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Blood plasma coagulation studied by surface plasmon resonance
T P Vikinge1, K M Hansson, J Benesch
1IFM, Linköping University, Laboratory of Applied Physics, Sweden. trine@ifm.liu.se
Journal of Biomedical Optics
|August 12, 2000
Summary
Surface plasmon resonance (SPR) and atomic force microscopy (AFM) revealed how thromboplastin and heparin affect blood plasma coagulation. Higher thromboplastin increased clotting time, while heparin counteracted this effect, showing distinct fibrin network structures.
Area of Science:
- Biophysics
- Hematology
- Biomaterials Science
Background:
- Blood plasma coagulation is a complex process vital for hemostasis.
- Understanding coagulation dynamics is crucial for diagnosing and treating bleeding disorders.
- Current methods for analyzing coagulation have limitations in real-time monitoring.
Purpose of the Study:
- To investigate blood plasma coagulation in real-time using surface plasmon resonance (SPR).
- To analyze the effects of varying thromboplastin and heparin concentrations on coagulation.
- To correlate SPR findings with fibrin network structures observed via atomic force microscopy (AFM).
Main Methods:
- Utilized a surface plasmon resonance (SPR) apparatus for real-time coagulation monitoring.
- Analyzed SPR response curves by fitting to a sigmoid equation to extract time constants.
- Employed atomic force microscopy (AFM) to examine fibrin network structures on sensor surfaces post-clotting.
Main Results:
- Thromboplastin dose-dependently increased the time constant of blood plasma coagulation.
- Heparin addition counteracted the pro-coagulant effect of thromboplastin.
- AFM revealed that decreased thromboplastin concentration led to increased fibrin fiber thickness.
Conclusions:
- SPR and AFM provide complementary insights into blood coagulation dynamics.
- The study demonstrates a correlation between SPR-derived parameters and fibrin network morphology.
- These findings support the utility of SPR and AFM as valuable tools for analyzing blood coagulation.