Abstract :
[en] This work investigates the synthesis of polypeptoid nanoparticles through Ugi-mediated polymerization-induced self-assembly (U-PISA), combining aqueous Ugi four-component polycondensation with PEG-based stabilization. Polypeptoid nano-objects were produced directly from amino acid-derived building blocks via a one-pot process under mild, open-air conditions. The effects of PEG molar mass and feed composition on particle formation and morphology were systematically examined, providing access to tunable spherical and worm-like nanostructures. The in situ formation of amphiphilic PEG-polypeptoid species suggests that nanoparticle formation proceeds through a PISA-like mechanism. However, the step-growth nature of the Ugi polycondensation implies that both PEG-functionalized and unconjugated polypeptoid chains may participate in nanoparticle assembly and stabilization. These results demonstrate that multicomponent polymerizations, such as Ugi polymerization, can be integrated into a PISA strategy, offering a simple route to polypeptoid nanoparticles with tunable morphologies and potential biomedical applications.
Funding text :
This work was supported by financial funding from CNRS INC Emer- gence. We also acknowledge the support of the CAP and MIC ICMPE platforms, DIM MaTerRe, and the Île-de-France region. China Scholar- ship Council (CSC, project 202208420008) is thanked for funding a PhD scholarship for the first author, L. LEI. A.D. thanks the F.R.S.-FNRS. Sylvain Prévost is gratefully acknowledged for his assistance during the SANS experiment at the ILL
Scopus citations®
without self-citations
0