4.7 Article

Study of double-bonded carboxymethyl chitosan/cysteamine-modified chondroitin sulfate composite dressing for hemostatic application

Journal

EUROPEAN POLYMER JOURNAL
Volume 162, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.eurpolymj.2021.110875

Keywords

Carboxymethyl chitosan; Chondroitin sulfate; Hydrogel; Freeze-dried dressing; Rapid hemostasis

Funding

  1. National Key R&D Program of China [2019YFD0901805]
  2. 111 Project [B18022]
  3. Fundamental Research Funds for the Central Universities [22221818014]

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A novel hemostatic dressing, Me-CMC/CSS, developed using thiol-ene click chemistry, showed rapid water absorption and transformation into soft hydrogels for wound sealing. The dressing achieved good hemostasis with significantly reduced blood clotting index and total blood loss in a rat liver hemorrhage model compared to untreated or gelatin sponge-treated groups. The excellent platelet adhesion ability of Me-CMC/CSS dressing suggests its potential application as a rapid hemostatic material.
Stanching severe traumatic bleeding requires hemostatic materials that can provide rapid and efficient hemostasis. However, most currently available hemostatic agents exhibit low efficiency and poor biocompatibility. In this study, a novel carboxymethyl chitosan modified with methacrylic anhydride (double-bonded carboxymethyl chitosan)/cysteamine-modified chondroitin sulfate (Me-CMC/CSS) rapid hemostatic dressing was developed using thiol-ene click chemistry. The freeze-dried Me-CMC/CSS dressings absorbed water rapidly and transformed into soft hydrogels that could seal wounds, achieving good hemostasis. The relative blood clotting index of the optimal Me-CMC/CSS dressing was decreased by 53% (p < 0.001) and 29% compared with a pure Me-CMC dressing and a commercial hemostatic gelatin sponge, respectively. In a rat liver hemorrhage model, the MeCMC/CSS dressing stopped bleeding rapidly, and the total blood loss was significantly decreased by 92% (p < 0.0001) compared with the untreated group and was lower than that with gelatin sponge treatment. The MeCMC/CSS dressing also exhibited a higher ability to adhere to platelets than the gelatin sponge. Furthermore, the Me-CMC/CSS dressing exhibited good hemocompatibility and cytocompatibility. The results indicate that the composite dressings can be potentially applied as rapid hemostatic materials.

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