Page 210 - Analytical Electrochemistry 2d Ed - Jospeh Wang
P. 210

6-3  SOLID-STATE DEVICES                                        195

            the laboratory to be transported to the sample. A range of assays have already been
            adapted to the microchip format. These possibilities have led to the concepts of
            mTAS (micro-total analytical systems) and ``Lab-on-a-Chip'', which are hot topics of
            analytical chemistry. The extremely small dimensions of electrochemical detectors,
            coupled with their remarkable sensitivity and compatibility with microfabrication
            technologies, make them very suitable for adaptation for ``Lab-on-a-Chip'' analytical
            microsystems. Microsystems relying on electrosmotic ¯ow obviate the needs for
            pumps or valves but require proper attention to the decoupling of the detector
            potential from the high voltage used to control the micro¯uidics. Such precise ¯uid
            control is accomplished by regulating the applied potentials at the terminus of each
            channel of the microchip (81). The channel networks of these chips include mixing
            tees and cross intersections for mixing reagents and injecting samples with high
            reproducibility (e.g., Figure 6-22). Particularly powerful is the use of electrochemical
            detectors for monitoring on-chip electric-®eld-driven separations (see Section 3-6).
              Large-scale sensor fabrication can be accomplished not only by lithographic
            techniques but also using modern screen-printing (thick-®lm) processes (82,83). The
            screen-printing technology relies on printing patterns of conductors and insulators
            onto the surface of planar (plastic or ceramic) substrates. Various conducting and
            insulating ink materials are available for this task. The screen-printing process
            involves several steps (as illustrated in Figure 6-23 for the fabrication of carbon
            electrodes), including placement of the ink onto a patterned screen or stencil,
            followed by forcing it through the screen with the aid of a squeegee, and
            drying=curing the printed patterns. Such a process yields mass-producible (uniform




























            FIGURE 6-22 Schematic of a microchip system for enzymatic assays. The channels
            terminate at reservoirs containing the indicated solutions. (Reproduced with permission
            from reference 81.)
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