4.7 Article

Monitoring Hg2+and MeHg+ poisoning in living body with an activatable near-infrared II fluorescence probe

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JOURNAL OF HAZARDOUS MATERIALS
卷 445, 期 -, 页码 -

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DOI: 10.1016/j.jhazmat.2022.130612

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Mercury poisoning; Brain toxicity; in vivo imaging; Fluorescent probes; Near-infrared II

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Noninvasively imaging mercury poisoning in living organisms is critical to understanding its toxicity and treatments. Especially, simultaneous fluorescence imaging of Hg2+ and MeHg+ in vivo is helpful to disclose the mysteries of mercury poisoning. A new near-infrared II (NIR II) emissive probe, NIR-Rh-MS, has been designed to visualize mercury toxicity in mice. The probe produces a marked fluorescence signal and displays good sensitivity to Hg2+ and MeHg+. It can penetrate deep into simulated tissues and has successfully monitored the toxicity of Hg2+ in mouse livers and the accumulation of MeHg+ in mouse brains via intravital NIR-II imaging.
Noninvasively imaging mercury poisoning in living organisms is critical to understanding its toxicity and treatments. Especially, simultaneous fluorescence imaging of Hg2+ and MeHg+ in vivo is helpful to disclose the mysteries of mercury poisoning. The key limitation for mercury imaging in vivo is the low imaging signal-to-background ratio (SBR) and limited imaging depth, which may result in unreliable detection results. Here, we designed and prepared a near-infrared II (NIR II) emissive probe, NIR-Rh-MS, leveraging the spirolactam ring-open tactic of xanthene dyes for in situ visualization of mercury toxicity in mice. The probe produces a marked fluorescence signal at 1015 nm and displays good linear responses to Hg2+ and MeHg+ with excellent sensitivity, respectively. The penetration experiments elucidate that the activated NIR-II fluorescence signal of the probe penetrates to a depth of up to 7 mm in simulated tissues. Impressively, the probe can monitor the toxicity of Hg2+ in mouse livers and the accumulation of MeHg+ in mouse brains via intravital NIR-II imaging for the first time. Thus, we believe that detecting Hg2+ and MeHg+ in different organs with a single NIR-II fluorescence probe in mice would assuredly advance the toxicologic study of mercury poisoning in vivo.

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