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CdSe量子点荧光猝灭法测定尿嘧啶 被引量:1

Uracil Determination Based on Fluorescence Quenching of CdSe Quantum Dots
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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pH7.4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3.23×10-6mol/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. 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: Fo/F = 0.992 + 3.35 × 10^4 Q (mol/L) with the correlation coefficient of 0.999 1. The method has a detection limit of 3.23× 10^-6 mol/L (0.36 μg/ml). These results show that CdSe QDs can be potentially used as luminescent probe for detecting U.
出处 《中国生物化学与分子生物学报》 CAS CSCD 北大核心 2009年第10期963-968,共6页 Chinese Journal of Biochemistry and Molecular Biology
基金 国家自然科学基金(No.30670522) 国家重点基础研究发展规划(973计划 No.2006CB705602 2006CB933205)~~
关键词 CDSE量子点 尿嘧啶 荧光猝灭 含量测定 CdSe quantum dots uracil fluorescence quenching determination
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  • 1Morgan A R, Chlebek J. Uracil-DNA glycosylase in insects: Drosophila and the locust[ J]. J Biol Chem, 1989, 264(17) : 9911- 9914.
  • 2Stasolla C, Yeung E C. Endogenous ascorbic acid modulates meristem reactivation in white spruce somatic embryos and affects thymidine and uridine metabolism [ J ]. Tree Physiol, 2006, 26 ( 9 ) : 1197-1206.
  • 3陈晓光,王本祥,张洁,张宏.尿嘧啶对单胺氧化酶的抑制作用[J].生物化学杂志,1992,8(1):81-85. 被引量:19
  • 4Eliseev V V, Rodionova O M, Sapronov NS, et al. The effect of uridine and uridine nucleotides on isolated rat heart performance in regional myocardial ischemia[J]. Patol Fiziol Eksp Ter, 2002, (2):13-18.
  • 5Gamelin E, Boisdron-Celte M, Larra F, et al. A simple chromatographic method for the analysis of pyrimidines and their dihydrogenated metabolites [ J ]. J Liq Chromatogr Relat Technol,1997, 20(19): 3155-3172.
  • 6Yu L, Zhao J, Li S P, et al. Quality evaluation of Cordyceps through simultaneous determination of eleven nucleosides and bases by RP-HPLC[J]. J Sep Sci, 2006, 29(7) : 953-958.
  • 7Yang F Q, Li S, Li P, et al. Optimization of CEC for simultaneous determination of eleven nucleosides and nucleobases in Cordyceps using central composite design[J]. Electrophoresls, 2007, 28(11) : 1681-1688.
  • 8于文静,王焕群.HPLC法测定花鹿茸饮片中尿嘧啶及次黄嘌呤的含量[J].中国药品标准,2006,7(5):45-47. 被引量:10
  • 9Martins T B, Hillyard D R, Litwin C M, et al. Evaluation of a PCR probe capture assay for the detection of toxoplasma gondii - incorporation of uracil N-glycosylase for contamination control [ J ]. Am J Clin Pathol, 2000, 113(5): 714-721.
  • 10Sparidans R W, Bosch T M, Jorger M, et al. Liquid chromatographytandem mass spectrometric assay for the analysis of uracil, 5, 6- dihydrouracil and beta-ureidopropionic acid in urine for the measurement of the activities of the pyrimidine catabolic enzymes [ J]. J Chromatogr B Analyt Technol Biomed Life Sci, 2006, 839 (1-2) : 45-53.

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