2023
DOI: 10.1016/j.ccr.2023.215336
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Review: Recent progress in fluorescent molecular systems for the detection of disease-related biomarkers in biofluids

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Cited by 28 publications
(7 citation statements)
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“…The NPSseries (NPS-A, -B, and -C) was prepared from 3fluorobenzene-1,2-diamine using three steps synthesis: (i) selenadiazole ring formation via the reduction of SeO 2 with a reaction of diamine, (ii) nitration reaction using the product of (i), and (iii) nucleophilic substitution reaction targeting the hydroxy group in various aromatic substitutes, with DIPEA. The NPO-series and NPS-series were verified by 1 H/ 13 C/ 19 F NMR, and MS (Supporting Figures, ESI).…”
Section: Synthesismentioning
confidence: 97%
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“…The NPSseries (NPS-A, -B, and -C) was prepared from 3fluorobenzene-1,2-diamine using three steps synthesis: (i) selenadiazole ring formation via the reduction of SeO 2 with a reaction of diamine, (ii) nitration reaction using the product of (i), and (iii) nucleophilic substitution reaction targeting the hydroxy group in various aromatic substitutes, with DIPEA. The NPO-series and NPS-series were verified by 1 H/ 13 C/ 19 F NMR, and MS (Supporting Figures, ESI).…”
Section: Synthesismentioning
confidence: 97%
“…Experimental details; absorption and emission spectra; analysis of peak area in LC; DFT calculations; FTIS analysis; and 1 H/ 13…”
Section: Uv/vis and Emission Measurementmentioning
confidence: 99%
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“…Fluorescent probes are widely employed as fluorescence indicators due to their advantages of fast detection, absence of radiation, and real-time processing. [1][2][3] Nevertheless, the presence of water as a common quencher 4 and the ability of polar solvents to stabilize the twisted intramolecular charge transfer (TICT) state result in a low fluorescence quantum yield of these probes in aqueous solution. 5 This limitation hinders the application of fluorescent probes in aqueous solution and biological systems.…”
Section: Introductionmentioning
confidence: 99%
“…However, these minor changes need to be detected in complex biological microenvironments with a broad range of interference, including nucleic acid (DNA) sequences, proteins, small molecules, and inorganic ions. Hence, ultrasensitive and unparalleled specificity diagnostic tools are required for quantified detection. Several analysis techniques including lateral flow immunoassay, polymerase chain reaction (PCR), and enzyme-linked immunosorbent assay (ELISA) have been widely used in clinical diagnosis. However, these techniques suffer from temporal heterogeneities, complex pretreatment processes, and time-consuming nucleic acid amplification. By comparison, electrical sensing technology has attracted extensive interest due to its label-free, real-time, and easily operated detection capability.…”
mentioning
confidence: 99%