4.7 Article

Direct Access to Polysaccharide-Based Vesicles with a Tunable Membrane Thickness in a Large Concentration Window via Polymerization-Induced Self-Assembly

期刊

BIOMACROMOLECULES
卷 22, 期 7, 页码 3128-3137

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.biomac.1c00569

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资金

  1. French Agence Nationale de la Recherche (ANR JCJC, GlyNanEP) [18-CE06-0002]
  2. French Infrastructure for Integrated Structural Biology (FRISBI) [ANR-10-INSB-05-05]
  3. NSF [DMR-0520547]
  4. European Union's Horizon 2020 research and innovation programme under the SINE2020 project [654000]
  5. iBiSA

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In this study, pure vesicles were prepared in situ from a polysaccharide-grafted copolymer using polymerization-induced self-assembly technology. The vesicles were found to self-assemble over a wide range of solid concentrations, and an increase in the targeted average degree of polymerization led to an increase in vesicle membrane thickness.
Polymersomes are multicompartmental vesicular nano-objects obtained by self-assembly of amphiphilic copolymers. When prepared in the aqueous phase, they are composed of a hydrophobic bilayer enclosing water. Although such fascinating polymeric nano-objects have been widely reported with synthetic block copolymers, their formation from polysaccharide-based copolymers remains a significant challenge. In the present study, the powerful platform technology known as polymerization-induced self-assembly was used to prepare in situ pure vesicles from a polysaccharide-grafted copolymer: dextran-g-poly(2-hydroxypropyl methacrylate) (Dex-g-PHPMA). The growth of the PHPMA grafts was performed with a dextran-based macromolecular chain transfer agent in water at 20 degrees C using photomediated reversible addition fragmentation chain transfer polymerization at 405 nm. Transmission electron microscopy, cryogenic electron microscopy, small-angle X-ray scattering, atomic force microscopy, and dynamic light scattering revealed that amphiphilic Dex-g-PHPMA(X = 100-300) (X is the targeted average degree of polymerization, (X) over bar (-)(n), of each graft at full conversion) exhibit remarkable self-assembly behavior. On the one hand, vesicles were obtained over a wide range of solid concentrations (from 2.5% to 13.5% w/w), which can facilitate posterior targeting of such rare morphology. On the other hand, the extension of (X) over bar (-)(n) induces an increase in the vesicle membrane thickness, rather than a morphological evolution (spherical micelles to cylinders to vesicles).

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