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A small-volume voltammetric detection of 4-aminophenol (PAP) has been developed using an interdigitated array (IDA) microelectrode cell in order to apply the IDA to electrochemical enzyme immunoassay. The signal of PAP at the IDA was steady state, and its magnitude was amplified compared with that of the usual single electrode due to redox cycling of PAP between the two finger sets of the IDA. A linear relationship between PAP concentration and cathodic limiting current was obtained from 1 to 1000 microM, reproducibly. The minimum sample volume in the measurement was reduced to 800 nL. High sample throughput of less than 1-min detection time per sample was achieved on 2-10-microL PAP samples. This IDA cell was applied to the electrochemical enzyme immunoassay of mouse IgG. Alkaline phosphatase was used as the enzyme label. The mouse IgG concentration was evaluated by detecting the concentration of PAP, which is the product of enzymatic reaction of the substrate, 4-aminophenyl phosphate (PAPP). Anti-mouse IgG was covalently immobilized on the glass surface of the small-volume immunowells by carbodiimide coupling. The assay range was 10-1000 ng/mL using 10-microL sample and 20-microL substrate solutions.

A method for the highly sensitive determination of acetylcholine (ACh) and choline (Ch) that employs a graphite-like carbon film electrode containing 6.5% platinum (Pt) nanoparticles was developed for use as a detector in microbore liquid chromatography (LC) with a postcolumn enzyme reactor. The film electrode was prepared by RF cosputtering carbon and Pt, which requires only a one-step formation process. This method can control the Pt content of the film at a relatively low deposition temperature (below 200 degrees C). The average size of the Pt nanoparticles was 2.5 nm. The film electrode showed excellent electrocatalytic activity, high sensitivity, and negligible baseline drift when detecting hydrogen peroxide. The electrode was modified with glucose oxidase and responded rapidly to glucose with a much more stable baseline current than at a Pt bulk electrode based sensor. Therefore, it is appropriate to employ the electrode to detect trace amounts of biomolecules, such as neurotransmitters and hormones combined with various oxidase enzymes. We used the electrode as a detector for microbore LC and observed a low detection limit of 2.5 and 2.3 fmol (10-microL injection) for ACh and Ch, respectively, which is approximately 1 order of magnitude lower than that of a Pt bulk electrode.

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