Comparative efficacy of hemorrhage control of a novel mesoporous bioactive glass versus two commercial hemostats

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 A...

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Main Authors: Pourshahrestani, Sara, Kadri, Nahrizul Adib, Zeimaran, Ehsan, Gargiulo, Nicola, Samuel, Shani, Naveen, Sangeetha Vasudevaraj, Hasikin, Khairunnisa, Kamarul, Tunku, Towler, Mark Robert
Format: Article
Published: IOP Publishing 2018
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Online Access:http://eprints.um.edu.my/21013/
https://doi.org/10.1088/1748-605X/aa9b3e
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Summary: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.