Abstract

Abstract Two Divisions of the International Union of Pure and Applied Chemistry (IUPAC), namely Physical Chemistry (Commission I.7 on Biophysical Chemistry formerly Steering Committee on Biophysical Chemistry) and Analytical Chemistry (Commission V.5 on Electroanalytical Chemistry) have prepared recommendations on the definition, classification and nomenclature related to electrochemical biosensors; these recommendations could, in the future, be extended to other types of biosensors. An electrochemical biosensor is a self-contained integrated device, which is capable of providing specific quantitative or semi-quantitative analytical information using a biological recognition element (biochemical receptor) which is retained in direct spatial contact with an electrochemical transduction element. Because of their ability to be repeatedly calibrated, we recommend that a biosensor should be clearly distinguished from a bioanalytical system, which requires additional processing steps, such as reagent addition. A device which is both disposable after one measurement, i.e., single use, and unable to monitor the analyte concentration continuously or after rapid and reproducible regeneration should be designated a single use biosensor. Biosensors may be classified according to the biological specificity-conferring mechanism or, alternatively, to the mode of physico-chemical signal transduction. The biological recognition element may be based on a chemical reaction catalysed by, or on an equilibrium reaction with macromolecules that have been isolated, engineered or present in their original biological environment. In the latter cases, equilibrium is generally reached and there is no further, if any, net consumption of analyte(s) by the immobilized biocomplexing agent incorporated into the sensor. Biosensors may be further classified according to the analytes or reactions that they monitor: direct monitoring of analyte concentration or of reactions producing or consuming such analytes; alternatively, an indirect monitoring of inhibitor or activator of the biological recognition element (biochemical receptor) may be achieved. A rapid proliferation of biosensors and their diversity has led to a lack of rigour in defining their performance criteria. Although each biosensor can only truly be evaluated for a particular application, it is still useful to examine how standard protocols for performance criteria may be defined in accordance with standard IUPAC protocols or definitions. These criteria are recommended for authors, referees and educators and include calibration characteristics (sensitivity, operational and linear concentration range, detection and quantitative determination limits), selectivity, steady-state and transient response times, sample throughput, reproducibility, stability and lifetime.

Highlights

  • Abbre6iations: Ab, antibody; Ag, antigen; bilayer lipid membranes (BLMs), bilayer lipid membrane; BSA, bovine serum albumin; chemically modified electrodes (CME), chemically modified electrode; enzyme field-effect transistors (FETs) (ENFET), enzyme field-effect transistor; FET, field-effect transistor; FIA, flow injection analysis; HPLC, high performance liquid chromatography; IMFET, immunological field-effect transistor; ion-selective electrode (ISE), ion selective electrode; ion-sensitive field effect transistor (ISFET), ion sensitive field-effect transistor; LP, lactose permease; tL, life time; LOD, limit of detection; LOQ, limit of quantification; NAD, nicotinamide adenine dinucleotide; PU, polyurethane; PVAL, poly(vinyl alcohol); self assembled monolayers (SAMs), self assembled monolayer; SPR, surface plasmon resonance; TCNQ, tetracyanoquinodimethane; TTF +, tetrathiafulvalene

  • Since a biosensor is a self contained integrated device, we recommend that it should be clearly distinguished from an analytical system which incorporates additional separation steps such as high performance liquid chromatography (HPLC), or additional hardware and/or sample processing such as specific reagent introduction, as flow injection analysis (FIA)

  • The situation is more complex for enzyme-labelled immuno-sensors: the Ab-Ag complex is expected to reach an equilibrium and reactions to be either reversible or irreversible, the labelled enzyme activity is measured under steady-state analyte consumption conditions

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Summary

Biosensor

A chemical sensor is a device that transforms chemical information, ranging from the concentration of a specific sample component to total composition analysis, into an analytically useful signal. Chemical sensors contain usually two basic components connected in series: a chemical (molecular) recognition system (receptor) and a physico-chemical transducer. The biological recognition system translates information from the biochemical domain, usually an analyte concentration, into a chemical or physical output signal with a defined sensitivity. Various proteins and low molecular weight substrates, ions mixed valence metal oxides permselective, ion-conductive inorganic crystals trapped mobile synthetic or biological ionophores ion exchange glasses enzyme(s) bilayer lipid or hydrophobic membrane inert metal electrode enzyme(s) antibody, receptor enzyme(s) whole cells membrane receptors plant or animal tissue antigen/antibody oligonucleotide duplex, aptamer enzyme labelled chemiluminescent or fluorescent labelled specific ligands protein receptors and channels enzyme labelled fluorescent labelled potentiometric, voltammetric in series with 1. Besides quantification of the above mentioned analytes, biosensors are used for detection and quantification of micro-organisms: receptors are bacteria, yeast or oligonucleotide probes coupled to electrochemical, piezoelectric, optical or calorimetric transducers

Amperometric
Electrochemical biosensor
Limitations in the use of the term ‘biosensor’
Classification
Receptor: biological recognition element
Detection or measurement mode: electrochemical transduction or detection
Analytes or Reactions monitored
Indirect monitoring of inhibitor or acti6ator of the biochemical receptor
Immobilization of biological receptors
Selecti6ity and reliability
Findings
Conclusion
Full Text
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