RESUMO
A simple, versatile approach for the roughening of polymer microparticles surfaces via a deformation technique in the presence of an inorganic matrix is presented here. The process consists of straightforward steps: (1) preparation of a bicomposite colloidal sol, that is polymer particles and inorganic particles, dispersed in a liquid, (2) drying of the mixture onto a suitable hard substrate, (3) heating the dried film above the glass transition temperature of the polymer, and (4) re-dispersion and chemical etching of the inorganic medium. The primary driver is capillary imbibition of the polymer melt into the inorganic colloidal template. In addition, 2D particle tracking experiments of dispersed rough particles in water were performed to probe the diffusional behaviour of the roughened objects in comparison with their smooth precursors. We show that, despite large scale roughness (up to 10% asperity size with respect to particle diameter), Stokes law is obeyed and the particle motion can be modelled simply with the Stokes-Einstein-Sutherland relation.
RESUMO
Polymer chemistry, composition and molar mass are factors that are known to affect cytotoxicity, however the influence of polymer architecture has not been investigated systematically. In this study the influence of the position of the cationic charges along the polymer chain on cytotoxicity was investigated while keeping constant the other polymer characteristics. Specifically, copolymers of various architectures, based on a cationic pH responsive monomer, 2-(dimethylamino)ethyl methacrylate (DMAEMA) and a non-ionic hydrophilic monomer, oligo(ethylene glycol)methyl ether methacrylate (OEGMA) were engineered and their toxicity towards a panel of cell lines investigated. Of the seven different polymer architectures examined, the block-like structures were less cytotoxic than statistical or gradient/tapered architectures. These findings will assist in developing future vectors for nucleic acid delivery.