Abstract
Dopamine (1) and tyrosinase (TR) activities were analyzed by using chemically modified ion-sensitive fieldeffect transistor (ISFET) devices. In one configuration, a phenylboronic acid functionalized ISFET was used to analyze 1 or TR. The formation of the boronate-1 complex on the surface of the gate altered the electrical potential associated with the gate, and thus enabled 1 to be analyzed with a detection limit of 7×10-5 M. Similarly, the TR-induced formation of 1, and its association with the boronic acid ligand allowed a quantitative assay of TR to be performed. In another configuration, the surface of the ISFET gate was modified with tyramine or 1 to form functional surfaces for analyzing TRactivities. The TR-induced oxidation of the tyramine- or 1-functionalized ISFETs resulted in the formation of the redox-active dopaquinone units. The control of the gate potential by the redox-active dopaquinone units allowed a quantitative assay of TR to be performed. The dopaquinone-functionalized ISFETs could be regenerated to give the 1-modified sensing devices by treatment with ascorbic acid.
| Original language | English |
|---|---|
| Pages (from-to) | 7288-7293 |
| Number of pages | 6 |
| Journal | Chemistry - A European Journal |
| Volume | 13 |
| Issue number | 26 |
| DOIs | |
| State | Published - 2007 |
Keywords
- Biosensors
- Enzymes
- Ion-sensitive field-effect transistors
- Monolayers
- Tyrosinase
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