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A Microfluidic Flow Chamber Model for Platelet Transfusion and Hemostasis Measures Platelet Deposition and Fibrin Formation in Real-time
Published on: February 14, 2017
Platinoid effects on human plasmatic coagulation kinetics: a viscoelastic analysis.
1Department of Anesthesiology, The University of Arizona College of Medicine, 1501 North Campbell Avenue, P.O. Box 245114, Tucson, AZ, 85724-5114, USA. vgnielsen333@gmail.com.
Platinum and ruthenium compounds were tested for their effects on blood clotting. Ruthenium chloride significantly increased clotting by enhancing prothrombin activation, unlike platinum compounds.
Area of Science:
- Biochemistry
- Hematology
- Oncology
Background:
- Metals like cadmium, chromium, copper, and iron are known to affect blood coagulation.
- Platinum-based chemotherapy is associated with thromboembolic events, yet platinoids' effects on coagulation are unstudied.
Purpose of the Study:
- To investigate the impact of platinum (carboplatin, cisplatin) and ruthenium (ruthenium chloride, NAMI-A) compounds on human plasma coagulation.
- To determine if platinum and ruthenium compounds influence blood clotting parameters.
Main Methods:
- Human plasma was treated with equimolar concentrations of platinum and ruthenium compounds.
- Thrombelastography was used to assess changes in plasmatic coagulation.
- Specialized thrombelastography techniques were employed to investigate ruthenium chloride's effects.
Main Results:
- Platinum compounds (carboplatin, cisplatin) did not significantly alter coagulation.
- NAMI-A showed mild hypercoagulability, while ruthenium chloride induced marked hypercoagulability.
- Ruthenium chloride was found to enhance prothrombin activation, indicating procoagulant properties.
Conclusions:
- The hypercoagulability linked to platinum compounds in vivo may not stem from direct effects on plasma coagulation.
- Ruthenium compounds can promote blood clotting by enhancing the common coagulation pathway.
- Further research on ruthenium-based chemotherapeutics is recommended to evaluate their procoagulant activity and clinical safety.
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