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A Micro-Extraction Technique Using a New Digitally Controlled Syringe Combined with UHPLC for Assessment of Urinary Biomarkers of Oxidatively Damaged DNA

机译:微萃取技术使用新的数字控制注射器结合UHpLC的氧化受损DNa的生物标志物尿评估

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摘要

The formation of reactive oxygen species (ROS) within cells causes damage to biomolecules, including membrane lipids, DNA, proteins and sugars. An important type of oxidative damage is DNA base hydroxylation which leads to the formation of 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxodG) and 5-hydroxymethyluracil (5-HMUra). Measurement of these biomarkers in urine is challenging, due to the low levels of the analytes and the matrix complexity. In order to simultaneously quantify 8-oxodG and 5-HMUra in human urine, a new, reliable and powerful strategy was optimised and validated. It is based on a semi-automatic microextraction by packed sorbent (MEPS) technique, using a new digitally controlled syringe (eVol®), to enhance the extraction efficiency of the target metabolites, followed by a fast and sensitive ultrahigh pressure liquid chromatography (UHPLC). The optimal methodological conditions involve loading of 250 µL urine sample (1∶10 dilution) through a C8 sorbent in a MEPS syringe placed in the semi-automatic eVol® syringe followed by elution using 90 µL of 20% methanol in 0.01% formic acid solution. The obtained extract is directly analysed in the UHPLC system using a binary mobile phase composed of aqueous 0.1% formic acid and methanol in the isocratic elution mode (3.5 min total analysis time). The method was validated in terms of selectivity, linearity, limit of detection (LOD), limit of quantification (LOQ), extraction yield, accuracy, precision and matrix effect. Satisfactory results were obtained in terms of linearity (r2 > 0.991) within the established concentration range. The LOD varied from 0.00005 to 0.04 µg mL−1 and the LOQ from 0.00023 to 0.13 µg mL−1. The extraction yields were between 80.1 and 82.2 %, while inter-day precision (n = 3 days) varied between 4.9 and 7.7 % and intra-day precision between 1.0 and 8.3 %. This approach presents as main advantages the ability to easily collect and store urine samples for further processing and the high sensitivity, reproducibility, and robustness of eVol®MEPS combined with UHPLC analysis, thus retrieving a fast and reliable assessment of oxidatively damaged DNA.
机译:细胞内活性氧(ROS)的形成会损坏生物分子,包括膜脂质,DNA,蛋白质和糖。氧化损伤的一种重要类型是DNA碱基羟基化,它导致形成8-oxo-7,8-dihydro-2'-deoxyguanosine(8-oxodG)和5-羟甲基尿嘧啶(5-HMUra)。由于分析物的含量低且基质复杂,因此尿液中这些生物标记物的测量具有挑战性。为了同时定量人类尿液中的8-oxodG和5-HMUra,优化并验证了一种新的,可靠且功能强大的策略。它基于使用新型数字控制注射器(eVol ®)的填充吸附剂(MEPS)技术进行的半自动微萃取,可提高目标代谢物的提取效率,然后快速,高效灵敏的超高压液相色谱(UHPLC)。最佳方法学条件包括将250 µL尿液样品(1∶10的稀释度)通过C8吸附剂加载到置于半自动eVol ®注射器中的MEPS注射器中,然后使用90 µL 20%的溶液进行洗脱甲醇于0.01%甲酸溶液中。在UHPLC系统中,使用由0.1%甲酸水溶液和甲醇组成的二元流动相,在等度洗脱模式下直接分析获得的提取物(总分析时间为3.5分钟)。该方法在选择性,线性,检测限(LOD),定量限(LOQ),提取率,准确性,精密度和基质效应方面得到了验证。在设定浓度范围内的线性(r 2 -1 变化,LOQ从0.00023到0.13 µg mL -1 变化。提取率在80.1%至82.2%之间,而日间精度(n = 3天)在4.9%至7.7%之间变化,日内精度在1.0%至8.3%之间变化。这种方法的主要优点是可以轻松收集和存储尿液样本以进行进一步处理,并且eVol ® MEPS的高灵敏度,可重复性和耐用性与UHPLC分析相结合,从而实现了快速,可靠的评估氧化损伤的DNA。

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