Acta Chimica Sinica ›› 2026, Vol. 84 ›› Issue (9): 1435-1441.DOI: 10.6023/A26040114 Previous Articles     Next Articles

Article

新型喹啉基近红外HSO3-双模式探针的构建及生物成像

田明玉a, 孟令莹a, 钟克利a, 汤立军a,*(), 宋锋玲b,*()   

  1. a 渤海大学 化学学院 化学学院 辽宁锦州 121013
    b 山东大学 化学与化工学院前沿化学研究所 化学与化工学院前沿化学研究所 山东青岛 266237
  • 投稿日期:2026-04-08 发布日期:2026-06-30
  • 通讯作者: 汤立军, 宋锋玲
  • 基金资助:
    国家自然科学基金(22278038); 辽宁省教育厅科研项目(LJ212410167066)

Construction of a Novel Near-Infrared Dual-Mode Probe Based on Quinoline for HSO3- and Its Imaging Applications

Mingyu Tiana, Lingying Menga, Keli Zhonga, Lijun Tanga,*(), Fengling Songb,*()   

  1. a College of Chemistry, Bohai University, Jinzhou 121013, Liaoning, China
    b Institute of Frontier Chemistry, College of Chemistry and Chemical Engineering, Shandong University, Qingdao 266237, Shandong, China
  • Received:2026-04-08 Published:2026-06-30
  • Contact: Lijun Tang, Fengling Song
  • Supported by:
    The National Natural Science Foundation of China(22278038); The project of Liaoning Provincial Department of Education(LJ212410167066)

SO2 is an important gaseous signaling molecule in living organisms, and its abnormal concentration is closely associated with various physiological and pathological processes, including respiratory and central nervous system diseases. SO2 exists mainly as HSO3⁻ in aqueous solution, making the development of highly specific and high-contrast detection methods for HSO3⁻ crucial for studying the physiological functions of SO2 and the early diagnosis of related diseases. In this study, a quinoline-based near-infrared fluorescent probe, QS-EC, with an A-π-A structure was designed and synthesized. The probe initially exists in a fluorescent "dark state." Upon specific 1,4-nucleophilic addition with HSO3⁻, its structure transforms into a D-π-A configuration, restoring the intramolecular charge transfer (ICT) effect and resulting in a dual-mode response of solution color deepening and fluorescence turn-on. The optical performance of QS-EC was systematically evaluated using UV-Vis and fluorescence spectroscopy. Spectroscopic results showed that the QS-EC responded to HSO3⁻ within 3 s, with a detection limit of 14.69 nmol/L, and remains stable within a pH range of 6~13. Competitive experiments demonstrated that QS-EC exhibits high selectivity for HSO3⁻ without interference from other anions or biothiols. It is worth emphasizing that QS-EC enables efficient detection of HSO3⁻, which not only simplifies the detection process but also significantly enhances the probe's practicality and biocompatibility. Furthermore, MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetra- zolium bromide) assays were used to evaluate its biocompatibility, revealing that cell viability remained above 80% after incubation with 0~20 μmol/L of QS-EC for 24 h, confirming its low cytotoxicity. For cellular imaging, QS-EC successfully enabled dynamic monitoring of both exogenous and endogenous HSO3⁻ in live cells. Further in vivo imaging experiments in zebrafish model showed a high signal-to-noise ratio red fluorescence turn-on signal, with fluorescence intensity increasing as the HSO3⁻ concentration rose. This indicates that QS-EC is capable of visually tracking HSO3⁻ distribution in complex living environments. Through systematic evaluation from molecular design and spectral performance to cellular and in vivo applications, this study fully demonstrates the potential of QS-EC for early diagnosis research in SO2-related diseases.

Key words: sulfur dioxide, fluorescent probe, dual-mode, intramolecular charge transfer, cellular imaging