Department of Chemistry, Razi University, Kermanshah, Iran; Faculty of Chemistry, Institute for Advanced Studies in Basic Sciences, Zanjan, Iran.
Department of Chemistry, Razi University, Kermanshah, Iran.
Biosens Bioelectron. 2015 Sep 15;71:470-475. doi: 10.1016/j.bios.2015.04.073. Epub 2015 Apr 24.
Herein, we have described the application of high fluorescent carbon dots (CDs) without any surface modification as a simple and fast responding fluorescence probe for sensitive and selective determination of hemoglobin (Hb) in the presence of H2O2. Although Hb itself was able to quench the fluorescence of CDs, based on the inner filter effect (IFE) of the protein that affects both excitation and emission spectra of CDs, the presence of H2O2 resulted in further improvement of the sensitivity of Hb detection. The assay is based on the reaction of Hb with H2O2 that generates reactive oxygen species including hydroxyl (OH•) and superoxide (O2(•-)) radicals under heme degradation and/or iron release from Hb and the subsequent reaction of hydroxyl radicals, as strong oxidizing agents, with CDs resulting in high fluorescence quenching. The proposed probe was used for determination of Hb in concentration range of 1-100 nM with a detection limit of 0.4 nM. The method was successfully applied to the determination of Hb in human blood samples.
在此,我们描述了高荧光碳点(CDs)的应用,无需任何表面修饰,即可作为一种简单、快速响应的荧光探针,用于在 H2O2 存在下灵敏、选择性地测定血红蛋白(Hb)。虽然 Hb 本身能够猝灭 CDs 的荧光,但基于蛋白质的内滤效应(IFE),该效应同时影响 CDs 的激发和发射光谱,H2O2 的存在进一步提高了 Hb 检测的灵敏度。该测定法基于 Hb 与 H2O2 的反应,在血红素降解和/或铁从 Hb 释放的过程中生成包括羟基(OH•)和超氧自由基(O2(•-))在内的活性氧物质,随后羟基自由基作为强氧化剂与 CDs 反应,导致高荧光猝灭。该探针用于测定 1-100 nM 浓度范围内的 Hb,检测限为 0.4 nM。该方法成功地应用于人血样中 Hb 的测定。
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