Simultaneous determination of multibenzodiazepines by HPLC/UV: Investigation of liquid-liquid and solid-phase extractions in human plasma

被引:72
作者
Borges, Keyller Bastos [1 ]
Freire, Ellen Figueiredo [2 ]
Martins, Isarita [3 ]
Pereira Bastos de Siqueira, Maria Elisa [3 ]
机构
[1] Univ Sao Paulo, Fac Pharmaceut Sci Ribeirao Preto, Dept Phys Chem, BR-14040903 Ribeirao Preto, Brazil
[2] Univ Sao Paulo, Fac Pharmaceut Sci Ribeirao Preto, Dept Pharmaceut Sci, BR-14040903 Ribeirao Preto, Brazil
[3] Univ Fed Alfenas, Lab Toxicol Anal, Alfenas, Brazil
基金
巴西圣保罗研究基金会;
关键词
Benzodiazepines; Flunitrazepam; Clonazepam; Oxazepam; Lorazepam; Chlordiazepoxide; Nordiazepam; Diazepam; N-Desalkylflurazepam; Human plasma; HPLC; LLE; SPE; CHROMATOGRAPHY-MASS SPECTROMETRY; NITROGEN-PHOSPHORUS DETECTION; COLUMN-SWITCHING TECHNIQUE; GAS-CHROMATOGRAPHY; WHOLE-BLOOD; HUMAN URINE; HUMAN-SERUM; POTENTIOMETRIC DETERMINATION; CAPILLARY-ELECTROPHORESIS; QUANTITATIVE-ANALYSIS;
D O I
10.1016/j.talanta.2008.11.003
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method for simultaneous determination of seven benzodiazepines (BZPs) (flunitrazepam, clonazepam, oxazepam, lorazepam, chlordiazepoxide, nordiazepam and diazepam using N-desalkylflurazepam as internal standard) in human plasma using liquid-liquid and solid-phase extractions followed by high-performance liquid chromatography (HPLC) is described. The analytes were separated employing a LC-18 DB column (250 mm x 4.6 mm, 5 mu m) at 35 degrees C under isocratic conditions using 5 mM KH2PO4 buffer solution pH 6.0: methanol: diethyl ether (55:40:5, v/v/v) as mobile phase at a flow rate of 0.8 mL min(-1). UV detection was carried out at 245 nm. Employing LLE, the best conditions were achieved with double extraction of 0.5 mL, plasma using ethyl acetate and Na2HPO4 pH 9.5 for pH adjusting. Employing SPE, the best conditions were achieved with 0.5 mL plasma plus 3 mL 0.1 M borate buffer pH 9.5, which were then passed through a C18 cartridge previously conditioned, washed for 3 times with these solvents: 3 mL 0.1 M borate buffer pH 9.5,4 mL Milli-Q water and 1 mL acetonitrile 5%, finally the BZPs elution was carried with diethyl ether: n-hexane: methanol (50:30:20). In both methods the solvent was evaporated at 40 degrees C under nitrogen flow. The validation parameters obtained in LLE were linearity range of 50-1200 ng mL(-1) plasma (r >= 0.9927), limits of quantification of 50 ng mL(-1) plasma, within-day and between-day CV% and E% for precision and accuracy lower than 15%, and recovery above 65% for all BZPs. In SPE, the parameter obtained were linearity range of 30-1200 ng mL(-1) plasma (r >= 0.9900), limits of quantification of 30 ng mL(-1) plasma, within-day and between-day CV% and E% for precision and accuracy lower than 15% and recovery above 55% for all BZPs. These extracting procedures followed by HPLC analysis showed their suitable applicability in order to examine one or more BZPs in human plasma. Moreover, it could be suggested that these procedures might be employed in various analytical applications, in special for toxicological/forensic analysis. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:233 / 241
页数:9
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