利用氧化单壁碳纳米角和低温酶辅助信号放大技术灵敏、选择性地荧光检测啶虫脒

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2024-09-10 DOI:10.1016/j.jphotochem.2024.116025
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引用次数: 0

摘要

针对中药农药残留检测准确度低的问题,我们开发了一种用于检测啶虫脒的生物传感器。首先,制备了一种能够吸附和淬灭荧光的氧化单壁碳纳米角。其次,基于这种纳米材料构建了一种新型荧光传感系统。对传感器系统的检测性能进行了评估,结果表明生物传感器的荧光淬灭主要是由于纳米材料吸附了适配体。最佳条件是纳米材料的质量浓度为 800 毫微克/毫升,孵育时间为 70 分钟,这样可获得最佳荧光响应。在这些最佳条件下,该系统被用于检测中药中的啶虫脒残留。荧光强度与啶虫脒浓度呈很强的线性关系,相关系数为 0.9985,检测限为 6.33 ng/mL。在样品测试中,该生物传感器表现出较高的准确性,平均回收率高,相对标准偏差低。该系统显示出卓越的选择性和检测性能,不受其他农药的干扰。
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Sensitive and selective fluorescence detection of acetamiprid using oxidized single-walled carbon nanohorns and cryonase-assisted signal amplification

To address the low accuracy of pesticide residue detection in traditional Chinese medicine, we developed a biosensor for acetamiprid detection. First, an oxidized single-walled carbon nanohorn capable of adsorbing and quenching fluorescence was prepared. Second, a novel fluorescence sensing system was constructed based on this nanomaterial. The detection performance of the sensor system was evaluated, which revealed that fluorescence quenching by the biosensor was primarily due to the adsorption of the aptamer by the nanomaterials. Optimal conditions were found to be a nanomaterial mass concentration of 800 ng/mL and an incubation time of 70 min, which resulted in the best fluorescence response. Under these optimal conditions, the system was used to detect acetamiprid residues in traditional Chinese medicine. The fluorescence intensity showed a strong linear relationship with acetamiprid concentration, with a correlation coefficient of 0.9985 and a detection limit of 6.33 ng/mL. In the sample test, the biosensor demonstrated high accuracy, with good average recovery rates and low relative standard deviation. The system showed excellent selectivity and detection performance, with no interference from other pesticides.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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