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首页> 外文期刊>Analytical chemistry >Chromatographic detection using tris(2,2 '-bipyridyl)ruthenium(III) as a fluorogenic electron-transfer reagent
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Chromatographic detection using tris(2,2 '-bipyridyl)ruthenium(III) as a fluorogenic electron-transfer reagent

机译:使用三(2,2'-联吡啶基)钌(III)作为荧光电子转移试剂的色谱检测

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Tris(2,2'-bipyridyl)ruthenium can be excited to fluorescence by visible light (lambda(abs) 454 nm, lambda(em) 607 nn) when in the M(II) oxidation state, but not in the M(III) state. A novel chromatographic detection method using the non-fluorescent M(III) form of the complex as a postcolumn fluorogenic reagent is demonstrated. The M(III) form is a powerful oxidizing agent (E-o = 1.27 V vs NHE, 1.05 V vs Ag/AgCl). The M(nr) reagent is generated on-line from the M(II) form of the complex by a highly efficient porous carbon electrode and then reacted briefly with chromato-graphic effluent; the M(II) created by electron transfer from oxidation-susceptible analytes is then detected by fluorescence. The fluorescence detector can be calibrated for number of electrons transferred by injection of either M(II) or an oxidative standard such as ferrocyanide. It is hoped that this redox-based detection scheme will provide an alternative to electrochemical detection, Among the advantages are freedom fi om surface fouling and the potential for extremely low detection limits. The scheme was applied to detection of the peptide dynorphin A and several of its fragments. Dynorphin A contains tyrosine at the N-terminus (position 1) and tryptophan in position 15; these amino acid residues are susceptible to oxidation and peptides containing them can be detected on that basis. Flow injection testing of the model compounds Tyr-Gly-Gly-Phe-Leu and Gly-Gly-Trp-Gly indicated that tyrosine transferred similar to 1 electron to the M(III) reagent and that tryptophan transferred similar to 4 electrons, Similar results were obtained from the chromatographic runs. Dynorphin A and six dynorphin A fragments containing the N-terminal tyrosine were detected easily at 100 nM concentration (14 pmol) using laser-induced fluorescence. As expected, one fragment that did not contain tryptophan or tyrosine was not detected. A mass detection limit of 80 fmol was estimated far the tyrosine-containing fragments. [References: 34]
机译:当处于M(II)氧化态而不是M(III)氧化态时,三(2,2'-联吡啶)钌可以被可见光(λ454 nm,λ607 nn)激发为荧光。 )状态。展示了一种使用非荧光M(III)形式的配合物作为柱后荧光试剂的新型色谱检测方法。 M(III)形式是一种强大的氧化剂(E-o = 1.27 V(相对于NHE),1.05 V(相对于Ag / AgCl))。 M(nr)试剂通过高效的多孔碳电极从络合物的M(II)形式在线生成,然后与色谱流出物短暂反应;然后通过荧光检测由易氧化的分析物通过电子转移产生的M(II)。可以通过注入M(II)或氧化标准液(例如亚铁氰化物)来校准荧光检测器的转移电子数量。希望这种基于氧化还原的检测方案将提供电化学检测的替代方法,其中的优点是不受表面污染的影响以及潜在的极低检测限。该方案用于检测强啡肽A及其片段的检测。强啡肽A在N端(位置1)含有酪氨酸,在位置15处含有色氨酸。这些氨基酸残基易于氧化,因此可以检测到含有这些残基的肽。对模型化合物Tyr-Gly-Gly-Phe-Leu和Gly-Gly-Trp-Gly的流动注射测试表明,酪氨酸向M(III)试剂传递的电子相似,为1个,色氨酸与4个电子传递的相似。从色谱运行中获得。使用激光诱导的荧光,可以很容易地在浓度为100 nM(14 pmol)的条件下检测到含有N端酪氨酸的强啡肽A和六个强啡肽A片段。如预期的那样,未检测到一个不含色氨酸或酪氨酸的片段。估计含酪氨酸的片段的质量检测极限为80 fmol。 [参考:34]

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