Suppr超能文献

用于通过毛细管电泳-激光诱导荧光法分析尿样中8-羟基-2'-脱氧鸟苷的纸质固相微萃取

Paper-based solid-phase microextraction for analysis of 8-hydroxy-2'-deoxyguanosine in urine sample by CE-LIF.

作者信息

Meng Xiangying, Liu Qinrui, Ding Yongsheng

机构信息

College of Life Sciences, University of Chinese Academy of Sciences, Beijing, P. R. China.

出版信息

Electrophoresis. 2017 Feb;38(3-4):494-500. doi: 10.1002/elps.201600439. Epub 2016 Nov 28.

Abstract

An easy-to-do paper-based solid-phase microextraction (p-SPME) was developed for determination of 8-hydroxy-2'-deoxyguanosine (8-OHdG) in urine sample by CE-LIF. Small piece of filter paper was used as a solid phase to extract 8-OHdG from urine sample. Its primary mechanism is based on the hydrogen-bonding interaction between 8-OHdG and cellulose molecules. The effects of the pH of the sample solution, extraction time, and temperature on the peak area of the analyte were investigated in order to obtain the optimal p-SPME conditions. Comparing with the untreated sample, the p-SPME can significantly reduce the interference to the separation of 8-OHdG by CE-LIF. Meanwhile, the p-SPEM can provide more than three times concentrated effect. The developed method was evaluated according to an FDA guideline for biological analysis. The precisions (RSD%, n = 5) of the peak area and migration time of the analyte at three different concentrations were within 3.02-5.82% and 0.92-1.58%, respectively. The limit of identification of the method is about 5 nM according to the significant difference between two sets of the samples with and without spiking the standard (Student's t-test, p < 0.05). Good linearity was obtained in the range of 10-1000 nM (R >0.99) based on the standard addition. The recoveries at three different concentrations were within 99.8-103.5%. The results of the real sample analysis are consistent with those reported in our previous paper (Electrophoresis 2014, 35, 1873-1879).

摘要

开发了一种易于操作的纸质固相微萃取(p-SPME)方法,用于通过毛细管电泳-激光诱导荧光(CE-LIF)测定尿液样本中的8-羟基-2'-脱氧鸟苷(8-OHdG)。使用小片滤纸作为固相从尿液样本中萃取8-OHdG。其主要机理基于8-OHdG与纤维素分子之间的氢键相互作用。研究了样品溶液的pH值、萃取时间和温度对分析物峰面积的影响,以获得最佳的p-SPME条件。与未处理样品相比,p-SPME可显著降低CE-LIF对8-OHdG分离的干扰。同时,p-SPEM可提供超过三倍的浓缩效果。根据美国食品药品监督管理局(FDA)的生物分析指南对所开发的方法进行了评估。分析物在三种不同浓度下峰面积和迁移时间的精密度(相对标准偏差,n = 5)分别在3.02 - 5.82%和0.92 - 1.58%范围内。根据加标和未加标两组样品之间的显著差异(学生t检验,p < 0.05),该方法的鉴定限约为5 nM。基于标准加入法,在10 - 1000 nM范围内获得了良好的线性(R > 0.99)。三种不同浓度下的回收率在99.8 - 103.5%范围内。实际样品分析结果与我们之前论文(《电泳》2014年,35卷,1873 - 1879页)中报道的结果一致。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验