Department of Analytical Chemistry, Marie-Curie Building (Annex), Campus of Rabanales, University of Cordoba, E-14071 Cordoba, Spain.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Mar 1;878(7-8):653-8. doi: 10.1016/j.jchromb.2010.01.024. Epub 2010 Jan 25.
A simple and sensitive method is proposed for the determination of seven low-molecular mass aldehydes in human urine samples using liquid chromatography with tandem mass spectrometric detection. Urine samples diluted twofold with 0.3M hydrochloric acid are aspirated into a LiChrolut EN solid-phase extraction column impregnated with 2,4-dinitrophenylhydrazine for cleanup, derivatization and preconcentration of the aldehydes. After elution of the hydrazones with acetonitrile, an aliquot is injected directly into the chromatograph. Identification and quantification of aldehydes was performed with electrospray in negative ion mode by selected reaction monitoring. By using synthetic urine samples, linearity is established over the concentration range 0.1-30 microg/l and limits of detection from 15 to 65 ng/l. The intra- and inter-day precision (RSD, %) of the aldehydes ranged from 2.9% to 6.4% and 3.6% to 9.3%, respectively, and specific uncertainties were ca. 5.0+/-0.3 ng for all aldehydes. Average recoveries performed on two levels by enriching synthetic urine samples ranged between 92% and 100%. The method was also validated in terms of study sample stability including long-term and short-term analyte stability, freeze-thaw and extract stability. In summary, the method proposed surpasses other recent chromatographic alternatives in terms of the limit of detection and sample requirements for analysis.
本文提出了一种简单灵敏的测定人尿液中七种低分子量醛类化合物的方法,采用液相色谱-串联质谱检测。尿液样品用 0.3M 盐酸稀释两倍后,用 2,4-二硝基苯肼浸渍的 LiChrolut EN 固相萃取柱进行净化、衍生和预浓缩。将腙用乙腈洗脱后,直接进样到色谱仪中。采用电喷雾负离子模式,通过选择反应监测对醛类化合物进行鉴定和定量。在合成尿液样品中,线性范围为 0.1-30 μg/l,检出限为 15-65 ng/l。醛类化合物的日内和日间精密度(RSD,%)分别为 2.9%-6.4%和 3.6%-9.3%,所有醛类化合物的特定不确定度约为 5.0+/-0.3 ng。通过对两种水平的合成尿液样品进行富集,平均回收率在 92%-100%之间。该方法还在研究样品稳定性方面进行了验证,包括长期和短期分析物稳定性、冻融和提取稳定性。综上所述,与其他最近的色谱替代方法相比,该方法在检测限和分析样品要求方面具有优势。