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Immobilized thrombin on X-ray radiopaque polyvinyl alcohol/chitosan embolic microspheres for precise localization and topical blood coagulation

Trans-catheter arterial embolization (TAE) plays an important role in treating various diseases. The available embolic agents lack X-ray visibility and do not prevent the reflux phenomenon, thus hindering their application for TAE therapy. Herein, we aim to develop a multifunctional embolic agent th...

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Detalles Bibliográficos
Autores principales: Li, Xiaohong, Ji, Xiongfa, Chen, Kun, Ullah, Muhammad Wajid, Li, Basen, Cao, Jiameng, Xiao, Lin, Xiao, Jun, Yang, Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807145/
https://www.ncbi.nlm.nih.gov/pubmed/33511310
http://dx.doi.org/10.1016/j.bioactmat.2020.12.013
Descripción
Sumario:Trans-catheter arterial embolization (TAE) plays an important role in treating various diseases. The available embolic agents lack X-ray visibility and do not prevent the reflux phenomenon, thus hindering their application for TAE therapy. Herein, we aim to develop a multifunctional embolic agent that combines the X-ray radiopacity with local procoagulant activity. The barium sulfate nanoparticles (BaSO(4) NPs) were synthesized and loaded into the polyvinyl alcohol/chitosan (PVA/CS) to prepare the radiopaque BaSO(4)/PVA/CS microspheres (MS). Thereafter, thrombin was immobilized onto the BaSO(4)/PVA/CS MS to obtain the thrombin@BaSO(4)/PVA/CS MS. The prepared BaSO(4)/PVA/CS MS were highly spherical with diameters ranging from 100 to 300 μm. In vitro CT imaging showed increased X-ray visibility of BaSO(4)/PVA/CS MS with the increased content of BaSO(4) NPs in the PVA/CS MS. The biocompatibility assessments demonstrated that the MS were non-cytotoxic and possessed permissible hemolysis rate. The biofunctionalized thrombin@BaSO(4)/PVA/CS MS showed improved hemostatic capacity and facilitated hemostasis in vitro. Additionally, in vivo study performed on a rabbit ear embolization model confirmed the excellent X-ray radiopaque stability of the BaSO(4)/PVA/CS MS. Moreover, both the BaSO(4)/PVA/CS and thrombin@BaSO(4)/PVA/CS MS achieved superior embolization effects with progressive ischemic necrosis on the ear tissue and induced prominent ultrastructural changes in the endothelial cells. The findings of this study suggest that the developed MS could act as a radiopaque and hemostatic embolic agent to improve the embolization efficiency.