Hierarchical Fractal Assemblies from Poly(ethylene oxide- b-lysine- b-leucine).
Craig A MachadoKyle C BentzRoger TranTaylor A JenkinsBrooke E BarnesLily E DiodatiDaniel A SavinPublished in: Biomacromolecules (2019)
Poly(ethylene oxide43- b-lysine62- b-leucine72) (wherein subscripts denote the degree of polymerization) was synthesized via ring-opening polymerization of N-carboxyanhydrides using an amine-terminated poly(ethylene oxide) macroinitiator, with polypeptide blocks produced by sequential monomer addition. Infrared and circular dichroism spectroscopy indicated that the peptide blocks in this polymer formed α-helices in the solid and solution states, respectively. In the aqueous solution, this polymer self-assembled into spherical micelles with a hydrodynamic radius of approximately 90 nm at concentrations between 0.05 and 0.20% w/w and pH values between 2 and 6.5. Upon preparation of transmission electron microscopy (TEM) grids, the micelles at pH 2 underwent hierarchical assembly to produce fractal assemblies, whereas small clusters were observed for micellar solutions at pH 6.5. Cryogenic-TEM of solutions showed spherical micelles, and dynamic light scattering showed no large (∼1 μm) aggregates in the solution, which suggests that fractal formation was a result of the drying process, and that fractals were not present in the solution. This system provides a facile route to nanostructured surfaces, which can be used for applications such as modulating cell adhesion or promoting the growth of neurons.
Keyphrases
- electron microscopy
- drug delivery
- cell adhesion
- aqueous solution
- drug release
- cancer therapy
- solid state
- hyaluronic acid
- molecularly imprinted
- spinal cord
- high resolution
- photodynamic therapy
- oxide nanoparticles
- signaling pathway
- reduced graphene oxide
- single molecule
- biofilm formation
- highly efficient
- liquid chromatography