Activatable Nanoprobes for Dual‐Modal NIR‐II Photoacoustic and Fluorescence Imaging of Hydrogen Sulfide in Colon Cancer

Author:

Wang Shuhan1,Zhang Xuan1,Zhang Yiping2,Zhu Kang3,Liu Xing3,Zhang Jieping2,Wang Guoyu2,Liu Daojia2,Zhao Kuaile4,Wang Xin5,Chen Junqiang2,Song Jibin3ORCID

Affiliation:

1. College of Chemistry Fuzhou University Fuzhou 350108 P. R. China

2. Department of Radiation Oncology, Department of Nuclear Medicine, Clinical Oncology School of Fujian Medical Univercity Fujian Cancer Hospital(Fujian Branch of Fudan University Shanghai Cancer Center) Fuzhou 350014 P. R. China

3. State Key Laboratory of Chemical Resource Engineering, College of Chemistry Beijing University of Chemical Technology Beijing 100029 P. R. China

4. Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai Clinical Research Center for Radiation Oncology Shanghai Key Laboratory of Radiation Oncology Shanghai 200032 P. R. China

5. Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital Chinese Academy of Medical Sciences and Peking Union Medical College No.17 Panjiayuan Nanli Chaoyang Beijing 100021 P. R. China

Abstract

AbstractHigh hydrogen sulfide (H2S) expression has been shown to play a crucial role in tumor growth and proliferation in colon cancer. So far, most probes used for monitoring H2S offer single‐modal imaging, which makes the collection of accurate information for tumor diagnosis difficult. In the present study, a novel dual‐modal imaging probe in the second near‐infrared (NIR‐II, 950‐1700) window is proposed and constructed by coating a uniform shell of polydopamine (PDA) on the surface of cuprous oxide (Cu2O)‐conjugated downconversion nanoparticles (DCNPs). Of note, DCNP‐Cu2O@PDA is in the “on” state, with emission centered at 1550 nm (irradiation using a 980nm laser) in non‐neoplastic tissues. Colon tumors with endogenous H2S overexpression can induce the in situ transformation of Cu2O to copper sulfide (Cu2‐XS). Owing to the competitive absorption between Cu2‐XS and DCNPs at a wavelength of 980 nm, the generated DCNP‐Cu2‐XS@PDA exhibits a quenched NIR‐II fluorescence (FL) signal. Meanwhile, Cu2‐XS exhibits a strong absorbance at 1250 nm, enhancing the NIR‐II photoacoustic (PA) signal accompanied by NIR‐II FL attenuation. The switching in PA and FL signals at the tumor site offered “double assurances” for the accurate monitoring of H2S.

Funder

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Natural Science Foundation of Fujian Province

China Postdoctoral Science Foundation

Publisher

Wiley

Subject

Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials

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