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The optode sensors can however work in the whole region 0–100% oxygen saturation in water, and the calibration is done the same way as with the Clark type sensor. No oxygen is consumed and hence the sensor is stirring insensitive, but the signal will stabilize more quickly if the sensor is stirred after being put into the sample.
The optode sensors can, however, work in the whole region 0% to 100% oxygen saturation in water, and the calibration is done the same way as with the Clark-type sensor. No oxygen is consumed, and hence the sensor is insensitive to stirring, but the signal will stabilize more quickly if the sensor is stirred after being put in the sample.
It can be measured with a dissolved oxygen probe such as an oxygen sensor or an optode in liquid media, usually water. [1] The standard unit of oxygen saturation is percent (%). Oxygen saturation can be measured regionally and noninvasively. Arterial oxygen saturation (SaO 2) is commonly measured using pulse oximetry.
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Quenching is made use of in optode sensors; for instance the quenching effect of oxygen on certain ruthenium complexes allows the measurement of oxygen saturation in solution. Quenching is the basis for Förster resonance energy transfer (FRET) assays.
The Clark oxygen electrode laid the basis for the first glucose biosensor (in fact the first biosensor of any type), invented by Clark and Lyons in 1962. [6] This sensor used a single Clark oxygen electrode coupled with a counter-electrode. As with the Clark electrode, a permselective membrane covers the Pt electrode.
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