In Situ Ionically Cross-Linkable Benzaldehyde-Modified Alginate and Its Bilayer Structure as a Tissue Sealant for Dural Closure

Effective tissue adhesives are vital for surgical applications. We synthesized <i>p</i>-aminobenzaldehyde-modified alginate (AL-ABA) with controlled degrees of substitution (DS, 3.8-13.7%) and cross-linked it ionically using CaCl<sub>2</sub>. AL-ABA solutions (3 w/v %) gelled rapidly (3-50 s), similar to unmodified alginate. Increasing DS reduced hydrogel stiffness but enhanced dura adhesiveness via Schiff's base formation with tissue amines, reaching 32 kPa at 9% DS. To optimize both adhesion and mechanical integrity, bilayer hydrogels were developed using an AL-ABA primer and AL cover layer, seamlessly bonded by ionic cross-linking. These AL-ABA/AL hydrogels showed strong dural adhesion and high burst pressure resistance (up to 406 mmHg). AL-ABA retained a low cytotoxicity and hemocompatibility. Ionically cross-linked AL-ABA and its bilayer configuration offer promising potential as biocompatible and efficient tissue sealants.

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Publication Details

Journal
Biomacromolecules
Published
2025-08-25
DOI
https://doi.org/10.1021/acs.biomac.5c00748
Citations
1
Primary Topic
Surgical Sutures and Adhesives
Type
article
Field-Weighted Citation Impact
2.01

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article

In Situ Ionically Cross-Linkable Benzaldehyde-Modified Alginate and Its Bilayer Structure as a Tissue Sealant for Dural Closure

Satoshi Fukushima, Taichi Ito, I‐Hsuan Yang, Norimasa Iwasaki et al.
1 citations
Biomacromolecules
Surgical Sutures and Adhesives
2.01
article

In Situ Ionically Cross-Linkable Benzaldehyde-Modified Alginate and Its Bilayer Structure as a Tissue Sealant for Dural Closure

Satoshi Fukushima, Taichi Ito, I‐Hsuan Yang, Norimasa Iwasaki, Seiichi Ohta, Kazuki Matsumiya, Mitsuko Isaji, Arvind K. Singh Chandel, Natsuko F. Inagaki, Masahiko Takahata, Kotaro Onishi, Satoshi Shimizu, Mineo Matsumoto, Atsushi Mizushima, Mai Yamada, Yizhou Dai, T. Iwabuchi
article en
1 citations

Abstract

Effective tissue adhesives are vital for surgical applications. We synthesized <i>p</i>-aminobenzaldehyde-modified alginate (AL-ABA) with controlled degrees of substitution (DS, 3.8-13.7%) and cross-linked it ionically using CaCl<sub>2</sub>. AL-ABA solutions (3 w/v %) gelled rapidly (3-50 s), similar to unmodified alginate. Increasing DS reduced hydrogel stiffness but enhanced dura adhesiveness via Schiff's base formation with tissue amines, reaching 32 kPa at 9% DS. To optimize both adhesion and mechanical integrity, bilayer hydrogels were developed using an AL-ABA primer and AL cover layer, seamlessly bonded by ionic cross-linking. These AL-ABA/AL hydrogels showed strong dural adhesion and high burst pressure resistance (up to 406 mmHg). AL-ABA retained a low cytotoxicity and hemocompatibility. Ionically cross-linked AL-ABA and its bilayer configuration offer promising potential as biocompatible and efficient tissue sealants.

BiomacromoleculesVol. 26(9)
Mochida Pharmaceutical (Japan) (JP), Hokkaido University (JP), The University of Tokyo (JP)
Japan Agency for Medical Research and Development, Mochida Pharmaceutical Company, National Science and Technology Council
Openalex Percentile: Top 12%
Surgical Sutures and Adhesives
2.01
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