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 in | Journal of materials chemistry. B, Materials for biology and medicine Vol. 13; no. 12; pp. 3959 - 3966 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
20.03.2025
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Subjects | |
Online Access | Get full text |
ISSN | 2050-750X 2050-7518 2050-7518 |
DOI | 10.1039/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. |
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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 |
AuthorAffiliation_xml | – name: First Hospital of Jilin University – name: Shanxi University – name: The First Hospital of Jilin University – name: Joint Laboratory of Opto-Functional Theranostics in Medicine and Chemistry – name: Department of Neurosurgery – name: Jilin Institute of Chemical Technology – name: Institute of Environmental Science – name: Department of Obstetrics and Gynecology – name: School of Chemistry and Pharmaceutical Engineering – name: Department of Emergency |
Author_xml | – sequence: 1 givenname: Tianyang surname: Han fullname: Han, Tianyang – sequence: 2 givenname: Lihao surname: Lin fullname: Lin, Lihao – sequence: 3 givenname: Huizhong surname: Jiang fullname: Jiang, Huizhong – sequence: 4 givenname: Li surname: Fan fullname: Fan, Li – sequence: 5 givenname: Yuewei surname: Zhang fullname: Zhang, Yuewei |
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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 |
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