We report the reversible addition-fragmentation chain transfer (RAFT) dispersion polymerization of 2-hydroxyethyl methacrylate (HEMA) in -dodecane using a poly(lauryl methacrylate) (PLMA) precursor at 90 °C. This formulation is an example of polymerization-induced self-assembly (PISA), which leads to the formation of a colloidal dispersion of spherical PLMA-PHEMA nanoparticles at 10-20% w/w solids. PISA syntheses involving polar monomers in non-polar media have been previously reported but this particular system offers some unexpected and interesting challenges in terms of both synthesis and characterization.
View Article and Find Full Text PDFHypothesis: Supra-particle formation by evaporation of an aqueous aerosol droplet containing nano-colloidal particles is challenging to investigate but has significant applications. We hypothesise that the Peclet number, Pe, which compares the effectiveness of evaporation-induced advection to that of colloidal diffusion, is critical in determining supra-particle morphology and can be used to predict the dried morphology for droplet containing polydisperse nanoparticles.
Experiments: Sterically-stabilized diblock copolymer nanoparticles were prepared via polymerization-induced self-assembly (PISA).
Peptides are important biomarkers for various diseases, however distinguishing specific amino-acid sequences using artificial receptors remains a major challenge in biomedical sensing. This study introduces a new approach for creating highly selective recognition surfaces using phage display biopanning against metal-organic nanosheets (MONs). Three MONs (ZIF-7, ZIF-7-NH and Hf-BTB-NH) are added to a solution containing every possible combination of seven-residue peptides attached to bacteriophage hosts.
View Article and Find Full Text PDFWe report the effect of added salt on the reversible addition-fragmentation chain transfer (RAFT) polymerization of 2-hydroxyethyl methacrylate (HEMA) in aqueous media. More specifically, poly(2-(methacryloyloxy)ethyl phosphorylcholine) (PMPC) was employed as a salt-tolerant water-soluble block for chain extension with HEMA targeting PHEMA DPs from 100 to 800 in the presence of NaCl. Increasing the salt concentration significantly reduces the aqueous solubility of both the HEMA monomer and the growing PHEMA chains.
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