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Biomedical subjects

M Marek

Publications and source records attributed to M Marek.

At least 37 records · Page 2Linked to original sources
PubMed1997

Connections between polarization curves and log(a[i]/a[ref])-pe diagram.

When reading papers concerning studies of corrosion of dental amalgam and its phases by means of polarization curves, one often finds it difficult to understand the reasons for the chemical reactions proposed from the form of the polarization curve. Thermodynamic data represented in the form of log(a[i]/a[ref])-pe diagrams, i.e., the logarithm of the activity of a metal or an alloy with reference to the activity of the corresponding metal ion, as a function of pe (a recalculated form of the potential), make it possible for one to determine which chemical reactions can occur on the specimen surface or in the solution within the potential difference used in the polarization experiment and to decide which of these reactions is the most probable. The hypothesis examined in this study is that a log(a[i]/a[ref])-pe diagram can be used in the interpretation of polarization curves. Potentiodynamic polarization curves and log(a[i]/a[ref])-pe diagrams were compared for the corrosion of Ag, Hg, and gamma 1 with and without Sn. It was found that there was a connection between the polarization curves and the log(a[i]/a[ref])-pe diagrams. From the composition of the specimens and the solution and by means of thermodynamic data, pe values for solid corrosion products and relative concentrations of soluble complexes at these pe values were obtained independently of the polarization curves. A much more reliable value for the nobility of metals and alloys was attained by use of the log(a[i]/a[ref])-pe diagrams than by use of the potential of the starting point of the polarization curves. It was found that pe corresponding to the potential of the starting point of the polarization curves in de-aerated synthetic saliva was obtained about two pe units before pe of the most insoluble solid compound formed on the specimen surface or in the solution.

Corrosion↗
PubMed1995

Effect of mercury on corrosion of eta' Cu-Sn phase in dental amalgams.

OBJECTIVES: The eta' Cu-Sn phase is the most corrosion-susceptible major component of the microstructure in high-copper dental amalgams, even though metallurgically prepared specimens of the phase are corrosion-resistant. The purpose of this study was to determine if mercury is the cause of the degradation. METHODS: Specimens of metallurgically prepared eta' Cu-Sn phase were tested in synthetic saliva using electrochemical methods. Mercury was adsorbed on the surface by exposure to mercury vapor, and the changes in the corrosion potential and anodic polarization characteristics were determined. Galvanic currents between eta' specimens and a high-copper dental amalgam were measured for both Hg-free and Hg-contaminated eta' electrodes. RESULTS: The Hg-free eta' phase showed a wide region of passivity. Exposure to mercury made the eta' phase electrochemically more active, and current peaks appeared on the polarization curves. The Hg-free eta' electrode was a cathode to a high-copper dental amalgam. The Hg-contaminated eta' electrode started also as a cathode, but became anode after a period of exposure. SIGNIFICANCE: It was concluded that mercury destabilizes the protective passive film on the eta' phase, making the phase more susceptible to corrosion in the oral environment. The results of the galvanic current measurements seem to indicate that the galvanic interaction between eta' and the other phases facilitates the mercury-related degradation.

Chemical Phenomena↗
PubMed1993

Influence of food deprivation on SCFA and electrolyte transport across sheep reticulorumen.

Net absorption rates for SCFA, sodium, chloride, magnesium, and water were measured in the temporarily isolated and washed reticulorumen of sheep. The animals were either fed hay ad lib. plus concentrates once daily or were deprived of food for two days. Food deprivation led to decreased net absorption of all the substances tested. Comparing the solutes, the relative decreases varied between 43% (butyrate) and 56% (acetate). The decrease in solute absorption was accompanied by diminished water absorption. It is concluded that the reduction in absorption may be beneficial for the animal in that energy consumption is diminished and the reservoir function of the forestomach will be maintained longer. However, the reduced absorptive capacity may lead to a deficiency of magnesium, which is thought to be absorbed mainly by the forestomachs.

Absorption↗
PubMed1993

The effect of the electrode potential on the release of mercury from dental amalgam.

The effect of the electrode potential on the rate of mercury dissolution from the matrix phase (gamma 1) of dental amalgam was investigated. Specimens of the Ag-Hg phase, with and without dissolved tin, were exposed to synthetic saliva and maintained at various potentials by means of a potentiostat. The amount of dissolved mercury was determined after 24 h by cold-vapor Atomic Absorption Spectrophotometry. Anodic polarization curves for the gamma 1 specimens and pure silver and mercury were also recorded. The results for the Ag-Hg phase showed a potential-independent dissolution rate between -0.6 and -0.1 V (SCE), followed by a sharp increase. Mercury dissolution from the Ag-Hg-Sn phase was much slower than from the tin-free gamma 1 phase, and potential-independent to +0.05 V (SCE); a sharp increase in mercury dissolution was observed at +0.1 V (SCE). The anodic polarization curves for the Ag-Hg-Sn phase indicated passivity between -0.67 V and +0.1 V (SCE), but no clear passivation for the Ag-Hg specimen, silver, or mercury. The results show that in the potential-independent region, mercury dissolved in the atomic form from both the tin-free and tin-containing gamma 1 phase. The increase in dissolution in the upper range of potentials was tentatively attributed to selective anodic dissolution of silver and an onset of electrochemical dissolution. The results indicate that the rate of mercury release from the gamma 1 phase of dental amalgam was not affected by potential changes due to alloying or galvanic contacts unless the potential exceeded some critical value.

Dental Amalgam↗
PubMed1992

Interactions between dental amalgams and the oral environment.

Dental amalgam fillings interact in a complex way with the environment in the oral cavity as they are subjected to chemical, biological, mechanical, and thermal forces. These forces change the restoration's appearance and properties, while metal ions, amalgam debris, non-metallic corrosion products, and mercury vapor are released into the oral cavity. The phenomena and conditions that affect the amalgam/environment interaction include the chemistry and biochemistry of the environment, formation of biofilms on the amalgam surfaces, existence of localized corrosion cells, galvanic contacts with other metallic restorations, abrasion during mastication, and synergistic effects of the different forces. Corrosion processes result in a degradation of the functional amalgam properties, while tarnishing reactions cause discoloration. Corrosion degradation of amalgam fillings is due mainly to localized corrosion cells in pores and crevices. Corrosion on occlusal surfaces is accelerated by abrasion during mastication, which removes the protective surface films. The average total amounts of metal species, including mercury, released per day in vivo from a restoration have not been determined. Much of the reported indirect evidence for high mercury release rates is either unreliable or controversial. A more detailed investigation is needed and will require the development of more sophisticated techniques of sampling in vivo, as well as both experimental and theoretical modeling in vitro.

Copper↗
PubMed1991

[A screening method for simultaneous immunochemical detection of aflatoxins and ochratoxin A in cereals and feed].

An immunochemical method was proposed for simultaneous determination of aflatoxin and ochratoxin A with the use of mixed solutions of the following reagents: standards of both mycotoxins, antiserums against the mycotoxins, and radioligands of 125I-aflatoxin B1 and 125I-ochratoxin A. The result of the analytical procedure is the value of concentration of the aflatoxin + ochratoxin A sum in the sample. The procedure needs half the amount of reagents as separate determination of each of the two mycotoxin, and is far less laborious. The proposed simultaneous immunoanalysis is suitable for large-are inspection of grain and feed safety from the viewpoint of aflatoxin and ochratoxin A levels.

Aflatoxins↗
PubMed1990

Corrosion behavior of Pd-Cu and Pd-Co alloys in synthetic saliva.

Pd-based alloys are major alternatives to gold-based alloys for PFM applications. In electrolytes simulating oral fluids, these alloys exhibit electrode behavior similar to passivity of active metals, i.e., a potential region of almost constant current density up to a critical potential, above which the current increases. The objective of this study was to correlate the electrode behavior with the results of solution analyses and changes in the surface composition of the alloys. Binary alloys Pd-15 wt% Cu and Pd-19 wt% Co, as well as the pure components, were examined. Corrosion potentials vs. time, potentiodynamic anodic polarization curves, polarization resistances vs. time, and potentiostatic anodic charges were measured with synthetic saliva used as the electrolyte. The concentrations of Pd, Cu, and Co in the solution after various exposures were determined by atomic absorption. The surfaces of the alloys were examined by x-ray photoelectron spectroscopy before and after the exposures. The results show that selective dissolution of the less-noble components occurred on the surfaces of both alloys for all the exposures, leaving the surfaces highly enriched in Pd. This enrichment contributed to the potential changes and the passive-type behavior. Copper dissolved more than cobalt at longer exposures and higher potentials, in spite of its higher nobility. Dissolution of cobalt seemed to be limited by the formation of a surface film, which may be related to the transition character of this element.

Cobalt↗
PubMed1990

The release of mercury from dental amalgam: the mechanism and in vitro testing.

Dissolution of mercury from the Ag-Hg matrix phase of dental amalgam is distilled water and synthetic saliva, and the mercury evaporation from the solutions, were studied in vitro. The main objectives of the study were to evaluate the factors that affect the results of the mercury release tests, and to consider the possible mechanisms of the release in vivo. Specimens were exposed to the liquids in open or closed bottles, and the changes in the mercury concentration were determined by cold-vapor Atomic Absorption Spectrophotometry. Concentration vs. time tests showed the dissolution rate decreasing with time. Tests involving sequences of short and long exposures with solution changes showed higher average rates for short-term dissolution into the fresh solution than for the longer preceding exposures. The differences were attributed to a stifling effect of the concentration of elemental mercury on the dissolution. It is believed that mercury dissolved mainly in the elemental form and that a continuous increase in the concentration was made possible by oxidation in the solution. In open cells, some of the mercury was lost by evaporation. The analysis showed that the results of mercury dissolution tests depend on many test variables, such as time, solution volume, oxidation and evaporation conditions, etc. Evaporation, dissolution, and evaporation/dissolution mechanisms of the mercury release in vivo were considered. It was concluded that the dissolution/evaporation model best described the mercury release from dental amalgam restorations.

Chemical Phenomena↗
PubMed1990

The effect of tin on the corrosion behavior of the Ag-Hg phase of dental amalgam and dissolution of mercury.

The anodic polarization behavior of the Ag-Hg matrix phase of dental amalgam (gamma 1) and the rate of mercury dissolution were examined as a function of the tin content. The objectives were to determine the effect of tin on the electrochemical behavior and dissolution of mercury and to provide evidence on whether tin dissolves in the gamma 1 phase or precipitates as a tin-rich phase. Anodic polarization curves were recorded for specimens of the gamma 1 phase containing 0-1.5% Sn and for the gamma 2 phase and a gamma 2-containing dental amalgam, in synthetic saliva. Mercury dissolved in synthetic saliva in 24 h was determined for the gamma 1 phase containing 0-1.0% Sn, with cold-vapor Atomic Absorption Spectrophotometry used for mercury analysis. Tin induced passive behavior of the gamma 1 phase and suppressed mercury dissolution. The passive gamma 1 phase did not exhibit a breakdown of passivity occurring at the gamma 2 phase. The results were consistent with the tin presence in gamma 1 in a solid solution, rather than in tin-rich precipitates, and indicated that at least 1.5% Sn can be dissolved in gamma 1 at 37 degrees C.

Corrosion↗
PubMed1989

[Primary lung cancer from biopsy material of the Pathomorphology Department of the Silesian Medical Academy in Zabrze].

An analysis was carried out of material biopsied during fiberoptic bronchoscopic examination of 289 patients suspected of lung malignant disorders were present more often in males. In the group of patients older than 40 years the most often diagnosed malignant process was squamous cell carcinoma. A high correlation of clinical suspicion of malignant process and histopathological diagnosis was found. A low rate of diagnosis of operable cases was found.

Adult↗
PubMed1988

Effect of detergents on aspartate ammonia-lyase activity in Escherichia alcalescens.

The effect of twelve detergents on aspartate ammonia-lyase activity of Escherichia alcalescens used for the production of L-aspartic acid was tested. Best permeabilization was found with Triton X-100, Slovafol 910 and Corona, a mixed commercial preparation. In contrast to Triton X-100 and Slovafol 910, a much narrower range of suitable concentrations was observed with Corona.

Ammonia-Lyases↗
PubMed1986

Glycidyl methacrylate copolymers as suitable supports for immobilizing antigens and antibodies.

Glycidyl methacrylate copolymers modified with 1,6-diaminohexane were activated with glutaraldehyde. Such activated supports were directly bound to the chosen antisera. Prepared immunosorbents contained ca. 40 mg of bound protein and were able to purify 2-5 mg of antigen (alkaline proteinases Esperase and Maxatase) per 1 g of solid support. Chaotropic agent (2.5 M ammonium thiocyanate in phosphate or Tris buffer) enabled antigen to be released quickly, the properties of the immunosorbent remaining unchanged.

Acrylates↗