Search PubMed⌕ Search

Biomedical subjects

SM Park

Publications and source records attributed to SM Park.

5 recordsLinked to original sources

An electrochemical impedance measurement technique employing Fourier transform

We describe a novel technique for measuring electrochemical impedance, in which the electrode potential is ramped to a desired bias potential and a small potential step is applied to the working electrode after a short time delay. Fourier transform of the first derivative of the current signal thus obtained provides ac currents in the frequency domain, which allows the computation of impedances of the electrode/electrolyte interface in the whole frequency range. A home-built data acquisition system for these measurements and the results obtained therefrom were used for the measurements. The advantage of the technique includes an extremely short time of less than 1 ms for impedance measurements in the whole frequency region while equilibrium conditions of the electrochemical system are being maintained before and after the measurements, among many others. This technique is expected to revolutionize electrochemical measurements and to find important applications such as in situ measurements during battery cycling, corrosion testing, and other electrochemical experiments.

Journal Article↗

Metabolite and isotopomer balancing in the analysis of metabolic cycles: I. Theory.

Proper analysis of label distribution in metabolic pathway intermediates is critical for correct interpretation of experimental data and strategic experimental design. While, for example, 13C nuclear magnetic resonance (NMR) spectroscopy is usually limited to the measurement of degrees of 13C enrichment, more information about metabolic fluxes can be extracted from the fine structure of NMR spectra, or molecular weight distributions of isotopomers of metabolic intermediates (measured by gas chromatography-mass spectrometry). For this purpose, rigorous accounting for the contribution of all pathways to label distribution is required, especially contributions resulting from multiple turns of metabolic cycles. In this paper we present a mathematical model developed to analyze isotopomer distributions of tricarboxylic acid cycle (TCA) intermediates following the administration of 13C (or 14C) labeled substrates. The theory presented provides the basis to analyze 13C NMR spectra and molecular weight distributions of metabolites. In a companion paper (Park et al., 1999), the theory is applied to the analysis of several cases of biological significance. Copyright 1999 John Wiley & Sons, Inc.

Journal Article↗

A Rational Approach to Selective Recognition of NH(4)(+) over K(+).

An ion-selective electrode (ISE) based on receptor 1 is highly selective for binding NH(4)(+) over K(+) (lg K(NH(4)(+)/K(+))=-2.6); the three imine nitrogen atoms in 1 are ideally positioned for hydrogen bonding with the tetrahedral NH(4)(+) ion. This selectivity is considerably greater than that found for commercial ISEs based on nonactin (lg K(NH(4)(+)/K(+))=-1.0).

Journal Article↗