Sambiagio Nicolas, Sauvain Jean-Jacques, Berthet Aurélie, Auer Reto, Schoeni Anna, Hopf Nancy B
Center for Primary Care and Public Health (Unisanté), University of Lausanne, Route de la Corniche 2, 1066 Epalinges-Lausanne, Switzerland.
Institute of Primary Health Care (BIHAM), University of Bern, Mittelstrasse 43, 3012 Bern, Switzerland.
Antioxidants (Basel). 2020 Dec 31;10(1):38. doi: 10.3390/antiox10010038.
Human biomonitoring of oxidative stress relies on urinary effect biomarkers such as 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG), and 8-iso-prostaglandin F2α (8-isoprostane); however, their levels reported for similar populations are inconsistent in the scientific literature. One of the reasons is the multitude of analytical methods with varying degrees of selectivity used to quantify these biomarkers. Single-analyte methods are often used, requiring multiple injections that increase both time and cost. We developed a rapid ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method to quantify both urinary biomarkers simultaneously. A reversed-phase column using a gradient consisting of 0.1% acetic acid in water and 0.1% acetic acid in methanol/acetonitrile (70:30) was used for separation. The MS detection was by positive (8-oxodG) and negative (8-isoprostane) ion-mode by multiple reaction monitoring. Very low limit of detection (<20 pg/mL), excellent linearity (R2 > 0.999), accuracy (near 100%), and precision (CV < 10%) both for intra-day and inter-day experiments were achieved, as well as high recovery rates (>91%). Matrix effects were observed but were compensated by using internal standards. Our newly developed method is applicable for biomonitoring studies as well as large epidemiological studies investigating the effect of oxidative damage, as it requires only minimal clean up using solid phase extraction.
人类氧化应激生物监测依赖于尿液效应生物标志物,如8-氧代-7,8-二氢-2'-脱氧鸟苷(8-氧代脱氧鸟苷)和8-异前列腺素F2α(8-异前列腺素);然而,科学文献中报道的类似人群的这些生物标志物水平并不一致。原因之一是用于量化这些生物标志物的分析方法众多,选择性程度各不相同。通常使用单分析物方法,这需要多次进样,增加了时间和成本。我们开发了一种快速超高效液相色谱-串联质谱(UPLC-MS/MS)方法,可同时对两种尿液生物标志物进行定量。使用由水相中0.1%乙酸和甲醇/乙腈(70:30)中0.1%乙酸组成的梯度的反相柱进行分离。通过多反应监测,以正离子模式(8-氧代脱氧鸟苷)和负离子模式(8-异前列腺素)进行质谱检测。实现了非常低的检测限(<20 pg/mL)、出色的线性(R2>0.999)、日内和日间实验的准确度(接近100%)和精密度(CV<10%),以及高回收率(>91%)。观察到基质效应,但通过使用内标进行了补偿。我们新开发的方法适用于生物监测研究以及调查氧化损伤影响的大型流行病学研究,因为它仅需要使用固相萃取进行最少的净化。