2006
DOI: 10.1016/j.jchromb.2006.06.017
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Enantiomeric separation of norgestrel by reversed phase high-performance liquid chromatography using eluents containing hydroxypropyl-beta-cyclodextrin in stereoselective skin permeation study

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Cited by 16 publications
(5 citation statements)
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“…For example, ion-pairing reagent (octanesulfonic acid) was added to the eluent for the determination of the quaternary ammonium derivative pancuronium bromide [91] and hydroxypropyl-␤-cyclodextrin for the separation of norgestrel enantiomers [92]. A special branch of HPLC, micellar liquid chromatography where micelle forming agents such as in this case cetyl trimethyl ammonium bromide are added to the eluent was applied to the determination of betamethasone and dexamethasone in tablets and in a cocktail containing both drugs [93].…”
Section: Hplc Methodsmentioning
confidence: 99%
“…For example, ion-pairing reagent (octanesulfonic acid) was added to the eluent for the determination of the quaternary ammonium derivative pancuronium bromide [91] and hydroxypropyl-␤-cyclodextrin for the separation of norgestrel enantiomers [92]. A special branch of HPLC, micellar liquid chromatography where micelle forming agents such as in this case cetyl trimethyl ammonium bromide are added to the eluent was applied to the determination of betamethasone and dexamethasone in tablets and in a cocktail containing both drugs [93].…”
Section: Hplc Methodsmentioning
confidence: 99%
“…In vitro skin permeation studies of S-, R-and RS-PL hydrochloride across the excised rat dorsal skin were carried out according to the procedures described in our previous study. 19 The skin was mounted on the receptor compartment of a two-chambered Valia-Chien glass diffusion cell at 32 C with stirring at a constant rate of 500 rpm. The Valia-Chien cell was composed of a receptor compartment and a donor compartment, with a volume of 4 ml for each compartment, and an effective diffusion area of approximately 0.65 cm 2 .…”
Section: Application Of the Assaymentioning
confidence: 99%
“…The survey of literature revealed that there are chromatographic methods for enantiomeric separation of chiral drugs using β-cyclodextrin as chiral mobile phase additives [7][8][9][10][11][12][13][14]. But there are no reported methods for enantiomeric separation of milnacipran using chiral mobile phase additives.…”
Section: Introductionmentioning
confidence: 99%