首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >A vinyl sulfone clicked carbon dot-engineered microfluidic paper-based analytical device for fluorometric determination of biothiols
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A vinyl sulfone clicked carbon dot-engineered microfluidic paper-based analytical device for fluorometric determination of biothiols

机译:一种乙烯基砜点击碳点工程的微流体纸 - 基于荧光素的分析装置,用于荧光测定生物硫醇

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摘要

A microfluidic paper-based analytical device integrating carbon dot (CDs) is fabricated and used for a fluorometric off-on assay of biothiols. Vinyl sulfone (VS) click immobilization of carbon dots (CDs) on paper was accomplished by a one-pot simplified protocol that uses divinyl sulfone (DVS) as a homobifunctional reagent. This reagent mediated both the click oxa-Michael addition to the hydroxyl groups of cellulose and ulterior covalent grafting of the resulting VS paper to NH2-functionalized CDs by means of click aza-Michael addition. The resulting cellulose nanocomposite was used to engineer an inexpensive and robust microfluidic paper-based analytical device (mu PAD) that is used for a reaction-based off-on fluorometric assay of biothiols (GSH, Cys, and Hcy). The intrinsic blue fluorescence of CDs (with excitation/emission maxima at 365/450 nm) is turned off via the heavy atom effect of an introduced iodo group. Fluorescence is turned on again due to the displacement of iodine by reaction with a biothiol. The increase in fluorescence is related to the concentration over a wide range (1 to 200 mu M for GSH and 5-200 mu M for Cys and Hcy, respectively), and the assay exhibits a low detection limit (0.3 mu M for GSH and Cys and 0.4 mu M for Hcy). The method allows for rapid screening and can also be used in combination with a digital camera readout.
机译:制造了一种基于微流体纸纸的分析装置,并用于生物硫醇的荧光离子测定。通过使用二乙烯基砜(DVS)作为同偶官能试剂的单盆简化方案,在纸上单击纸点(CDS)的固定碳砜(CDS)的固定化。该试剂介导通过点击AZA-Michael添加到NH 2官能化Cds的纤维素和Ulidorior的羟基的羟基和Ulidorior的羟基加入的咔啉和Ulidorior的羟基加来。得到的纤维素纳米复合材料用于工程师工程师,其基于廉价的微流体纸的分析装置(MU PAD),其用于基于反应的生物硫醇(GSH,Cys和Hcy)的反应的荧光测定。通过引入的Iodo组的重原子效应关闭Cds的固有蓝色荧光(365/450nm处的激发/发射最大值)。由于碘与生物硫醇的反应,荧光再次接通。荧光的增加与宽范围内的浓度有关(对于GSH的1至200μm,分别为Cys和Hcy的5-200μm),并且测定表现出低的检测极限(对于GSH,0.3μm,并且Hcy的Cys和0.4亩m)。该方法允许快速筛选,也可以与数码相机读数组合使用。

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