Determination of sodium cromoglycate in human plasma by liquid chromatography-mass spectrometry in the turbo ion spray mode

被引:20
作者
Ozoux, ML [1 ]
Girault, J
Malgouyat, JM
Pasquier, O
机构
[1] Aventis Pharma, Dept Drug Metab & Pharmacokinet, DMPK France, F-92165 Antony, France
[2] Bioanalyt Labs, F-86000 Poitiers, France
来源
JOURNAL OF CHROMATOGRAPHY B | 2001年 / 765卷 / 02期
关键词
sodium cromoglycate;
D O I
10.1016/S0378-4347(01)00420-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A highly sensitivity liquid chromatography-tandem mass spectrometry method has been developed for the quantitation of sodium cromoglycate (SCG) in human plasma. The method was validated over a linear range of 0.100-50.0 ng/ml, using C-13(4) sodium cromoglycate as the internal standard. Compounds were extracted from 1.0 ml of lithium heparin plasma by methanol elution of C-18 solid-phase extraction cartridges. The dried residue was reconstituted with 100 mul of 0.01 N HCl, and 30 mul was injected onto the LC-MS-MS system. Chromatographic separation was achieved on a C8 (3.5 mum) column with an isocratic mobile phase of methanol-water-0.5 M ammonium acetate (35:64.8:0.2, v/v/v). The analytes were detected with a PE Sciex API 3000 mass spectrometer using turbo ion spray with positive ionization. Ions monitored in the multiple reaction monitoring (MRM) mode were m/z 469.2 (precursor ion) to m/z 245.1 (product ion) for SCG and m/z 473.2 (precursor ion) to m/z 247.1 (product ion) for C-13(4) SCG (I.S.). The average recoveries of SCG and the I.S. from human plasma were 91 and 87%, respectively. The low limit of quantitation was 0.100 ng/ml. Results from a 4-day validation study demonstrated excellent precision (C.V.% values were between 1.9 and 6.5%) and accuracy (-5.4 to -1.2%) across the calibration range of 0.100-50.0 ng/ml. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:179 / 185
页数:7
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