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Comparison of animal and human blood for in vitro dynamic thrombogenicity testing of biomaterials

血栓形成 血栓 高密度聚乙烯 生物医学工程 血栓形成 全血 血小板 肝素 人类血液 硅酮 医学 外科 材料科学 免疫学 聚乙烯 生理学 复合材料
作者
Megan A. Jamiolkowski,Mehulkumar Patel,Madelyn D. Golding,Richard A. Malinauskas,Qijin Lu
出处
期刊:Artificial Organs [Wiley]
卷期号:46 (12): 2400-2411 被引量:8
标识
DOI:10.1111/aor.14366
摘要

To determine suitable alternatives to human blood for in vitro dynamic thrombogenicity testing of biomaterials, four different animal blood sources (ovine, bovine, and porcine blood from live donors, and abattoir porcine blood) were compared to fresh human blood.To account for blood coagulability differences between individual donors and species, each blood pool was heparinized to a donor-specific concentration immediately before testing in a dynamic flow loop system. The target heparin level was established using a static thrombosis pre-test. For dynamic testing, whole blood was recirculated at room temperature for 1 h at 200 ml/min through a flow loop containing a single test material. Four materials with varying thrombotic potentials were investigated: latex (positive control), polytetrafluoroethylene (PTFE) (negative control), silicone (intermediate thrombotic potential), and high-density polyethylene (HDPE) (historically thromboresistant). Thrombus weight and surface area coverage on the test materials were quantified, along with platelet count reduction in the blood.While donor-specific heparin levels varied substantially from 0.6 U/ml to 7.0 U/ml among the different blood sources, each source was able to differentiate between the thrombogenic latex and the thromboresistant PTFE and HDPE materials (p < 0.05). However, only donor ovine and bovine blood were sensitive enough to differentiate an increased response for the intermediate thrombotic silicone material compared to PTFE and HDPE.These results demonstrated that multiple animal blood sources (particularly donor ovine and bovine blood) may be suitable alternatives to fresh human blood for dynamic thrombogenicity testing when appropriate control materials and donor-specific anticoagulation levels are used.
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