Related Experiment Video
Updated: May 18, 2026

Extracellular Vesicle Tissue Factor Activity Assay
Published on: December 29, 2023
Tick-derived protein Qinghaienin-based anticoagulant coating inhibits activation of the zymogen FXII
Yanan Zhao1, Kaiting Chen2, Xiaofei He1
1Laboratory of Molecular Medicine, Ordos Central Hospital, Inner Mongolia Autonomous Region, Ordos, 017000, China; Ordos Clinical Medical College, Inner Mongolia Medical University, Ordos, 017000, China.
Thrombus formation and thrombosis-related complications have consistently limited the safe use of blood-contacting medical devices in clinical practice. Qinghaienin, a novel tick-derived protein, inhibits activation of the intrinsic coagulation pathway by competing with factor XII for anionic surfaces. In this study, to create an anticoagulant coating, Qinghaienin was grafted onto the surface of commonly used medical polyvinyl chloride (PVC) material, which was premodified by polydopamine-polyethyleneimine (PDA-PEI). A series of studies verified that Qinghaienin immobilized on the PVC surface significantly enhanced the hydrophilicity of the material while retaining its biological activity. The PDA-PEI/Qinghaienin coating inhibited nonspecific protein adsorption, platelet adhesion, and thrombus formation in vitro. Furthermore, the PDA-PEI/Qinghaienin coating exhibited outstanding anticoagulant performance, which was superior to that of the PDA-PEI/Hep coating in static whole blood tests. In a rabbit arteriovenous shunt model, the coating effectively prolonged extracorporeal blood circulation time compared with control trials. These results demonstrate that the PDA-PEI/Qinghaienin coating exhibits excellent hemocompatibility and anticoagulant activity, highlighting its potential use in blood-contacting medical devices.
Thrombus formation and thrombosis-related complications have consistently limited the safe use of blood-contacting medical devices in clinical practice. Qinghaienin, a novel tick-derived protein, inhibits activation of the intrinsic coagulation pathway by competing with factor XII for anionic surfaces. In this study, to create an anticoagulant coating, Qinghaienin was grafted onto the surface of commonly used medical polyvinyl chloride (PVC) material, which was premodified by polydopamine-polyethyleneimine (PDA-PEI). A series of studies verified that Qinghaienin immobilized on the PVC surface significantly enhanced the hydrophilicity of the material while retaining its biological activity. The PDA-PEI/Qinghaienin coating inhibited nonspecific protein adsorption, platelet adhesion, and thrombus formation in vitro. Furthermore, the PDA-PEI/Qinghaienin coating exhibited outstanding anticoagulant performance, which was superior to that of the PDA-PEI/Hep coating in static whole blood tests. In a rabbit arteriovenous shunt model, the coating effectively prolonged extracorporeal blood circulation time compared with control trials. These results demonstrate that the PDA-PEI/Qinghaienin coating exhibits excellent hemocompatibility and anticoagulant activity, highlighting its potential use in blood-contacting medical devices.
Related Concept Videos
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Venous Thrombosis III: Interprofessional Care
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...

