Mechanistic study of tumor fluorescence response signals based on a near-infrared viscosity-sensitive probe
- Tianyang Han 1,2, Lihao Lin 3, Huizhong Jiang 4, Li Fan 5, Yuewei Zhang 1,6
- Tianyang Han 1,2, Lihao Lin 3, Huizhong Jiang 4
- 1Joint Laboratory of Opto-Functional Theranostics in Medicine and Chemistry, First Hospital of Jilin University, Changchun 130021, P. R. China. zhangyueweichem@163.com.
- 2Department of Obstetrics and Gynecology, First Hospital of Jilin University, Changchun 130021, P. R. China.
- 3Department of Emergency, The First Hospital of Jilin University, Changchun 130021, P. R. China.
- 4Department of Neurosurgery, The First Hospital of Jilin University, Changchun 130021, P. R. China.
- 5Institute of Environmental Science, Shanxi University, Taiyuan 030006, P. R. China. fanli128@sxu.edu.cn.
- 6School of Chemistry and Pharmaceutical Engineering, Jilin Institute of Chemical Technology, Jilin 132022, P. R. China.
- 0Joint Laboratory of Opto-Functional Theranostics in Medicine and Chemistry, First Hospital of Jilin University, Changchun 130021, P. R. China. zhangyueweichem@163.com.
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View abstract on PubMed
Summary
This summary is machine-generated.This study introduces a new near-infrared fluorescence probe for measuring viscosity. The research reveals that cellular state, not the tumor microenvironment, primarily influences probe signals, advancing viscosity probe applications.
Area Of Science
- Biomedical Engineering
- Chemical Biology
- Molecular Imaging
Background
- Viscosity is a key physiological parameter linked to cellular functions and diseases.
- Existing viscosity-sensitive fluorescence probes show promise for tumor imaging but lack mechanistic clarity due to environmental interference.
Purpose Of The Study
- To develop and characterize a novel viscosity-responsive fluorescence probe.
- To elucidate the primary mechanism driving fluorescence changes in viscosity probes within complex biological systems.
Main Methods
- Development of a near-infrared (700-1200 nm) fluorescence probe utilizing the twisted intramolecular charge transfer (TICT) mechanism.
- Evaluation of probe photostability and dual targeting of mitochondria and lysosomes.
- In-depth analysis to differentiate contributions of cellular state, tumor microenvironment, and cell type to probe response.
Main Results
- The developed probe exhibits an ultra-wide emission range in the near-infrared spectrum with strong photostability.
- The probe successfully targets both mitochondria and lysosomes.
- Cellular intrinsic state was identified as the dominant factor influencing probe fluorescence changes, outweighing microenvironmental or cell-type effects.
Conclusions
- The developed TICT-based probe offers a robust tool for viscosity sensing with advanced spectral properties and organelle targeting.
- Understanding the primary role of cellular state provides crucial theoretical insights for the rational design and application of future viscosity-responsive probes in biomedical research.
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