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Chlortetracycline (CTC), one of the tetracyclic antibiotics, has been widely employed for the inhibition of bacteria. Due to the potential threat to human health posed by the residual CTC, the development of ratiometric fluorescent probes that can achieve accurate measurement and in-situ imaging is urgently needed but remains challenged. Here, a bovine serum albumin (BSA)-involved host-guest system was designed as the novel ratiometric probe (C3@BSA) for CTC based on the indicator-displacement assay principle. Significantly, the fluorescence difference between the CTC@BSA complex and other tetracyclic@BSA complexes ensured high selectivity of this probe. The indicator (C3) was rationally derived from a simple chalcone dye with weak binding affinity to BSA (1.7 × 10 M) compared with CTC (2.2 × 10 M). The sensing process can finish in 10 s with sensitive response (detection limit: 0.23 μM) and anti-interference capacities over common ions and amino acids. On this basis, the probe was successfully used to detect CTC in HeLa cells and B16 cells, where the distributions of CTC were displayed under a dual-channel imaging mode for the first time. Our research provided a novel ratiometric probe for CTC and an effective strategy for designing ratiometric fluorescent indicator-displacement assays.
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http://dx.doi.org/10.1016/j.talanta.2024.127251 | DOI Listing |
Eur J Med Chem
November 2025
Department of Chemistry and Molecular Biology, University of Gothenburg, Medicinaregatan 7B, 413 90, Gothenburg, Sweden. Electronic address:
Environment-sensitive fluorescent probes are indispensable tools for studying biological systems and advancing drug discovery. This study reports the development of 4-sulfamoyl-7-aminobenzoxadiazole (SBD)-based fluorescent probes for the allosteric site of the liver isoform of pyruvate kinase (PKL). By integrating SBD moieties into known activator scaffolds, such as mitapivat and diarylsulfonamide (DASA) ligands, probes for indicator displacement assays were designed to quantify ligand interactions in the allosteric site.
View Article and Find Full Text PDFMikrochim Acta
July 2025
Department of Materials and Textile Technology, Faculty of Science and Technology, Thammasat University, Pathumtani, 12120, Thailand.
Cellulose nanocrystals (CNCs) were successfully extracted and purified from cotton fabric waste via alkali treatment and acid hydrolysis. The resulting nanostructure was characterized using transmission electron microscopy (TEM) and X-ray diffraction spectroscopy (XRD), confirming the successful isolation of CNCs. A PV/Cu-CNCs/CNFs/PVA hydrogel was then synthesized through chemical crosslinking of polyvinyl alcohol (PVA), cellulose nanofibrils (CNFs), cellulose nanocrystals (CNCs), and borax.
View Article and Find Full Text PDFDalton Trans
August 2025
Institute of Chemistry, National Autonomous University of Mexico, Ciudad Universitaria, México, 04510, CDMX, Mexico.
Selective recognition and sensing of neurotransmitters in aqueous media using artificial receptors is an attractive but challenging goal in modern supramolecular chemistry. Despite advances in the development of optical receptors for some neurotransmitters, such as dopamine, limited efforts have been invested in developing receptors for epinephrine, a neurotransmitter of paramount importance and a widely used drug for heart attacks. Herein, a new fluorescent molecular receptor (referred to as 1) based on a 1,3-bis-benzimidazole-benzene derivative covalently linked to two phenyl boronic acids was synthesized, structurally characterized single-crystal X-ray diffraction, and studied in-depth as a receptor for four catecholamine-based neurotransmitters as well as several nucleosides, monosaccharides and L-tyrosine in water at physiological pH.
View Article and Find Full Text PDFACS Omega
July 2025
Departamento de Química Física, Escuela de Química, Facultad de Química y de Farmacia, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile.
In this work, two 7-(diethylamino)-quinolin-2-(1)-one derivatives ( and ) were synthesized and characterized both structurally and physicochemically. The interaction of these derivatives with cucurbit[7]-uril () was explored through combined experimental and approaches, highlighting their unique behavior and practical potential. Experimentally, the complexes exhibited a 1:1 stoichiometry, as confirmed by fluorescence spectroscopy and isothermal titration calorimetry (ITC).
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
January 2026
Guizhou Key Laboratory of Macrocyclic and Supramolecular Chemistry, School of Chemistry and Chemical Engineering, Guizhou University, Guiyang 550025, China. Electronic address:
The supramolecular fluorescent probe exhibited promising application in the field of detection and analysis, but developing supramolecular fluorescent probes with long wavelength emission and enhancement functions for the detection of phenylethylamines is a challenge. In this work, the guest molecule SPn with a D-π-A structure was designed and synthesized, and supramolecular fluorescent probe (SPn/Q[8]) with long wavelength emission was constructed by the host-guest interaction with cucurbit[8]uril (Q[8]). This probe detects phenethylamines based on an indicator displacement assay, which is a process characterized by a fast effect rate (within 6.
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