Removal of electrochemically active compounds |
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In serum/plasma [31]:
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Uric acid
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Ascorbic acid
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Dopamine
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L-cysteine
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Acetaminophen
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Salicylic acid
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In urine [32]:
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Urea
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Tartaric acid
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Citric acid
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Glucose
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Leucine
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Proline
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Tyrosine
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In saliva [33]:
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Uric acid
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Ascorbic acid
|
Removal of particulate to avoid clogging of microchannels and microvalves [34] |
Blood cells may form aggregates clogging the microchannels during separation of plasma from blood [35] |
|
Adjustment of ionic strength and temperature [36,37] |
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Variable ionic strength influence potentiometric, conductimetric and also voltammetric measurements. In addition, ionic strength and nature affects biological reactions [36]
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Temperature affects the slope of the electrode response according to the Nernst equation [37]
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Reducing non specific absorption of hydrophobic material such as PDMS [38] |
Adsorption of fluorescence markers can cause a drift in the background fluorescence intensity [38] |
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Removal of surface fouling compounds [39] |
Fouling cause by plasma proteins, lipids, and other biochemical components of the biological fluids [39] |
Removal of compounds interfering with the biorecognition or signal amplification mechanisms [40] |
PCR inhibitors in blood sample such as heme, hemoglobin, lactoferrin and immunoglobulin G [40] |
|
Adjustment of pH [41] |
A pH buffer can be used to reduce hydroxyl ion (OH−) effects that interfere ISE electrodes [41] |
Adjustment of pH [42] |
Surface charge (Zeta potential) of the microchannels' walls is generally a function of the pH thus, the electroosmotic pumping process can be enhanced or degraded by changes in pH [42] |