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Table 4 Regression and validation parameters of the proposed HPLC method for quantitative determination of Metoprolol, Nebivolol, carvedilol and atenolol enantiomers using mobile phase n-hexane: ethanol: DEA (75: 25: 0.1by volume)

From: Enantioseparation, quantification, molecular docking and molecular dynamics study of five β-adrenergic blockers on Lux-Cellulose-2 column

Parameters

Metoprolol

Nebivolol

Carvedilol

Atenolol

Enant.1

Enant.2

Enant.1

Enant.2

Enant.1

Enant.2

Enant.1

Enant.2

Linearity

 Slope (Au-Sec.ml/µg)

3.2903

3.3722

1.0659

1.1315

11.3710

11.4470

3.8646

3.6325

 Intercept (Au-Sec)

− 3.3282

− 6.3580

− 4.4288

− 2.0739

− 13.5980

− 17.7210

17.4170

25.2190

 Correlation coefficient r

0.9996

0.9995

0.9995

0.9997

0.9996

0.9996

0.9995

0.9995

 Range (\(\upmu \)g/ml)

50–250

50–250

50–250

50–250

20–100

20–100

50–250

50–250

 Accuracy (Mean + R.S.D.%)

99.96 + 1.022

100.21 + 0.867

99.90 + 0.587

100.40 + 0.898

100.29 + 1.088

99.94 + 1.000

100.29 + 0.898

100.12 + 1.405

 *Robustness (RSD %)

0.996

0.853

0.531

0.832

0.992

0.997

0.845

0.998

 **Robustness (RSD %)

0.931

0.792

0.622

0.774

0.832

0.851

0.641

0.826

Precision (RSD %)

 Repeatabiltya

0.821

0.612

0.481

0.765

0.851

0.805

0.733

0.914

 Reproducibilityb

0.933

0.693

0.531

0.801

0.942

0.912

0.799

0.982

 LODc (\(\upmu \)g/mL)

6.7

6.7

6.7

6.7

2.7

2.7

6.7

6.7

 LOQc (\(\upmu \)g/mL)

20

20

20

20

8

8

20

20

  1. aIntra-day (n = 3), average of three concentrations of each drug, repeated three times within the same day
  2. bInter-day (n = 3), average of three concentrations of each drug repeated three times in three consecutive days
  3. cLOD = 3.3 (SD/S), LOQ = 10(SD/S), where SD is the standard deviation of regression residuals and S is the slope of calibration curves
  4. *The robustness of the proposed method was investigated by analysis of samples under deliberate change in flow rate ± 0.1 mL/min
  5. **The robustness of the proposed method was investigated by analysis of samples under deliberate change in Temperature ± 0.1 °C