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Table 7 Comparison of the proposed HPLC method to the reported HPLC methods

From: Validated HPLC–PDA methodology utilized for simultaneous determination of Etoricoxib and Paracetamol in the presence of Paracetamol toxic impurities

Reported methods

Analytes separated

Linearity (µg/mL) of the drugs

Retention time

Impurities

Drugs

Ref (49)

PCM

5–30

3.07

 

ETO

5–30

5.72

Ref (50)

PCM

50–150

3.27

 

ETO

6–18

6.12

Ref (51)

PCM

8.3–41.5

3.12

 

ETO

1–5

6.82

Ref (52)

PCM

48–146

8.34

 

ETO

6 -19

18.45

Ref (53)

PCM

1200–3600

2.460

 

ETO

1000 -3000

1.189

Proposed method

PAP, PHA

PCM

1.5–30 μg /mL

3.41

 

ETO

1.5–30 μg /mL

7.27