A Ratiometric SERS Probe for Imaging the Macrophage Phenotypes in Live Mice with Epilepsy and Brain Tumor

Author:

Duan Wenjia12,Wang Cong13,Jiang Yiqing1,Sui An4,Li Zhi5,Wang Lu1,Lei Zuhai1,Aime Silvio6,Yu Jinhua4,Li Cong13ORCID

Affiliation:

1. Key Laboratory of Smart Drug Delivery Ministry of Education; Innovative Center for New Drug Development of Immune Inflammatory Diseases Ministry of Education School of Pharmacy Fudan University Shanghai 201203 China

2. Department of Forensic Toxicology Academy of Forensic Science, Ministry of Justice Shanghai Key Laboratory of Forensic Medicine Shanghai Forensic Science Platform Shanghai 200063 China

3. State Key Laboratory of Medical Neurobiology Zhongshan Hospital Shanghai Fifth People's Hospital Fudan University Shanghai 201203 China

4. School of Information Science and Technology Fudan University Shanghai 200433 China

5. Department of Neurosurgery Huashan Hospital Fudan University Shanghai 200040 China

6. Department of Molecular Biotechnologies Health Sciences Molecular Imaging Center University of Torino Torino 10126 Italy

Abstract

AbstractMacrophage performs multiple functions such as pathogen phagocytosis, antigen presentation, and tissue remodeling by polarizing toward a spectrum of phenotypes. Dynamic imaging of macrophage phenotypes is critical for evaluating disease progression and the therapeutic response of drug candidates. However, current technologies cannot identify macrophage phenotypes in vivo. Herein, a surface‐enhanced Raman scattering nanoprobe, AH1, which enables the accurate determination of physiological pH with high sensitivity and tissue penetration depth through ratiometric Raman signals is developed. Due to the phenotype‐dependent metabolic reprogramming, AH1 can effectively identify macrophage subpopulations by measuring the acidity levels in phagosomes. After intravenous administration, AH1 not only visualizes the spatial distribution of macrophage phenotypes in brain tumors and epileptic regions of mouse models, but also reveals the repolarization of macrophages in brain lesions after drug intervention. This work provides a new tool for dynamically monitoring the disease‐associated immune microenvironment and evaluating the efficacy of immune‐therapeutics in vivo.

Funder

National Natural Science Foundation of China

National Science Fund for Distinguished Young Scholars

National Postdoctoral Program for Innovative Talents

China Postdoctoral Science Foundation

Shanghai Rising-Star Program

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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