0.1% Na2S only exhibited any significant change in appearance after 24 h of storage at 37 degrees C. However, specimens exposed first to the Pb (NO3)2 solutions showed discernible delta E values after exposure to the Na2S solution. Delta E was greatest for specimens exposed to the more concentrated Pb (NO3)2 solution. Most of the discoloration in both thin and intact tooth specimens was confined to the outermost layers of the tooth structure. For the intact specimens, the greatest degree of discoloration occurred in the cementum, the most permeable part of the tooth structure.

Adult↗

Dental research at the National Bureau of Standards: how it changed the practice of dental health service.

A history of dental research at the National Bureau of Standards since its inception in 1919 is presented. The initial thrust on dental amalgam by the US Army Dental Corps, the assignment of Dr. William Souder to the project, and subsequent developments are traced. Difficulties in obtaining support for the early stages of the program following World War I are described. The involvement of the American Dental Association in 1928, issuance of the first ADA specification on dental amalgam, and the ultimate ramifications on dental (and medical) standards programs throughout the world are described. Benefits to patients, dentists, and taxpayers from support of the dental research program have been calculated as exceeding the combined budgets of the currently supporting institutions--NBS, ADA, and National Institute of Dental Research.

Chemistry, Physical↗

Dimensional changes of a high-tin content amalgam.

Amalgam made with Brewster Alloy (62% Ag, 33% Sn, 5% Cu, and 0.2% Zn) had little or no dimensional change during 24 h at 23 degrees C. Brewster amalgam stored for five yr in air expanded 186, 68, and 14 microns/cm at 60, 37, and 23 degrees C, respectively. Nearly "stable" conditions were approached at about 50 mo.

Chemical Phenomena↗

The role of zinc in dental amalgams.

Twenty-five AG-Sn alloys containing various additions of Zn were amalgamated and the amalgams tested for physical properties pertinent to dental restoration use. The mercury retained, dimensional change, compressive strength, and creep were all functions of the Zn content.

Corrosion↗

Effect of residual mercury content on creep in dental amalgams.

For most of the tested amalgams, the increased mercury content caused by delayed compaction increases the flow or creep. The amalgams that had high creep values when packed early were decidedly affected by the increase in mercury content caused by delay in compaction. Amalgams made with Dispersalloy, Tytin, Sybraloy, and New True Dentalloy are not as sensitive to the mercury content as are some of the others tested. Tests for creep may be related more to clinical practice if they are performed on specimens compacted three minutes after trituration rather than on specimens compacted immediately (a half minute) after trituration. In clinical practice, small amounts of amalgam should be mixed and used immediately after trituration. If the delay between trituration and compaction is longer than three minutes, additional mixes are required. We therefore conclude that, in making a large amalgam restoration, many small mixes have superior results over one large mix.

Chemical Phenomena↗

Linear dimensional change of copper-rich dental amalgam.

Copper-rich amalgams made from alloy mixtures have large expansions in air at 105 +/- 2 weeks that range from 100 to 194 micrometers/cm at 60 C, from 36 to 101 micrometers/cm at 37 C, and from 14 to 44 micrometers/cm at 23 C on unrestricted 8- x 4-mm cylinders (Dispersalloy, Micro II, and Optaloy II). Other copper-rich amalgams made from one alloy usually had a slight shrinkages at the three temperatures with an exception, a slight expansion of 12 micrometers/cm at 60 C (Aristaloy CR, Indilogy non-zinc, Sybraloy, and Tytin). Dimensional changes during hardening ranged,on the average, from -3 to +19 micrometers/cm when measured by ADA Specification methods and from -2 to +25 micrometers/cm when measured by an indirect method. The clinical significance of the foregoing findings is unknown; nor is a relationship known among dimensional change of unrestricted specimens, dimensional change of restricted specimens, creep value, and clinical behavior of amalgams generally. In specific instances, however, a relationship is sometimes shown.

Chemical Phenomena↗