CE Determination of 8-Hydroxy-2′-deoxguanosine in Urine Samples Based on Enrichment by Online Sweeping with Nanogold
摘 要
提出了纳米金在线富集-毛细管电泳法测定尿样中8-羟基-2′脱氧鸟嘌呤核苷(8-OHdG)的方法。试验选择了以下的分析条件:① 运行电压-20 kV;② 背景电解质为pH 8.2的20 mmol·L-1硼砂(含粒径10 nm纳米金溶液200 μL和0.1 mmol·L-1 CTMAB);③ 检测波长254 nm。试验证明背景电解质中的纳米金粒子与CTMAB形成胶束,提高了对8-OHdG的扫集能力,8-OHdG与dG在10 min内可实现基线分离。8-OHdG浓度在0.50~50.0 μmol·L-1范围内呈线性,检出限(3S/N)为39 nmol·L-1。方法用于尿样中8-OHdG含量的测定,所得加标回收率在90.0%~104.6%之间。
Abstract
A method for the determination of 8-hydroxy-2′-deoxguanosine (8-OHdG) in urine sample by CE based on enrichment by online sweeping with nanogold was proposed. Analytical conditions were studied and following optimized parameters were given: ① moving voltage: -20 kV; ② electrophoretic medium: 20 mmol·L-1 of borax solution (pH 8.2, including 10 nm nanogold solution of 200 μL and 0.1 mmol·L-1 CTMAB; ③ wavelength of detection: 254 nm. It was shown that micelle was formed between nanogold and CTMAB in the electrophoretic medium, which conduced to the sweeping of 8-OHdG. The baseline resolution was attained within 10 min. Linearity range between 0.50 and 50.0 μmol·L-1 was obtained with detection limit (3S/N) of 39 nmol·L-1. The proposed method was used in the determination of 8-OHdG in a urine samples, gving recovery found by standard addition method in the range of 90.0%-104.6%.
中图分类号 O657.8
所属栏目
基金项目 国家自然科学基金资助项目(20765003)
收稿日期 2011/3/5
修改稿日期
网络出版日期
作者单位点击查看
备注颜流水(1964-),男,江西进贤人,博士,教授,主要研究方向为毛细管电泳及色谱分析。
引用该论文: YAN Liu-shui,REN Yan,GUO Hui-qin,XIONG Meng-yao,HUANG Yan,XUE Kun-peng. CE Determination of 8-Hydroxy-2′-deoxguanosine in Urine Samples Based on Enrichment by Online Sweeping with Nanogold[J]. Physical Testing and Chemical Analysis part B:Chemical Analysis, 2011, 47(11): 1253~1255
颜流水,任艳,郭会琴,熊萌瑶,黄燕,薜昆鹏. 基于纳米金在线扫集-毛细管电泳法测定尿样中8-羟基-2′脱氧鸟嘌呤核苷[J]. 理化检验-化学分册, 2011, 47(11): 1253~1255
共有人对该论文发表了看法,其中:
人认为该论文很差
人认为该论文较差
人认为该论文一般
人认为该论文较好
人认为该论文很好
参考文献
【1】KASAI H, NISHIMURA S. Hydroxylation of deoxyguanosine at the C-8 position by ascorbic acid and other reducing agents[J]. Nuclear Acids Res, 1984,12:2137-2145.
【2】DEVASAGAYAM T P A, STEENKEN S, OBENDORF M S W, et al. Formation of 8-hydroxy(deoxy) guanosineandgeneration of strand break at guanine residues in DNA by singlet oxygen[J]. Biochemistry, 1991,30:6283-6289.
【3】梅素容,许国旺,吴采樱.人尿中8-羟基脱氧鸟苷的气相色谱分析方法[J].分析化学, 2001,29(12):1394-1397.
【4】SPERATI A, ABENI D D, TAGASSON C, et al. Exposure to indoor background radiation and urinary concentrations of 8-hydroxydeoxyguanosine, a marker of oxidative DNA damage[J]. Eur J Cancer, 1995,31A:934-940.
【5】MECOCCI P, MACGARVEY U, KAUFMAN A E, et al. Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain[J]. Ann Neurol, 1993,34(4):609-616.
【6】WU Lin-lin, Chiou Congeng, CHANG Pin-yan, et al. Urinary 8-OHdG: a marker of oxidative stress to DNA and a risk factor for cancer, atherosclerosis and diabetics[J]. Clinica Chimica Acta, 2004,339:1-9.
【7】WANG Xin-yi, ZOU Ming-jian. Determination of human urinary kanamycin in one step using urea-enhanced surface plasmon resonance light-scattering of gold nanoparticles[J]. Anal Bioanal Chem, 2009,395:2397-2403.
【2】DEVASAGAYAM T P A, STEENKEN S, OBENDORF M S W, et al. Formation of 8-hydroxy(deoxy) guanosineandgeneration of strand break at guanine residues in DNA by singlet oxygen[J]. Biochemistry, 1991,30:6283-6289.
【3】梅素容,许国旺,吴采樱.人尿中8-羟基脱氧鸟苷的气相色谱分析方法[J].分析化学, 2001,29(12):1394-1397.
【4】SPERATI A, ABENI D D, TAGASSON C, et al. Exposure to indoor background radiation and urinary concentrations of 8-hydroxydeoxyguanosine, a marker of oxidative DNA damage[J]. Eur J Cancer, 1995,31A:934-940.
【5】MECOCCI P, MACGARVEY U, KAUFMAN A E, et al. Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain[J]. Ann Neurol, 1993,34(4):609-616.
【6】WU Lin-lin, Chiou Congeng, CHANG Pin-yan, et al. Urinary 8-OHdG: a marker of oxidative stress to DNA and a risk factor for cancer, atherosclerosis and diabetics[J]. Clinica Chimica Acta, 2004,339:1-9.
【7】WANG Xin-yi, ZOU Ming-jian. Determination of human urinary kanamycin in one step using urea-enhanced surface plasmon resonance light-scattering of gold nanoparticles[J]. Anal Bioanal Chem, 2009,395:2397-2403.
相关信息