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Updated: Feb 11, 2026

Determination of the Excitation and Coupling Rates Between Light Emitters and Surface Plasmon Polaritons
Published on: July 21, 2018
Distinguishing between whole cells and cell debris using surface plasmon coupled emission
Muhammad Anisuzzaman Talukder1,2,3, Curtis R Menyuk3, Yordan Kostov4,5
1Department of Electrical and Electronic Engineering, Bangladesh University of Engineering and Technology, Dhaka 1205, Bangladesh.
Distinguishing whole cells from cell debris is crucial for diagnosing diseases like tuberculosis. A new method uses surface plasmon coupled emission patterns to differentiate them, potentially enabling microscope-free detection.
Area of Science:
- Optical Physics
- Biomedical Imaging
- Nanotechnology
Background:
- Accurate differentiation between whole cells and cell debris is vital for diagnostic microscopy, particularly in identifying infectious agents like Mycobacterium tuberculosis in pulmonary samples.
- Current methods may require complex microscopy setups, limiting accessibility and speed.
Purpose of the Study:
- To theoretically demonstrate a novel method for distinguishing whole cells from cell debris using surface plasmon coupled emission (SPCE).
- To explore the potential of this technique for label-free, microscope-free cellular analysis.
Main Methods:
- Theoretical modeling of SPCE patterns generated by fluorescently-labeled whole cells and cell debris on a thin metal film.
- Analysis of far-field emission patterns, specifically the number and angular separation of emitted rings.
Main Results:
- Whole cells produce SPCE at multiple angles, resulting in two or more distinct far-field rings.
- Cell debris generate SPCE at a single angle, creating only one far-field ring.
- The angular separation of rings from whole cells is distinct enough for reliable differentiation.
Conclusions:
- The number of rings in the SPCE far-field pattern serves as a reliable indicator to distinguish whole cells from cell debris.
- This technique offers a promising avenue for simplified, potentially microscope-free cellular analysis and diagnostics.
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