Mechanistic study of tumor fluorescence response signals based on a near-infrared viscosity-sensitive probe

Viscosity is an important physiological parameter closely associated with various cellular processes and diseases. Several fluorescence probes responsive to viscosity have been developed, demonstrating high sensitivity specifically towards tumor tissues. However, the underlying core mechanism of thi...

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Published inJournal of materials chemistry. B, Materials for biology and medicine Vol. 13; no. 12; pp. 3959 - 3966
Main Authors Han, Tianyang, Lin, Lihao, Jiang, Huizhong, Fan, Li, Zhang, Yuewei
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 20.03.2025
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ISSN2050-750X
2050-7518
2050-7518
DOI10.1039/d4tb02067g

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Abstract Viscosity is an important physiological parameter closely associated with various cellular processes and diseases. Several fluorescence probes responsive to viscosity have been developed, demonstrating high sensitivity specifically towards tumor tissues. However, the underlying core mechanism of this highly potential responsive signal has been a subject of debate, as highly sensitive probes encounter excessive environmental interferences in complex tumor tissues. Therefore, we have developed a viscosity-responsive fluorescence probe based on the classical TICT mechanism (twisted intramolecular charge transfer) as a research tool. This probe features an ultra-wide emission range of 700-1200 nm in the near-infrared spectrum, strong photostability, and simultaneous targeting of mitochondria and lysosomes. Through in-depth analysis, we have revealed the intrinsic mechanisms underlying its functionality, demonstrating that the major contributor to the fluorescence change of responsive probes during imaging is the inherent state of cells rather than the tumor microenvironment or the cell type. Our findings provide a theoretical foundation for the continued exploration and application of viscosity-responsive probes. A highly specific viscosity-responsive probe with NIR-II emission for in-depth analysis of tumor cells versus microenvironment fluorescence signals.
AbstractList Viscosity is an important physiological parameter closely associated with various cellular processes and diseases. Several fluorescence probes responsive to viscosity have been developed, demonstrating high sensitivity specifically towards tumor tissues. However, the underlying core mechanism of this highly potential responsive signal has been a subject of debate, as highly sensitive probes encounter excessive environmental interferences in complex tumor tissues. Therefore, we have developed a viscosity-responsive fluorescence probe based on the classical TICT mechanism (twisted intramolecular charge transfer) as a research tool. This probe features an ultra-wide emission range of 700–1200 nm in the near-infrared spectrum, strong photostability, and simultaneous targeting of mitochondria and lysosomes. Through in-depth analysis, we have revealed the intrinsic mechanisms underlying its functionality, demonstrating that the major contributor to the fluorescence change of responsive probes during imaging is the inherent state of cells rather than the tumor microenvironment or the cell type. Our findings provide a theoretical foundation for the continued exploration and application of viscosity-responsive probes.
Viscosity is an important physiological parameter closely associated with various cellular processes and diseases. Several fluorescence probes responsive to viscosity have been developed, demonstrating high sensitivity specifically towards tumor tissues. However, the underlying core mechanism of this highly potential responsive signal has been a subject of debate, as highly sensitive probes encounter excessive environmental interferences in complex tumor tissues. Therefore, we have developed a viscosity-responsive fluorescence probe based on the classical TICT mechanism (twisted intramolecular charge transfer) as a research tool. This probe features an ultra-wide emission range of 700-1200 nm in the near-infrared spectrum, strong photostability, and simultaneous targeting of mitochondria and lysosomes. Through in-depth analysis, we have revealed the intrinsic mechanisms underlying its functionality, demonstrating that the major contributor to the fluorescence change of responsive probes during imaging is the inherent state of cells rather than the tumor microenvironment or the cell type. Our findings provide a theoretical foundation for the continued exploration and application of viscosity-responsive probes. A highly specific viscosity-responsive probe with NIR-II emission for in-depth analysis of tumor cells versus microenvironment fluorescence signals.
Viscosity is an important physiological parameter closely associated with various cellular processes and diseases. Several fluorescence probes responsive to viscosity have been developed, demonstrating high sensitivity specifically towards tumor tissues. However, the underlying core mechanism of this highly potential responsive signal has been a subject of debate, as highly sensitive probes encounter excessive environmental interferences in complex tumor tissues. Therefore, we have developed a viscosity-responsive fluorescence probe based on the classical TICT mechanism (twisted intramolecular charge transfer) as a research tool. This probe features an ultra-wide emission range of 700-1200 nm in the near-infrared spectrum, strong photostability, and simultaneous targeting of mitochondria and lysosomes. Through in-depth analysis, we have revealed the intrinsic mechanisms underlying its functionality, demonstrating that the major contributor to the fluorescence change of responsive probes during imaging is the inherent state of cells rather than the tumor microenvironment or the cell type. Our findings provide a theoretical foundation for the continued exploration and application of viscosity-responsive probes.Viscosity is an important physiological parameter closely associated with various cellular processes and diseases. Several fluorescence probes responsive to viscosity have been developed, demonstrating high sensitivity specifically towards tumor tissues. However, the underlying core mechanism of this highly potential responsive signal has been a subject of debate, as highly sensitive probes encounter excessive environmental interferences in complex tumor tissues. Therefore, we have developed a viscosity-responsive fluorescence probe based on the classical TICT mechanism (twisted intramolecular charge transfer) as a research tool. This probe features an ultra-wide emission range of 700-1200 nm in the near-infrared spectrum, strong photostability, and simultaneous targeting of mitochondria and lysosomes. Through in-depth analysis, we have revealed the intrinsic mechanisms underlying its functionality, demonstrating that the major contributor to the fluorescence change of responsive probes during imaging is the inherent state of cells rather than the tumor microenvironment or the cell type. Our findings provide a theoretical foundation for the continued exploration and application of viscosity-responsive probes.
Author Fan, Li
Lin, Lihao
Han, Tianyang
Zhang, Yuewei
Jiang, Huizhong
AuthorAffiliation The First Hospital of Jilin University
Department of Neurosurgery
First Hospital of Jilin University
Joint Laboratory of Opto-Functional Theranostics in Medicine and Chemistry
School of Chemistry and Pharmaceutical Engineering
Shanxi University
Department of Obstetrics and Gynecology
Jilin Institute of Chemical Technology
Department of Emergency
Institute of Environmental Science
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Snippet Viscosity is an important physiological parameter closely associated with various cellular processes and diseases. Several fluorescence probes responsive to...
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crossref
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StartPage 3959
SubjectTerms Charge transfer
Fluorescence
Fluorescent Dyes - chemical synthesis
Fluorescent Dyes - chemistry
Fluorescent indicators
Humans
I.R. radiation
Infrared Rays
Infrared spectra
Lysosomes
Near infrared radiation
Neoplasms - diagnostic imaging
Optical Imaging
Parameter sensitivity
Probes
Tumor microenvironment
Tumors
Viscosity
Title Mechanistic study of tumor fluorescence response signals based on a near-infrared viscosity-sensitive probe
URI https://www.ncbi.nlm.nih.gov/pubmed/40028911
https://www.proquest.com/docview/3179114371
https://www.proquest.com/docview/3173400884
Volume 13
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linkProvider Royal Society of Chemistry
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