Nanomedicine for targeting brain Neurodegeneration: Critical barriers and circadian rhythm Considerations

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Abstract

The development of novel therapies for central nervous system (CNS) diseases, particularly neurodegenerative disorders like Alzheimer’s disease (AD), is a critical global health priority. Biotherapeutics, such as monoclonal antibodies (mAbs) and RNA-based therapies, have shown potential for treating brain disorders. However, their clinical progress is limited by their difficult access to their brain targets. At the preclinical level, nanotechnology has been shown, to help these molecules overcome the biological barriers that imped their adequate brain delivery. This review highlights advances in this area and the challenges for the translation to the clinic. Key nanotechnology-based strategies, such as surface modifications utilizing endogenous protein corona, functionalization with targeting ligands, therapeutic ultrasound-mediated microbubble oscillation were particularly analyzed. Additionally, in line with the focus of the Special Issue, this review integrates the concept of chronotherapy, with a focus on AD treatment, highlighting the idea that, by aligning nanoparticle (NP)-based drug delivery with circadian rhythms, it may be possible to improve therapeutic outcomes. Finally, the article analyzes current strategies in CNS drug delivery in clinical trials and provides future directions within this frame, notably in the area of AD.

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Pineiro-Alonso, L., Rubio-Prego, I., Lobyntseva, A., González-Freire, E., Langer, R., & Alonso, M. J. (2025). Nanomedicine for targeting brain Neurodegeneration: Critical barriers and circadian rhythm Considerations. Advanced Drug Delivery Reviews, 222, 115606. 10.1016/j.addr.2025.115606

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This work was supported by the government of Xunta de Galicia (Competitive Reference Groups, Consellería de Educación e Ordenación Universitaria, Xunta de Galicia, Ref: ED431C 2021/17); by the FEDER/ Spanish Ministry of Science, Innovation and Universities (AEI/ Project- PID2020-119368RB-I00) and by Xunta de Galicia (Centro singular de Investigación de Galicia accreditation 2019-2022) and the European Union (European Regional Development Fund (ERDF), Ref: ED431G 2019/02). This work is part of the projects Targeting Circadian Clock Dysfunction in Alzheimer’s Disease (HORIZON-MSCA-2021-DN-01, Ref:101073474) financed by the European Union; and DIAGBI (PLEC2021-008034) funded by MICIU/AEI/ 10.13039/501100011033 and by the “European Union NextGenerationEU/PRTR”. Laura Pineiro-Alonso acknowledges a grant (ED481A 2022/237) from Xunta de Galicia “Axudas de apoio á etapa predoutoral 2021”. Inés Rubio-Prego acknowledges a grant (IFI23/00035) from Instituto de Salud Carlos III “Contratos i-PFIS: Doctorados ISS-empresa en Ciencias y Tecnologías de la Salud”. Alexandra Lobyntseva acknowledges a grant (101072895) funded within Horizon Europe Marie Skłodowska-Curie Doctoral Net- works. Figures have been created with BioRender.com.

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© 2025 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by- nc-nd/4.0/).
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