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
- oxidative stress
- induced apoptosis
- small molecule
- loop mediated isothermal amplification
- photodynamic therapy
- cerebral ischemia
- cognitive impairment
- aqueous solution
- high resolution
- label free
- high fat diet induced
- high intensity
- brain injury
- wastewater treatment
- adipose tissue
- skeletal muscle
- fluorescence imaging
- metabolic syndrome
- poor prognosis
- insulin resistance
- cell death
- optical coherence tomography
- real time pcr
- energy transfer
- drug delivery
- room temperature
- endoplasmic reticulum stress