Aggregation-induced emission carbon dots as Al3+-mediated nanoaggregate probe for rapid and selective detection of tetracycline

Authors
Seo, Young HunEstrada, Diana Elizabeth AguilarJang, DohyubBaik, SeungyunLee, JaehoKim, Dong HaKim, Sehoon
Issue Date
2024-04
Publisher
Pergamon Press Ltd.
Citation
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, v.310
Abstract
Worldwide abuse of tetracycline (TC) seriously threatens environmental safety and human health. Metal-TC complexes formed by residual TC in the environment can also contribute to the spread of antibiotic resistance. Therefore, monitoring of TC residues is still required. Here, we report novel aggregation -induced emission carbon dots (AIE-Cdots) as nanoaggregate probes for the rapid and selective detection of TC residue. Riboflavin precursors with rotational functional groups led to the development of AIE-Cdots. The aggregation of AIE-Cdots was induced selectively for Al3+, amplifying the fluorescence signals owing to the restricted rotation of the side chains on the AIE-Cdot surface. The fluorescence signal of such Al3+-mediated nanoaggregates (Al3+-NAs) was further triggered by the structural fixation of TC at the Al3+ active sites, suggesting the formation of TCcoordinated Al3+-NAs. A linear correlation was observed in the TC concentration range of 0-10 mu M with a detection limit of 42 nM. In addition, the strong Al3+ binding affinity of AIE-Cdots produced similar NAs and enhanced fluorescence signals in Al3+-TC mixtures. These AIE-Cdots-based nanoplatforms have a rapid response, good selectivity, and reliable accuracy for detecting TC or aluminum complexes, meeting the requirements for hazardous substance monitoring and removal in environmental applications.
Keywords
ULTRASENSITIVE DETECTION; LIQUID-CHROMATOGRAPHY; ANTIBIOTICS; RESIDUES; SOIL; METALS; FATE; Carbon dots; Aggregation induced emission; Rotational functional group; Nanoaggregates; Al 3+ion; Tetracycline
ISSN
1386-1425
URI
https://pubs.kist.re.kr/handle/201004/149453
DOI
10.1016/j.saa.2024.123925
Appears in Collections:
KIST Article > 2024
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