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Table 1 Assay and method validation parameters for the determination of flutamide and its metabolites in plasma and urine samples by the proposed methods

From: Determination of flutamide and two major metabolites using HPLC–DAD and HPTLC methods

Parameters

HPTLC method

HPLC method

Spiked human plasma samples

Spiked urine samples

Spiked human plasma samples

Spiked urine samples

Flutamide

Flu-1

Flu-3

Flutamide

Flu-1

Flu-3

Flutamide

Flu-1

Flu-3

Flutamide

Flu-1

Flu-3

Rangea

0.30–3.0

0.30–3.0

0.30–3.0

0.3–4.0

0.3–2.5

0.3–4.0

2–50

2–50

15–200

2–50

2–50

15–200

Slope

− 655.53b

5414.98c

− 1659.60c

12446.00d

− 455.09c

2573.60d

− 261.41c

41861.50d

− 2182.80c

13125.00d

− 139.66c

1829.70d

60.0650

41.5830

5.8755

51.8810

37.2350

6.3446

Intercept

665.50

3039.00

1240.80

1385.10

3066.40

305.60

− 13.2490

− 2.8848

25.9910

− 21.3530

− 0.8850

35.0270

Correlation (r)

0.9998

0.9998

0.9992

0.9997

0.9994

0.9996

0.9999

0.9997

0.9999

0.9998

0.9999

0.9997

LLOQ

0.30

0.30

0.30

0.30

0.30

0.30

2.0

2.0

15.0

2.0

2.0

15.0

  1. aRange: for HPTLC, it is measured by µg/band and for HPLC method in µg/mL
  2. The linearity was achieved using the polynomial regression equation: A = aX2 + bX + C
  3. bCoefficient 1, cCoefficient 2X = concentration µg/band, C = intercept