Enzymatic Crosslinking of Coacervates Yields High‐Strength and Reconstitutable Biomedical Adhesives

Biomedical adhesives are emerging as an effective wound treatment option. The current cyanoacrylate or fibrin-based adhesives falter in either being ineffective in high moisture regions due to their hydrophobic character or producing very weak adhesion due to rapid degradation in the biological milieu. To overcome these impediments in the practical application of biomedical adhesives, water-based biomedical adhesives are prepared through enzymatic crosslinking of polyelectrolyte complexes (PECs) that not only offer high adhesion strength but also work well in high relative humidity environments and sustain during the wound healing process. The adhesive is prepared from oppositely charged polyelectrolytes (PEs) having a polyamide backbone and containing ca. 25 mol% phenolic pendants as the Horseradish Peroxidase (HRP)-responsive residues. Excellent formulation stability, rapid curing, optical clarity of the adhesive layer, and high-strength adhesion of diverse substrates are the key advantages of this PEC adhesive. The strongest adhesion is found for wood with adhesive strength up to 10 MPa. The adhesive can be lyophilized to a powder form and reconstituted, fully retaining its adhesive performance. It is hemostatic and exhibited a promising surface wound-healing outcome in mice, significantly outperforming the commercial cyanoacrylate-based tissue adhesives. These findings position the enzyme-cured PEC adhesives as a promising contender in advanced wound care applications.

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Publication Details

Journal
Advanced Healthcare Materials
Published
2025-11-12
DOI
https://doi.org/10.1002/adhm.202502990
Citations
1
Primary Topic
Polymer Surface Interaction Studies
Type
article
Field-Weighted Citation Impact
0.66

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article

Enzymatic Crosslinking of Coacervates Yields High‐Strength and Reconstitutable Biomedical Adhesives

Aasheesh Srivastava, Tanmay Dutta, Debasis Nayak, Paramita Das et al.
1 citations
Advanced Healthcare Materials
Polymer Surface Interaction Studies
0.66
article

Enzymatic Crosslinking of Coacervates Yields High‐Strength and Reconstitutable Biomedical Adhesives

Aasheesh Srivastava, Tanmay Dutta, Debasis Nayak, Paramita Das, Roop Singh Lodhi, Drishiya Vats, Bhanwar Lal
article en
1 citations

Abstract

Biomedical adhesives are emerging as an effective wound treatment option. The current cyanoacrylate or fibrin-based adhesives falter in either being ineffective in high moisture regions due to their hydrophobic character or producing very weak adhesion due to rapid degradation in the biological milieu. To overcome these impediments in the practical application of biomedical adhesives, water-based biomedical adhesives are prepared through enzymatic crosslinking of polyelectrolyte complexes (PECs) that not only offer high adhesion strength but also work well in high relative humidity environments and sustain during the wound healing process. The adhesive is prepared from oppositely charged polyelectrolytes (PEs) having a polyamide backbone and containing ca. 25 mol% phenolic pendants as the Horseradish Peroxidase (HRP)-responsive residues. Excellent formulation stability, rapid curing, optical clarity of the adhesive layer, and high-strength adhesion of diverse substrates are the key advantages of this PEC adhesive. The strongest adhesion is found for wood with adhesive strength up to 10 MPa. The adhesive can be lyophilized to a powder form and reconstituted, fully retaining its adhesive performance. It is hemostatic and exhibited a promising surface wound-healing outcome in mice, significantly outperforming the commercial cyanoacrylate-based tissue adhesives. These findings position the enzyme-cured PEC adhesives as a promising contender in advanced wound care applications.

Advanced Healthcare MaterialsVol. 15(7)
Indian Institute of Science Education and Research, Bhopal (IN)
Indian Institute of Science Education and Research Bhopal, Indian Institute of Science Education and Research Mohali
Openalex Percentile: Top 25%
Polymer Surface Interaction Studies
0.66
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