Table 6.
Electrochemical characteristics of other carbon-based electrodes as sensors for caffeine determination.
| Medium | Electrohemical Sensor | Method | LOD | CV Oxidation Peaks | Linear Range | Real Sample | References |
|---|---|---|---|---|---|---|---|
| 0.5 M H2SO4 | GrRAC GrRGC |
DPV | 2.9 µM 6.1 µM |
/ | 5–1000 μM | Soft drinks and pharmaceutical formulations | [93] |
| 0.5 M H2SO4 | GrRAC GrRGC |
CV DPV |
2.31 µM 6.33 µM |
+1.54 V | 0–50 μM | Pharmaceutical formulations and synthetic urine | [92] |
| 0.5 M H2SO4 | GrRAC-50% GrRAC-70% |
CV, DPV | 2.94 μM for GrRAC-70% | +1.51 V for both sensors | 2.5–1000 μM | Pharmaceutical formulations and beverages | [91] |
| 0.1 M PBS pH 6 |
MWCNT-AuNP-CCE | CV DPV |
0.354 µM | +0.1 V (DPV) | 10–1500 µM | Human serum and urine | [97] |
| 0.1 M PBS pH 7.4 |
AgNPs:ErGO/PG | CV, SWV | 0.54 nM | +1.275 V ** | 0.001–200 μM | Human urine and serum samples | [99] |
| 0.1 M acetate buffer pH 3 |
TX-100-MWCNTs/Au | DPV | 0.08 µM | +1.45 V (DPV) | 0.58–11.50 µM | Tea samples | [98] |
**—simultaneously.