Liquid chromatography determination of citalopram enantiomers using β-cyclodextrin as a chiral mobile phase additive

被引:0
|
作者
Suez Canal University, Faculty of Pharmacy, Pharmaceutical Analytical Chemistry Department, Ismailia 41522, Egypt [1 ]
不详 [2 ]
机构
来源
J AOAC Int | 2006年 / 1卷 / 65-70期
关键词
Acetic acid - Graph theory - Isomers - pH effects - Ultraviolet detectors;
D O I
暂无
中图分类号
学科分类号
摘要
A reliable and specific method for the determination of citalopram enantiomers was developed and validated. Chromatographic resolution of citalopram enantiomers was made on a Shim-pack (5 μm particle size) cyanopropyl column with β-cyclodextrin (β-CD) as an effective chiral mobile phase additive. The composition of the mobile phase was (90 + 10, v/v) aqueous 0.1% triethylammonium acetate buffer, pH 4.0 (adjusted with acetic acid), and acetonitrile, containing 12 mM β-CD. The flow rate was 0.8 mL/min with ultraviolet detection at 240 nm. The effects of the mobile phase composition, concentration of β-CD, and pH of the triethylammonium acetate buffer on peak shape and resolution of the enantiomers were investigated. The calibration graphs were linear (r = 0.9999, n = 8) in the range of 1-40 μg/mL for S-(+) citalopram and R-(-) citalopram. The limit of detection values were 5.51 × 10-3 and 4.35 × 10-3 μg/mL, while the limit of quantification values were found to be 1.84 × 10-2 and 1.45 × 10-2 μg/mL for S-(+) citalopram and R-(-) citalopram, respectively.
引用
收藏
相关论文
共 50 条
  • [31] Chiral liquid chromatography contribution to the determination of the absolute configuration of enantiomers
    Roussel, C
    Del Rio, A
    Pierrot-Sanders, J
    Piras, P
    Vanthuyne, N
    JOURNAL OF CHROMATOGRAPHY A, 2004, 1037 (1-2) : 311 - 328
  • [32] Simultaneous determination of pirlindole enantiomers and dehydropirlindole by chiral liquid chromatography
    Ceccato, A
    Hubert, P
    de Tullio, P
    Liégois, JF
    Stachow, M
    Géczy, J
    Crommen, J
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1998, 17 (6-7) : 1071 - 1079
  • [33] Separation of the enantiomers of β-blocking drugs by TLC with a chiral mobile phase additive
    Tlvert, A.M.
    Backman, A.
    Journal of Planar Chromatography - Modern TLC: JPC, 1993, 6 (03):
  • [34] Separation of enantiomers by high performance liquid chromatography using derivants of L-proline as chiral mobile phase additives
    Chang Yinxia
    Hou Zhilin
    Li Qiwan
    Gao Tianrong
    Yuan Liming
    CHINESE JOURNAL OF ANALYTICAL CHEMISTRY, 2006, 34 : S100 - S104
  • [35] Resolution of racemic thyroxine with chiral additive as mobile phase by high performance liquid chromatography
    Wang, R
    Xie, JW
    Jia, ZP
    Hu, XL
    Chen, LR
    CHINESE JOURNAL OF ANALYTICAL CHEMISTRY, 2001, 29 (04) : 406 - 409
  • [36] A covalent organic framework for chiral capillary electrochromatography using a cyclodextrin mobile phase additive
    Gao, Lidi
    Zhao, Xuan
    Qin, Shili
    Dong, Qing
    Hu, Xingfang
    Chu, Hongtao
    CHIRALITY, 2022, 34 (03) : 537 - 549
  • [37] Effect of mobile phase composition on the separation of propranolol enantiomers using a perphenylcarbamate β-cyclodextrin bonded chiral stationary phase
    Ching, CB
    Fu, P
    Ng, SC
    Xu, YK
    JOURNAL OF CHROMATOGRAPHY A, 2000, 898 (01) : 53 - 61
  • [38] Determination of Atropine Enantiomers in Ophthalmic Solutions by Liquid Chromatography Using a Chiral AGP® Column
    Soares, Renata
    Singh, Anil Kumar
    Maria Kedor-Hackmann, Erika Rosa
    Rocha Miritello Santoro, Maria Ines
    JOURNAL OF AOAC INTERNATIONAL, 2009, 92 (06) : 1663 - 1672
  • [39] Enantiomeric resolution of dansyl phenylalanine and analogs by microcolumn liquid chromatography with γ-cyclodextrin as mobile phase additive
    Takeuchi, T.
    Nagae, N.
    HRC Journal of High Resolution Chromatography, 1992, 15 (02):
  • [40] Simultaneous determination of three alkaloids in Huangbo using an ionic liquid as a mobile phase additive in reversed-phase liquid chromatography
    Ding, Xiaoyuan
    Tang, Yan
    Sun, Ailing
    Liu, Renmin
    JOURNAL OF SEPARATION SCIENCE, 2015, 38 (03) : 374 - 380