首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >A rapid and sensitive liquid chromatographyegative ion tandem mass spectrometry method for the determination of an indolocarbazole in human plasma using internal standard (IS) 96-well diatomaceous earth plates for solid-liquid extraction
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A rapid and sensitive liquid chromatographyegative ion tandem mass spectrometry method for the determination of an indolocarbazole in human plasma using internal standard (IS) 96-well diatomaceous earth plates for solid-liquid extraction

机译:使用内标(IS)96孔硅藻土板进行固液萃取的快速灵敏液相色谱/负离子串联质谱法测定人血浆中的吲哚咔唑

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摘要

A sensitive liquid chromatography/tandem mass spectrometry (LC/MS/MS) method for the quantitation of a novel topoisomerase I inhibitor (indolocarbazole derivative I) in human plasma was developed to support clinical studies. Drug and internal standard were isolated from plasma by solid-liquid extraction using 96-well diatomaceous earth plates. Various extraction solvents were evaluated for extraction of I and 9% isopropyl alcohol (IPA) in methyl-tert-butyl ether (MtBE) was chosen as the optimal extraction solvent. The sensitivity of this LC/MS/MS method is 10x higher in negative ion mode using alkaline conditions than in positive ion mode using a wide range of pH's. A mobile phase with 2 mM ammonium hydroxide enhanced the sensitivity in negative ion mode over other volatile bases. The calibration curve for compound I is linear over the range 0.05-200 ng/mL in plasma and the lower limit of quantification (LLOQ) of the assay is 0.05 ng/mL, when 0.25 mL of plasma is processed. The method was fully validated and successfully applied to plasma samples from clinical studies. Performing chromatography at high pH, for enhanced negative ion sensitivity, eliminates the need for post-column addition of base. Furthermore, the 96-well diatomaceous earth plate extraction offers the following advantages over liquid-liquid extraction (LLE) or solid-phase extraction (SPE): clean sample extracts with reduced sample preparation time; increased sample throughput; no conditioning or washing steps; and a neutral eluate applicable to acid/base labile compounds. Copyright (C) 2002 John Wiley Sons, Ltd. [References: 9]
机译:建立了用于定量测定人血浆中新型拓扑异构酶I抑制剂(吲哚并咔唑衍生物I)的灵敏液相色谱/串联质谱(LC / MS / MS)方法,以支持临床研究。使用96孔硅藻土板通过固液萃取从血浆中分离出药物和内标。评估了各种萃取溶剂对I的萃取,选择了在甲基叔丁基醚(MtBE)中的9%异丙醇(IPA)作为最佳萃取溶剂。这种LC / MS / MS方法在碱性条件下在负离子模式下的灵敏度比在宽pH值下在正离子模式下的灵敏度高10倍。与其他挥发性碱相比,含有2 mM氢氧化铵的流动相提高了负离子模式的灵敏度。当处理0.25 mL血浆时,化合物I的校准曲线在血浆中0.05-200 ng / mL范围内呈线性,测定的下限(LLOQ)为0.05 ng / mL。该方法已得到充分验证,并成功应用于临床研究中的血浆样品。在高pH下进行色谱分析,可增强负离子敏感性,因此无需在柱后添加碱。此外,与液液萃取(LLE)或固相萃取(SPE)相比,96孔硅藻土板萃取具有以下优势:清洁的样品萃取物,减少了样品制备时间;增加样品通量;没有调节或洗涤步骤;以及适用于酸/碱不稳定化合物的中性洗脱液。版权所有(C)2002 John Wiley Sons,Ltd. [参考:9]

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