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Published on: May 24, 2020
In vitro and ex vivo Flow Models for Arterial Thrombosis: A Systematic Review.
Hande Eyisoylu1, Rachele Cagnazzo2, Gijsje H Koenderink3
1Department of Hematology, Erasmus MC Cardiovascular Institute, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
This review examines flow-based models for studying arterial thrombosis, finding both macro- and microfluidic approaches offer valuable insights into platelet aggregation and fibrin deposition for cardiovascular research.
Area of Science:
- Cardiovascular Research
- Biomedical Engineering
- Hematology
Background:
- Arterial thrombosis involves platelet aggregation and fibrin deposition, leading to vessel occlusion and critical in cardiovascular diseases like heart attack and stroke.
- Understanding arterial thrombosis mechanisms is vital for developing effective preventative treatments and reducing disease burden.
- In vitro and ex vivo flow-based models are essential tools for studying thrombus formation under controlled conditions.
Purpose of the Study:
- To systematically review and classify in vitro and ex vivo flow-based models used for studying arterial thrombosis.
- To evaluate the design, physiological relevance, and experimental utility of these models.
- To provide a comprehensive overview for researchers investigating arterial thrombosis.
Main Methods:
- A systematic literature search was performed across Medline, Embase, and Web of Science using terms for arterial thrombosis and flow/shear stress models.
- Two independent reviewers screened articles, including studies with dynamic flow in vitro or ex vivo models.
- Eighty-two studies met the inclusion criteria, excluding static, venous, or in vivo models.
Main Results:
- Macro-scale models replicate complex arterial flow and thrombus formation similar to clinical findings.
- Microfluidic models offer precise control over shear stress and geometry, ideal for high-resolution imaging and patient-specific designs.
- Both model types have limitations in replicating in vivo hemodynamics but provide valuable platforms for mechanistic studies and drug testing.
Conclusions:
- No single model perfectly replicates the in vivo environment for studying arterial thrombosis.
- Continuous innovation in microfabrication and standardization enhances the physiological relevance and clinical translatability of these models.
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