Literature DB >> 35619425

Striking Effect of Polymer End-Group on C60 Nanoparticle Formation by High Shear Vibrational Milling with Alkyne-Functionalized Poly(2-oxazoline)s.

Joachim F R Van Guyse1, Victor R de la Rosa1, Reidar Lund2, Michiel De Bruyne3,4, Riet De Rycke3,4, Sergey K Filippov5, Richard Hoogenboom1.   

Abstract

Buckminsterfullerene (C60) has a large potential for biomedical applications. However, the main challenge for the realization of its biomedical application potential is to overcome its extremely low water solubility. One approach is the coformulation with biocompatible water-soluble polymers, such as poly(2-oxazoline)s (PAOx), to form water-soluble C60 nanoparticles (NPs). However, uniform and defined NPs have only been obtained via a thin film hydration method or using cyclodextrin-functionalized PAOx. Here, we report the mechanochemical preparation of defined and stable C60:PAOx NPs by the introduction of a simple alkyne group as a polymer end-group. The presence of this alkyne bond is proven to be crucial in the mechanochemical synthesis of stable, defined sub-100 nm C60:PAOx NPs, with high C60 content up to 8.9 wt %.

Entities:  

Year:  2019        PMID: 35619425     DOI: 10.1021/acsmacrolett.8b00998

Source DB:  PubMed          Journal:  ACS Macro Lett        ISSN: 2161-1653            Impact factor:   6.903


  1 in total

1.  A solvent-free mechanochemical synthesis of polyaromatic hydrocarbon derivatives.

Authors:  Cong Wang; Malik Hill; Brandon Theard; James Mack
Journal:  RSC Adv       Date:  2019-09-04       Impact factor: 4.036

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.