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In this work, a ratiometric electrochemical sensor was developed for the detection of perphenazine (PPZ). The sensor was constructed by electrodepositing Cu-coordinated molecularly imprinted polymer (Cu-MIP) on Ag nanoparticles (NPs) modified flexible porous carbon cloth. The Cu-MIP showed highly electrochemical response because of the enhanced adsorptive ability and electronic properties of Cu chelation; Ag NPs could provide a stable and effective reference signal for ratiometric quantification. Thus the resulted sensor not only displayed high selectivity and sensitivity, but also exhibited satisfactory reproducibility and anti-interference ability. Under the optimum conditions, the quantitative detection of PPZ was performed with differential pulse voltammetry. It was found that the peak current ratio of PPZ and Ag NP was linear to the concentration of PPZ in the range of 1-700 nmol L (R = 0.9968), and the limit of detection was 0.43 nmol L (S/N = 3). The practicability of the sensor was examined by determining human serum and pharmaceutical samples, and satisfactory results and recoveries (ranging from 92.46% to 104.90%) were achieved.
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http://dx.doi.org/10.1016/j.aca.2022.340301 | DOI Listing |
J Fluoresc
September 2025
School of Life and Environmental Sciences, Guilin University of Electronic Technology, Guilin, 541004, China.
The pervasive concern regarding veterinary drug residues in food necessitates advanced detection solutions, particularly addressing limitations of conventional methods reliant on large-scale instrumentation that incur prolonged analysis duration, complex sample preparation, and lack of real-time on-site capability. A portable "single response-on" molecularly imprinted ratiometric fluorescent paper-based sensor was developed for quantifying fleroxacin (FLX) residues in animal-derived foods, wherein B, N-co-doped MXene quantum dot (B, N-MQD) was synthesized and combined with BCP-Eu as dual-emission fluorophores, while FLX- molecularly imprinted polymer (FLX-MIP) was engineered using functionalized Nano-SiO as the carrier. Concentration-dependent fluorescence enhancement at 574 nm was exhibited with invariant reference signal at 411 nm, achieving a 36-fold lower detection limit (0.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Department of Chemistry, School of Chemistry and Chemical Engineering, Key Laboratory of Surface & Interface Science of Polymer Materials of Zhejiang Province, Zhejiang Sci-Tech University, Hangzhou 310018, China. Electronic address:
Developing iron-based nanozymes with highly active sites and elucidating their catalytic mechanisms hold great promise for advancing applications in food safety, environmental monitoring and clinical medicine. Herein, vanadium (V)-doped FeO (V-FeO) nanozymes with peroxidase (POD)-mimetic activity were fabricated using a post-doping method and employed to construct a colorimetric/electrochemical dual-mode sensor for quantitative analysis of nitrite (NO). Experimental and density functional theory data show that the dopant of V into the structure of V-FeO nanozymes can enhance their POD-mimetic activity due to the increased oxygen vacancies and the improved adsorption ability for HO.
View Article and Find Full Text PDFAnal Chem
August 2025
Key Laboratory for Biorheological Science and Technology of Ministry of Education, Bioengineering College of Chongqing University, Chongqing 400044, PR China.
Continued development of high-performance, low-cost, in vitro diagnostic tools is critical for cancer diagnosis and therapeutic prognosis. Herein, we propose a four-response ratiometric electrochemical homogeneous biosensor based on positive MOF biomaterial for detection of the estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor-2 (HER2), and cell proliferation index (Ki67) protein biomarkers, and for simultaneous diagnosis of 10 types of breast cancer directly in human serum using a single electrode within one system. The principle of this specific four-response ratiometric electrochemical biosensor relied on neutral red (NR), tolonium blue (TB), tetramethylbenzidine (TMB), and malachite green (MG) loaded on the surface of UiO-66-NH.
View Article and Find Full Text PDFMikrochim Acta
August 2025
Department of Chemistry, Liaocheng University, Liaocheng, Shandong, 252059, People's Republic of China.
Ratiometric electrochemiluminescence (ECL) aptasensors have garnered significant interest in bioanalysis by simultaneously measuring two distinct emission signals and utilizing their intensity ratio for quantitative output. However, conventional designs face critical limitations. Mandatory aptamer functionalization elevates fabrication complexity and costs.
View Article and Find Full Text PDFEnviron Sci Technol
August 2025
State Key Laboratory of Regional Environment and Sustainability, School of Environment, Tsinghua University, Beijing 100084, PR China.
Accurately characterizing the proton's spatiotemporal distribution is critical for elucidating proton/electron generation and transfer mechanisms in electroactive biofilms (EABs). This study employed ratiometric fluorescence sensing for nondestructive, real-time pH mapping in current-producing EABs. The distribution of protons in EABs is determined by both their generation, which is electron donor-dependent, and their transfer, mediated by concentration gradients and buffering effects.
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