Recent investigations have suggested that abnormally elevated levels of HOCl may be tightly related to the severity of neuroinflammation. Although some successes have been achieved, fluorescent probes with far-red fluorescence emission and capable of detecting HOCl with high specificity in pure aqueous solution are still urgently needed. Herein, a responsive far-red fluorescent probe, DCI-H, has been constructed to monitor HOCl activity in vivo and in vitro . DCI-H could rapidly respond to HOCl within 120 s and had a low detection limit for HOCl of 1.5 nM. Importantly, physiologically common interfering species, except for HOCl, did not cause a change in the fluorescence intensity of DCI-HOCl at 655 nm. The results of confocal imaging demonstrated the ability of DCI-H to visualize endogenous HOCl produced by MPO-catalyzed H 2 O 2 /Cl - and LPS stimulation. With the assistance of DCI-H, upregulation of HOCl levels was observed in the mice model of LPS-induced neuroinflammation. Thus, we believed that DCI-H provided a valuable tool for HOCl detection and diagnosis of inflammation-related diseases.
Keyphrases
- fluorescent probe
- living cells
- lps induced
- inflammatory response
- single molecule
- traumatic brain injury
- lipopolysaccharide induced
- loop mediated isothermal amplification
- cognitive impairment
- high resolution
- photodynamic therapy
- poor prognosis
- fluorescence imaging
- signaling pathway
- long non coding rna
- drug delivery
- wastewater treatment
- anti inflammatory
- cancer therapy
- energy transfer