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Biomedical subjects

Andrzej S Baranski

Publications and source records attributed to Andrzej S Baranski.

4 recordsLinked to original sources

Cyclic chronopotentiometry as a detection tool for flowing solution systems.

Cyclic chronopotentiometry provides a very simple detection method, which may be particularly useful in capillary electrophoresis (CE) and microseparation systems. It has been shown that for disk microelectrodes it is possible to define safe reduction and oxidation currents that would never lead to the formation of H2 or O2 gas bubbles, even if they are applied for an indefinitely long time period. During end-column CE detection, currents passing through the working microelectrode can be completely controlled by the external electronic circuit and they are not affected by the separation current. Consequently, problems created by the offset potential in CE can be completely eliminated. The detection can be accomplished through a variety of different mechanisms; however, generation of the electrode response as a result of analyte adsorption seems to be most common. The method is applicable to many analytes, which do not have to be electroactive. The analytical signal is obtained by monitoring the change in the average electrode potential (calculated for either a cathodic or an anodic half-cycle) caused by an analyte interacting with the electrode. The analytical signal is proportional to the analyte concentration, within a concentration range extending over approximately 2 orders of magnitude.

Journal Article↗

Cyclic chronopotentiometric determination of sugars at Au and Pt microelectrodes in flowing solutions.

The main advantage of the application of cyclic chronopotentiometry (CCP) in end-column CE detection arises from the fact that the detection parameters and the magnitude of the analytical signal are (in contrast with other electrochemical detection methods) independent of the ohmic polarization of the solution caused by the separation current at the detection end of the capillary. CCP was used to determine sugars on platinum and gold microelectrodes after separation by CE. The results obtained with a gold microelectrode were better. Subsequently this detection method was used for quantitative determination of sugars in honeys and for their authentication.

Carbohydrates↗

High frequency faradaic rectification voltammetry at microelectrodes.

An experimental setup for carrying out faradaic rectification measurements at micrometer-sized electrodes under potential control is described. A new method of data analysis is proposed that allows the determination of the standard rate constant and the electron-transfer coefficient of a fast charge transfer process without knowing the impedance of the microelectrode. This method is based on the frequency dependence of the shape of the faradaic rectification voltammograms (i.e., the average width of the peaks and the ratio of the peak heights) rather than on the magnitude of the faradaic rectification signal. The method was tested in the determination of heterogeneous electron transfer kinetics of Fe(CN)6(3-/4-) and Ru(NH3)6(2+/3+) in aqueous solutions on a platinum microelectrode (12.5 microm in radius) and ferrocene/ferrocinum redox couple in a dimethylformamide solution on a gold microelectrode (12.5 microm in radius).

Journal Article↗

Hot microelectrodes.

Heat generation at disk microelectrodes by a high-amplitude (few volt) and high-frequency (0.1-2 GHz) alternating voltage is described. This method allows changing electrode temperature very rapidly and maintaining it well above the boiling point of solution for a very long time without any indication of boiling. The size of the hot zone in solution is determined by the radius of the electrode. There is no obvious limit in regard to the electrode size, so theoretically, by this method, it should be possible to create hot spots that are much smaller than those created with laser beams. That could lead to potential applications in medicine and biology. The heat-generating waveform does not electrically interfere with normal electroanalytical measurements. The noise level at hot microelectrodes is only slightly higher, as compared to normal microelectodes, but diffusion-controlled currents at hot microelectrodes may be up to 7 times higher, and an enhancement of kinetically controlled currents may be even larger. Hot microelectrodes can be used for end-column detection in capillary electrophoresis and for in-line or in vivo analyses. Temperature gradients at hot microelectrodes may exceed 1.5 x 10(5) K/cm, which makes them useful in studies of Soret diffusion and thermoelectric phenomena.

Journal Article↗