A fluorescent signal amplification strategy via host-guest recognition for cortisol detection

被引:0
|
作者
Wang, Jiao [1 ]
Kong, Jinming [1 ]
Zhang, Xueji [2 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Environm & Biol Engn, Nanjing 210094, Jiangsu, Peoples R China
[2] Shenzhen Univ, Sch Biomed Engn, Hlth Sci Ctr, Shenzhen 518060, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Stress biomarker; Fluorescence sensing; Host-guest recognition; ATRP;
D O I
10.1016/j.saa.2024.125611
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Psychological stress is a major contributor to individual health disparities. Accurate and quantitative detection of stress markers is crucial preventing mental health related problems. Supramolecular chemistry is widely used in drug delivery, catalysis, sensors and other applications. However, due to the difficulty of host functionalization such as cyclodextrins and solid-state pillar[n], it is still a challenge to directly realize the detection of guests through host-guest recognition behavior. Here, we reported an atom transfer radical polymerization (ATRP) fluorescent biosensor for direct and selective detection of guest molecule stress marker cortisol, translating molecular recognition behavior into quantifiable detection signals. Realizes quantitative chemical detection and builds a portable and affordable sensing platform for quantitative detection of target molecules without complex cross-linking steps. Overcomes the disadvantages of traditional methods that require the use of antibodies or are difficult to functionalize during the host-guest recognition process. This ATRP fluorescent biosensor was fabricated by employing zinc phthalocyanine (ZnPc) as a photocatalyst under 630 nm wavelength radiation, beta-CDBr15 as a macromolecular initiator, and fluorescein O-methacrylate (FMA-O) as a monomer for polymerization. The system provides ultra-high sensitivity for the detection of cortisol (limit of detection 0.47 ng/mL) and specificity for the detection of cortisol in the presence of interfering substances such as progesterone and urea. Selective and real sample experiments confirm the specificity and scalability of this mechanism can also be customized by the rational design of the host-guest complex to quantitatively detect various molecules. This
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页数:9
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