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Updated: Jul 29, 2025

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Published on: August 26, 2014
SERS Endoscopy for Monitoring Intracellular Drug Dynamics
Beatrice Fortuni1, Monica Ricci1, Raffaele Vitale2
1Molecular Imaging and Photonics, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, 3001 Leuven, Belgium.
Surface-enhanced Raman scattering (SERS) endoscopy with plasmonic nanowires tracks the common chemotherapy drug doxorubicin inside cancer cells. This method reveals drug localization, DNA intercalation, and interactions, advancing drug mechanism studies.
Area of Science:
- Biomedical Optics
- Nanotechnology
- Pharmacology
Background:
- Understanding intracellular drug dynamics is crucial for developing effective cancer treatments.
- Current tools for monitoring drug behavior within cells are limited.
- Doxorubicin is a widely used chemotherapy agent whose precise intracellular actions require further elucidation.
Purpose of the Study:
- To apply surface-enhanced Raman scattering (SERS) endoscopy for real-time monitoring of doxorubicin's intracellular fate.
- To investigate the spatio-temporal dynamics and mechanism of action of doxorubicin in A549 cancer cells.
- To differentiate drug behavior upon direct administration versus delivery system use.
Main Methods:
- Utilized plasmonic nanowires as SERS probes for enhanced signal detection.
- Employed SERS endoscopy for high-resolution imaging of drug distribution within living cells.
- Analyzed doxorubicin's localization, complexation, and DNA intercalation over time.
Main Results:
- Achieved unprecedented spatio-temporal resolution of doxorubicin's intracellular journey.
- Identified nuclear localization and time-dependent DNA intercalation of doxorubicin.
- Distinguished the intracellular dynamics of doxorubicin when administered directly versus via a delivery system.
Conclusions:
- SERS endoscopy provides critical insights into drug mechanisms of action at the cellular level.
- This technique offers a powerful new tool for medicinal chemistry and drug discovery.
- The findings pave the way for improved therapeutic strategies by understanding drug-cell interactions.
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