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Biomedical subjects

H R Stanley

Publications and source records attributed to H R Stanley.

At least 19 recordsLinked to original sources

Local and systemic responses to dental composites and glass ionomers.

For many years, the dental profession worked mainly with rather inert restorative materials that had a limited contact with vital tissue, and the opportunity for local and systemic complications was minimal. However, conditions have changed in recent years where the two leading non-mercury-containing materials, resin composites and glass-ionomer cements, are chemically active compounds and can have detrimental effects on pulp tissue. With the advent of light-curing techniques with incremental layering, resin component formulae that were formerly found to be quite irritating to the pulp have become less so with the elimination of the need for matrices and pressure for good adaptation to be gained. As experience revealed the deficiencies and dangers of ultraviolet-light-curing techniques, visible-light-curing systems were developed that provided greater depth of cure, a higher degree of polymerization with less shrinkage with incremental layers, and less porosity. When glass-ionomer cements (GICs) were first introduced, with just one acid (polyacrylic), pulpal responses were classified as bland. With the addition of many more acids to enhance certain characteristics and reduce the setting time, GICs have become more irritating, especially when used as luting agents in areas where the remaining dentin thickness is 0.5 mm or less. Gold foil and amalgam are inert and innocuous restorative materials but require pressure for condensation which creates an exaggerated inflammatory response. This presentation emphasizes the pulpal responses and side-effects of these non-mercury-containing restorative materials and how to keep them within an acceptable range of biocompatibility. Despite the lack of any substantial appearance of soft tissue and systemic responses to resin composites and GICs, the results of a survey of recent literature are included.

Composite Resins

Pulp reactions to resin cements.

Several formulas of a resin-filled cement that successfully passed a series of laboratory tests were evaluated for their pulp reactions in primates. Their performance was compared to three controls: a positive control (silicate cement), a negative control (zinc oxide-eugenol) and a control group with the protection of calcium hydroxide. The chemical cure resin cement scored the lowest reactions for the 5-day evaluation. The intermediate and prolonged periods demonstrated no significant differences while average, acceptable responses were recorded. No resin cement formula scored as low as the negative control for the three time periods. Silicate cement, the positive control, scored the greatest inflammatory reaction of any material in the intermediate period, but this response was resolved after 60 days. When the resin cements were used with calcium hydroxide, the traditional reactions to calcium hydroxide were observed; an initial mild irritation that diminished with time and was completely resolved after 60 days. The resin cements, with or without the calcium hydroxide, compared favorably to the negative control IRM after 60 days. If the resin cements are appropriately applied, they are expected to be well tolerated by the human pulp. The microorganisms associated with microleakage (MLM) were minimal and there appeared to be no correlation between the MLM and pulp inflammation.

Analysis of Variance

Biological evaluation of dental materials.

Dental materials and devices are being treated more like drugs and now have to meet the safety and efficacy requirements of drugs and medical devices. Biocompatibility is the key word. The history of the development of controls, standards, and guidelines began almost 500 years ago and is detailed in a chronological fashion up to the present time. An outline of the latest revised draft of the international document (ISO Technical Report No. 7405), to be completed hopefully by 1993 in time for the harmonization of the European Standards within the EC, is presented. The types of tests (initial, secondary, and preclinical usage tests) are listed and described. No amount of experimental study can guarantee absolute safety for any substance. However, toxicological investigations provide data from which reasonable projections and predictions can be made about the conditions under which the product can be safely used. It is the intent that this Technical Report be reviewed regularly and revised, with the ultimate objective of converting it to an International Standard.

Animals

Biocompatibility of a glass ionomer luting agent. 2. Crown cementation.

In this experiment, 64 crown preparations were made in four primates. Final impressions, die fabrication, wax patterns and castings were achieved using conventional established clinical and laboratory techniques. Vented and unvented crowns were cemented with a glass ionomer cement (GI) and a zinc phosphate cement (ZOP). Some preparations were protected with calcium hydroxide liquid. On the same animals, in teeth not used for crowns, Class V cavities were prepared and GI and ZOP inserted by means of a pressure technique imitating hydraulic pressure generated during crown cementation. After periods of 5 and 60 days, the animals were sacrificed, the jaws dissected, fixed in formalin and prepared for histological evaluation. Of the 64 cemented crowns, one was unaccounted for. Of the unvented crowns with GI (5 days), vented crowns with GI (60 days), unvented crowns with ZOP (60 days), Class V with ZOP (5 days) and GI (60 days) with a remaining dentin thickness (RDT) of less than 1 mm, inflammatory responses of greater than or equal to 1 degree (on a scale 1-4 degrees) were observed. The use of liquid calcium hydroxide reduced the intensity of the reactions, in particular when small RDTs were present. It can be concluded that when RDTs of 1 mm or more were present, the cements in all groups were non-toxic. When it is estimated that the RDT is less than or equal to 1 mm, the use of a calcium hydroxide liner is recommended. Placement of luting agents in Class V preparations with pressure resulted in reactions resembling crown cementation.(ABSTRACT TRUNCATED AT 250 WORDS)

Analysis of Variance

Pulpal responses to ionomer cements--biological characteristics.

When glass ionomer cements were initially introduced, the pulpal responses were considered milder relative to other cements. However, the results mainly came from the application of glass ionomer cements as restorative materials. When ultimately tested with the basic laws of biocompatibility required of other cements, especially a luting agents, little difference has been shown. The judicious use of calcium hydroxide is highly recommended.

Biocompatible Materials

Human pulp response to a new composite system. Vytol composite restorative and bonding agent.

A new two-paste composite system (Vytol and Vytol Bonding Agent) was evaluated to establish its level of pulpal response in human teeth and to determine whether a calcium hydroxide base is required. Class V cavity preparations were cut in seventy-two teeth of ten male patients whose ages averaged 52.5 years. The teeth were restored and extracted at 1 to 7 days, 12 to 14 days, and 47 to 56 days. Histologic evaluation indicated that the unlined Vytol System reacted very similarly to other commercially available composite restorative materials and that a calcium hydroxide base is effective in reducing or eliminating adverse pulp responses.

Acid Etching, Dental

Direct pulp capping treatment: a long-term follow-up.

In reviewing 356 instances of pulp capping during the past 25 years, 149 cases were recalled with posttreatment intervals greater than five years. One hundred thirty teeth (87.3%) were still vital and functioning with an average posttreatment interval of 11.7 years. The criteria for pulp capping procedures are in need of revision. Restrictions based on tooth size and age of the patient are unfounded.

Adolescent

The implantation of natural tooth form bioglasses in baboons. A preliminary report.

This report describes a 6-month screening study comparing the tissue responses of several bioglass natural tooth implants in adult female baboons. The dental implants were designed to elicit osteogenesis at the interface of the implant and the oral tissues. This is in contrast to those types of implant materials that are merely biologically acceptable. Incisor teeth were extracted, dupplicated in bioglass, returned to the natural sockets, and splinted to the adjacent natural tooth, where they remained splinted for 3 months and then free standing for an additional 3 months. Microscopic evaluation revealed distinct histopathologic characteristics with certain bioglass formulas, such as ankylosis, a pseudofibrous capsule with fibers running parallel to the root surface, or an apparently true periodontal membrane with properly oriented Sharpey's fibers. True cementogenesis was not found.

Animals