# Dialdehyde Alginate as a Crosslinker for Chitosan/Starch Films: Toward Biocompatible and Antioxidant Wound Dressing Materials

**Authors:** Sylwia Grabska-Zielińska, Marek Pietrzak, Lidia Zasada, Krzysztof Łukowicz, Agnieszka Basta-Kaim, Marta Michalska-Sionkowska, Marcin Wekwejt, Beata Kaczmarek-Szczepańska

PMC · DOI: 10.3390/ijms27031174 · International Journal of Molecular Sciences · 2026-01-23

## TL;DR

Researchers developed biocompatible wound dressing films using chitosan, starch, and dialdehyde alginate, showing good mechanical and antioxidant properties.

## Contribution

The study introduces dialdehyde alginate as a crosslinker to enhance the stability and antioxidant properties of chitosan/starch films.

## Key findings

- ADA crosslinking improved the hydrophilicity and antioxidant behavior of CTS-ST films.
- Films showed non-hemolytic and non-cytotoxic properties, indicating good biocompatibility.
- CTS-ST ratio and ADA variant significantly influenced crosslinking efficiency and material performance.

## Abstract

Biopolymer-based films have attracted increasing attention as sustainable and bioactive materials for wound management. Among them, chitosan (CTS) and starch (ST) blend represent promising candidate due to their natural origin, biodegradability, and intrinsic biological activity; however, their mechanical weakness and limited stability necessitate additional modification. This study reports the development and characterization of CTS-ST thin films crosslinked with dialdehyde alginate (ADA), synthesized via controlled oxidation. Two ADA variants differing in aldehyde group content were prepared to investigate the effect of crosslinking on the structural, physicochemical, and biological performance of the materials. The films were fabricated by blending 2% w/v CTS and ST in varying mass ratios (75/25, 50/50, and 25/75), followed by the addition of ADA (5% w/w) and glycerol (5% w/w) as a plasticizer. The mixtures were then cast onto plates and dried under ambient conditions. Comprehensive characterization included Fourier-transform infrared spectroscopy, moisture content analysis, contact angle measurements, antioxidant activity assay, hemolysis testing, and cytotoxicity evaluation using human keratinocyte cells. The results demonstrated that both the ADA variant and CTS/ST ratio significantly influenced crosslinking efficiency, hydrophilicity, and antioxidant behavior. All samples exhibited non-hemolytic behavior and no significant cytotoxic effects, indicating their favorable biocompatibility. The combination of biostability, antioxidant ability, and absence of cytotoxic effects highlights the potential of ADA-crosslinking CTS/ST films for further development as wound dressing materials and other biomedical applications.

## Linked entities

- **Chemicals:** chitosan (PubChem CID 129662530), glycerol (PubChem CID 753)

## Full-text entities

- **Genes:** ADA (adenosine deaminase) [NCBI Gene 100] {aka ADA1}
- **Diseases:** cytotoxic (MESH:D064420), hemolysis (MESH:D006461)
- **Chemicals:** glycerol (MESH:D005990), ST (MESH:D013213), aldehyde (MESH:D000447), CTS (MESH:D048271), Dialdehyde Alginate (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12897587/full.md

## References

95 references — full list in the complete paper: https://tomesphere.com/paper/PMC12897587/full.md

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Source: https://tomesphere.com/paper/PMC12897587