首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Quantification of malondialdehyde in exhaled breath condensate using pseudo two-dimensional ultra-performance liquid chromatography coupled with single quadrupole mass spectrometry
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Quantification of malondialdehyde in exhaled breath condensate using pseudo two-dimensional ultra-performance liquid chromatography coupled with single quadrupole mass spectrometry

机译:使用伪二维超高性能液相色谱法与单Quadrupole质谱法耦合呼吸呼吸凝结物中丙二醛的定量

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We developed a robust analytical method for quantification of malondialdehyde (MDA) in exhaled breath condensate (EBC) via derivatization with 2,4-dinitrophenylhydrazine (DNPH). The target MDA-DNPH hydrazone was separated by ultra-performance liquid chromatography using two reversed-phase analytical columns (C-18 and phenyl-hexyl) inter-connected via a two-position, six-port switching valve to a single-quadrupole mass spectrometer. The target derivative was analyzed under positive electrospray ionization using single ion monitoring mode (m/z = 235 for the target derivative, and m/z = 237 for its labeled isotopic analog). This pseudo two-dimensional chromatographic separation provided optimum separation conditions for the target derivative resulting in the limit of detection of 0.58 nM in EBC sample (or 36.2 pmol on-column amount), which is comparable to those reported previously using different techniques, including tandem mass spectrometry. Based on the calibration solutions, the method had a linear quantification range of 1.0-200 nM (r2 = 0.998). The method showed good relative recoveries (92.2-102.0%) and acceptable precisions (3.6-12.2% for inter-day precision, and 4.3-12.4% for intra-day precision for two quality control levels, prepared from 5 nM and 25 nM solutions). The derivative was found to be stable at room temperature for 48 h or during analysis. The method was used to analyze 205 exhaled breath condensate samples collected from individuals from a healthy population of student athletes. MDA was detected in approximately 95% of these samples, with concentrations ranging from 1.16 to 149.63 nM. The median concentration was 6.82 nM, (IQR 4.08-9.88). These data demonstrate that our method can be successfully used to measure MDA in population studies.
机译:我们通过用2,4-二硝基苯基肼(DNPH)通过衍生化进行了一种稳健的分析方法,用于通过衍生化衍生化呼出呼吸凝结物(EBC)。通过通过双向六端口切换阀相互连接到单Quadrupole质量的两个反相分析柱(C-18和苯基 - 己基)通过超级性能液相色谱法分离靶MDA-DNPH腙。光谱仪。使用单离子监测模式(用于靶衍生物M / z = 235,对于其标记的同位素类似物的M / Z = 237,在正电喷雾电离下分析靶衍生物。该假二维色谱分离为靶衍生物提供了最佳的分离条件,该衍生物导致EBC样品中的0.58nm的检测极限(或36.2pmol柱量),其与先前使用不同技术的那些相当,包括串联质谱。基于校准溶液,该方法的线性定量范围为1.0-200nm(R2 = 0.998)。该方法表现出良好的相对回收率(92.2-102.0%)和可接受的精度(日常精度3.6-12.2%,用于两种质量控制水平的日内精确度为4.3-12.4%,由5 nm和25 nm溶液制备)。发现衍生物在室温下稳定48小时或分析期间。该方法用于分析从学生运动员的健康人群中收集的205次呼出的呼吸凝结水样。 MDA在大约95%的这些样品中检测到,浓度范围为1.16至149.63nm。中值浓度为6.82nm,(IQR 4.08-9.88)。这些数据表明,我们的方法可以成功地用于测量人口研究中的MDA。

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