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Home >> Biotechnology and Genomics >> Biosensors as Biotechnology Tools >> History of the Development of Biosensors

History of the Development of Biosensors
The development of biosensors began in 1950, when a biosensors with an oxygen electrode (sometimes described as Clark electrode) was developed by L. L. Clark in Cincinnati, USA to measure the dissolved oxygen in blood. Later, glucose oxidase enzyme in a gel was coated and immobilized on the oxygen electrode to measure blood sugar. Similarly, enzyme urease was used (in combination with an electrode specific for NH4++ ions) for measuring urea in body fluids like blood and urine. These two biosensors developed in early years of the history of biosensors made use of two different transducer technologies.

In the first case, the estimates were made by measurement of electric current (amperometric) and in the second case for urea measurements, the estimates were based on the measurement of charge on the electrode (potentiometric). The biosensors based on the use of enzymes involving catalytic action are described as catalytic biosensors as against bioaffinity biosensors developed later, which do not make use of enzymes, but instead make use of antibodies, receptor molecules, etc., which have high affinity with the analyte. In 1980s, the first bioaffinity biosensors were developed, in which radiolabelled receptors were immobilized on to a tranducer surface. Biosensors based on ELISA have also been developed using labelled antibody or labelled antigen coupled with a suitable transducer.

Whole cell biosensors were also developed during 1980s, making use of whole microbial cells or organelles. Similarly, small sensing organs like antennule have been used, to measure the level of various drugs or environmental toxicants. As mentioned above, receptor molecules located in cell membranes have also been isolated and used in biosensors.

 

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