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首页> 外文期刊>European journal of mass spectrometry >Rapid and sensitive determination of diacetylpolyamines in human fingernail by ultraperformance liquid chromatography coupled with electrospray ionization tandem mass spectrometry
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Rapid and sensitive determination of diacetylpolyamines in human fingernail by ultraperformance liquid chromatography coupled with electrospray ionization tandem mass spectrometry

机译:超高效液相色谱-电喷雾串联质谱法快速灵敏地测定人指甲中的二乙酰基多胺

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A rapid and sensitive ultraperformance Liquid chromatography coupled with electrospray ionization tandem mass spectrometry (UPLC-ESI-MS/MS) method has been developed and validated for quantitatively determining diacetylpolyamines in the human fingernail. N-1,N-8-diacetylspermidine (DiAct-Spd), N-1,N-12-lacetylspermine (DiAct-Spm) and 1,6-diam'nohexane WAN; [the internal standard [ISI] were extracted from human fingernail samples by a MeOH:MHCl solution, followed by 4-(N,N-dimethylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole [DBD-F] derivatization, and then separated on an ACQUITY BEH C18 column with a gradient elution of acetonitrile and water containing 0.1% formic acid. The derivatives of the diacetylpolyamines were fully separated within a short run time (3.0 min). The triple quadrupole mass spectrometric detection was performed in the multiple reactions monitoring (MRM) mode by the UPLC-ESI-MS/MS system in the positive ionization mode. MRM using the fragmentation transitions of m/z 455.20 -> 100.07, 737.25 -> 100.07 and 567.10 -> 3479.07 in the positive ESI mode was performed to quantify DiAct-Spd, DiAct-Spm and IS, respectively. The calibration curve is between 0.04 ng mL(-1) and 10 ng mL(-1) for DiAct-Spd and DiAct-Spm. The detection limits (signal to noise ratio of five) were 5-10 pg mL(-1). A good linearity was achieved from the calibration curves (r(2) > 0.9999), and the intra-day and inter-day assay precisions were less than 7.06%. Furthermore, the recoveries (%) of the diacetylpolyamines spiked in the human fingernails were 79.18-97.11. The present method proved that the high sensitivity is characterized by the specificity and feasibility of the sample analysis. Consequently, the proposed method was used to analyze human fingernail samples from 15 lung-cancer patients and 22 healthy volunteers. Diacetylpolyamines were detected from the fingernails of the lung-cancer patients for the first time. The concentration of DiAct-Spd in the lung-cancer patient group tended to be higher than those in the healthy volunteers.
机译:快速灵敏的超高性能液相色谱与电喷雾电离串联质谱法(UPLC-ESI-MS / MS)相结合,已开发并验证了用于定量测定人指甲中二乙酰基多胺的方法。 N-1,N-8-二乙酰基亚精胺(DiAct-Spd),N-1,N-12-乙酰基亚精胺(DiAct-Spm)和1,6-二氨基壬烷WAN; [内标[ISI]通过MeOH:MHCl溶液从人指甲样品中提取,然后进行4-(N,N-二甲基氨基磺酰基)-7-氟-2,1,3-苯并恶二唑[DBD-F]衍生化,然后在ACQUITY BEH C18色谱柱上进行分离,用乙腈和含有0.1%甲酸的水进行梯度洗脱。二乙酰基多胺的衍生物在短时间内(3.0分钟)被完全分离。 UPLC-ESI-MS / MS系统以正电离模式在多反应监测(MRM)模式下进行三重四极杆质谱检测。在正ESI模式下使用m / z 455.20-> 100.07、737.25-> 100.07和567.10-> 3479.07的片段化转移进行MRM分别定量DiAct-Spd,DiAct-Spm和IS。对于DiAct-Spd和DiAct-Spm,校准曲线在0.04 ng mL(-1)和10 ng mL(-1)之间。检出限(信噪比为5)为5-10 pg mL(-1)。从校准曲线获得了良好的线性度(r(2)> 0.9999),并且日内和日间测定精度均小于7.06%。此外,在人的指甲中加成的二乙酰基多胺的回收率(%)为79.18-97.11。本方法证明了高灵敏度的特点是样品分析的特异性和可行性。因此,该方法被用于分析15名肺癌患者和22名健康志愿者的人指甲样品。首次从肺癌患者的指甲中检测到二乙酰基多胺。肺癌患者组中DiAct-Spd的浓度往往高于健康志愿者中的浓度。

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