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Activation dynamics study of trapped platelets using a lab-built optical tweezers micro-raman spectrometer
N Mithun1, Shamee Shastry2, Ganesh Mohan2
1Centre of Excellence for Biophotonics, Department of Atomic and Molecular Physics, Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India.
Scientific Reports
|February 19, 2025
Summary
Raman tweezers spectroscopy offers a rapid and reliable method for studying platelet activation, revealing biochemical and morphological changes crucial for diagnosing diseases like cardiovascular diseases and Alzheimer's disease.
Area of Science:
- Biophysics
- Spectroscopy
- Cell Biology
Background:
- Platelet disorders are linked to various diseases, including cardiovascular diseases (CVDs), Alzheimer's disease (AD), and cancer.
- Current diagnostic methods (imaging, clinical analysis, neuropsychological tests) can be time-consuming and prone to errors.
- Raman tweezers spectroscopy presents a faster, more accurate alternative for diagnosis.
Purpose of the Study:
- To investigate platelet activation dynamics using Raman tweezers spectroscopy.
- To establish a novel method for real-time analysis of platelet activation in a clinical setting.
Main Methods:
- Utilized an in-house assembled optical tweezers micro-Raman spectrometer.
- Trapped live platelets to study their activation dynamics.
- Analyzed biochemical and morphological changes during platelet activation.
Main Results:
- Observed significant biochemical and morphological changes upon platelet activation.
- Documented the formation of filopodia, shape transformation (discoid to spherical), and aminophospholipid translocation.
- Detected notable intensity variations in Raman bands corresponding to phospholipids during activation.
Conclusions:
- Raman tweezers spectroscopy provides trustworthy and timely results for platelet activation analysis.
- Understanding platelet activation dynamics is vital for monitoring diseases like CVDs and ADs.
- This prospective method holds potential for future clinical applications in analyzing platelet activation.

