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Separation of corticosteroids by microemulsion EKC with diethyl L-tartrate as the oil phase.

Electrophoresis (2007-09-26)
Chi-Hung Wu, Tse-Hsien Chen, Kuan-Pin Huang, Guan-Ren Wang, Chuen-Ying Liu
RESUMO

A novel microemulsion based on a mixture of diethyl L-tartrate (DET) and SDS was developed for the microemulsion EKC (MEEKC) determination of structurally related steroids. The system consisted of 0.5% w/w DET, 1.7% w/w SDS, 1.2% w/w 1-butanol, 89.6% w/w phosphate buffer (40 mM, pH 7.0), and 7% w/w ACN. With an applied voltage of +10 kV, a baseline separation of aldosterone (A), cortisone acetate (CA), dexamethasone (D), hydrocortisone (H), hydrocortisone acetate (HA), prednisolone (P), prednisolone acetate (PA), prednisone (Ps), triamcinolone (T), and triamcinolone acetonide (TA) could be achieved. Under the optimized conditions, the reproducibility of the retention time (n = 4) for most of the compounds was less than +/-0.8% with the exception of A, Ps, and T. The average number of theoretical plates was 18 800 plates/m. The results were compared with those achieved by the modified micellar EKC (MEKC). MEEKC showed obvious advantages over MEKC for the separation of highly hydrophobic substances. To further evaluate the system, we tested the MEEKC method by analyzing corticosteroids in a spiked urine sample.

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Sigma-Aldrich
(+)-Diethyl L-tartrate, ≥99%
Sigma-Aldrich
(−)-Diethyl D-tartrate, ≥99%
Sigma-Aldrich
Cortisone 21-acetate, ≥99%
Sigma-Aldrich
Diethyl L-tartrate, ≥99%, FG
Cortisone acetate, European Pharmacopoeia (EP) Reference Standard