Jul 2026· Analytical Methods· Vol 18, pp. 6919-6928· 0 citations
Medicine
Abstract
Bisulfite (HSO3-), which exists in equilibrium with sulfite and sulfur dioxide derivatives, plays significant roles in food preservation and biological systems. However, elevated levels of bisulfite are associated with various physiological disorders. Therefore, the development of reliable methods for monitoring bisulfite is of considerable importance. Herein, we report a flavonol-based fluorescent probe, 4-(3-hydroxy-4-oxo-4H-chromen-2-yl) benzaldehyde (BSP), synthesized via a simple two-step reaction using 1-(2-hydroxyphenyl)ethan-1-one and 4-(diethoxy methyl)benzaldehyde. BSP exhibits excellent water solubility and a strong turn-on fluorescence response toward HSO3- in PBS buffer (pH 5.0), with green emission at 515 nm and a large Stokes shift of 155 nm. The probe shows high selectivity and sensitivity with a detection limit of 0.19 µM. The sensing mechanism is attributed to nucleophilic addition of HSO3- to the aldehyde group, suppressing the n → π* transition and enhancing intramolecular charge transfer (ICT), resulting in significant fluorescence enhancement. BSP was successfully applied for bisulfite detection in onion epidermal cells and environmental water samples.
Bisulfite (HSO3−) is widely used as a preservative and antioxidant in the food industry and chemical manufacturing, yet its excessive residues pose risks to food quality, environmental safety, and human health. To achieve rapid, selective, and quantitative detection of HSO3−, a ratiometric fluorescent probe based on a benzothiazole–carbazole unit and a benzoindole ion was developed. Upon reaction with HSO3−, the probe exhibits a distinct dual-emission response, fluorescence intensity decreases at 612 nm and increases at 467 nm, enabling robust ratiometric sensing (F467/F612). Owing to its pronounced fluorescence modulation (emission signal change > 145 nm) and high sensitivity (limit of detection = 0.62 μM), the probe demonstrates reliable performance in aqueous samples and has been successfully integrated into portable test strips and swabs. Furthermore, when coupled with a smartphone-based colorimetric application software, the probe allows convenient and real-time quantification of both gaseous SO2 and aqueous HSO3− across environmental and food-related matrices. This work thus delivers a practical, instrument-free platform for sulfite monitoring in complex real-world settings.
Chunling Zhou, Yanxin Zhang, Ying Sun et al.· Methods and Applications in...· 0 citations
Sulfites are widely used as preservatives and antioxidants in food, but excessive intake poses health risks. Therefore, rapid, sensitive, and on‑site detection of sulfites is essential for food safety. In this work, a cationic small‑molecule fluorescent probe was synthesized via the condensation of
N
‑ethylcarbazole (electron donor) and a benzoindolium ion (electron acceptor). It exhibits a D–π–A architecture with an intramolecular charge transfer (ICT) effect, showing red fluorescence at 617 nm. Upon reaction with HSO
3
−
through Michael addition at the conjugated C═C bond, the ICT pathway is blocked, leading to fluorescence quenching. The probe displays excellent selectivity for HSO
3
−
(limit of detection = 0.1 µM). Significantly, it can be simply deposited onto filter paper to fabricate easy‐to‐use test strips. Under a 365 nm UV lamp, the test strips exhibit a visible color change from red to blue with increasing HSO
3
−
concentration, allowing naked‑eye detection. Coupled with a smartphone color‑reading application, a linear relationship between the blue‐to‐red intensity ratio (B/R) and HSO
3
−
concentration enables rapid on‑site quantitative analysis. The test strips were successfully applied to detect residual HSO
3
−
in various dried fruit samples. This work provides a simple, low‑cost, and practical method for detecting sulfite levels in food and environmental samples.
Kanli Wang, Chenle Liao, Qian Cao et al.· ChemistrySelect· 0 citations
Experimental data indicate that probe CDP can effectively detect N2H4 across a broad pH range (5-12) and demonstrates significant potential for imaging N2H4 in living cells and mice models.
Zhuoran Song, Haoqi Zhang, Xiaoqing Yang et al.· Ecotoxicology and Environmen...· 0 citations
Herein, we have developed a novel ratiometric fluorescent probe through rational design and synthesis, named 2-((5-(4-(3,3-dimethyl-1,2,3,4-tetrahydro-2,4-methoxyacridin-9-yl) phenyl) thiophen-2-yl) methylene)-1H-indene-1,3 (2H)-dione, abbreviated as TA-PT-ID. TA-PT-ID is based on the nopinone skeleton and utilizes a Michael addition reaction as the GSH recognition mechanism. TA-PT-ID exhibits excellent photophysical properties, including a rapid response to GSH (within 1 min), a good linear correlation (R2 = 0.9919), and a low detection limit of 50 nM. TA-PT-ID was successfully applied to the detection of GSH in soil and water samples. Furthermore, ratiometric imaging of endogenous GSH was achieved using TA-PT-ID in HeLa cells, RAW264.7 cells, and zebrafish. In summary, TA-PT-ID provides a powerful new tool for the real-time detection of GSH in complex environments, and its rapid response and broad pH adaptability make it highly promising for applications in biological imaging and environmental monitoring.
Mengdi Zhao, Yue Gu, Yueyin Liang et al.· Spectrochimica Acta Part A -...· 0 citations
A novel near-infrared ratiometric fluorescent probe designed and synthesized by rationally linking dicyanoisophorone with 2-(2-hydroxyphenyl)benzothiazole provides a reliable and versatile tool for the visual monitoring of fluoride ions in both environmental and biological contexts.
Qi Zhou, Wen-Hao Hu, Ke Xiao et al.· Analytical Methods· 0 citations
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