4.7 Article

In Vivo Toxicity Assessment of Chitosan-Coated Lignin Nanoparticles in Embryonic Zebrafish (Danio rerio)

Journal

NANOMATERIALS
Volume 11, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/nano11010111

Keywords

toxicology; development; biocompatibility; nanotoxicology; sustainability

Funding

  1. United States Department of Agriculture National Institute of Food and Agriculture (USDA-NIFA) [2013-67021-21181]
  2. Oregon State University Agricultural Research Foundation [ARF8301A]
  3. National Institute of Environmental and Health Sciences [R01ES017552]
  4. Molecular Biotechnology Training Program (MBTP) - National Institutes of Health
  5. Graduate School at North Carolina State University [5 T32 GM008776-15]
  6. NSF [CMMI-1825476]

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The study found that chitosan-coated lignin nanoparticles were more toxic at high concentrations compared to plain nanoparticles, resulting in higher mortality rates and significant sublethal endpoints. Further research is needed to fully understand the mechanisms of toxicity of chitosan-coated lignin nanoparticles.
Lignin is the second most abundant biopolymer on Earth after cellulose. Since lignin breaks down in the environment naturally, lignin nanoparticles may serve as biodegradable carriers of biocidal actives with minimal environmental footprint compared to conventional antimicrobial formulations. Here, a lignin nanoparticle (LNP) coated with chitosan was engineered. Previous studies show both lignin and chitosan to exhibit antimicrobial properties. Another study showed that adding a chitosan coating can improve the adsorption of LNPs to biological samples by electrostatic adherence to oppositely charged surfaces. Our objective was to determine if these engineered particles would elicit toxicological responses, utilizing embryonic zebrafish toxicity assays. Zebrafish were exposed to nanoparticles with an intact chorionic membrane and with the chorion enzymatically removed to allow for direct contact of particles with the developing embryo. Both mortality and sublethal endpoints were analyzed. Mortality rates were significantly greater for chitosan-coated LNPs (Ch-LNPs) compared to plain LNPs and control groups. Significant sublethal endpoints were observed in groups exposed to Ch-LNPs with chorionic membranes intact. Our study indicated that engineered Ch-LNP formulations at high concentrations were more toxic than plain LNPs. Further study is warranted to fully understand the mechanisms of Ch-LNP toxicity.

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