Journal article Characterization and evaluation of the ability of graphene quantum dots to affect α-synuclein aggregation in synucleinopathy models
Tuba Oz (author) (Search by this author)
a Department of Toxicology, Poznan University of Medical Sciences
;
Anna Alwani (author) (Search by this author)
;
Agnieszka Kamińska (author) (Search by this author)
;
Barbara Jachimska (author) (Search by this author)
;
Makoto Timmon Tanaka (author) (Search by this author)
;
Yasuo Miki (author) (Search by this author)
;
Koichi Wakabayashi (author) (Search by this author)
;
Katarzyna Maziarz (author) (Search by this author)
;
Sheetal Kaushik Bhardwaj (author) (Search by this author)
;
Ajeet Kaushik (author) (Search by this author)
;
Małgorzata Figiel (author) (Search by this author)
;
Piotr Chmielarz (author) (Search by this author)
;
Małgorzata Kujawska (author) (Search by this author)
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Citation
Tuba Oz, Anna Alwani, Agnieszka Kamińska, Barbara Jachimska, Makoto Timmon Tanaka, Yasuo Miki, Koichi Wakabayashi, Katarzyna Maziarz, Sheetal Kaushik Bhardwaj, Ajeet Kaushik, Małgorzata Figiel, Piotr Chmielarz, Małgorzata Kujawska. Characterization and evaluation of the ability of graphene quantum dots to affect α-synuclein aggregation in synucleinopathy models. Science and Technology of Advanced Materials. 2026, 27 (1), 2662693. https://doi.org/10.1080/14686996.2026.2662693

Description:

(abstract)

Synucleinopathies, including Parkinson’s disease and multiple system atrophy (MSA), are neurodegenerative disorders characterized by aggregation of α-synuclein (ASN). Nanomaterials capable of modulating protein misfolding represent a potential intervention strategy. Here, we synthesized graphene quantum dots (GQDs) and systematically evaluated their physicochemical properties and biological activity against ASN aggregation. The GQDs were characterized using spectroscopic, electron microscopy, and colloidal techniques to determine surface chemistry, charge, optical properties, and crystalline structure. Biological evaluation demonstrated cytocompatibility in human dermal fibroblasts (IC50 = 90 µg mL−1 at 24 h) with assessments of DNA damage and inflammatory responses. Functionally, GQDs destabilized preformed ASN fibrils in a cell-free assay, as evidenced by reduced Thioflavin-T fluorescence. In primary murine dopaminergic neurons, GQDs decrease pS129-ASN inclusion formation without compromising neuronal viability. Most importantly, intranasal administration of GQDs in an MSA mouse model reduced ASN immunoreactivity in the brain. Collectively, our data indicate that the synthetized GQDs are bioactive and can modulate ASN aggregation across cell-free, neuronal, and in vivo models. Importantly, physicochemical properties govern nano – bio interactions, providing a rationale for further refinement of GQDs as a biomaterial platform for synucleinopathy-related applications.

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Keyword: Graphene quantum dots, bioactive nanomaterials, Nano–bio interactions, amyloid inhibition, nanotoxicology, cytocompatibility, nano–bio interface

Date published: 2026-12-31

Publisher: Taylor & Francis

Journal:

  • Science and Technology of Advanced Materials (ISSN: 14686996) vol. 27 issue. 1 2662693

Funding:

Manuscript type: Author's version (Accepted manuscript)

MDR DOI: https://doi.org/10.48505/nims.6305

First published URL: https://doi.org/10.1080/14686996.2026.2662693

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Updated at: 2026-05-21 11:41:20 +0900

Published on MDR: 2026-05-21 14:27:40 +0900