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Experimental Assessment of Hemostatic Agents: Comparison with New Developed Chitosan-Based Material  

Cho, Young-Kyoo (Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Kyungpook National University)
Lee, Sang-Yun (Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Kyungpook National University)
Kim, Tae-Jung (Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Kyungpook National University)
Lim, Hyun-Ju (Department of Advanced Organic Materials Science and Engineering, Kyungpook National University)
Oh, Eun-Jung (Department of Advanced Organic Materials Science and Engineering, Kyungpook National University)
Lee, Soo-Bok (Fiber & Tech Co.)
Choi, Kang-Young (Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Kyungpook National University)
Yang, Jung-Dug (Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Kyungpook National University)
Cho, Byung-Chae (Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Kyungpook National University)
Chung, Ho-Yun (Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Kyungpook National University)
Publication Information
Archives of Plastic Surgery / v.38, no.4, 2011 , pp. 369-375 More about this Journal
Abstract
Purpose: Many hemostatic agents and dressings have been tested with variable degree of success. Chitosan has a positive charge, it attracts red blood cells, which have a negative charge. Our goal is to test the efficacy of new developed chitosan-based hemostatic materials in providing durable hemostasis in a high-flow arterial wound model. Methods: We compared each group with SD rats motality tests and in vitro blood compatibility test by blood clotting index (BCI). We devided the SD rats into 6 groups (N =15) by type of hemostatic agents. A: 100% nonwoven chitosan (degree of the deacetylation: 90%). B: 50% N-acetylation on nonwoven of chitosan gel (degree of the deacetylation: 50%). C: 60% N-acetylation on nonwoven of chitosan ge (degree of the deacetylation: 40%)l. D: Cutanplast$^{(R)}$. E: HemCon$^{(R)}$ F: Gauze. In vivo test, a proximal arterial injury was created in unilateral femoral arteries of 90 anesthetized SD rats. Each materials was made same size and thickness then applied to the injury site for 3 minutes. In vitro test, we compared each group with BCI in human blood. Results: In vivo test, group A showed lower motality rate of 46% than any other groups, Group B and C showed lower motality rate of 60% than group D and E's motality rate of 66%. In vitro test, BCI of group A ($30.6{\pm}1.2$) and B ($29.3{\pm}1.0$) were showed nearly about group D ($29.1{\pm}1.8$) and E ($27.4{\pm}1.6$). Group C ($37.1{\pm}2.0$) showed higher BCI than group A and B, it means group C decreased blood clotting. Conclusion: In conclusion, this study suggests a newly developed chitosan-based hemostatic materials induced durable hemostasis and increased blood clotting, and are considered as effective biologic hemostatic agents.
Keywords
Hemostatic agents; Chitosan; Blood clotting;
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