Chitosan-Based Nanocomposite Dressings Loaded with Zinc Oxide and Camphor for Hemostatic Applications

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Authors: Ioanna Koumentakou, Theodora Adamantidi, Marios Argyrios Finos, Pavlos Efthymiopoulos, Ramonna Kosheleva, Ioannis Tsamesidis, Eleana Kontonasaki, George Z. Kyzas
Cited by: 1
References: 103

Abstract

Two hemostatic bionanocomposite dressings were developed using natural, semi-natural (or semi-synthetic) and synthetic polymers. The first system consisted of chitosan (CS), polyvinyl alcohol (PVA), and carboxymethyl cellulose (CMC) (CS/PVA/CMC), while the second was based on CS, PVA, and starch (SR) (CS/PVA/SR). Zinc oxide (ZnO) nanoparticles and bicyclic monoterpene camphor (CP) ketone were incorporated as bioactive agents in order to enhance antimicrobial and hemostatic performance. FTIR spectroscopy confirmed the successful solvent casting synthesis of the dressings and the interactions between the biopolymers and additives. XRD analysis indicated a predominantly amorphous structure, while SEM images and EDS analysis revealed uniform dispersion of ZnO particles within the polymer matrices without aggregation. Furthermore, the CS/PVA/CMC-1ZnO/CP sample exhibited a water sorption of 12,666 ± 126%, while CS/PVA/SR-1ZnO/CP reached 7013 ± 215%. ZnO incorporation also improved mechanical performance, with CS/PVA/SR-2ZnO/CP displaying the highest tensile strength (39.18 ± 0.2 MPa) and elongation at break (9.54 ± 1.04%). ZnO incorporation also led to a concentration-dependent increase in antibacterial activity, with SR-based dressings achieving near-complete bacterial reduction at higher ZnO loadings. All the dressings demonstrated good biocompatibility, while CS/PVA/SR-1ZnOCP showed the fastest clotting time (420 s ± 40), highlighting its potential for hemostatic applications.

Fields of Study & Subjects

Hemostasis and retained surgical items Wound Healing and Treatments Surgical Sutures and Adhesives

Publication details

Journal / source
Processes
Publisher
MDPI AG
Volume
14
Issue
9
Pages
1470–1470
Publication date
30 April 2026
Language
EN