1. Sodium alginate/carboxycellulose/polydopamine composite microspheres for rapid hemostasis of deep irregular wounds.
- Author
-
Hu J, Hu Y, Kang M, Liu X, Wu B, Wang L, Wei Y, and Huang D
- Subjects
- Animals, Mice, Male, Porosity, Alginates chemistry, Alginates pharmacology, Microspheres, Polymers chemistry, Polymers pharmacology, Hemostasis drug effects, Hemostatics chemistry, Hemostatics pharmacology, Indoles chemistry, Indoles pharmacology
- Abstract
Hemostasis of deep irregular wounds is a severe problem in clinical practice. The development of rapid-acting hemostatic agents for deep and irregular wound is urgently needed. Here, sodium alginate/carboxycellulose/polydopamine (SA/CNF/PDA) microspheres was prepared by reverse emulsification and crosslinking with Ca
2+ , and SA/CNF/PDA composite hemostatic microspheres with porous structure were obtained by freeze-drying. SA/CNF/PDA composite hemostatic microspheres exhibited excellent porosity and water absorption which could rapidly absorb blood on the wound surface. Moreover, SA/CNF/PDA composite microspheres demonstrated remarkable hemostatic capabilities both in vitro and in vivo. It exhibited strong hemostatic performance in models of mouse tail-break and liver damage. Especially in liver injury model, it was completely hemostatic in 95 s, and blood loss (19.3 mg). The hemostatic efficacy of the SA/CNF/PDA composite microspheres was amplified through the stimulation of both exogenous and endogenous coagulation pathways. Therefore, SA/CNF/PDA composite hemostatic microspheres are suitable for rapid hemostasis of deep irregular wounds which are potential rapid hemostatic material for surgical application., Competing Interests: Declaration of Competing Interest We declare that we have no financial and personal relationships with other people or organizations that can influence our work, there is no professional or other personal interest of any nature or kind in any product, service and/or company that could be construed as influencing the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)- Published
- 2024
- Full Text
- View/download PDF