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Intracellular localization of nanoparticle dimers by chirality reversal
Maozhong Sun1,2, Liguang Xu1,2, Joong Hwan Bahng3,4
1State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, 214122, China.
Chiroptical activity of DNA-bridged plasmonic nanoparticle dimers allows real-time tracking of cellular uptake. This breakthrough enables precise intracellular localization for enhanced photodynamic cancer therapy.
Area of Science:
- Nanotechnology
- Biomedical Engineering
- Spectroscopy
Background:
- Plasmonic nanoparticle (NP) localization (intracellular vs. extracellular) critically impacts therapeutic and diagnostic outcomes.
- Current spectroscopic methods fail to differentiate NP location during transmembrane transport.
- Distinguishing NP location is essential for effective nanomedicine and understanding cellular interactions.
Purpose of the Study:
- To develop a real-time spectroscopic method for tracking plasmonic nanoparticle internalization into mammalian cells.
- To differentiate between extracellular and intracellular localization of DNA-bridged NP dimers.
- To demonstrate the application of this technique in targeted photodynamic cancer therapy.
Main Methods:
- Utilizing the chiroptical activity of DNA-bridged plasmonic nanoparticle dimers.
- Employing real-time ensemble spectroscopy to monitor changes in circular dichroism during cellular uptake.
- Investigating the correlation between NP twisting motion, electrostatic repulsion changes, and transmembrane transport.
Main Results:
- Chiroptical activity, specifically circular dichroism peaks, changes sign (negative to positive) during NP internalization.
- A spontaneous twisting motion around the DNA bridge, driven by altered electrostatic repulsion, accompanies transmembrane transport.
- The study demonstrated enhanced cervical cancer cell elimination using photodynamic therapy when photon polarization matched intracellular NP dimer absorption.
Conclusions:
- Chiroptical activity of DNA-bridged NP dimers provides a novel spectroscopic tool for real-time monitoring of nanoparticle cellular internalization.
- This method allows for accurate differentiation of intracellular versus extracellular NP localization.
- Spectroscopic targeting of chiral nanostructures shows significant potential for improving the efficacy of nanomedicine, particularly in photodynamic therapy for cancer treatment.
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