In Vivo NIR‐II Fluorescence Lifetime Imaging of Whole‐Body Vascular Using High Quantum Yield Lanthanide‐Doped Nanoparticles

Author:

Guo Yongwei123,Hu Jie123ORCID,Wang Peiyuan234ORCID,Yang Hongyi23,Liang Sisi23,Chen Dejian23,Xu Kunyuan23,Huang Yingping235,Wang Qinglai123,Liu Xiaolong234ORCID,Zhu Haomiao123ORCID

Affiliation:

1. College of Chemistry Fuzhou University Fuzhou 350108 China

2. CAS Key Laboratory of Design and Assembly of Functional Nanostructures Fujian Key Laboratory of Nanomaterials Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences Fuzhou 350002 China

3. Xiamen Key Laboratory of Rare Earth Photoelectric Functional Materials Xiamen Research Center of Rare Earth Materials Haixi Institutes Chinese Academy of Sciences Xiamen 361021 China

4. The United Innovation of Mengchao Hepatobiliary Technology Key Laboratory of Fujian Province Mengchao Hepatobiliary Hospital of Fujian Medical University Fuzhou 350025 China

5. Fujian Provincial Key Laboratory of Polymer Materials College of Chemistry and Materials Science Fujian Normal University Fuzhou 350007 China

Abstract

AbstractSecond near infrared (NIR‐II, 1000–1700 nm) fluorescence lifetime imaging is a powerful tool for biosensing, anti‐counterfeiting, and multiplex imaging. However, the low photoluminescence quantum yield (PLQY) of fluorescence probes in NIR‐II region limits its data collecting efficiency and accuracy, especially in multiplex molecular imaging in vivo. To solve this problem, lanthanide‐doped nanoparticles (NPs) β‐NaErF4: 2%Ce@NaYbF4@NaYF4 with high PLQY and tunable PL lifetime through multi‐ion doping and core–shell structural design, are presented. The obtained internal PLQY can reach up to 50.1% in cyclohexane and 9.2% in water under excitation at 980 nm. Inspired by the above results, a fast NIR‐II fluorescence lifetime imaging of whole‐body vascular in mice is successfully performed by using the homebuilt fluorescence lifetime imaging system, which reveals a murine abdominal capillary network with low background. A further demonstration of fluorescence lifetime multiplex imaging is carried out in molecular imaging of atherosclerosis cells and different organs in vivo through NPs conjugating with specific peptides and different injection modalities, respectively. These results demonstrate that the high PLQY NPs combined with the homebuilt fluorescence lifetime imaging system can realize a fast and high signal‐to‐noise fluorescence lifetime imaging; thus, opening a road for multiplex molecular imaging of atherosclerosis.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Fujian Province

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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