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Fluorogenic atom transfer radical polymerization in aqueous media as a strategy for detection

机译:含水介质中的荧光原子转移自由基聚合作为检测策略

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The development of novel approaches to signal amplification in aqueous media could enable new diagnostic platforms for the detection of water-soluble analytes, including biomolecules. This paper describes a fluorogenic polymerization approach to amplify initiator signal by the detection of visible fluorescence upon polymerization in real-time. Fluorogenic monomers were synthesized and co-polymerized by atom transfer radical polymerization (ATRP) in water to reveal increasing polymer fluorescence as a function of both reaction time and initiator concentration. Optimization of the fluorogenic ATRP reaction conditions allowed for the quantitative detection of a small-molecule initiator as a model analyte over a broad linear concentration range (pM to mM). Raising the reaction temperature from 30 degrees C to 60 degrees C facilitated sensitive initiator detection at sub-picomolar concentrations in as little as 1 h of polymerization. This method was then applied to the detection of streptavidin as a model biological analyte by fluorogenic polymerization from a designed biotinylated ATRP initiator. Taken together, these studies represent the first example of a fluorogenic ATRP reaction and establish fluorogenic polymerization as a promising approach for the direct detection of aqueous analytes and biomolecular recognition events.
机译:在水性介质中发出信号扩增的新方法的开发可以使新的诊断平台用于检测水溶性分析物,包括生物分子。本文描述了通过在实时聚合时通过检测可见光荧光来扩增引发剂信号的荧光聚合方法。通过原子转移自由基聚合(ATRP)在水中合成荧光单体并共聚合,以显示随着反应时间和引发剂浓度的函数的增加。优化荧光ATRP反应条件的优化允许在宽线性浓度范围(PM至Mm)上为模型分析物进行定量检测。将反应温度从30℃升高至60℃的促进敏感引发剂检测,在亚微微摩尔浓度下,只为聚合的1小时。然后将该方法应用于通过设计的生物素化的ATRP引发剂的荧光聚合检测链霉抗生物素蛋白作为模型生物分析物的检测。总之,这些研究代表了荧光ATRP反应的第一实例,并建立了荧光聚合作为直接检测水性分析物和生物分子识别事件的有希望的方法。

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