Scientists at Texas A&M University has used the functionalities of organic nanomaterials-based chemistry and chitosan to help bring emergency medicine one step closer to a viable solution for alleviating blood loss, from the hospital to the battlefield.
Hemorrhage is a leading cause of death in traumatic injuries, ranking fourth in the United States at a total cost of $671 billion in 2013. Working with an interdisciplinary team involving collaborators from Assiut University in Egypt, Texas A&M chemist Karen Wooley’s research group has developed a bioabsorbable wound dressing that advances on the proven haemostatic properties of chitosan. They synthesized chitosan into chitosan nanoparticles while crosslinking with cylcodextrin polyester. The result was an advanced functionalized biocompatible, biodegradable nanomaterial which bolstered the efficacy of their wound dressing.
Wooley’s team, led by Texas A&M chemistry Ph.D. student and NASA Space Technology Research Fellow Eric Leonhardt, encapsulated chitosan nanofibers within a sugar-based hydrogel which dissolves at the site of application in seven days. It enabled a wider surface area for wound-healing while eliminating the need for removing the material from the site of adminstration. Their results are published in Nature Communications.
“Bioabsorbable wound dressings that can be applied and left in the injury site are desirable for a variety of blood loss scenarios — for example, to control bleeding in traumatic injuries and to save lives on both civilian and military fronts,” said Leonhardt, a member of the research team and co-author on the paper. “The composite materials we’ve developed are malleable and could be easily administered to wound sites. They have also performed significantly better in terms of reducing the amount of blood loss and the time required to achieve hemostasis against commercially available bioabsorbable wound dressing in several animal models.”
Other team members in addition to Leonhardt include Texas A&M materials science and engineering Ph.D. student Nari Kang; Dr. Mahmoud Elsabahy, assistant director of the Texas A&M Laboratory for Synthetic-Biologic Interactions and director of the Assiut Clinical Center of Nanomedicine at Al-Rajhy Liver Hospital; and Dr. Mostafa A. Hamad, a professor in the Department of Surgery within the Assuit Faculty of Medicine.
Elsabahy recognized that, while chitosan is a desirable option in such dressings due to its proven efficacy in slowing blood flow and because it offers bonus antimicrobial properties, it also has a tendency to clump, rendering it difficult to incorporate into a bioabsorbable material. The team overcame that obstacle by loading chitosan into a nanostructured template scaffold to better disperse it and increase its interaction with blood components, thereby speeding up both absorption and healing.
As a first step in their discovery process, the researchers developed hydrogels from cyclodextrins – a type of saccharide with hydrolytically degradable linkages – designed with sites that were capable of ionically interacting with and binding to chitosan molecules. After freeze-drying the resulting composite material, they exposed it to a solution that removed the template scaffold. They then used scanning electron microscopy to further analyze the chitosan, which assembled into mats of highly entangled nanofibers measuring about 10-to-20 nanometers in diameter.
“Not only are these fibers considerably smaller than what has been previously reported for chitosan, they also are highly desirable, given that the corresponding increase in surface area is expected to greatly enhance hemostatic effect,” said Elsabahy, who conceived the project. “We believe this work will enhance the scope of chitosan as a hemostatic technology through the demonstration of its fabrication and use as a bioabsorbable wound dressing.”
To date, the team has applied their composite wound dressings to liver injuries in rats, rabbits and pigs. The key endpoints assessed were the amount of blood loss, time to hemostasis, and mean arterial pressure. The dressings were also implanted in damaged liver and imaged it after 7 days to evaluate the biodegradation of the chitosan nanoparticle composite material. Complete degradation (no residues) was observed in all experiments.
“Hemorrhage is responsible for more than 35 percent of pre-hospital deaths and more than 40 percent of deaths within the first 24 hours of injury,” Leonhardt said. “Hemostatic dressings have the potential to reduce morbidity and mortality through the early control of hemorrhage. These dressings can be included in first aid kits and carried by soldiers to save lives in the battlefield, and they can be also utilized to control bleeding in various injury scenarios and surgical procedures in hospitals. Absorbable hemostatic dressing can be left in the injury site and eliminate the necessity for carrier removal, which reduces the risk of re-bleeding — in case of carrier removal of non-absorbable dressings — and decreases the duration required for the surgical interventions.”
Wooley intends to extend this initial work to the evaluation of the materials in studies that simulate lethal hemorrhage scenarios, followed by clinical trials. In addition, she would like to conduct future fundamental studies to further explore the mechanism of chitosan nanofiber formation within the template scaffolds, with the aim of ultimately achieving control over the assembly to enable tuning and optimization of the resulting morphology of the wound dressings.
The team’s work was supported by the NASA Space Technology Research Fellowship Program (Grant No. NNX15AQ08H) and the Welch Foundation through Wooley’s W. T. Doherty-Welch Chair in Chemistry (Grant No. A-0001).
Their Nature Communications paper, “Absorbable hemostatic hydrogels comprising composites of sacrificial templates and honeycomb-like nanofibrous mats of chitosan,” can be viewed online along with related figures and captions.
For additional information on Wooley and her related research, visit http://www.chem.tamu.edu/faculty/karen-wooley/.
