# Comparative Biofunctionality Assessment of Lignin and Lignin/Chitosan Nanoparticles: Impact of Chitosan Co-Assembly on Cytotoxicity, Cytocompatibility, Radical-Scavenging Activity, and Antimicrobial Performance

**Authors:** Tsvetelina Zagorcheva, Boika Andonova-Lilova, Denitsa Georgieva, Silviya Hristova, Zhani Yanev, Nikolina Rusenova, Georgi Beev, Kamelia Petkova-Parlapanska, Galina Nikolova, Yanka Karamalakova, Zvezdelina Yaneva

PMC · DOI: 10.3390/pharmaceutics18030350 · Pharmaceutics · 2026-03-11

## TL;DR

This study compares the biofunctional properties of lignin and lignin-chitosan nanoparticles, showing that the latter are more biocompatible and effective in scavenging radicals and fighting microbes.

## Contribution

The study introduces lignin-chitosan nanoparticles as a novel, sustainable nanoplatform with enhanced biomedical properties.

## Key findings

- LCNPs showed higher long-term cell viability compared to LNPs in fibroblasts and keratinocytes.
- LCNPs exhibited improved lipid peroxidation and superoxide inhibition compared to LNPs.
- LCNPs demonstrated up to 8–13-fold higher antimicrobial activity compared to lignin solutions.

## Abstract

Background/Objectives: The aim of the present study was to conduct a systematic in vitro assessment of the biofunctionalities of newly synthesized lignin (LNPs) and lignin–chitosan nanoparticles (LCNPs) via a comparative in vitro estimation of their cytotoxicity, cytocompatability potential, radical-scavenging activity, and antimicrobial performance, thereby establishing a benchmark for their sustainable design and biomedical applications. Methods: LNPs and LCNPs were synthesized via “green” self-assembly and co-assembly methods. Results: In vitro cytotoxicity studies on L929 fibroblasts and HaCaT keratinocytes demonstrated higher long-term viability for LCNPs (half-maximal inhibitory concentration IC50 = 3.05 mg/mL at 72 h) compared with LNPs (IC50 = 1.37 mg/mL), while both formulations maintained >76% viability at a concentration of 0.5 mg/mL. Electron Paramagnetic Resonance (EPR) and spectrophotometric antioxidant assays displayed strong radical scavenging activity, with LNPs excelling in ●OH, NO, and ABTS scavenging and LCNPs exhibiting enhanced lipid peroxidation and superoxide inhibition potential. Antimicrobial testing revealed minimal inhibitory concentration (MIC) reductions of the nanoparticles up to 8–13-fold compared to lignin solutions, with LCNPs showing higher activity against Gram-positive and Gram-negative microbial strains. Conclusions: These results highlight LCNPs as biocompatible, antioxidant, and antimicrobial nanoplatforms with potential for regenerative medicine, oxidative stress mitigation, and infection control.

## Linked entities

- **Chemicals:** lignin (PubChem CID 175586), chitosan (PubChem CID 129662530), ●OH (PubChem CID 961), NO (PubChem CID 24822), ABTS (PubChem CID 35688)

## Full-text entities

- **Diseases:** Cytotoxicity (MESH:D064420), infection (MESH:D007239)
- **Chemicals:** NO (MESH:D009614), OH (MESH:C031356), lipid (MESH:D008055), ABTS (MESH:C002502), Chitosan (MESH:D048271), superoxide (MESH:D013481), LNPs (-), Lignin (MESH:D008031)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028907/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028907/full.md

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Source: https://tomesphere.com/paper/PMC13028907