Abstract:A reusable fiber optic enzyme biosensor provided rapid detection of acetylcholinesterase (AChE) inhibitors and fast regeneration of the sensor for reuse. However, while highly sensitive in detection of oxyphosphate AChE inhibitors, it was insensitive in detection of the less active thiophosphates. It was generic in its identification and did not identify the chemical structure of the analyte. A fiber optic immunosensor, using polyclonal antiparathion antibodies (Abs) was very selective (could differentiate bet… Show more
“…Changes in the absorbance, luminescence, polarization or refractive index are then detected. For more information on fibre optic biosensor design, advantages, limitations and other technical aspects see [2,[52][53][54]. As an example, benzopyrene bound to antibodies immobilized on the distal part of a fibre optic has been detected due to its intrinsic fluorescence when excited by laser radiation (He-Cd) transmitted inside the fibre [55,56].…”
Section: Conductimetric and Impedimetric Immunosensorsmentioning
A review of the fundamental aspects and environmental applications of biosensors is presented. The bases of different transducer principles such as electrochemical, optical and piezoelectric are discussed. Various examples are given of the applications of such principles to develop immunosensor devices to determine common environmental contaminants. Attention is also paid to catalytic biosensors, using enzymes as sensing elements. Biosensor devices based on the use of cholinesterase and various oxidase enzymes such as tyrosinase, laccase, peroxidase and aldehyde dehydrogenase are reported. Some examples are given of the applications of other biomolecules such as whole cells, DNA or proteins, to determine pollution. Validation studies are presented comparing biosensors with chromatographic techniques to determine organophosphorus pesticides and phenolic compounds in environmental samples.
“…Changes in the absorbance, luminescence, polarization or refractive index are then detected. For more information on fibre optic biosensor design, advantages, limitations and other technical aspects see [2,[52][53][54]. As an example, benzopyrene bound to antibodies immobilized on the distal part of a fibre optic has been detected due to its intrinsic fluorescence when excited by laser radiation (He-Cd) transmitted inside the fibre [55,56].…”
Section: Conductimetric and Impedimetric Immunosensorsmentioning
A review of the fundamental aspects and environmental applications of biosensors is presented. The bases of different transducer principles such as electrochemical, optical and piezoelectric are discussed. Various examples are given of the applications of such principles to develop immunosensor devices to determine common environmental contaminants. Attention is also paid to catalytic biosensors, using enzymes as sensing elements. Biosensor devices based on the use of cholinesterase and various oxidase enzymes such as tyrosinase, laccase, peroxidase and aldehyde dehydrogenase are reported. Some examples are given of the applications of other biomolecules such as whole cells, DNA or proteins, to determine pollution. Validation studies are presented comparing biosensors with chromatographic techniques to determine organophosphorus pesticides and phenolic compounds in environmental samples.
“…Detection and quantification of biomolecular interactions have benefited greatly from the incorporation of fiber-optic technology . A variety of optical sensing strategies have been developed, which are capable of detecting a broad range of biologicals including, but not limited to antibodies, , nucleic acids, , toxins, pesticides, , explosives, and numerous other small molecules.…”
An immunosensor using a long-period grating (LPG) was used for sensitive detection of antibody-antigen reactions. Goat anti-human IgG (antibody) was immobilized on the surface of the LPG, and detection of specific antibody-antigen binding was investigated. This sensor operates using total internal reflection where an evanescent field interacts with bound antibody immobilized over the grating region. The reaction between antibody and antigen altered the LPG transmission spectrum and was monitored in real time as a change in refractive index, thereby eliminating the need for labeling antigen molecules. Human IgG binding was observed to be concentration dependent over a range of 2-100 microg mL-1, and equilibrium bound antigen levels could be attained in approximately 5 min using an initial rate determination. Binding specificity was confirmed using human interleukin-2 and bovine serum albumin as controls, and nonspecific adsorption of proteins did not significantly interfere with detection of binding. Antigen detection in a heterogeneous protein mixture and in crude cell lysate from Escherichia coli was also confirmed. Moreover, regeneration of the LPG surface via diethylamine treatment resulted in approximately 80% removal of bound antigen. Subsequently, fibers reexposed to antigen retained greater than 85% of the initial signal after five consecutive regeneration cycles.
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