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基于山竹果皮衍生的氮掺杂碳量子点的分子印迹荧光传感器对链霉素的选择性检测

Selective detection of streptomycin using a molecularly imprinted fluorescence sensor based on mangosteen peel-derived nitrogen-doped carbon quantum dots.

作者信息

Pham Bach, Tran Dong Duong, Nguyen Thi Phuong Anh, Nguyen Quang Khanh, Ung Thi Dieu Thuy, Tran Ngoc Bich, Vu Duy Tung, Nguyen Thi Kim Thuong, Nguyen Thi Anh Huong, Pham Thi Ngoc Mai

机构信息

Faculty of Chemistry, University of Science, Vietnam National University, 19 Le Thanh Tong, Hoan Kiem, Hanoi 11000, Viet Nam.

Department of Chemistry, College of Natural Sciences, Hanyang University, Seoul 04763, Republic of Korea.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2025 Dec 15;343:126622. doi: 10.1016/j.saa.2025.126622. Epub 2025 Jun 30.

Abstract

Streptomycin, a broad-spectrum aminoglycoside antibiotic, is widely used in both human and veterinary medicine. Its overuse and environmental accumulation pose serious health risks, underscoring the need for sensitive and selective detection methods. In this study, we developed a molecularly imprinted fluorescence sensor (MIP-FS) by integrating nitrogen-doped carbon quantum dots (N-CQDs) with molecularly imprinted polymers (MIPs) for the selective detection of streptomycin. The N-CQDs were synthesized via a green microwave-assisted method using mangosteen peel as a sustainable and low-cost carbon source, representing an alternative biomass-based route for nanomaterial production. The resulting N-CQDs@MIPs displayed excellent fluorescence properties, high photostability, and strong selectivity for streptomycin through a fluorescence enhancement mechanism. Under optimized conditions, the sensor achieved a low detection limit of 3.2 nM (1.8 ppb) and a wide linear range from 0.01 to 8.00 μM. It also exhibited high selectivity against structurally similar antibiotics and common interfering ions. The method was successfully applied to pharmaceutical and environmental water samples, yielding results consistent with LC-MS/MS. These findings highlight the potential of the developed sensor as a rapid, sensitive, and eco-friendly tool for streptomycin detection in complex matrices.

摘要

链霉素是一种广谱氨基糖苷类抗生素,广泛应用于人类医学和兽医学。其过度使用和在环境中的积累带来了严重的健康风险,这凸显了对灵敏且具选择性的检测方法的需求。在本研究中,我们通过将氮掺杂碳量子点(N-CQDs)与分子印迹聚合物(MIPs)相结合,开发了一种用于选择性检测链霉素的分子印迹荧光传感器(MIP-FS)。N-CQDs是通过绿色微波辅助法,以山竹果皮作为可持续且低成本的碳源合成的,这代表了一种基于生物质的纳米材料生产替代路线。所得的N-CQDs@MIPs通过荧光增强机制表现出优异的荧光性能、高光稳定性以及对链霉素的强选择性。在优化条件下,该传感器实现了3.2 nM(1.8 ppb)的低检测限以及0.01至8.00 μM的宽线性范围。它对结构相似的抗生素和常见干扰离子也表现出高选择性。该方法成功应用于药物和环境水样,结果与液相色谱 - 串联质谱法(LC-MS/MS)一致。这些发现突出了所开发传感器作为一种用于在复杂基质中快速、灵敏且环保地检测链霉素的工具的潜力。

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