首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of intact oxaliplatin in human plasma using high performance liquid chromatography-tandem mass spectrometry
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Determination of intact oxaliplatin in human plasma using high performance liquid chromatography-tandem mass spectrometry

机译:高效液相色谱-串联质谱法测定人血浆中完整的奥沙利铂

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A HPLC-tandem mass spectrometry method was developed and validated for the quantitation of intact oxaliplatin in human plasma. Plasma ultrafiltrates were precipitated with acetonitrile and separation was performed on a 250 mm Beckman ODS reverse phase column using a gradient mobile phase. The mass spectrometer was operated in positive ionization mode using TurboionSpray and p recursor-production combinations of m/z 391.1 -> 305.1 and 371.1 -> 247.0 were monitored for oxaliplatin and carboplatin, the internal standard, respectively. The lower limit of quantitation for oxaliplatin was 20 ng/ml. The linear range of the method was 20-1000 ng/ml. The between- and within-day relative standard deviations ranged from 3.1 to 7.7%, and accuracy was within 5%. This method was successfully applied in a clinical study of oxaliplatin. (C) 2008 Elsevier B.V. All rights reserved.
机译:建立了高效液相色谱串联质谱法,并验证了人血浆中完整奥沙利铂的定量方法。用乙腈沉淀血浆超滤液,并使用梯度流动相在250 mm Beckman ODS反相色谱柱上进行分离。质谱仪使用TurboionSpray在正电离模式下运行,并分别监测m / z 391.1-> 305.1和371.1-> 247.0的p前体生成物的内标物奥沙利铂和卡铂。奥沙利铂的定量下限为20 ng / ml。该方法的线性范围是20-1000 ng / ml。日间和日间相对标准偏差在3.1到7.7%之间,准确度在5%之内。该方法已成功应用于奥沙利铂的临床研究。 (C)2008 Elsevier B.V.保留所有权利。

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