Safwat Nardine, Mahmoud Amr M, Ayad Miriam F, Abdel-Ghany Maha F, Gomaa Mohammed M, Yamani Hend Z
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Ain Shams University, Cairo, 11566, Egypt.
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, 11562, Egypt.
Talanta. 2025 Aug 6;297(Pt B):128683. doi: 10.1016/j.talanta.2025.128683.
Dopamine (DPA) plays a critical role in regulating various physiological systems, and its abnormal levels are associated with disorders such as neurodegenerative diseases, psychiatric disorders, drug addiction, and certain cancers. Therefore, the development of reliable, rapid, and sensitive methods for DPA determination is crucial for early diagnosis and effective treatment, particularly in clinical settings and point-of-care testing (POCT). In this study, a "turn-on" fluorescent probe was developed using a terbium-based metal-organic framework (Tb-MOF) constructed from dual ligands. This design addresses the drawbacks of traditional turn-off MOF sensors by enabling fluorescence enhancement upon dopamine (DPA) recognition, leading to improved sensitivity and selectivity. The dual-ligand Tb-MOF design strategically combines terephthalic acid for efficient Tb sensitization with 2-methylimidazole facilitating selective dopamine recognition. After only 3 min of incubation in phosphate buffer (pH 7.00) at room temperature, the assay enables immediate detection of DPA in plasma and urine samples following simple protein precipitation, supporting its suitability for POCT. This represents a clear advantage over many previously reported fluorescent probes that require longer incubation times or elevated temperatures. The proposed probe demonstrated high selectivity and sensitivity for DPA determination in human plasma and urine, with a wide linear range of 1.00 × 10 - 1.00 × 10 M and a low limit of detection of 2.05 × 10 M. These advantages highlight the potential of this dual-ligand Tb-MOF probe as a valuable platform for point-of-care testing aimed at early detection and monitoring of DPA-related disorders.
多巴胺(DPA)在调节各种生理系统中起着关键作用,其异常水平与神经退行性疾病、精神疾病、药物成瘾和某些癌症等疾病相关。因此,开发可靠、快速且灵敏的DPA检测方法对于早期诊断和有效治疗至关重要,尤其是在临床环境和即时检测(POCT)中。在本研究中,使用由双配体构建的基于铽的金属有机框架(Tb-MOF)开发了一种“开启”荧光探针。这种设计通过在多巴胺(DPA)识别时实现荧光增强,解决了传统关闭型MOF传感器的缺点,从而提高了灵敏度和选择性。双配体Tb-MOF设计策略性地将用于有效铽敏化的对苯二甲酸与促进选择性多巴胺识别的2-甲基咪唑结合。在室温下于磷酸盐缓冲液(pH 7.00)中孵育仅3分钟后,该测定法能够在简单的蛋白质沉淀后立即检测血浆和尿液样本中的DPA,支持其适用于POCT。这相对于许多先前报道的需要更长孵育时间或更高温度的荧光探针具有明显优势。所提出的探针在人血浆和尿液中对DPA测定表现出高选择性和灵敏度,线性范围宽,为1.00×10⁻⁶ - 1.00×10⁻⁴ M,检测限低至2.05×10⁻⁷ M。这些优势突出了这种双配体Tb-MOF探针作为用于早期检测和监测与DPA相关疾病的即时检测有价值平台的潜力。