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. 2021 Dec 2;12:751321. doi: 10.3389/fphar.2021.751321

TABLE 4.

Main validation parameters of the high-performance liquid chromatography (HPLC) method applied to quantify paroxetine in plasma, brain, and lung matrices.

Validation parameter Mouse matrices (n = 3)
Plasma Brain homogenate Lung homogenate
Calibration range (µg/ml) 0.0500–2.00 0.0250–1.00 0.0500–2.00
Regression equation a Y = 1.19–0.00671 Y = 1.96 + 0.00428 Y = 1.14–0.0158
Coefficient of determination (r 2) b 0.994 0.996 0.994
LLOQ (µg/ml) 0.0500 0.0250 0.0500
Intra-day
 Precision (%CV) 7.07–14.3 1.25–7.98 10.0–13.4
 Accuracy (%RE) −10.9–0.865 −3.11–13.2 −9.84–9.72
Intra-day
 Precision (%CV) 6.90–12.2 4.97–9.94 5.73–14.6
 Accuracy (%RE) 0.974–14.9 −3.31–12.5 −14.7 to −1.71

LLOQ, lower limit of quantification; CV, coefficient of variation; %RE, deviation from nominal value.

a

Equation of the calibration curve is given by the general equation of y = mx + b, with m corresponding to the slope and b to the intercept. The equation represents the peak areas signals of paroxetine to that of the internal standard (y), versus the corresponding concentration of paroxetine (x).

b

Weighted linear regression using 1/×2 as the best weighting factor.