Table 1. Figures of merit obtained from the calibration curves used for quantitation.
Analyte | Calibration range | Retention Time (min)a | Concentration range (LLOQ – ULOQ) | R2, b | LOD (nM) | LOQ (nM) |
p-Tyr | 0.4 – 200 μM | 1.452±0.003 | 0.44 – 220 μM | 0.996 | 39.0 | 129.9 |
m-Tyr | 16 – 250 nM | 1.889±0.012 | 17 – 275 nM | 0.996 | 1.2 | 3.9 |
o-Tyr | 16 – 1000 nM | 2.733±0.009 | 17 – 1100 nM | 0.998 | 2.8 | 9.5 |
Phe | 0.2 – 200 μM | 3.100±0.003 | 0.22 – 220 μM | 0.9991 | 14.4 | 48.0 |
3NO2-Tyr | 16 – 1000 nM | 3.415±0.004 | 17 – 1100 nM | 0.995 | 4.2 | 14.0 |
3Cl-Tyr | 7 – 2000 nM | 3.211±0.008 | 8 – 2200 nM | 0.997 | 0.9 | 3.0 |
2dG | 7 – 1000 nM | 2.51±0.02 | 8 – 1100 nM | 0.996 | 0.7 | 2.5 |
8OHdG | 2 – 250 nM | 3.263±0.010 | 2.2 – 275 nM | 0.993 | 0.2 | 0.6 |
: mean values ± standard deviation;
: Regression coefficient for the linear regression curves calculated using (Peak Area Metabolite)/(Peak Area of the Internal standard).as response, and ((Metabolite)/(Internal standard)) as independent variable. Internal standard: Phe-D5