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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Liquid chromatography/tandem mass spectrometry method for simultaneous determination of risperidone and its active metabolite 9-hydroxyrisperidone in human plasma
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Liquid chromatography/tandem mass spectrometry method for simultaneous determination of risperidone and its active metabolite 9-hydroxyrisperidone in human plasma

机译:液相色谱/串联质谱法同时测定人血浆中的利培酮及其活性代谢物9-羟基利培酮

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A rapid and sensitive liquid chromatography/tandem mass spectrometry (LC/MS/MS) method has been developed and validated for simultaneous quantification of risperidone (RSP) and its active metabolite 9-hydroxyrisperidone (9-OH-RSP) in human plasma. The analytes were extracted from human plasma by using the protein precipitation extraction technique. Methyl risperidone was used as internal standard for RSP and 9-OH-RSP. A Betasil C18 column provided chromatographic separation of analytes followed by detection with mass spectrometry. The mass transition ion-pair was followed as m/z 411.28 -> 191.15 for RSP and m/z 427.30 -> 207.10 for 9-OH-RSP. The method involves a simple extraction, isocratic chromatography conditions and mass spectrometric detection that enable detection at sub-nanogram levels. The proposed method has been validated with a linear range of 0.10-15.0 ng/mL for RSP and 9-OH-RSP. The intrarun and interrun precision and accuracy values were within 15%. The overall recoveries for RSP and 9-OH-RSP were 82.1% and 83.2%, respectively. The total analysis time was as low as 3.0 min only. The developed method was applied for the determination of the pharmacokinetic parameters of RSP and 9-OH-RSP following a single oral administration of a 1 mg RSP tablet in 24 healthy male volunteers. Copyright (c) 2006 John Wiley & Sons, Ltd.
机译:已开发出一种快速灵敏的液相色谱/串联质谱(LC / MS / MS)方法,并已验证可同时定量人血浆中的利培酮(RSP)及其活性代谢物9-羟基利培酮(9-OH-RSP)。使用蛋白质沉淀提取技术从人血浆中提取分析物。甲基利培酮用作RSP和9-OH-RSP的内标。 Betasil C18色谱柱提供了分析物的色谱分离,然后进行了质谱检测。对于RSP,质量转移离子对遵循m / z 411.28-> 191.15,对于9-OH-RSP,遵循m / z 427.30-> 207.10。该方法涉及简单的提取,等度色谱条件和质谱检测,可实现亚纳米级的检测。对于RSP和9-OH-RSP,所提出的方法已经在0.10-15.0 ng / mL的线性范围内进行了验证。批内和批间精度和准确性值均在15%以内。 RSP和9-OH-RSP的总回收率分别为82.1%和83.2%。总分析时间仅为3.0分钟。在24名健康男性志愿者中单次口服1 mg RSP片剂后,将开发的方法用于测定RSP和9-OH-RSP的药代动力学参数。版权所有(c)2006 John Wiley&Sons,Ltd.

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