Bola-amphiphilic glycodendrimers for targeting glial cells in the brain

Abstract

Targeting the glial cells in the brain constitutes a formidable challenge due to the presence of the blood-brain barrier (BBB) and the difficulty in achieving specific targeting. Intranasal (IN) administration offers a promising solution to bypass the BBB for delivery directly to the brain, while nanotechnology-based delivery provides tailored targeting capabilities. Here, we report dendrimer-based nanosystems developed for IN administration to target astrocytes and microglia, two types of glial cells that play important roles in maintaining brain homeostasis. Specifically, we demonstrate that bola-amphiphilic glycodendrimers, Ia and Ib, which bear glucose and mannose terminals, respectively target astrocytes and microglia in mouse brain. These two glycodendrimers, composed of a hydrophobic bola-lipid in the middle connected with two hydrophilic poly(amidoamine) dendrons, were effectively synthesized via click reaction using unprotected carbohydrate building units, and self-assembled into small and spherical nanoparticles by virtue of their amphiphilicity. In a mouse model, both dendrimer nanoparticles successfully reached the brain following IN administration, where the glucose-dendrimer Ia selectively targeted astrocytes, and the mannose-dendrimer Ib microglia. These findings highlight the potential of glycodendrimer-based nanosystems for precise targeting in the brain and offer a promising perspective for treating central nervous system (CNS) diseases.

Supplementary files

Article information

Article type
Paper
Submitted
17 Jul 2025
Accepted
24 Oct 2025
First published
27 Oct 2025
This article is Open Access
Creative Commons BY license

Nanoscale, 2025, Accepted Manuscript

Bola-amphiphilic glycodendrimers for targeting glial cells in the brain

L. Peng, Z. BIAN, W. Zhang, S. Garofalo, D. M. Dhumal, J. Zheng, T. Roussel, E. Laurini, C. Galanakou, C. Lauro, M. Maresca, Y. Xia, D. Zhu, S. Pricl, X. Liu and C. Limatola, Nanoscale, 2025, Accepted Manuscript , DOI: 10.1039/D5NR03017J

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