Jing Zhu, Peiming Yang, Qinghong Zhang, Wenwu Wang
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引用次数: 0
Abstract
Multiple CuNCs with modulable spectra were obtained by selecting nucleoside molecules as ligands. C-series CuNCs showed strong and discrepant emission intensities which were selected as the recognition elements of a three-channel fluorescent sensor array after surface modification with SH-β-cyclodextrin. Leveraging differences in host-guest recognition between various tetracyclines and the β-cyclodextrin cavity, the array generated distinct fluorescence response fingerprint patterns, enabling high-throughput discrimination of six structurally similar tetracycline antibiotics at different concentrations. Linear discriminant analysis revealed a linear relationship between the most influential discrimination factor and the antibiotic concentrations, allowing for highly sensitive and specific detection. And we obtained the satisfactory detection limits for tetracycline, aureomycin, oxytetracycline, doxycycline hydrochloride, minocycline and methacycline and they were 0.61 µM, 0.48 µM, 0.53 µM, 0.51 µM, 1.2 µM and 1.4 µM, respectively. Furthermore, the sensor array successfully identified spiked six antibiotics at different concentrations in environmental water and commercial milk samples, and achieved 100% accuracy in double-blind screening of unknown samples. This work provides an efficient sensing strategy for detecting structural analogs in complex matrices, with promising potential in environmental monitoring and food safety.
期刊介绍:
As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.