Dual emissive nanoprobe for reliable detection of antipsychotic drug fluphenazine using silicon nanoparticles and eosin dye

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
Yousef A. Bin Jardan , Mohamed M. El-Wekil , Mohamed R. Elmasry , Al-Montaser Bellah H. Ali
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Abstract

Fluphenazine (FLU) is a widely used antipsychotic drug associated with significant extrapyramidal side effects, including dystonia, akathisia, and Parkinsonism. As such, the development of innovative and reliable sensors for its precise determination is of critical importance. In this study, a robust ratiometric fluorescent sensor was designed for accurate sensing of FLU. The probe utilizes a combination of fluorescent silicon nanoparticles (fSiNPs) and eosin, which exhibit dual emissions at 430 nm (blue) and 512 nm (green) upon excitation at 330 nm. The addition of FLU resulted in a significant quenching of eosin fluorescence at 512 nm, attributed to electrostatic interactions, hydrogen bonding, and π–π stacking interactions between the aromatic systems. Meanwhile, the fluorescence emission of the silicon nanoparticles (fSiNPs) at 430 nm remained unaffected, serving as a stable internal reference signal for ratiometric measurements. The fluorescence intensity ratio (F430/F512) exhibited a linear response to FLU concentrations in the range of 0–400 µM, with a calculated detection limit of 1.5 nM (S/N = 3). The fluorescent system was successfully applied for the detection of FLU in pharmaceutical tablets and human biological fluids, including serum and urine samples. The method achieved recovery rates ranging from 95.5 % to 103.7 %, with RSDs between 2.54 % and 4.03 %. The results highlight the high accuracy, precision, and reproducibility of the method for FLU quantification across diverse sample matrices. This robust performance underscores the system’s potential as a reliable analytical tool for pharmaceutical quality control and clinical diagnostics.
用硅纳米粒子和伊红染料双发射纳米探针可靠地检测抗精神病药物氟非那嗪
氟非那嗪(FLU)是一种广泛使用的抗精神病药物,与显著的锥体外系副作用相关,包括肌张力障碍、静坐症和帕金森病。因此,开发创新和可靠的传感器来精确测定它是至关重要的。本研究设计了一种鲁棒的比例荧光传感器,用于流感的精确检测。该探针利用荧光硅纳米粒子(fSiNPs)和伊红的组合,在330 nm激发时表现出430 nm(蓝色)和512 nm(绿色)的双重发射。在512 nm处,由于静电相互作用、氢键和芳香体系之间的π -π堆叠相互作用,FLU的加入导致伊红荧光明显猝灭。同时,硅纳米颗粒(fSiNPs)在430 nm处的荧光发射不受影响,可作为比率测量的稳定内参信号。荧光强度比(F430/F512)对FLU浓度在0 ~ 400µM范围内呈线性响应,计算出的检出限为1.5 nM (S/N = 3)。该荧光系统已成功应用于药物片剂和人体生物体液(包括血清和尿液样本)中的流感检测。加样回收率为95.5% ~ 103.7%,rsd为2.54% ~ 4.03%。结果强调了流感定量方法在不同样品基质中的高准确性、精密度和可重复性。这种强大的性能强调了该系统作为药物质量控制和临床诊断的可靠分析工具的潜力。
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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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