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Urinary 8-oxo-7,8-dihydro-2 '-deoxyguanosine analysis by an improved ELISA: An inter-laboratory comparison study

机译:改进的ELISA法测定尿中的8-oxo-7,8-dihydro-2'-deoxyguanosine:实验室间比较研究

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摘要

ELISA is commonly used for the detection of urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG), a marker of whole body oxidative stress. However, the method has been criticized for high inter-laboratory variability and poor agreement with chromatographic techniques. We performed an inter-laboratory comparison of 8-oxodG assessed in 30 urine samples and a urine spiked with four different concentrations of 8-oxodG by ELISA using standardized experimental conditions, including: sample pretreatment with solid-phase extraction (SPE), performing analysis using a commercial kit from a single manufacturer and strict temperature control during the assay. We further compared the ELISA results with high-performance liquid chromatography-tandem mass spectrometry (HPLC MS/MS) and performed tentative identification of compounds that may contribute to the discrepancy between both methods. For all but one participating laboratory (Data 1) we observed consistent ELISA results lying mostly within 1 SD of the mean 8-oxodG concentration. Mean 8-oxodG levels assessed by ELISA correlated with the data obtained by HPLC MS/MS (R=0.679, p < 0.001). The correlation improved when Data 1 were excluded from the analysis (R=0.749, p < 0.001). We identified three outlying urine samples; one with an ELISA 8-oxodG concentration lower, and two with 8-oxodG levels higher, than those measured by HPLC MS/MS. Omitting these samples further improved inter-methodology agreement (R=0.869, p <0.001). In the outliers with high 8-oxodG estimates various aromatic and heterocyclic compounds were tentatively identified using gas chromatography-mass spectrometry (GC MS). Application of authentic standards revealed the presence of saccharides, including D-glucose and D-galactose as putative interfering substances. In summary, assay standardization improved ELISA inter-laboratory agreement, although some variability is still observed. There are still compounds contributing to overestimation of 8-oxodG by ELISA, but only in some urine samples. Thus, despite significant improvement, ELISA still should not be considered a robust alternative to chromatographic techniques. (C) 2016 Elsevier Inc. All rights reserved.
机译:ELISA通常用于检测尿液中的8-oxo-7,8-dihydro-2'-deoxyguanosine(8-oxodG),这是全身氧化应激的标志。但是,该方法因实验室间变异性高和与色谱技术的一致性差而受到批评。我们使用标准化实验条件通过ELISA对30个尿液样品和掺有四种不同浓度的8-oxodG的尿液进行了实验室间比较,其中包括:固相萃取(SPE)样品预处理,进行分析在分析过程中使用单一制造商的商业试剂盒并进行严格的温度控制。我们进一步将ELISA结果与高效液相色谱-串联质谱(HPLC MS / MS)进行了比较,并对可能导致这两种方法之间差异的化合物进行了初步鉴定。对于除一个参与实验室外的所有实验室(数据1),我们观察到一致的ELISA结果大部分位于平均8-oxodG浓度的1 SD之内。通过ELISA评估的平均8-oxodG水平与通过HPLC MS / MS获得的数据相关(R = 0.679,p <0.001)。当从分析中排除数据1时,相关性得到改善(R = 0.749,p <0.001)。我们确定了三个外围尿液样本;与通过HPLC MS / MS测定的结果相比,一种具有较低的ELISA 8-oxodG浓度,而两种具有较高的8-oxodG水平。省略这些样本可进一步改善方法间的一致性(R = 0.869,p <0.001)。在使用高8-oxodG估计的异常值中,使用气相色谱-质谱(GC MS)初步确定了各种芳族​​和杂环化合物。可靠标准品的应用表明存在糖类,包括D-葡萄糖和D-半乳糖是假定的干扰物质。总而言之,尽管仍观察到一些可变性,测定法标准化改善了ELISA实验室间的一致性。仍然有一些化合物通过ELISA导致高估了8-oxodG,但仅在某些尿液样品中。因此,尽管有了重大改进,但仍不应将ELISA视为色谱技术的可靠替代品。 (C)2016 Elsevier Inc.保留所有权利。

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