Self-Assembly of PEG-b-PTMC Copolymers: Micelles and Polymersomes Size Control - Archive ouverte HAL
Article Dans Une Revue Langmuir Année : 2019

Self-Assembly of PEG-b-PTMC Copolymers: Micelles and Polymersomes Size Control

Résumé

Poly(ethylene glycol)45-b-poly(trimethylene carbonate)n PEG45-b-PTMCn diblock copolymers were synthesized with five different PTMC degrees of polymerization (n = 38, 96, 144, 170, 332) and their self-assembly properties in water were studied using a manual nanoprecipitation procedure. We confirmed that the copolymer’s hydrophilic weight fraction (fPEG) is controlling nanoparticles morphology. We determined that the PEG45-b-PTMC96 with fPEG ≈ 17% is the optimal hydrophilic fraction for the stabilization of well-defined unilamellar vesicles with a membrane thickness of δ ≈ 14.6 nm. Maintaining this fraction constant and modulating the overall molar mass of the block copolymers allowed the establishment of a power law of which provides a robust correlation between the molar mass of PTMC and vesicles’ membrane thickness. Finally, we proved that controlling nanoprecipitation’s conditions by microfluidics allowed fine-tuning and control of the nanoparticles size and polydispersity index while maintaining their shape with a perfect batch-to-batch reproducibility.
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Dates et versions

hal-02306925 , version 1 (13-03-2020)

Identifiants

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Coralie Lebleu, Laura Rodrigues, Jean-Michel Guigner, Annie Brûlet, Elisabeth Garanger, et al.. Self-Assembly of PEG-b-PTMC Copolymers: Micelles and Polymersomes Size Control. Langmuir, 2019, 35 (41), pp.13364-13374. ⟨10.1021/acs.langmuir.9b02264⟩. ⟨hal-02306925⟩
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