Modification of AgNP-Decorated PET: A Promising Strategy for Preparation of AgNP-Filled Nuclear Pores in Polymer Membranes.

Polymer-based membranes represent an irreplaceable group of materials that can be applied in a wide range of key industrial areas, from packaging to high-end technologies. Increased selectivity to transport properties or the possibility of controlling membrane permeability by external stimuli represents a key issue in current material research. In this work, we present an unconventional approach with the introduction of silver nanoparticles (AgNPs) into membrane pores, by immobilising them onto the surface of polyethyleneterephthalate (PET) foil with subsequent physical modification by means of laser and plasma radiation prior to membrane preparation.

A New Promising Material for Biological Applications: Multilevel Physical Modification of AgNP-Decorated PEEK.

In the case of polymer medical devices, the surface design plays a crucial role in the contact with human tissue. The use of AgNPs as antibacterial agents is well known; however, there is still more to be investigated about their anchoring into the polymer surface. This study describes the changes in the surface morphology and behaviour in the biological environment of polyetheretherketone (PEEK) with immobilised AgNPs after different surface modifications.

Laser-Promoted Immobilization of Ag Nanoparticles: Effect of Surface Morphology of Poly(ethylene terephthalate).

In the last two decades, the importance of nanomaterials in modern technologies has been unquestionable. Metal nanoparticles are frequently used in many areas of science and technology, delivering unprecedented improvements to properties of the conventional materials. This work introduces an effective tool for preparing a highly enriched poly (ethylene terephthalate) (PET) surface with silver nanoparticles, firmly immobilized in the same surface area on polymer.

Conformational differences between surface-bound and fluid-phase complement-component-C3 fragments. Epitope mapping by cDNA expression.

In previous studies a subset of complement-component-C3 (C3) epitopes, C3(D), expressed in denatured and surface-bound C3 and C3 fragments, has been described. These epitopes were detected by antibodies raised against denatured C3. In the present study we used a cDNA expression strategy to localize epitopes recognized by monoclonal and polyclonal anti-C3(D) antibodies.