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Bioanalysis

Source Compiled from Cammann, K. Working with ion-Seiective Eiectrodes. Springer-Verlag Berlin, 1977 and Lunte, C. E. Heineman, W. R. "Electrochemical Techniques in Bioanalysis." In Steckham, E., ed. Topics in Current Chemistry, Vol. 143, Springer-Verlag Berlin, 1988, p. 8. - Abbreviations E = enzyme B = bacterial particle T = tissue. [Pg.486]

Figure 11.16 Chromatograms of plasma samples obtained by using SPE-SFC with super-aitical desorption of the SPE cartridge (a) blank plasma (20 p.1), UV detection at 215 nm (b) blank plasma (20 p.1), UV detection at 360 nm (c) plasma (1 ml) containing 20 ng mitomycin C (MMC), UV detection at 360 nm. Reprinted from Journal of Chromatography, 454, W. M. A. Niessen et al., Phase-system switching as an on-line sample pretreatment in the bioanalysis of mitomycin C using supercritical fluid cliromatography, pp. 243-251, copyright 1988, with permission from Elsevier Science. Figure 11.16 Chromatograms of plasma samples obtained by using SPE-SFC with super-aitical desorption of the SPE cartridge (a) blank plasma (20 p.1), UV detection at 215 nm (b) blank plasma (20 p.1), UV detection at 360 nm (c) plasma (1 ml) containing 20 ng mitomycin C (MMC), UV detection at 360 nm. Reprinted from Journal of Chromatography, 454, W. M. A. Niessen et al., Phase-system switching as an on-line sample pretreatment in the bioanalysis of mitomycin C using supercritical fluid cliromatography, pp. 243-251, copyright 1988, with permission from Elsevier Science.
W. J. Lough and T. A. G. Noctor, Multi-column approaches to chhal bioanalysis by liquid cliromatogruphy . Prog. Pharm. Biomed. Anal. 1 241 -257 (1994). [Pg.293]

A. Walhagen and L.-E. Edholm, Chiral separation on acliiral stationary phases with different functionalities using /3-cyclodextiin in the mobile phase and application to bioanalysis and coupled columns , Chromatographia 32 215-223 (1991). [Pg.294]

K. S. Boos and C. H. Grimm, High performance liquid chromatography integated with solid-phase exti action in bioanalysis using resti icted access precolumn packings . Trends Anal. Chem. 18 175-180(1999). [Pg.298]

W. M. A. Niessen, R J. M. Bergers, U. R. Tjaden and J. van der Greef, Phase-system switclring as an on-line sample preti eatment in the bioanalysis of mitomycin C using supercritical fluid clrromatogi aphy , 7. Chromatogr. 454 243-251 (1988). [Pg.300]

Chronoamperometry is often used for measuring the diffusion coefficient of electroactive species or the surface area of the working electrode. Analytical applications of chronoamperometry (e.g., in-vivo bioanalysis) rely on pulsing of the potential of the working electrode repetitively at fixed tune intervals. Chronoamperometry can also be applied to the study of mechanisms of electrode processes. Particularly attractive for this task are reversal double-step chronoamperometric experiments (where the second step is used to probe the fate of a species generated in the first step). [Pg.61]

Health Technology Research Center Nano-bioanalysis Team 2217-14 Hayashi-cho, Takamatsu Kagawa 761-0395 Japan... [Pg.339]

A significant development in the methodology of potentiometry that paved the way for its utility in bioanalysis was the discovery of the ion selective electrode (ISE). Conceptually, the ISE involves the measurement of a membrane potential. The response of the electrochemical cell is therefore based on an interaction between the membrane and the analyte that alters the potential across the membrane. The selectivity of the potential response to the analyte depends on the specificity of the membrane interaction for the analyte. [Pg.4]


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