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. 2022 Jun 29;2022:6909528. doi: 10.1155/2022/6909528

Table 2.

Micellar electrokinetic chromatographic methods for determination of CP.

Technique Column (C) Mobile phase or eluent Conditions Matrices Reference
MEKC Uncoated FSC of 50 μm 6 mM Na2B4O7, 10 mM Na2HPO4, 75 mM SDS pH 9.1 257∗∗, V of 15 kV Human serum and plasma [50]
MEKC Uncoated FSC of 40.2 cm × 50 μm id Tris with SDS : MeOH 214∗∗, V of 15 kV Plasma and cerebrospinal fluid [51]
MEKC Uncoated FSC of 31.2 cm (21 cm × 675 mm ID) 10 mM tris buffer pH 8.0 + 150 mM SDS and 20 mM tris buffer pH 9.0 + 200 mM SDS 254∗∗, V was 8 kV Plasma and cerebrospinal fluid [52]
MEKC Bare FSC of 50 µm, 5 mmol with length 56 cm Imidazole buffer pH 5.1 240∗∗, V of 25 kV NMP in CP for injection [53]
MEKC Uncoated FSC length 31.2 cm Tris buffer + SDS as an electrolyte solution 214∗∗, V of 15 kV Commercial injections [54]
MEKC + indirect UV MEKC [A 50 lm i.d 64.5 cm (56 cm detection length) bare FSC]
IC [Gel IC-Cation-SW C (4.6 50 mm, 5 lm) supported by a water's cation GC (4.6·50 mm, 10 lm)]
MEKC (10 mM creatinine pH 3.8)
IC (ACN: 0.01 mM nitric acid) (1 : 100)
225∗∗
MEKC (V of 30 kV)
IC (1)
NMP in CP for injection [55]
CZE FSC (48.6 cm × 50 µm i.d.) with 40.2 cm as a detection length 40.2 cm) 15 mm sodium borate buffer pH 9.3 215∗∗, V was 20 kV Pharmaceutical formulations and
human plasma
[56]

(ml/min); ∗∗ (nm).