Rapid Hemostasis Resulting from the Synergism of Self-Assembling Short Peptide and O‑Carboxymethyl Chitosan

The development of novel hemostatic agents with distinct modes of action from traditional ones remains a formidable challenge. Self-assembling peptide hydrogels have emerged as a new hemostatic material, not only because of their inherent biocompatibility and biodegradability but also their designab...

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Veröffentlicht in:ACS applied materials & interfaces 2020-12, Vol.12 (50), p.55574-55583
Hauptverfasser: Hao, Ruirui, Peng, Xiaoting, Zhang, Yan, Chen, Jiaxi, Wang, Tong, Wang, Wenxin, Zhao, Yurong, Fan, Xinglong, Chen, Cuixia, Xu, Hai
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Sprache:eng
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Zusammenfassung:The development of novel hemostatic agents with distinct modes of action from traditional ones remains a formidable challenge. Self-assembling peptide hydrogels have emerged as a new hemostatic material, not only because of their inherent biocompatibility and biodegradability but also their designability. Especially, rational molecular design can make peptides and their hydrogelation responsive to biological cues. In this study, we demonstrated that transglutaminase-catalyzed reactions not only occurred among designed short peptide I3QGK molecules but also between the peptide and a natural polysaccharide O-carboxymethyl chitosan. Because Factor XIII in the blood can rapidly convert into activated transglutaminase (Factor XIIIa) upon bleeding, these enzymatic reactions, together with the electrostatic attraction between the two hemostatic agents, induced a strong synergetic effect in promoting hydrogelation, blood coagulation, and platelet adhesion, eventually leading to rapid hemostasis. The study presents a promising strategy for developing alternative hemostatic materials and methods.
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.0c15480