Comparative Efficacy of Hemorrhage Control of a Novel Mesoporous Bioactive Glass Versus Two Commercial Hemostats
Abstract
Mesoporous bioactive glass containing 1% Ga 2 O 3 (1%Ga-MBG) is attractive for hemorrhage control because of its surface chemistry which can promote blood-clotting. The present study compares this proprietary inorganic coagulation accelerator with two commercial hemostats, Celox™ (CX) and QuikClot Advanced Clotting Sponge Plus™ (ACS + ). The results indicate that the number of adherent platelets were higher on the 1%Ga-MBG and CX surfaces than ACS + whereas a greater contact activation was seen on 1%Ga-MBG and ACS + surfaces than CX. 1%Ga-MBG not only resulted in larger platelet aggregates and more extensive platelet pseudopodia compared to CX and ACS + but also significantly accelerated the intrinsic pathways of the clotting cascade. In vitro thrombin generation assays also showed that CX and ACS + induced low levels of thrombin formation while 1%Ga-MBG had significantly higher values. 1%Ga-MBG formed a larger red blood cell aggregate than both CX and ACS + . Direct exposure of 1%Ga-MBG to fibroblast cells increased cell viability after 3 days relative to CX and ACS + , inferring excellent cytocompatibility. The results of this study promote 1%Ga-MBG as a promising hemostat compared to the commercially available products as it possesses essential factors required for coagulation activation.
Recommended Citation
S. Pourshahrestani et al., "Comparative Efficacy of Hemorrhage Control of a Novel Mesoporous Bioactive Glass Versus Two Commercial Hemostats," Biomedical Materials (Bristol), vol. 13, no. 2, article no. 025020, IOP Publishing, Feb 2018.
The definitive version is available at https://doi.org/10.1088/1748-605X/aa9b3e
Department(s)
Chemical and Biochemical Engineering
International Standard Serial Number (ISSN)
1748-605X; 1748-6041
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2023 IOP Publishing, All rights reserved.
Publication Date
08 Feb 2018
PubMed ID
29148431
Comments
Ministry of Higher Education, Grant UM.C/625/1/HIR/MoE/ ENG/58