Glycosylated polyplex micelles from oppositely charged block copolymers

Glycosylated nanoparticles hold significant promise for applications in biomedicine, because of their ability to mimic complex carbohydrate interactions. Herein, we report the synthesis of block copolymers featuring both a glycosylated segment and a charged block <i>via</i> RAFT polymerization and postpolymerization modifications. Additionally, we prepared glycosylated polyplex micelles by mixing oppositely charged glycosylated block copolymers in aqueous media. Electrostatic interactions between the charged segments occur, triggering the formation of glycosylated nanoparticles with a polyplex core. The resulting nanoparticles were characterized <i>via</i> dynamic light scattering (DLS), <i>ζ</i>-potential measurements and transmission electron microscopy (TEM), which confirmed their nonspherical morphology. Furthermore, we expanded this strategy by incorporating oppositely charged homopolymers, highlighting the versatility of our approach. These findings demonstrate a robust and modular platform for the design of glycosylated nanoparticles, paving the way for future exploration of their dynamic properties and potential use as responsive carriers for drug delivery.

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Publication Details

Journal
Journal of Materials Chemistry B
Published
2025-01-01
DOI
https://doi.org/10.1039/d4tb02760d
Citations
2
Primary Topic
biodegradable polymer synthesis and properties
Type
article
Field-Weighted Citation Impact
1.19

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article

Glycosylated polyplex micelles from oppositely charged block copolymers

Mokun Chen, Rudy Folkersma, Théophile Pelras, Katja Loos et al.
2 citations
Journal of Materials Chemistry B
biodegradable polymer synthesis and properties
1.19
article

Glycosylated polyplex micelles from oppositely charged block copolymers

Mokun Chen, Rudy Folkersma, Théophile Pelras, Katja Loos, Vincent S. D. Voet, Joël Benninga
article en
2 citations

Abstract

Glycosylated nanoparticles hold significant promise for applications in biomedicine, because of their ability to mimic complex carbohydrate interactions. Herein, we report the synthesis of block copolymers featuring both a glycosylated segment and a charged block <i>via</i> RAFT polymerization and postpolymerization modifications. Additionally, we prepared glycosylated polyplex micelles by mixing oppositely charged glycosylated block copolymers in aqueous media. Electrostatic interactions between the charged segments occur, triggering the formation of glycosylated nanoparticles with a polyplex core. The resulting nanoparticles were characterized <i>via</i> dynamic light scattering (DLS), <i>ζ</i>-potential measurements and transmission electron microscopy (TEM), which confirmed their nonspherical morphology. Furthermore, we expanded this strategy by incorporating oppositely charged homopolymers, highlighting the versatility of our approach. These findings demonstrate a robust and modular platform for the design of glycosylated nanoparticles, paving the way for future exploration of their dynamic properties and potential use as responsive carriers for drug delivery.

Journal of Materials Chemistry BVol. 13(16)
University of Groningen (NL), Stenden University of Applied Sciences (NL)
Rijksuniversiteit Groningen, Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Openalex Percentile: Top 24%
biodegradable polymer synthesis and properties
1.19
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Glycosylated polyplex micelles from oppositely charged block copolymers — Mokun Chen, Rudy Folkersma, et al. · Journal of Materials Chemistry B (2025) | TGRS Research Map | TGRS