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Table 8 Ruggedness, Robustness, and stability of analytical solution of the proposed UPLC and UV methods

From: Facile synthesis and eco-friendly analytical methods for concurrent estimation of selected pharmaceutical drugs in their solutions: application to quality by design, lean six sigma, and stability studies

Parameter

UPLC

UV

Limit %

RS

MCR

CFZ

PYD

CFZ

PYD

CFZ

PYD

Day to Day

0.82

0.93

0.63

0.81

0.56

0.77

RSD ≤ 2.0%

Analyst to Analyst

0.78

1.20

0.55

0.79

0.71

0.89

Column to Column

0.54

1.12

–

–

–

–

Flow rate change (± 0.1 mL/min)

0.95

1.27

–

–

–

–

pH changes of mobile phase (± 0.2)

0.83

0.88

–

–

–

–

Wavelength change (± 2.0) nm

0.90

0.96

0.78

0.88

0.83

0.91

Column temperature change (± 2.0) °C

0.69

0.84

–

–

–

–

Fresh Sample

0.11

0.20

0.10

0.14

0.13

0.15

Stored Sample in fridge

0.43

0.56

0.23

0.31

0.25

0.34

Stored Sample in room temperature

0.74

0.89

0.45

0.52

0.47

0.66