Highly Absorbent Ultrafast Self‐Gelling Starch Microparticles for Robust Wet‐Tissue Adhesion and Instant Hemostasis

Rapid and effective hemostasis of mass bleeding from irregularly shaped wounds remains a critical clinical challenge. Herein, a highly absorbent and self-gelling microparticle (MP) is reported based on modified starch as a hemostatic material with robust wet tissue adhesiveness. The aldehyde- and catechol-modified starch (ACS) is synthesized via partial oxidation of starch for the reduction of dense intermolecular interactions within starch, thereby significantly enhancing its interaction with water molecules. Moreover, the conjugated catechol group strengthens the affinity to various biomolecules. The ACS microparticle (ACS-MP) prepared by calcium intercalation into the polysaccharide chains and subsequent freeze-milling rapidly converts to a stable hydrogel within seconds upon hydration, exhibiting superior water absorption capacity and tissue adhesion. The ACS-MP demonstrates excellent in vivo biocompatibility in local and systemic administration. The application of ACS-MP to bleeding wounds enables rapid blood absorption and accumulation of blood components and coagulation factors. The ACS-MP can fill irregularly shaped wounds, forming a tissue-adhesive hydrogel in situ, thereby creating a physical barrier for non-compressible hemostasis. The superior hemostatic performance of ACS-MP against massive hemorrhage from liver injuries in mice and pigs is confirmed. The ACS-MP will be a promising hemostat for effectively controlling mass bleeding in various tissues in clinical settings.

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Publication Details

Journal
Advanced Science
Published
2025-03-24
DOI
https://doi.org/10.1002/advs.202501857
Citations
3
Primary Topic
Hemostasis and retained surgical items
Type
article
Field-Weighted Citation Impact
5.31
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article

Highly Absorbent Ultrafast Self‐Gelling Starch Microparticles for Robust Wet‐Tissue Adhesion and Instant Hemostasis

Soohwan An, Seung Yeop Han, Seung‐Woo Cho, Dong Jin Joo et al.
3 citations
Advanced Science
Hemostasis and retained surgical items
5.31
article

Highly Absorbent Ultrafast Self‐Gelling Starch Microparticles for Robust Wet‐Tissue Adhesion and Instant Hemostasis

Soohwan An, Seung Yeop Han, Seung‐Woo Cho, Dong Jin Joo, Mi‐Jeong Lee, Tae Woo Oh, Eun Je Jeon, Jihoon Jeon
article en
3 citations

Abstract

Rapid and effective hemostasis of mass bleeding from irregularly shaped wounds remains a critical clinical challenge. Herein, a highly absorbent and self-gelling microparticle (MP) is reported based on modified starch as a hemostatic material with robust wet tissue adhesiveness. The aldehyde- and catechol-modified starch (ACS) is synthesized via partial oxidation of starch for the reduction of dense intermolecular interactions within starch, thereby significantly enhancing its interaction with water molecules. Moreover, the conjugated catechol group strengthens the affinity to various biomolecules. The ACS microparticle (ACS-MP) prepared by calcium intercalation into the polysaccharide chains and subsequent freeze-milling rapidly converts to a stable hydrogel within seconds upon hydration, exhibiting superior water absorption capacity and tissue adhesion. The ACS-MP demonstrates excellent in vivo biocompatibility in local and systemic administration. The application of ACS-MP to bleeding wounds enables rapid blood absorption and accumulation of blood components and coagulation factors. The ACS-MP can fill irregularly shaped wounds, forming a tissue-adhesive hydrogel in situ, thereby creating a physical barrier for non-compressible hemostasis. The superior hemostatic performance of ACS-MP against massive hemorrhage from liver injuries in mice and pigs is confirmed. The ACS-MP will be a promising hemostat for effectively controlling mass bleeding in various tissues in clinical settings.

Advanced ScienceVol. 12(19)
Yonsei University (KR), Severance Hospital (KR), Institute for Basic Science (KR)
Clean water and sanitation
Openalex Percentile: Top 5%
Hemostasis and retained surgical items
5.31
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