# Modified Chitosan-Based Hemostatic Dressings Incorporating Heparin-Loaded Nanoparticles for Enhanced Hemostatic Activity

**Authors:** Despoina Meimaroglou, Evi Christodoulou, Rizos Evangelos Bikiaris, Ioanna Koumentakou, Michiel Jan Noordam, Amalia Oikonomou, Ioannis Taitzoglou, Ioannis Tsamesidis, Eleana Kontonasaki, Zoi Terzopoulou, Lysimachos G. Papazoglou, George Z. Kyzas, Dimitrios N. Bikiaris

PMC · DOI: 10.3390/pharmaceutics18030373 · Pharmaceutics · 2026-03-18

## TL;DR

A new wound dressing combines modified chitosan and heparin-loaded nanoparticles to improve hemostasis and healing.

## Contribution

A dual-function hemostatic dressing integrating modified chitosan and heparin-loaded nanoparticles is developed.

## Key findings

- Modified chitosan provides rapid topical hemostasis.
- Controlled heparin release modulates fibrin deposition and supports healing.
- In vitro and in vivo studies show potential for effective wound care.

## Abstract

Background/Objectives: Achieving effective hemostasis is a vital step in wound healing, particularly in cases of severe bleeding caused by surgical procedures or trauma. This study focuses on the development of chitosan-based dressings enriched with Heparin (hep)-loaded poly(butylene succinate) (PBSu) nanoparticles to combine hemostatic and anticoagulant properties. Methods: Chitosan, a biocompatible and biodegradable carbohydrate with inherent antibacterial and hemostatic properties, was chemically modified with 2-(N-morpholino)ethanesulfonic acid (MES) and 2-acrylamido-2-methylpropane sulfonic acid (AMPS) to enhance its swelling ability and hemostatic activity. PBSu nanoparticles were synthesized using an oil-in-water emulsification method and loaded with Hep to achieve controlled anticoagulant release. The dressings of the modified chitosan derivatives with the nanoparticles which were systematically characterized for morphology, chemical structure, swelling ability, loading capacity, and Hep release kinetics. Results: This dual-function system is designed to decouple local surface hemostasis from thrombotic processes: the chitosan matrix provides rapid topical hemostasis, while controlled heparin release from the nanoparticles aims to modulate excessive fibrin deposition, support microvascular perfusion, and exploit the pro-healing benefits of low-dose heparin reported in advanced wound dressings, particularly in high-risk or thrombotic-prone patients. In vitro and in vivo studies demonstrated their potential for promoting rapid hemostasis. Conclusions: These findings suggest that the integration of modified chitosan and Hep-loaded nanoparticles is a promising strategy for advancing wound care and hemostatic technologies.

## Linked entities

- **Chemicals:** chitosan (PubChem CID 129662530), 2-(N-morpholino)ethanesulfonic acid (PubChem CID 78165), 2-acrylamido-2-methylpropane sulfonic acid (PubChem CID 65360)

## Full-text entities

- **Diseases:** trauma (MESH:D014947), bleeding (MESH:D006470), thrombotic (MESH:D013927)
- **Chemicals:** Heparin (MESH:D006493), Chitosan (MESH:D048271), 2-acrylamido-2-methylpropane sulfonic acid (-), 2-(N-morpholino)ethanesulfonic acid (MESH:C004550), water (MESH:D014867), carbohydrate (MESH:D002241), PBSu (MESH:C089797), oil (MESH:D009821)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13030816/full.md

## References

65 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030816/full.md

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Source: https://tomesphere.com/paper/PMC13030816