Electrochemical detection amperometry

Figure 3.21 Properties measured during electrochemical detection. Amperometry measures the current or charge transferred between neutral or ionic analytes and the electrode. Conductivity measures the mobility of ions in an electric field. (Reprinted from Ref. 49 with permission.)...

Electrochemical Detectors Another common group of HPLC detectors are those based on electrochemical measurements such as amperometry, voltammetry, coulometry, and conductivity. Figure 12.29b, for example, shows an amperometric flow cell. Effluent from the column passes over the working electrode, which is held at a potential favorable for oxidizing or reducing the analytes. The potential is held constant relative to a downstream reference electrode, and the current flowing between the working and auxiliary electrodes is measured. Detection limits for amperometric electrochemical detection are 10 pg-1 ng of injected analyte. 

Monitoring enzyme catalyzed reactions by voltammetry and amperometry is an extremely active area of bioelectrochemical interest. Whereas liquid chromatography provides selectivity, the use of enzymes to generate electroactive products provides specificity to electroanalytical techniques. In essence, enzymes are used as a derivatiz-ing agent to convert a nonelectroactive species into an electroactive species. Alternatively, electrochemistry has been used as a sensitive method to follow enzymatic reactions and to determine enzyme activity. Enzyme-linked immunoassays with electrochemical detection have been reported to provide even greater specificity and sensitivity than other enzyme linked electrochemical techniques. 

Figure 1 Electrochemical detection of catechol, acetaminophen, and 4-methyl catechol, demonstrating the selectivity of differential pulse detection vs. constant potential detection. (A) Catechol, (B) acetaminophen, and (C) 4-methylcatechol were separated by reversed phase liquid chromatography and detected by amperometry on a carbon fiber electrode. In the upper trace, a constant potential of +0.6 V was used. In the lower trace, a base potential of +425 mV and a pulse amplitude of +50 mV were used. An Ag/AgCl reference electrode was employed. Note that acetaminophen responds much more strongly than catechol or 4-methylcatechol under the differential pulse conditions, allowing highly selective detection. (Reproduced with permission from St. Claire, III, R. L. and Jorgenson, J. W., J. Chromatogr. Sci. 23, 186, 1985. Preston Publications, A Division of Preston Industries, Inc.)...

One of these is electrochemical detection, which can be used with traditional CE as well as with the microchip design. Electrochemical detection generally provides good sensitivity and bulk property response (conductivity, potentiometry), and can be selectively tuned to a certain class of compounds (amperometry). ... 

Another recent development is the advent of pulse amperometry in which the potential is repeatedly pulsed between two (or more) values. The current at each potential or the difference between these two currents ( differential pulse amperometry ) can be used to advantage for a number of applications. Similar advantages can result from the simultaneous monitoring of two (or more) electrodes poised at different potentials. In the remainder of this chapter it will be shown how the basic concepts of amperometry can be applied to various liquid chromatography detectors. There is not one universal electrochemical detector for liquid chromatography, but, rather, a family of different devices that have advantages for particular applications. Electrochemical detection has also been employed with flow injection analysis (where there is no chromatographic separation), in capillary electrophoresis, and in continuous-flow sensors. 

All of the fat-soluble vitamins, including provitamin carotenoids, exhibit some form of electrochemical activity. Both amperometry and coulometry have been applied to electrochemical detection. In amperometric detectors, only a small proportion (usually <20%) of the electroactive solute is reduced or oxidized at the surface of a glassy carbon or similar nonporous electrode in coulometric detectors, the solute is completely reduced or oxidized within the pores of a graphite electrode. The operation of an electrochemical detector requires a semiaqueous or alcoholic mobile phase to support the electrolyte needed to conduct a current. This restricts its use to reverse-phase HPLC (but not NARP) unless the electrolyte is added postcolumn. Electrochemical detection is incompatible with NARP chromatography, because the mobile phase is insufficiently polar to dissolve the electrolyte. A stringent requirement for electrochemical detection is that the solvent delivery system be virtually pulse-free. 

N. E. Hebert, W.G. Ruhr and S.A. Brazill, A microchip electrophoresis device with integrated electrochemical detection A direct comparison of constant potential amperometry and sinusoidal voltammetry, Anal. Chem., 75 (2003) 3301-3307. 

Rocklin, R., Conductivity and Amperometry Electrochemical Detection in Liquid Chromatography. Dionex Corporation, Sunnyvale, California, 1989. 

Immunoassays, electrochemical — A quantitative or qualitative assay based on the highly selective antibody-antigen binding and electrochemical detection. Poten-tiometric, capacitive, and voltammetric methods are used to detect the immunoreaction, either directly without a label or indirectly with a label compound. The majority of electrochemical immunoassays are based on -> voltammetry (-> amperometry) and detection of redox-active or enzyme labels of one of the immunochemical reaction partners. The assay formats are competitive and noncompetitive (see also -> ELISA). 

There are many substances which would appear to be good candidates for LC-EC from a thermodynamic point of view but which do not behave well due to kinetic limitations. Johnson and co-workers at Iowa State University used some fundamental ideas about electrocatalysis to revolutionize the determination of carbohydrates, nearly intractable substances which do not readily lend themselves to ultraviolet absorption (LC-UV), fluorescence (LC-F), or traditional DC amperometry (LC-EC) [2], At the time that this work began, the EC of carbohydrates was more or less relegated to refractive index detection (LC-RI) of microgram amounts. The importance of polysaccharides and glycoproteins, as well as traditional sugars, has focused a lot of attention on pulsed electrochemical detection (FED) methodology. The detection limits are not competitive with DC amperometry of more easily oxidized substances such as phenols and aromatic amines however, they are far superior to optical detection approaches. 

In electrochemical detection, the potential of a working electrode can be measured versus a reference electrode, usually while no net current is flowing between the electrodes. This type of detection is referred to as potentiometry. Alternatively, a potential is applied to the working electrode with respect to the reference electrode while the generated oxidation or reduction current is measured. This technique is referred to as amperometry. When applying a negative po-... 

The field of electrochemical detection in CE have been extensively reviewed in Refs. 1-3. Instructive applications can be found for amperometry in Ref. 4, for potentiometry in Ref. 5, and for conductometry in Ref. 6. 

To overcome the problem of detection in CE, many workers have used inductively coupled plasma-mass spectrometry (ICP-MS) as the method of detection. " Electrochemical detection in CE includes conductivity, amperometry, and potentiometry detection. The detection limit of amperometric detectors has been reported to be up to 10 M. A special design of the conductivity cell has been described by many workers. The pulsed-amperometric and cyclic voltametry waveforms, as well as multi step waveforms, have been used as detection systems for various pollutants. Potentiometric detection in CE was first introduced in 1991 and was further developed by various workers.8-Hydroxyquino-line-5-sulfonic acid and lumogallion exhibit fluorescent properties and, hence, have been used for metal ion detection in CE by fluorescence detectors.Over-... 

Electrochemical detection (using conductivity, amperometry, or potentiometry). 

This kind of amperometry is the most widely used electrochemical detection method in liquid chromatography. A constant DC potential is continuously applied to the electrodes of the detector cell. The theory of amperometry with constant working potential does not differ from the theory of hydrodynamic voltammetry, even though the applied potential remains constant. 

Electrochemical detection based on conductometry, amperometry or potentiometry is used to only a limited extent in capillary electrophoresis, with only conductivity detectors commercially available [13,475,508-511]. Conductivity is a universal method for... 

Electrochemical Detection. Two types of electrochemical detection have been used with CE conductivity and amperometry. One of the problems with electrochemical detection has been that of isolating the detector electrodes from the high voltage required for the separation. One method for isolation involves inserting a porous glass or graphite joint between the end of the capillary and a second capillary containing the detector electrodes. 

Scanning electrochemical detection has also been employed for single-cell CE separations. In contrast to amperometry, scanning electrochemical detection varies the voltage of the working electrode. As separated species pass the working electrode, a voltammogram is obtained for each... 

Sensitive and selective detection techniques are of crucial importance for capillary electrophoresis, microfluidic chips, and other microfluidic analysis systems. Electrochemical detector has attracted considerable interest in these fields owing to its high sensitivity, inherent miniaturization of both the detection and control instrumentation, low cost and power demands, and high compatibility with microfabrication technology. The commonly used electrochemical detection approaches can be classified into three general modes COTiductimetry, potentiometry, and amperometry. 

For the nonoptical detection method, electrochemistry is one of the most commonly used detection method, and it has played a major role in the microfiuidic immunoassays since it was firstly combined with the microfiuidic immunoassay technique in 1998. The principle of this method is to convert the analyte s chemical signal into the electrical signal via the electrodes. There are three categories of the electrochemical techniques amperometry, potentiometry, and conductometry. 

Recently, electrochemical detection methods, namely, conductimetry, amperometry, and potentio-metry, have also become accessible. All three variants of electrochemical detection are intrinsically simpler than the optical methods, and their success depends highly on the electrode materials and designs used. Conductivity detection relies on measurement of the differences between the conductivities of the analyte and the separation electrolyte this provides a direct relationship between migration times and response factor, and makes this detector universal. On the contrary, amperometric detection is restricted to electroactive species and potentiometric detection is not possible for certain small ions with multiple charges. Conductimetric detection works better for inorganic compounds since the higher mobility of... 

The highest sensitivity and selectivity in vitamin E LC assays are obtained by using fluorescence or electrochemical detection. In the former, excitation at the low wavelength (205 nm) leads to improved detection limits but at the expense of selectivity, compared with the use of 295 nm. Electrochemical detection in the oxidation mode (amperometry or coulometry) is another factor 20 times more sensitive. In routine practice, however, most vitamin E assays employ the less sensitive absorbance detection at 292-295 nm (variable wavelength instrument) or 280 nm (fixed wavelength detectors). If retinol and carotenoids are included, a programmable multichannel detector, preferably a diode array instrument, is needed. As noted previously, combined LC assays for vitamins A, E, and carotenoids are now in common use for clinical chemistry and can measure about a dozen components within a 10 min run. The NIST and UK EQAS external quality assurance schemes permit interlaboratory comparisons of performance for these assays. 

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