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Table 4 Stability of lenalidomide in plasma samples

From: Development and validation of a liquid chromatography-tandem mass spectrometric method for the determination of lenalidomide in human plasma and its application on bioequivalence studies

Nominal concentration (ng/mL)

Obtained concentration (ng/mL)

% CV

% RE

Autosampler stability

 26.25

26.63 ± 0.89

3.34

− 1.46

 807.64

815.27 ± 29.37

3.6

− 0.94

Freeze-thaw stability

 26.25

27.56 ± 0.70

2.54

− 4.99

 807.64

805.36 ± 29.96

3.72

0.28

Bench top stability

 26.25

27.02 ± 1.17

4.33

− 2.94

 807.64

808.84 ± 6.81

0.84

− 0.15

Dry extract stability in room temperature

 26.25

26.26 ± 1.26

4.81

− 0.04

 807.64

792.79 ± 30.55

3.85

1.84

Long term stability in plasma at 65 days in – 80 °C

 26.25

25.47 ± 0.36

1.42

2.95

 807.64

786.65 ± 6.01

0.76

2.60

Long term stability in plasma at 65 days in – 20 °C

 26.25

25.01 ± 0.49

1.96

4.71

 807.64

785.27 ± 0.82

0.82

2.75