首页 | 本学科首页   官方微博 | 高级检索  
   检索      

CdSe量子点荧光猝灭法测定尿嘧啶
引用本文:郑剑威,王 永,戎 非,付德刚.CdSe量子点荧光猝灭法测定尿嘧啶[J].中国生物化学与分子生物学报,2009,25(10):963-968.
作者姓名:郑剑威  王 永  戎 非  付德刚
作者单位:;1)东南大学生物电子学国家重点实验室,南京210096;2)苏州市环境与生物安全重点实验室,苏州215123
摘    要:以CdSe量子点为荧光探针,基于荧光猝灭法对碱基尿嘧啶进行了定量检测,考察了缓冲液体系、反应时间、量子点浓度等多种因素的影响. 实验结果表明,在pH 7.4的0.2 mol/L Na2HPO4-NaH2PO4缓冲液中,反应时间为60 min,尿嘧啶浓度为10-6~10-4mol/L范围时,其线性回归方程为F0/F =0.992+3.35×104Q (mol/L),检测限为3.23×10-6 mol/L(即0.36μg/ml). 该方法检测范围宽,灵敏度高,为尿嘧啶的测定提供了新的方法.

关 键 词:CdSe量子点  尿嘧啶  荧光猝灭  含量测定  
收稿时间:2009-4-15
修稿时间:2009-7-16

Uracil Determination Based on Fluorescence Quenching of CdSe Quantum Dots
ZHENG Jian-Wei,WANG Yong,RONG Fei,FU De-Gang.Uracil Determination Based on Fluorescence Quenching of CdSe Quantum Dots[J].Chinese Journal of Biochemistry and Molecular Biology,2009,25(10):963-968.
Authors:ZHENG Jian-Wei  WANG Yong  RONG Fei  FU De-Gang
Institution:1) State Key Laboratory of Bioelectronics, Southeast University, Nanjing 210096, China;2)Key Laboratory of Environmental and Bio-Safety in Suzhou, Southeast University, Suzhou 215123, China
Abstract:Uracil (U) was quantitatively detected based on its fluorescence (FL) quenching of CdSe quantum dots (QDs). The experimental conditions including buffer solution, concentration of CdSe QDs, and incubation time are optimized in view of their influence on the FL behavior of the QDs. Under the optimized conditions, i.e. Na2HPO4-NaH2PO4 buffer solution with pH 7.4 and 60 min of incubation, the emission intensity of CdSe QDs and the concentration of U follow the Stern-Volmer equation in the range of 10-6~10-4mol/L. The obtained linear fitting equation is: F0/F =0.992+3.35×104Q (mol/L) with the correlation coefficient of 0.9991. The method has a detection limit of 3.23×10-6 mol/L (0.36μg/ml). These results show that CdSe QDs can be potentially used as luminescent probe for detecting U.
Keywords:CdSe quantum dots  uracil  fluorescence quenching  determination
点击此处可从《中国生物化学与分子生物学报》浏览原始摘要信息
点击此处可从《中国生物化学与分子生物学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号