Simultaneous determination of fluvoxamine isomers and quetiapine in human plasma by means of high-performance liquid chromatography

被引:64
|
作者
Saracino, Maria Addolorata
Mercolini, Laura
Flotta, Giuseppina
Albers, Lawrence J.
Merli, Roberto
Raggi, Maria Augusta
机构
[1] Univ Bologna, Alma Mater Studiorum, Dipartimento Sci Farmaceut, I-40126 Bologna, Italy
[2] Univ Calif Irvine, Mental Hlth Care Grp, Long Beach, CA 90822 USA
[3] ASL 12 Biella, Dipartimento Salute Mentale, Unita Modulare Psichiatr 2, I-13836 Cossato, BI, Italy
关键词
quetiapine; fluvoxamine isomers; human plasma; liquid chromatography; solid-phase extraction;
D O I
10.1016/j.jchromb.2006.06.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An original HPLC-UV method has been developed for the simultaneous determination of the atypical antipsychotic quetiapine and the geometric isomers of the second-generation antidepressant fluvoxamine. The analytes were separated on a reversed-phase C8 column (150 mm x 4.6 mm W., 5 mu m) using a mobile phase composed of acetonitfile (30%) and a 10.5 mM, pH 3.5 phosphate buffer containing 0.12% triethylamine (70%). The flow rate was 1.2 mL min(-1) and the detection wavelength was 245 nm. Sample pretreatment was carried out by an original solid-phase extraction procedure using mixed-mode cation exchange (DSC-MCAX) cartridges; only 300 mu L of plasma were needed for one analysis. Citalopram was used as the internal standard. The method was validated in terms of linearity, extraction yield, precision and accuracy. Good linearity was obtained in plasma over the 5.0-160.0 ng mL(-1) concentration range for each fluvoxamine isomer and over the 2.5-400.0 ng mL(-1) concentration range for quetiapine. Extraction yield values were always higher than 93%, with precision (expressed as relative standard deviation values) better than 4.0%. The method was successfully applied to human plasma samples drawn from patients undergoing polypharmacy with the two drugs. Satisfactory accuracy values were obtained, with mean recovery higher than 94%. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:227 / 233
页数:7
相关论文
共 50 条
  • [31] Determination of saquinavir in human plasma by high-performance liquid chromatography
    Ha, HR
    Follath, F
    Bloemhard, Y
    Krahenbuhl, S
    JOURNAL OF CHROMATOGRAPHY B, 1997, 694 (02): : 427 - 433
  • [32] Determination of omeprazole in human plasma by high-performance liquid chromatography
    Macek, J
    Ptacek, P
    Klima, J
    JOURNAL OF CHROMATOGRAPHY B, 1997, 689 (01): : 239 - 243
  • [33] Determination of tallimustine in human plasma by high-performance liquid chromatography
    Marrari, P
    Pianezzola, E
    Benedetti, MS
    JOURNAL OF CHROMATOGRAPHY B-BIOMEDICAL APPLICATIONS, 1996, 677 (01): : 133 - 139
  • [34] Determination of acyclovir in human plasma by high-performance liquid chromatography
    Boulieu, R
    Gallant, C
    Silberstein, N
    JOURNAL OF CHROMATOGRAPHY B, 1997, 693 (01): : 233 - 236
  • [35] Determination of cisapride in human plasma by high-performance liquid chromatography
    Campanero, MA
    Calahorra, B
    Garcia-Quetglas, E
    Honorato, J
    Carballal, JJ
    CHROMATOGRAPHIA, 1998, 47 (9-10) : 537 - 541
  • [36] Determination of lamotrigine in human plasma by high-performance liquid chromatography
    Angelis-Stoforidis, P
    Morgan, DJ
    O'Brien, TJ
    Vajda, FJE
    JOURNAL OF CHROMATOGRAPHY B, 1999, 727 (1-2): : 113 - 118
  • [37] Determination of eltanolone in human plasma by high-performance liquid chromatography
    Jones, DJ
    Bjorksten, AR
    Crankshaw, DP
    JOURNAL OF CHROMATOGRAPHY B, 1997, 694 (02): : 467 - 470
  • [38] Simultaneous determination of cefotaxime and desacetylcefotaxime in human plasma and cerebrospinal fluid by high-performance liquid chromatography
    Scanes, T
    Hundt, AF
    Swart, KJ
    Hundt, HKL
    JOURNAL OF CHROMATOGRAPHY B, 2001, 750 (01): : 171 - 176
  • [39] Simultaneous Determination of Isoniazid, Pyrazinamide, Rifampicin and Acetylisoniazid in Human Plasma by High-Performance Liquid Chromatography
    Zhifeng Zhou
    Lingyun Chen
    Peng Liu
    Mei Shen
    Fei Zou
    Analytical Sciences, 2010, 26 : 1133 - 1138