Nguyen Van Anh Ngoc, Vu Trung Hieu, Nguyen Phuong Thy, Kim Moon Il
Department of BioNano Technology, Gachon University, 1342 Seongnamdae-ro, Sujeong-gu, Seongnam 13120, Republic of Korea.
Biosensors (Basel). 2025 Aug 13;15(8):528. doi: 10.3390/bios15080528.
We present a dual-mode optical sensing strategy for selective and sensitive detection of sulfide ions (S), employing copper-anchored nitrogen-doped graphene quantum dots (Cu@N-GQDs) as bifunctional nanozymes. The Cu@N-GQDs were synthesized via citric acid pyrolysis in the presence of ammonium hydroxide (serving as both nitrogen source and reductant) and copper chloride, leading to uniform incorporation of copper oxide species onto the N-GQD surface. The resulting nanohybrids exhibit two synergistic functionalities: intrinsic fluorescence comparable to pristine N-GQDs, and significantly enhanced peroxidase-like catalytic activity attributed to the anchored copper species. Upon interaction with sulfide ions, the system undergoes a dual-optical response: (i) fluorescence quenching via Cu-S complexation, and (ii) inhibition of peroxidase-like activity due to the deactivation of Cu catalytic centers via the interaction with S. This dual-signal strategy enables sensitive quantification of S, achieving detection limits of 0.5 µM (fluorescence) and 3.5 µM (colorimetry). The sensor demonstrates excellent selectivity over competing substances and high reliability and precision in real tap water samples. These findings highlight the potential of Cu@N-GQDs as robust, bifunctional, and field-deployable nanozyme probes for environmental and biomedical sulfide ion monitoring.
我们提出了一种用于选择性和灵敏检测硫化物离子(S)的双模式光学传感策略,采用铜锚定的氮掺杂石墨烯量子点(Cu@N-GQDs)作为双功能纳米酶。通过在氢氧化铵(用作氮源和还原剂)和氯化铜存在下柠檬酸热解合成Cu@N-GQDs,从而使氧化铜物种均匀地掺入到N-GQD表面。所得的纳米杂化物表现出两种协同功能:与原始N-GQDs相当的固有荧光,以及由于锚定的铜物种而显著增强的过氧化物酶样催化活性。与硫化物离子相互作用时,该系统会发生双光学响应:(i)通过Cu-S络合实现荧光猝灭,以及(ii)由于与S相互作用使Cu催化中心失活而抑制过氧化物酶样活性。这种双信号策略能够灵敏地定量S,实现0.5 μM(荧光)和3.5 μM(比色法)的检测限。该传感器对竞争物质表现出优异的选择性,并且在实际自来水样品中具有高可靠性和精密度。这些发现突出了Cu@N-GQDs作为用于环境和生物医学硫化物离子监测的强大、双功能且可现场部署的纳米酶探针的潜力。