1996
DOI: 10.1016/0021-9673(95)00810-1
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Optimized micellar electrokinetic chromatographic separation of benzodiazepines

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Cited by 31 publications
(18 citation statements)
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“…The migration velocity and hence the migration times of BZDs depends on the partitioning of the solute between the CD and the micelle (Figure 3). 8,15,16 This technique is limited to solutes, which can fit into the CD cavity. The ratio of the solute incorporated into the micelle depends on its hydrophobicity but the inclusion complex formation of the solute with CD depends on the concordance of the solute molecular size with the CD cavity diameter.…”
Section: 10mentioning
confidence: 99%
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“…The migration velocity and hence the migration times of BZDs depends on the partitioning of the solute between the CD and the micelle (Figure 3). 8,15,16 This technique is limited to solutes, which can fit into the CD cavity. The ratio of the solute incorporated into the micelle depends on its hydrophobicity but the inclusion complex formation of the solute with CD depends on the concordance of the solute molecular size with the CD cavity diameter.…”
Section: 10mentioning
confidence: 99%
“…The ratio of the solute incorporated into the micelle depends on its hydrophobicity but the inclusion complex formation of the solute with CD depends on the concordance of the solute molecular size with the CD cavity diameter. 13,15 Using a molecular modulation program, Chem3D (CambridgeSoft), we followed the molecular complexation of BZDs with CDs. Having a rigid structure with a benzene ring condesated to a diazepinic one the complexation process for BZDs is difficult and far from perfect.…”
Section: 10mentioning
confidence: 99%
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“…The weak solvent strength of purely micellar eluents in the reversed-phase liquid chromatography can be increased by the addition of an organic modifier [2,3], which can also improve the efficiency of the chromatographic peaks [4]. Micellar mobile phase shows several advantages compared to the conventional hydro-organic eluents such as low cost, low toxicity, the possibility of simultaneous separation of ionic and nonionic compounds without needing a gradient elution, direct injection of biological fluids due to the solubility of proteins in the micelles, low volatility, detection sensitivity enhancement, unique separation selectivity [5][6][7][8], application in quantitative structureactivity relationship studies [9].…”
Section: Introductionmentioning
confidence: 99%