首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Selective and sensitive liquid chromatography-tandem mass spectrometry method for the determination of levonorgestrel in human plasma
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Selective and sensitive liquid chromatography-tandem mass spectrometry method for the determination of levonorgestrel in human plasma

机译:选择性灵敏液相色谱-串联质谱法测定人血浆中左炔诺孕酮

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A selective, sensitive and rapid liquid chromatography-tandem mass spectrometry method for the determination of levonorgestrel in plasma was developed. An Applied Biosystems API 3000 triple quadrupole mass spectrometer set to multiple reaction monitoring (MRM) mode, using atmospheric pressure photospray ionisation (APPI) in the positive mode. Using 17-alpha-methyltestosterone as internal standard (IS), liquid-liquid extraction was followed by reversed phase liquid chromatography using a phenyl-hexyl column and tandem mass spectrometric detection. The mean recovery for levonorgestrel and 17-alpha-methyltestosterone was 99.5 and 62.9%, respectively. The method was validated from 0.265 to 130 ng levonorgestrel/ml plasma with the lower limit of quantification (LLOQ) set at 0.265 ng/ml. This assay method makes use of the increased sensitivity and selectivity of tandem mass spectrometric (MS/MS) detection, allowing for a rapid (extraction and chromatography) and selective method for the determination of levonorgestrel in human plasma. The assay method was used in a pharmacokinetic study to quantify levonorgestrel in human plasma samples generated after administrating a single oral dose of 1.5 mg levonorgestrel to healthy female volunteers for up to five half lives. The total chromatographic runtime of this method was 5.0 min per sample, allowing for analysis of a large number of samples per batch. (C) 2004 Elsevier B.V. All rights reserved.
机译:建立了选择性,灵敏,快速的液相色谱-串联质谱法测定血浆中左炔诺孕酮的方法。 Applied Biosystems API 3000三重四极杆质谱仪设置为多重反应监控(MRM)模式,在正模式下使用大气压光喷雾电离(APPI)。使用17-α-甲基睾丸酮作为内标(IS),进行液-液萃取,然后使用苯基己基柱和串联质谱检测进行反相液相色谱。左炔诺孕酮和17-α-甲基睾丸激素的平均回收率分别为99.5%和62.9%。该方法在0.265至130 ng左炔诺孕酮/ ml血浆中得到验证,定量下限(LLOQ)设置为0.265 ng / ml。这种测定方法利用了串联质谱(MS / MS)检测的更高的灵敏度和选择性,从而可以快速(萃取和色谱分析)选择性测定人体血浆中的左炔诺孕酮。该测定方法用于药代动力学研究中,对健康女性志愿者口服单剂量1.5 mg左炔诺孕酮长达五个半衰期后,在人体血浆样品中定量左炔诺孕酮。此方法的总色谱运行时间为每个样品5.0分钟,从而允许每批分析大量样品。 (C)2004 Elsevier B.V.保留所有权利。

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