Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, China.
State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Wuhan 430074, P.R. China.
Anal Chem. 2023 Aug 22;95(33):12550-12556. doi: 10.1021/acs.analchem.3c02911. Epub 2023 Aug 7.
The classes and forms of antibiotics directly determine their ecotoxicity and environmental chemical behavior, and developing a sensor array for simultaneous and in situ detection of antibiotics is highly anticipated. In this study, different morphologies of g-CN with different fluorescence properties and peroxidase activity were prepared by regulating the degree of interlayer stacking and planar connectivity. Subsequently, in order to enhance its enzyme activity and amplify the differences in response signals to different antibiotics, three morphologies of g-CN/MIL-101(Fe) were prepared by in situ growth of equivalent amounts of MIL-101(Fe) on g-CN, respectively. The sensor array constructed based on the cross-response signals between g-CN/MIL-101(Fe) and antibiotics not only realized the simultaneous detection of quinolones, furans, tetracyclines, and lincomamides but also could efficiently identify their seven different forms. In the range of 0.2-0.8 ppm, the minimum detection limit for antibiotics was 12 ppb. In addition, the recovery experiments of multicomponent-mixed antibiotics in environmental samples show that the recovery rate remained at 91.42-107.59%, confirming the reliability and practicality of the sensor array. This study not only revealed the influence of crystal morphology regulation on the optical properties and enzyme activities of nanozymes, but also provided support for tracing, ecological remediation, and in situ environmental chemical behavior research of antibiotics.
抗生素的种类和形式直接决定了它们的生态毒性和环境化学行为,因此,开发一种用于同时和原位检测抗生素的传感器阵列备受期待。在本研究中,通过调节层间堆积程度和平面连接性,制备了具有不同荧光性质和过氧化物酶活性的不同形态的 g-CN。随后,为了提高其酶活性并放大对不同抗生素的响应信号差异,分别通过原位生长等量的 MIL-101(Fe),制备了三种形态的 g-CN/MIL-101(Fe)。基于 g-CN/MIL-101(Fe)与抗生素之间的交叉响应信号构建的传感器阵列不仅实现了喹诺酮类、呋喃类、四环素类和林可酰胺类抗生素的同时检测,还能有效地识别它们的七种不同形式。在 0.2-0.8ppm 范围内,抗生素的最低检测限为 12ppb。此外,环境样品中多组分混合抗生素的回收实验表明,回收率保持在 91.42-107.59%,证实了传感器阵列的可靠性和实用性。本研究不仅揭示了晶体形态调节对纳米酶光学性质和酶活性的影响,还为抗生素的追踪、生态修复和原位环境化学行为研究提供了支持。