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Table 3 Analytical performance data for the determination of the PAR and DAN by the proposed HPLC method

From: Hydro-organic mobile phase and factorial design application to attain green HPLC method for simultaneous assay of paracetamol and dantrolene sodium in combined capsules

Parameter

PAR

DAN

Linearity range (µg/mL)

1.0–200

1.0–40.0

Intercept (a)

22.784

19.476

Slope (b)

7.058

24.975

Correlation coefficient (r)

0.9999

0.9999

S.D. of residuals (Sy/x)

1.99

5.446

S.D. of intercept (Sa)

0.806

3.068

S.D. of slope (Sb)

0.010

0.147

Percentage relative standard deviation, % RSD

1.133

1.28

Percentage relative error, % Error

0.356

0.48

Limit of detection, LOD (µg/mL)

0.15

0.18

Limit of quantitation, LOQ (µg/mL)

0.48

0.61