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Biomedical subjects

V Mornstein

Publications and source records attributed to V Mornstein.

5 recordsLinked to original sources
PubMed2006

Project support of practical training in biophysics.

The Department of Biophysics ensures practical training in biophysics and related subjects for students of medical and health study programmes. Demonstrations of medical technology are an important part of this training. Teaching for Faculty of Sciences in biophysical study programmes becomes also very important. Some lectures and demonstrations of technology are involved, but the practical trainig is missing. About 1 mil. CZK for additional laboratory equipment was obtained from the HEIDF project No. 1866/ 2005 "The demonstration and measuring technology for education in medical biophysics and radiological physics" for measuring system DEWETRON for high frequency signal analysis, Fluke Ti30 IR camera, PM 9000B patient monitor, ARSENAL AF 1 fluorescence microscope, and Nikon Coolpix 4500 digital camera with accessories for microphotography. At the present time, further financial resources are being provided by a development project of Ministry of Education "Inter-university co-operation in biomedical technology and engineering using top technologies" in total amount of almost 5 mil CZK, whereas over 2 mil CZK from this project are reserved for student laboratory equipment. The main goal of this project is to ensure the participation of Medical Faculty in educational co-operation in the biomedical technology and engineering, namely with the Faculty of Electrical Engineering and Communication (FEEC), Brno University of Technology. There will be taught those areas of biophysics which are not covered by FEEC, thus forming a separate subject "General Biophysics". The following instruments will be installed: UV-VIS spectrophotometers, rotation viscometers, tensiometers, microscopes with digital image processing, cooled centrifuge, optical benches, and some smaller instruments for practical measurements.

Biophysics↗
PubMed1995

Effect of ultrasound on DNA synthesis in tumor cells.

The objective of this study was to consider the influence of continuous-wave (CW) ultrasound (800 kHz) on DNA synthesis in Ehrlich ascitic tumor cells in vitro. The 10-min irradiation was carried out in rotating polyethylene tubes (5 rpm). Incorporation of 3H-thymidine was employed to detect DNA synthesis. Replication and unscheduled (repair) DNA synthesis were distinguished by means of hydroxyurea treatment before insonation. It was established that the use of 0.5 W/cm2 and 1.0 W/cm2 (ISA) CW ultrasound interfered with DNA synthesis showing up as inhibition. The inhibition became most noticeable when starting insonation in a sample cooled to 5 degrees C. During insonation, the sample temperature was allowed to increase to the ambient (water bath) temperature of 37 degrees C. However, at an ultrasound intensity (SA) of 0.1 W/cm2 such inhibition was not proven, but a moderate stimulation of DNA synthesis was demonstrated. Changes in DNA synthesis after insonation were found to be transient because of a lack of stimulatory and/or inhibitory ultrasound effects after 1-h incubation at 37 degrees C. In our experimental conditions no effects on DNA synthesis due to the effects of the insonated medium on the cells were discernible. No statistically significant changes in unscheduled DNA synthesis were observed. Possible action mechanisms are discussed.

Animals↗
PubMed1980

Electrochemical behaviour of proteins at graphite electrodes. I. Electrooxidation of proteins as a new probe of protein structure and reactions.

Electrochemical oxidation of proteins at a paraffin-wax-impregnated spectroscopic graphite electrode was studied by means of linear sweep and differential pulse voltametric techniques. It was found that proteins at the graphite electrode yield an oxidation current in the vicinity of potentials of 0.7-0.8 V in the range of neutral pH values. This current has the characteristics of adsorption currents. It was shown that irreversible electrooxidation of tyrosine or tryptophan residues is responsible for the occurrence of these protein currents. This previously undescribed electrochemical activity of proteins was exploited for the demonstration of the influence of urea on the accessibility of both tyrosine and tryptophan residues in protein molecules for interaction with their environment. It was also demonstrated that voltammetry at graphite electrodes permits an electrochemical analysis of proteins that do not contain cystine or cysteine residues.

Animals↗
PubMed1980

Electrochemical behaviour of proteins at graphite electrodes. II. Electrooxidation of amino acids.

Electrochemical oxidation of L,alpha-amino acids at a paraffin-wax impregnated spectroscopic graphite electrode (WISGE) was studied by means of linear sweep, cyclic, phase-sensitive alternating current and differential pulse voltammetric techniques. It was found that out of the amino acids usually occurring in proteins only tyrosine, tryptophan, histidine, cystine, cysteine and methionine were oxidized at the WISGE. At relatively low concentrations of amino acids (up to ca. 2 x 10(-4) M) the electrode process in which the amino acids are oxidized at the WISGE has the characteristics of an irreversible reaction controlled by diffusion. Coulometric measurements showed that oxidation of tyrosine and tryptophan at the WISGE, i.e. of amino acids which are responsible for the oxidizability of proteins at graphite electrodes, is a two-electron process. At higher concentrations of tyrosine-and tryptophan (above ca. 2 x 10(-4) M) adsorption of the oxidation product of these amino adds was demonstrated.

Journal Article↗