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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >A signal-on ratiometric fluorometric heparin assay based on the direct interaction between amino-modified carbon dots and DNA
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A signal-on ratiometric fluorometric heparin assay based on the direct interaction between amino-modified carbon dots and DNA

机译:基于氨基修饰的碳点和DNA之间的直接相互作用的基于直接相互作用的信号 - 用于比例的荧光血液测定

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摘要

Amino-modified carbon dots (C-dots) with positively charged surface were prepared. They display strong blue fluorescence and are shown to act as quenchers of the green fluorescence of FAM-labeled ssDNA such as the F-probe used in this work that was immobilized on the C-dots. On the addition of highly negatively charged heparin (Hep), it will interact with the C-dots and displace the F-probe from C-dots. Once the F-probe is displaced by Hep, its green fluorescence is restored. The intrinsic blue fluorescence of the C-dots remains stable after addition of Hep. Thus, a signal-on ratiometric fluorometric assay was developed for the ultra-sensitive detection of Hep. The underlying mechanisms of quenching and recovery are discussed. Under optimized conditions, the recovery of the ratiometric fluorescence of the system composed of C-dots and quenched F-probe is proportional to the Hep concentration in the range of 0.01-2.0 mu g.mL(-1) (=0.00125-0.25 U.mL(-1)). The method was successfully applied to the determination of Hep in spiked serum samples.
机译:制备具有带正电荷表面的氨基改性的碳点(C点)。它们显示强大的蓝色荧光,并且显示为FAM标记的SSDNA的绿色荧光的猝灭剂,例如在该工作中固定在C点上的该工作中使用的F探针。在添加高度带负电荷的肝素(HEP)上,它将与C点相互作用并置换来自C点的F探针。一旦F-探针被HEP移位,它会恢复其绿色荧光。在加入HEP后,C点的内在蓝色荧光保持稳定。因此,为HEP的超敏感检测开发了一种信号比率荧光测定法。讨论了淬火和恢复的潜在机制。在优化的条件下,由C点和淬火F探针组成的系统的比例荧光的回收与0.01-2.0μmmm1mml(-1)(= 0.00125-0.25 U.1)的恒温浓度成比例.ML(-1))。该方法成功地应用于尖刺血清样品中HEP的测定。

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