Establishing repeatability and ruggedness of chiral separations in micellar electrokinetic chromatography mass spectrometry: Combined use of covalently bonded capillary column and molecular micelles

• Published in: Journal of Chromatography A Vol. 1617; p. 460835
• Main Authors: Akter, Ferdoushi, Shamsi, Shahab A.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 26.04.2020
• Subjects: Adrenergic beta-Antagonists - analysis; Adrenergic beta-Antagonists - chemistry; AMPS bonded capillary column; Chiral analysis; Chromatography, Micellar Electrokinetic Capillary - methods; Leucine - analogs & derivatives; Leucine - chemistry; Micellar electrokinetic chromatography-mass spectrometry (MEKC-MS); Micelles; Poly-L-SUCL; Polymers - chemistry; Reproducibility of Results; Stereoisomerism; Tandem Mass Spectrometry - methods; β-blockers; Chiral analysis; β-blockers; Poly-L-SUCL; Micellar electrokinetic chromatography-mass spectrometry (MEKC-MS); AMPS bonded capillary column
• ISSN: 0021-9673; 1873-3778
• DOI: 10.1016/j.chroma.2019.460835

•A combination of covalently bonded AMPS capillary column and molecular micelles.•Optimize simultaneous chiral separations of three β-blockers.•A simple, precise and accurate MEKC-MS/MS for the quantitation of β-blockers in commercial tablets. Although micellar electrokinetic chromatography-mass spectrometry (MEKC-MS) using bare silica capillary filled with molecular micelles is an advantageous hyphenated technique for chiral analysis, it is still in the developmental stage. This is mainly because of the lower repeatability of retention time and peak area associated with the difficulty in controlling electroosmotic flow on bare silica capillaries. Besides the lower robustness and electrospray erosion of the fused-silica capillary tip, the lifetime is limited for 10–15 runs per capillary column. We have tested a new MEKC-MS method to eradicate this problem using a covalently bonded 2-acrylamido-2-methyl-1-propane-sulfonic acid (AMPS) column filled with free floating molecular micelles, polysodium N-undecenoxy carbonyl-L-leucinate (poly-L-SUCL). Simultaneous enantiomeric separations and MS/MS detection of three β-blockers [atenolol (ATEN), metoprolol (METO) and, pindolol (PINDO)] was achieved within 25 min with improved column lifetime of at least 45–50 runs. Excellent repeatability of retention time was observed for β-blockers, as evidenced by the relative standard deviation of less than 2% and 3% for intra-capillary and inter-capillary column, respectively. The linear calibration range of both β-blockers was simultaneously established using enantiomers of PINDO as an internal standard. The limit of detection and the lower limit of quantitation were 0.2 μg/mL and 0.5 μg/mL, respectively, for both ATEN and METO. Acceptable recovery of the enantiomeric content of the commercial METO tablet (98-99.5%) and ATEN tablet (89-92.5%) were obtained with adequate system suitability for the precision of peak area (≤10% RSD) under optimum conditions. The developed MEKC-MS approach was extended, which provided broader repeatibility of chiral separation to a panel of primary, secondary and tertiary amines as well as one anionic chiral compound.