Immunosensors electrodic surface

In amperometry, the current produced by the oxidation or reduction of an electroactive analyte species at an electrode surface is monitored under controlled potential conditions. The magnitude of the current is then related to the quantity of analyte present. However, as both antibody and antigen are not intrinsically electroactive, a suitable label must be introduced to the immunocomplex to promote an electrochemical reaction at the immunosensors. In this respect, enzyme labels including the... 

A comparison of the products of AP hydrolysis of HQDP (HQ), PP, and 1-NP using cyclic voltammetry revealed that HQ produced well-defined peaks, and that the oxidation of HQ is reversible. More importantly, no apparent passivation of the electrode surface was observed even at high millimolar concentrations after 50 scans. Following a series of investigations, this non-fouling nature of HQ was attributed to the non-accumulation of its oxidation products on the electrode surface and the good diffusional properties of HQ at the electrode-solution interface. Another positive feature of HQDP as a substrate for AP is a tenfold greater oxidation current response of HQ compared to those obtained in the presence of PP or 1-NP. Overall, HQDP provides a suitable and attractive alternative substrate system for AP in the development of amperometric immunosensors. 

In some instances, the design of an amperometric immunosensor may be such that the enzyme is located some distance away from the electrode surface, or the presence of interfering substances in biological samples may require using an alternative electron transfer pathway. This usually involves a redox-active species with a small molecular... 

Conductometric transducers, as the oldest electrochemical devices, seem not to enjoy wide applications due to their poor selectivity. For example, Yagiuda et al. proposed a conductometric immunosensor for the determination of methamphetamine (MA) in urine [89], The decrease in the conductivity between a pair of platinum electrodes might result from the direct attachment of MA onto the anti-MA antibodies immobilized on the electrode surface. The system was claimed to be a useful detection technique of MA in comparison with a gas chromatography-mass spectrometry method. 

Some electrochemically active substances that can generate photons on an electrode surface are suitable labels for homogeneous immunoassays. A labelled antigen exhibits an electrochemical reactivity and produces luminescence, but when it is immunochemically complexed, the labelled antigen loses its electrochemiluminescent properties. One optical immunosensor for homogeneous immunoassays was assembled by spattering platinum on the end surface of an optical fibre. Spattered platinum maintains optical transparency and functions as an electrode. An optical electrode efficiently... 

Electrochemical immunosensors based on screen-printed electrodes have recently been applied to the detection of environmental pollutants such as PCBs, PAHs, pesticides [17-20] and of important molecules in clinical and food field [21-23]. In this case, the screen-printed electrodes are both the solid-phase for the immunoassay and the electrochemical transducers antibody or antigen molecules are directly immobilised at the sensor surface (transducer) and one of these species is enzyme-labelled in order to generate an electroactive product which can be detected at the screen-printed electrode surface. 

The application of a potentiometric immunosensor for detecting the herbicide simazine in food was described by Yulaev et al. [113]. After a competitive immune reaction on the gold planar electrode surface, the... 

Electrochemical immunosensors have been widely used for environmental analysis in amperometric, potentiometric, and conductimetric configurations. Amperometric immunosensors measure the current generated by oxidation or reduction of redox substances at the electrode surface, which is held at an appropriate electrical potential. Wilmer et al. measured concentrations of 2,4-dichlorophenoxyacetic acid (2,4-D) in water by using an amperometric immunosensor with a limit of detection of 0.1 Jtg L-1 (Wilmer et al., 1997). Some examples of new developments are the disposable screen-printed electrodes for the detection of polycyclic aromatic hydrocarbons (PAHs)... 

The combination of a photoisomerizable spiropyran and Ab-DNP was also applied in the development of reversible amperometric immunosensors.49 The amperometric immunosensor was based on a 6,8-dinitrospiropyran-assembled monolayer on an Au electrode (Figure 6b). When Ab-DNP associated with the spiropyran monolayer as the electrode, the electrode surface was insulated toward the solubilized redox probe, and its amperometric response decreased. After irradiation (360nmantigen monolayer that resulted in a dissociation of Ab-DNP from the monolayer. The rinsed electrode revealed a high amperometric response, indicating that the Ab-DNP was washed off. Thus, the two-step illumination of the monolayer enables its reversible cyclic performance, which would demonstrate a general means for cyclic operation of an amperometric immunosensor. 

The selectivity of immunosensors for steroid analytes is achieved with the use of appropriately selected monoclonal antibodies. The carbon working electrode provides a suitable surface for passive adsorption of proteins, and can therefore be tailored with an appropriate antibody, so that it will act as an immunoactive surface upon which an immunoaffinity assay can be performed an electrochemical signal can then be generated by monitoring the production of an electroactive species at the underlying electrode surface. We and other workers have found that to retain maximum monoclonal antibody activity, it is desirable to use a primary antibody (rabbit IgG), which serves both to capture (e.g., from a culture medium) and to orientate the mAb. Hence this approach... 

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