An optimal concentration of phosphoric acid as an etching agent. Part II: Microleakage studies.
Explore the source record for details and available documents.
SEARCH · Search PubMed
Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
The growing proportion of older Americans and the projections in declining edentulousness in future cohorts of elderly necessitate elucidation of the responses of the aging human dentition to existing restorative techniques. This study investigated the results of the acid etch process as a function of age of specimen donors as well as a function of race, tooth type, and time between extraction and etch. Statistical analysis of data showed no significant effect on solubility by age, race, or length of time from extraction until etch. Molars were significantly less soluble than other teeth. The most frequently observed microscopic texture was an irregular, granular configuration termed 3g. Widely textural variation was observed in each specimen. A possible explanation for the observations is the distribution of prismless enamel. The widespread belief that older teeth are less efficaciously etched may be based on the greater frequency of composite restoration failures in the elderly, which in turn is more likely a factor of restoration size and changes in intraoral environment than of age.
STATEMENT OF PROBLEM: "Compomers" are being used with increasing frequency in Europe and North America. PURPOSE: This study evaluated the marginal seal of two compomers in vivo. MATERIAL AND METHODS: Periodontally involved teeth, scheduled for extraction, were selected. Four groups of a combination of materials were used (Dyract with Dyract-PSA primer, group 1; Dyract with Prime and Bond 2.0, group 2; Compoglass with SCA primer, group 3; and Compoglass with Syntac Single Component, group 4). The restorations were made in a standardized shaped cavity, across the cementoenamel junction, and the teeth were extracted after 2 to 3 months of clinical service. The specimens were kept in a solution of 2% methylene blue for 24 hours. After being embedded in epoxy resin, sections were made with a low speed saw along the longitudinal axis of the teeth. The examination of dye penetration was made with a microscope at a magnification of x20 and scoring was done at both coronal and apical sites. Kruskal-Wallis statistical analysis was performed at 5% significance level. RESULTS: Groups 2 and 4 scored significantly less than groups 1 and 3 and for groups 2 and 4, 30% of the restorations exhibited leakage. CONCLUSION: These restoration systems did not completely prevent leakage either at the incisal or the cervical margins. Therefore the use of an enamel-dentin bonding system in combination with the proprietary compomer is recommended.
The etching effect of 50% H-3PO-4 applied together with 2% NaF or SnF-2 was compared with the effect of H-3PO-4 on pre- and postfluoridated enamel by scanning electron microscopy. Substantial etching of enamel resulted with use of 50% H-3PO-4 with 2% NaF. High fluoride incorporation in the surface provided additional protection of the conditioned enamel.
The pretreatment of corn stover with H2SO4 and H3PO4 was investigated. Pretreatments were carried out from 30 to 120 min in a batch reactor at 121 degrees C, with acid concentrations ranging from 0 to 2% (w/v) at a solid concentration of 5% (w/v). Pretreated corn stover was washed with distilled water until the filtrate was adjusted to pH 7.0, followed by surfactant swelling of the cellulosic fraction in a 0-10% (w/v) solution of Tween-80 at room temperature for 12 h. The dilute acid treatment proved to be a very effective method in terms of hemicellulose recovery and cellulose digestibility. Hemicellulose recovery was 62-90%, and enzymatic digestibility of the cellulose that remained in the solid was >80% with 2% (w/v) acid. In all cases studied, the performance of H2SO4 pretreatment (hemicellulose recovery and cellulose digestibility) was significantly better than obtained with H3PO4. Enzymatic hydrolysis was more effective using surfactant than without it, producing 10-20% more sugar. Furthermore, digestibility was investigated as a function of hemicellulose removal. It was found that digestibility was more directly related to hemicellulose removal than to delignification.
We report the first case of a pharmaceutical cocrystal formed between an inorganic acid and an active pharmaceutical ingredient (API), which enabled us to develop a stable crystalline and bioavailable solid dosage form for pharmaceutical development where otherwise only unstable amorphous free form or salts could have been used.
To develop a new surface treatment agent which improves the bond strength of adhesive resin to both non-precious and precious metals, experimental treatment agents containing both an adhesive bonding promoter for precious metals and one for non-precious metals were prepared by dissolving epithioalkyl methacrylate (EP3MA or EP8MA) and 10-methacryloyloxydecyl dihydrogen phosphate (MDP) in acetone. The surfaces of dental metals were treated by the treatment agents and metal specimens were butt-jointed together with MMA-PMMA resins. After 2,000 thermal cyclings in water at temperatures of 4 and 60 degrees C, tensile bond strengths were measured. The effectiveness of surface treatments was evaluated by tensile bond strengths and microscopic failure mode analysis after the tensile test. The combined treatment of EP3MA-MDP or EP8MA-MDP was used effectively for non-precious metals as well as precious metals, and was shown to be extremely effective compared with the single treatment of EP3MA, EP8MA, or MDP.
A membrane-assisted solvent extraction (MASE) method is presented for the extraction of several non-ionic organophosphorus chemicals from wastewaters samples followed by LC-MS/MS determination. The method was developed for a variety of chlorinated phosphates (trichloroethyl, tichloropropyl) and non-chlorinated phosphates (triphenyl, tributyl) used as flame retardants and for plasticizers such as triethylhexyl and tris-butoxyethyl phosphate. Parameters such as extracting solvent, sample volume and ionic strength, extraction temperature and time were optimized. The final method provides good quantification limits (1-25 ng L(-1)) and linearity (R2>0.9978). Method precision was also good at high concentrations (5% mean RSD at the 500 ng L(-1) level) but decreased at lower concentrations (20% mean RSD at the 20 ng L(-1) level). MASE yields lower matrix effects than SPE in a successive LC-MS/MS analysis of these compounds, avoiding the need for standard addition for quantification. When applied to wastewater samples comparable results were obtained using either MASE with internal standard calibration or SPE with standard addition.