Synergistic Blend of <i>p</i> -Aminomethylbenzoic Acid in Electrohydrodynamically Atomized Chitosan–PVA Composite Particles for Hemostasis and Wound Healing

Electrohydrodynamic splitting was performed on a filament consisting of a blend of chitosan and poly(vinyl alcohol) (PVA), followed by ionotropic gelation to produce uniform microparticles with dimensions on the order of 400 μm. The trapped solvent was removed by lyophilization, which rendered ultraporous characteristics to these particles and thus enabled quick absorption of blood plasma, along with aggregation of platelets for hemostasis. The uniformity of the particles ensured uniform coverage of the wound space. The increase in the PVA fraction in the blend resulted in greater porosity and surface area, as evidenced by the SEM image and BET analysis, respectively, and in turn, led to faster clotting, as shown by thromboelastography and <i>in vivo</i> analysis on rat models. Furthermore, the introduction of <i>p</i>-aminomethylbenzoic acid (ABA) as a releasable solute resulted in hindered fibrinolysis in the coagulation cascade, producing a stable blood clot. The <i>in vivo</i> experiments on the rat model further demonstrated the synergistic contribution of chitosan as an antimicrobial and wound healing agent.

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Publication Details

Journal
ACS Applied Bio Materials
Published
2026-01-12
DOI
https://doi.org/10.1021/acsabm.5c02085
Primary Topic
Electrospun Nanofibers in Biomedical Applications
Type
article
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article

Synergistic Blend of p -Aminomethylbenzoic Acid in Electrohydrodynamically Atomized Chitosan–PVA Composite Particles for Hemostasis and Wound Healing

Pradyumna Kumar Sasmal, Sandip Saha, Somenath Ganguly
ACS Applied Bio Materials
Electrospun Nanofibers in Biomedical Applications
article

Synergistic Blend of p -Aminomethylbenzoic Acid in Electrohydrodynamically Atomized Chitosan–PVA Composite Particles for Hemostasis and Wound Healing

Pradyumna Kumar Sasmal, Sandip Saha, Somenath Ganguly
article en

Abstract

Electrohydrodynamic splitting was performed on a filament consisting of a blend of chitosan and poly(vinyl alcohol) (PVA), followed by ionotropic gelation to produce uniform microparticles with dimensions on the order of 400 μm. The trapped solvent was removed by lyophilization, which rendered ultraporous characteristics to these particles and thus enabled quick absorption of blood plasma, along with aggregation of platelets for hemostasis. The uniformity of the particles ensured uniform coverage of the wound space. The increase in the PVA fraction in the blend resulted in greater porosity and surface area, as evidenced by the SEM image and BET analysis, respectively, and in turn, led to faster clotting, as shown by thromboelastography and <i>in vivo</i> analysis on rat models. Furthermore, the introduction of <i>p</i>-aminomethylbenzoic acid (ABA) as a releasable solute resulted in hindered fibrinolysis in the coagulation cascade, producing a stable blood clot. The <i>in vivo</i> experiments on the rat model further demonstrated the synergistic contribution of chitosan as an antimicrobial and wound healing agent.

ACS Applied Bio MaterialsVol. 9(3)
Indian Institute of Technology Kharagpur (IN)
Openalex Percentile: Top 90%
Electrospun Nanofibers in Biomedical Applications
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