首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Exploiting the fluorescence resonance energy transfer (FRET) between CdTe quantum dots and Au nanoparticles for the determination of bioactive thiols
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Exploiting the fluorescence resonance energy transfer (FRET) between CdTe quantum dots and Au nanoparticles for the determination of bioactive thiols

机译:利用CDTE量子点和Au纳米粒子之间的荧光共振能量转移(FRET)以确定生物活性硫醇

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This work focused the implementation of FRET processes between CdTe quantum dots (QDs), acting as donors, and gold nanoparticles (AuNPs), behaving as acceptors, for the determination of several bioactive thiols such as captopril, glutathione, L-cysteine, thiomalic acid and coenzyme M. The surface chemistry of the QDs and AuNPs was adjusted with adequate capping ligands, i.e. mercaptopropionic acid and cysteamine, respectively, to guarantee the establishment of strong electrostatic interaction between them and promoting the formation of stable FRET assemblies. Under these circumstances the fluorescence emission of the QDs was completely suppressed by the AuNPs. The assayed target analytes were capable of disrupting the donor-acceptor assemblies yielding a concentration-related reversion of the FRET process and restoring QDs fluorescence emission. Distinct mechanisms, involving enhancing of the QDs quantum yield (QY), AuNPs agglomeration, nanoparticles detachment, etc., could be proposed to explain the referred FRET reversion. The developed approach assured good analytical working ranges and demonstrate adequate sensitivity for the assayed compounds, anticipating great prospective for implementing rapid, simple and reliable sensing methodologies for the monitoring of pharmaceutical, food and environmental species. However, selectivity could be a hindrance in the detection of these bioactive thiols in more complex matrices such as environmental and food samples. This problem could be circumvented through the employment of multivariate chemometric methods for the analysis and processing of whole fluorometric response. Moreover, the proposed methodology shows a great analytical versatility since it is possible to easily adapt the surface chemistry, of both QDs and AuNPs, to the chemical nature of the target analyte. (C) 2019 Elsevier B.V. All rights reserved.
机译:这项工作的重点是CDTE量子点(QDS)之间的FRET过程的实施,作用作供体,以及金纳米颗粒(AUNP),表现为受体,用于测定几种生物活性硫醇,如卡托普利,谷胱氨酸,L-半胱氨酸,硫代甲酸和辅酶M.用足够的覆盖配体,即巯基丙酸和半胱胺调节QDS和AUNP的表面化学,以保证在它们之间建立强的静电相互作用并促进形成稳定的FRET组件。在这种情况下,QDS的荧光发射完全被AUNP抑制。测定的靶分析物能够破坏供体 - 受体组件,从而产生浓度相关的FRET过程的逆转,并恢复QD荧光发射。可以提出涉及增强QDS量子产率(QY),AUNPS团聚,纳米粒子脱离等的不同机制来解释引用的FRET REFRAVER。开发的方法确保了良好的分析工作范围,并表现出对测定化合物的充分敏感性,预计实施用于监测药品,食品和环境物种的快速,简单可靠的传感方法。然而,在更复杂的基质(如环保和食物样品)中,选择性可能是检测这些生物活性硫醇的障碍。通过使用多元化学计量方法来避免这种问题,用于分析和加工整个缺汽反应。此外,所提出的方法表明了巨大的分析通用性,因为可以容易地使QD和AUNP的表面化学改善到目标分析物的化学性质。 (c)2019 Elsevier B.v.保留所有权利。

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