Basak Dipanwita, Gajurel Sushmita, Vashisht Aseem, Saikia Hemaprobha
Department of Chemistry, Bodoland University, Kokrajhar, BTR, Assam Pin, Kokrajhar, 783370, Assam, India.
University Center for Research and Development, Chandigarh University, Mohali, 140413, India.
J Fluoresc. 2025 Sep 4. doi: 10.1007/s10895-025-04544-z.
The real-time and selective detection of dopamine (DA) in complex biological systems remains a critical challenge due to its low physiological concentrations and interference from structurally similar biomolecules such as ascorbic acid and uric acid. Traditional analytical techniques often fall short in terms of specificity, cost-effectiveness, and ease of deployment in biological matrices. To address this gap, we developed a highly selective fluorescent nanosensor based on bentonite-supported Cu-based bimetallic nanoparticles (B/nZVCu-Ni/Ag), synthesized via a green route using Lawsonia inermis extract. The phytogenic synthesis facilitated the reduction and stabilization of the nanoparticles, yielding well-dispersed crystalline domains (10-13 nm) anchored uniformly on the bentonite layered sheets. Comprehensive characterization through PXRD, FTIR, TEM, UV-Vis, and fluorescence spectroscopy confirmed the formation and functional integration of the nanoparticles. Among the two variants, the B/nZVCu-Ni (D1) probe exhibited superior fluorescence enhancement upon interaction with DA, achieving a detection limit as low as 5.13 nM and a high binding constant (K = 1.47 × 10⁵ M⁻¹). The sensor demonstrated excellent selectivity, with negligible response to common interfering agents, and displayed a robust reversible on-off fluorescence behavior upon sequential addition and removal of DA using EDTA , confirming dynamic binding reversibility. These results establish the B/nZVCu-M nanoprobes, particularly D1, as promising candidates for ultrasensitive, interference-resistant, and reusable fluorescence-based detection of dopamine in synthetic urine sample.
由于多巴胺(DA)在复杂生物系统中的生理浓度较低,且易受结构相似的生物分子(如抗坏血酸和尿酸)的干扰,因此对其进行实时、选择性检测仍然是一项严峻挑战。传统分析技术在特异性、成本效益以及在生物基质中的易用性方面往往存在不足。为了填补这一空白,我们开发了一种基于膨润土负载的铜基双金属纳米粒子(B/nZVCu-Ni/Ag)的高选择性荧光纳米传感器,该纳米粒子通过使用无刺番荔枝提取物的绿色路线合成。植物源合成促进了纳米粒子的还原和稳定,产生了均匀锚定在膨润土层片上的分散良好的结晶域(10 - 13纳米)。通过粉末X射线衍射(PXRD)、傅里叶变换红外光谱(FTIR)、透射电子显微镜(TEM)、紫外可见光谱和荧光光谱进行的综合表征证实了纳米粒子的形成和功能整合。在这两种变体中,B/nZVCu-Ni(D1)探针在与DA相互作用时表现出优异的荧光增强,检测限低至5.13 nM,结合常数高(K = 1.47×10⁵ M⁻¹)。该传感器表现出优异的选择性,对常见干扰剂的响应可忽略不计,并且在使用乙二胺四乙酸(EDTA)依次添加和去除DA时表现出稳健的可逆开关荧光行为,证实了动态结合可逆性。这些结果表明,B/nZVCu-M纳米探针,特别是D1,有望成为用于合成尿液样本中多巴胺的超灵敏、抗干扰和可重复使用的基于荧光检测的候选物。