Developing Iron Nanochelating Agents: Preliminary Investigation of Effectiveness and Safety for Central Nervous System Applications.

DFO chelation iron nanobubbles neurodegeneration

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
05 Jan 2024
Historique:
received: 24 11 2023
revised: 31 12 2023
accepted: 02 01 2024
medline: 23 1 2024
pubmed: 23 1 2024
entrez: 23 1 2024
Statut: epublish

Résumé

Excessive iron levels are believed to contribute to the development of neurodegenerative disorders by promoting oxidative stress and harmful protein clustering. Novel chelation treatments that can effectively remove excess iron while minimizing negative effects on the nervous system are being explored. This study focuses on the creation and evaluation of innovative nanobubble (NB) formulations, shelled with various polymers such as glycol-chitosan (GC) and glycol-chitosan conjugated with deferoxamine (DFO), to enhance their ability to bind iron. Various methods were used to evaluate their physical and chemical properties, chelation capacity in diverse iron solutions and impact on reactive oxygen species (ROS). Notably, the GC-DFO NBs demonstrated the ability to decrease amyloid-β protein misfolding caused by iron. To assess potential toxicity, in vitro cytotoxicity testing was conducted using organotypic brain cultures from the substantia nigra, revealing no adverse effects at appropriate concentrations. Additionally, the impact of NBs on spontaneous electrical signaling in hippocampal neurons was examined. Our findings suggest a novel nanochelation approach utilizing DFO-conjugated NBs for the removal of excess iron in cerebral regions, potentially preventing neurotoxic effects.

Identifiants

pubmed: 38255803
pii: ijms25020729
doi: 10.3390/ijms25020729
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : San Paolo-UNITO
ID : S1921_EX-POST_21_01
Organisme : University of Turin
ID : C.G. F.D.A. RiLo22, C.G. RiLo23

Auteurs

Eleonora Ficiarà (E)

School of Pharmacy, Center for Neuroscience, University of Camerino, 62032 Camerino, Italy.

Chiara Molinar (C)

Department of Drug Science and Technology, University of Turin, 10125 Turin, Italy.

Silvia Gazzin (S)

Fondazione Italiana Fegato-Onlus, Bldg. Q, AREA Science Park, ss14, Km 163.5, Basovizza, 34149 Trieste, Italy.

Sri Jayanti (S)

Fondazione Italiana Fegato-Onlus, Bldg. Q, AREA Science Park, ss14, Km 163.5, Basovizza, 34149 Trieste, Italy.

Monica Argenziano (M)

Department of Drug Science and Technology, University of Turin, 10125 Turin, Italy.

Lucia Nasi (L)

Institute of Materials for Electronics and Magnetism (IMEM) CNR, Parco Area delle Scienze 37/A, 43124 Parma, Italy.

Francesca Casoli (F)

Institute of Materials for Electronics and Magnetism (IMEM) CNR, Parco Area delle Scienze 37/A, 43124 Parma, Italy.

Franca Albertini (F)

Institute of Materials for Electronics and Magnetism (IMEM) CNR, Parco Area delle Scienze 37/A, 43124 Parma, Italy.

Shoeb Anwar Ansari (SA)

Department of Neurosciences, University of Turin, 10124 Turin, Italy.

Andrea Marcantoni (A)

Department of Drug Science and Technology, University of Turin, 10125 Turin, Italy.

Giulia Tomagra (G)

Department of Drug Science and Technology, University of Turin, 10125 Turin, Italy.

Valentina Carabelli (V)

Department of Drug Science and Technology, University of Turin, 10125 Turin, Italy.

Caterina Guiot (C)

Department of Neurosciences, University of Turin, 10124 Turin, Italy.

Federico D'Agata (F)

Department of Neurosciences, University of Turin, 10124 Turin, Italy.

Roberta Cavalli (R)

Department of Drug Science and Technology, University of Turin, 10125 Turin, Italy.

Classifications MeSH