节点文献

核酸酶催化放大传感体系的设计及其在铅离子比色检测中的应用

Design of DNA Enzyme Catalytic Amplification-based BiosensingPlatform for Colorimetric Detection of Lead Ions (Ⅱ)

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 高晓霞贾玉华杨金凤李继山杨荣华

【Author】 GAO Xiao-Xia1,JIA Yu-Hua1,YANG Jin-Feng1,2,LI Ji-Shan1,YANG Rong-Hua11(State Key Laboratory for Chemo/Biosensing and Chemometrics,College of Chemistry and Chemical Engineering,Hunan University,Changsha 410082,China)2(Department of Anesthesiology,Tumor Hospital,Xiangya School of of Medicine of Central South University,Changsha 410013,China)

【机构】 湖南大学化学化工学院化学生物传感与计量学国家重点实验室中南大学湘雅医学院附属肿瘤医院

【摘要】 基于8-17 DNA酶的催化切割特性和类辣根过氧化物酶DNA酶的氧化还原反应催化特性,发展了一种新型核酸酶催化放大传感体系,并用于Pb2+的比色检测。考察了K+浓度,pH值及反应时间对检测体系的影响。ABTS吸光度变化与Pb2+浓度在5.0~100 nmol/L范围内呈良好的线性关系,检出限为3.0 nmol/L。此外,因Pb2+酶的特异性,本方法对Pb2+具有良好的选择性。

【Abstract】 Based on the catalytic cleavage of 8-17 DNA enzyme(DNAzyme) and the catalytic redox of horseradish peroxidase(HRP)-mimicking DNAzyme,a novel DNAzyme catalytic amplification biosensing platform has been proposed for the colorimetric detection of lead ions(Pb2+).The effects of K+ concentration,pH value and incubation time on the detection system were investigated.The system exhibited a dynamic response range for Pb2+ from 5 to 100 nmol/L with a detection limit of 3 nmol/L.In addition,the selectivity of the sensor for Pb2+ against other environmentally related metal ions was outstanding.

【基金】 国家自然科学基金(Nos.21075032,21005026,21135001)
  • 【文献出处】 分析化学 ,Chinese Journal of Analytical Chemistry , 编辑部邮箱 ,2013年05期
  • 【分类号】O657.3
  • 【被引频次】9
  • 【下载频次】211
节点文献中: 

本文链接的文献网络图示:

本文的引文网络