Tuning the Solid- and Solution-State Fluorescence of the Iron-Chelator Deferasirox

去铁斯若 化学 荧光 荧光团 组合化学 聚集诱导发射 抗生素 生物物理学 生物化学 光学 医学 生物 物理 内科学 地中海贫血
作者
Xi‐Le Hu,Adam C. Sedgwick,Daniel N. Mangel,Ying Shang,Axel Steinbrueck,Kai‐Cheng Yan,Ling Zhu,Dylan W. Snelson,Sajal Sen,Calvin V. Chau,Gabriel Juárez,Vincent M. Lynch,Xiao‐Peng He,Jonathan L. Sessler
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:144 (16): 7382-7390 被引量:31
标识
DOI:10.1021/jacs.2c01155
摘要

Deferasirox, an FDA-approved iron chelator, has gained increasing attention for use in anticancer and antimicrobial applications. Recent efforts by our group led to the identification of this core as an easy-to-visualize aggregation-induced emission platform, or AIEgen, that provides a therapeutic effect equivalent to deferasirox (J. Am. Chem. Soc. 2021, 143, 3, 1278–1283). However, the emission wavelength of the first-generation system overlapped with that of Syto9, a green emissive dye used to indicate live cells. Here, we report a library of deferasirox derivatives with various fluorescence emission profiles designed to overcome this limitation. We propose referring to systems that show promise as both therapeutic and optical imaging agents as "illuminoceuticals". The color differences between the derivatives were observable to the unaided eye (solid- and solution-state) and were in accord with the Commission Internationale de L'Eclairage (CIE) chromaticity diagram 1913. Each fluorescent derivative successfully imaged the respective spherical and rod shapes of methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa. They also displayed iron-dependent antibiotic activity. Three derivatives, ExNMe2 (3), ExTrisT (11), and ExDCM (13), display emission features that are sufficiently distinct so as to permit the multiplex (triplex) imaging of both MRSA and P. aeruginosa via stimulated emission depletion microscopy. The present deferasirox derivatives allowed for the construction of a multi-fluorophore sensor array. This array enabled the successful discrimination between Gram-positive/Gram-negative and drug-sensitive/drug-resistant bacteria. Antibiotic sensitivity and drug-resistant mutants from clinically isolated strains could also be identified and differentiated.
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