Department of Instrumentation and Analytical Chemistry, CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, 116023, China; College of Science, Northeastern University, Shenyang, 110819, China.
College of Science, Northeastern University, Shenyang, 110819, China.
Talanta. 2024 Dec 1;280:126763. doi: 10.1016/j.talanta.2024.126763. Epub 2024 Aug 24.
Norfloxacin (NOR) and levofloxacin (LEV) are the two most frequently used fluoroquinolones (FQs) in clinic. Their residues seriously endanger the ecosystem and human health. Due to their similarity in structure and properties, it is urgent to develop an efficient and sensitive strategy for detection and differentiation. Herein, we synthesized a novel ratiometric fluorescent sensor for the first time by combining N, S co-doped carbon dots (CDs) and the precursors of Tb-MOFs through a facile one-pot method. The introduction of CDs effectively facilitated the energy transfer between Tb and FQs, overcoming the limitation that single Tb-MOFs could not identify similar antibiotics. Specifically, the presence of NOR resulted in reverse signal response through the inner filter effect and antenna effect. The synergistic effect of these two mechanisms contributed to achieving signal amplification accompanied by a distinguishable color transition. The limit of detection (LOD) was 0.036 μM. Different from NOR, the addition of LEV reduced the electron density of the system, weakened the coordination ability of Tb with LEV, and induced a single signal response with Tb fluorescence intensity as a reference signal (LOD = 0.383 μM). Furthermore, the method proved to be rapid and visual, allowing for the straightforward analysis of FQs residues in water, food matrices, and biological samples with satisfactory precision. By integrating N, S-CDs@Tb-MOFs with flexible substrates, the paper-based sensor facilitated the visual quantitative determination of FQs by reading RGB values. The developed sensor presents a promising strategy for the identification and real-time monitoring of antibiotics.
诺氟沙星(NOR)和左氧氟沙星(LEV)是临床中使用最广泛的两种氟喹诺酮类药物(FQs)。它们的残留严重威胁着生态系统和人类健康。由于它们在结构和性质上的相似性,因此迫切需要开发一种高效、灵敏的检测和区分策略。在这里,我们首次通过简便的一锅法将 N、S 共掺杂碳点(CDs)和 Tb-MOFs 的前体结合起来,合成了一种新型的比率荧光传感器。CDs 的引入有效地促进了 Tb 和 FQs 之间的能量转移,克服了单一 Tb-MOFs 无法识别类似抗生素的局限性。具体来说,NOR 的存在通过内滤效应和天线效应产生反向信号响应。这两种机制的协同作用有助于实现信号放大,并伴有可区分的颜色转变。检测限(LOD)为 0.036 μM。与 NOR 不同,LEV 的加入降低了体系的电子密度,削弱了 Tb 与 LEV 的配位能力,并以 Tb 荧光强度作为参考信号产生单一信号响应(LOD=0.383 μM)。此外,该方法快速、直观,可用于水、食品基质和生物样品中 FQs 残留的直接分析,具有令人满意的精密度。通过将 N、S-CDs@Tb-MOFs 与柔性基底集成,纸基传感器通过读取 RGB 值实现了 FQs 的可视化定量测定。该开发的传感器为抗生素的识别和实时监测提供了一种有前途的策略。