Bioinspired large Stokes shift small molecular dyes for biomedical fluorescence imaging

Author:

Chen Hao12ORCID,Liu Lingjun13,Qian Kun1,Liu Hailong1,Wang Zhiming1,Gao Feng1ORCID,Qu Chunrong1ORCID,Dai Wenhao1ORCID,Lin Daizong1ORCID,Chen Kaixian123,Liu Hong1234ORCID,Cheng Zhen124ORCID

Affiliation:

1. State Key Laboratory of Drug Research, Molecular Imaging Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.

2. University of Chinese Academy of Sciences, No. 19A Yuquan Road, Beijing 100049, China.

3. State Key Laboratory of Natural Medicines and Department of Medicinal Chemistry, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing 210009, China.

4. Shandong Laboratory of Yantai Drug Discovery, Bohai Rim Advanced Research Institute for Drug Discovery, Yantai, Shandong 264117, China.

Abstract

Long Stokes shift dyes that minimize cross-talk between the excitation source and fluorescent emission to improve the signal-to-background ratio are highly desired for fluorescence imaging. However, simple small molecular dyes with large Stokes shift (more than 120 nanometers) and near-infrared (NIR) emissions have been rarely reported so far. Here, inspired by the chromophore chemical structure of fluorescent proteins, we designed and synthesized a series of styrene oxazolone dyes (SODs) with simple synthetic methods, which show NIR emissions (>650 nanometers) with long Stokes shift (ranged from 136 to 198 nanometers) and small molecular weight (<450 daltons). The most promising SOD9 shows rapid renal excretion and blood-brain barrier passing properties. After functioning with the mitochondrial-targeted triphenylphosphonium (TPP) group, the resulting SOD9-TPP can be engineered for head-neck tumor imaging, fluorescence image–guided surgery, brain neuroimaging, and on-site pathologic analysis. In summary, our findings add an essential small molecular dye category to the classical dyes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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