Novel MOF-integrated MXene-magnetite electrochemical platform for effective detection of chloramphenicol

Abstract

Chloramphenicol (CAP) contamination in natural waters presents an increasing concern due to its persistence and potential risks to ecosystems and human health. To address this challenge, an electrochemical sensing platform based on a Fe3O4@MXene@Fe-BDC composite modified screen-printed carbon electrode was developed and characterized. The hybrid material combines the high electrical conductivity of MXene, the magnetic and catalytic properties of Fe3O4, and the adsorption capabilities of the Fe-BDC metal–organic framework, resulting in a synergistic enhancement of sensing performance. Using differential pulse voltammetry, the sensor achieved a broad linear detection range from 1 to 309 µM, a low detection limit of 0.26 µM, and a high sensitivity of 0.95 µA µM−1 cm−2. X-ray photoelectron spectroscopy and electrochemical analyses revealed that functional groups such as carboxyl, phenolic, and Fe–O play a central role in CAP recognition through hydrogen bonding, π–π interactions, and metal–oxygen coordination pathways. The sensor also exhibited notable stability, retaining 95.7% of its initial response after 20 days, and performed reliably in complex water samples. These results demonstrate the potential of the Fe3O4@MXene@Fe-BDC architecture as an efficient and practical tool for monitoring chloramphenicol in environmental settings.

Graphical abstract: Novel MOF-integrated MXene-magnetite electrochemical platform for effective detection of chloramphenicol

Supplementary files

Article information

Article type
Paper
Submitted
16 Dec 2025
Accepted
06 Mar 2026
First published
16 Mar 2026
This article is Open Access
Creative Commons BY-NC license

Environ. Sci.: Adv., 2026, Advance Article

Novel MOF-integrated MXene-magnetite electrochemical platform for effective detection of chloramphenicol

R. Paz, H. Viltres, N. Gupta, C. Leyva, S. Srinivasan and A. R. Rajabzadeh, Environ. Sci.: Adv., 2026, Advance Article , DOI: 10.1039/D5VA00474H

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