Determination of ibuprofen and naproxen in tablets

被引:86
作者
Sádecká, J [1 ]
Cakrt, M [1 ]
Hercegová, A [1 ]
Polonsky, J [1 ]
Skacáni, I [1 ]
机构
[1] Slovak Univ Technol Bratislava, Fac Chem Technol, Dept Analyt Chem, SK-81237 Bratislava, Slovakia
关键词
capillary isotachophoresis; fluorescence spectrometry; ibuprofen; naproxen;
D O I
10.1016/S0731-7085(01)00374-0
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Ibuprofen and naproxen have been quantified in tablets by capillary isotachophoresis. Hydrochloric acid (10 mmol/l) adjusted with creatinine to pH 5.0 plus 0.1% polyvinylpyrrolidone was used as the leading electrolyte and 10 mmol-l 4-morpholineethanesulfonic acid as the terminating electrolyte. Linearity was observed from 40.0 to 200.0 mg,l of ibuprofen (naproxen), with a coefficient of determination (r(2)) of 0.999. Good quantitation was obtained in short analysis time. The isotachophoretic results were compared with those obtained by the fluorescence spectrometry. Experimental parameters for ibuprofen were: lambda (EX) = 224 nm and lambda (EM)= 290 nm. Experimental parameters For naproxen were. lambda (EX) = 230 nm and lambda (EM) = 355 nm. The calibration plot was Found to be linear in the range 0.4-2.4 mg,l for ibuprofen and 5.0-20.0 mug/l for naproxen. The minimal sample pretreatment and relatively low running cost make isotachophoresis a good alternative to existing methods. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:881 / 891
页数:11
相关论文
共 25 条
[1]   PHARMACOLOGICAL DIFFERENCES BETWEEN OPTICAL ISOMERS OF IBUPROFEN - EVIDENCE FOR METABOLIC INVERSION OF (-)-ISOMER [J].
ADAMS, SS ;
BRESLOFF, P ;
MASON, CG .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1976, 28 (03) :256-257
[2]   SEPARATION AND IDENTIFICATION OF NONSTEROIDAL ANTIRHEUMATIC DRUGS CONTAINING A FREE CARBOXYL FUNCTION USING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
BATTISTA, HJ ;
WEHINGER, G ;
HENN, R .
JOURNAL OF CHROMATOGRAPHY, 1985, 345 (01) :77-89
[3]  
BOYNTON C S, 1988, Journal of Clinical Pharmacology, V28, P512
[4]   The non-aqueous titrimetric assay of the selected anti-inflammatory agents using tetra-n-butylammonium hydroxide as titrant [J].
Çakirer, O ;
Kiliç, E ;
Atakol, O ;
Kenar, A .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1999, 20 (1-2) :19-26
[5]   Development and robustness testing of a nonaqueous capillary electrophoresis method for the analysis of nonsteroidal anti-inflammatory drugs [J].
Cherkaoui, S ;
Veuthey, JL .
JOURNAL OF CHROMATOGRAPHY A, 2000, 874 (01) :121-129
[6]   THE DETERMINATION OF NONSTEROIDAL ANTIINFLAMMATORY DRUGS IN PHARMACEUTICALS BY CAPILLARY ZONE ELECTROPHORESIS AND MICELLAR ELECTROKINETIC CAPILLARY CHROMATOGRAPHY [J].
DONATO, MG ;
BAEYENS, W ;
VANDENBOSSCHE, W ;
SANDRA, P .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1994, 12 (01) :21-26
[7]  
EAKRT M, 2000, IN PRESS J CHROMAT A
[8]   Enantioselective determination by capillary electrophoresis with cyclodextrins as chiral selectors [J].
Fanali, S .
JOURNAL OF CHROMATOGRAPHY A, 2000, 875 (1-2) :89-122
[9]   Stereoselective determination of S-naproxen in tablets by capillary electrophoresis [J].
Fillet, M ;
Fotsing, L ;
Bonnard, J ;
Crommen, J .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1998, 18 (4-5) :799-805
[10]   FIA-FT-IR DETERMINATION OF IBUPROFEN IN PHARMACEUTICALS [J].
GARRIGUES, S ;
GALLIGNANI, M ;
DELAGUARDIA, M .
TALANTA, 1993, 40 (01) :89-93