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Table 5 Comparison between the different reported LC–MS/MS methods for CAB in plasma [17, 18] and the new suggested one

From: A validated LC–MS/MS method for analysis of Cabergoline in human plasma with its implementation in a bioequivalent study: investigation of method greenness

Analyte/application

Volume of human plasma

Extraction solvent composition/volume

Blood Volume

Internal standard

Components of Mobile system

Flow rate (mL/min)

Retention time/total run time

Stationary phase

Linear range of CAB (pg/mL)

The AGREE score

References

CAB alone/applied for pure CAB only in plasma samples but not for human volunteers

150 µL

A mixture of methylene chloride/isooctane, 2:3/2.5 mL

1 mL

Deutrated C14 labeled CAB

Aqueous solution of ammonium formate (10 mM, pH 3): acetonitrile (70/30, v/v)

0.5

4.26 min/4.27 min

A µ-Bondapak C18 (3.9 × 150 mm, 10 μm)

1.86–124.0

0.36

Allievi and Dostert [21]

CAB and L-dopa/for schizophrenic patients

100 µL

Acetonitrile, 20 mM ammonium formate liquid (90:10, v/v)/50 µL

Not mentioned

Deutrated C14 CAB

Gradient elution mode started with 20; 80 V, V acetonitrile; water (containing 20 mM ammonium formate) for 3 min

0.2

7.4 min/2.5 min

RP-COSMOSIL C8-MS column (2 mm × 150 mm, 5-mm diameter, Kyoto, Japan)

5–250

0.47

Igarashi et al. [22]

CAB alone/in pharmaceutical product analysis and pharmacokinetics studies

500 µL

Diethyl ether/3 mL

5 mL

Quetiapine

Isocratic mode, methanol: 20 mm ammonium acetate (70: 30, V/V)

0.75

2.6 min/5.5 min

Agilent eclipse reversed-phase C18 (3.5 µm, 4.6 × 100 mm) column

2–200

0.63

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