Electronic polymers biocompatibility

The presence of polymer, solvent, and ionic components in conducting polymers reminds one of the composition of the materials chosen by nature to produce muscles, neurons, and skin in living creatures. We will describe here some devices ready for commercial applications, such as artificial muscles, smart windows, or smart membranes other industrial products such as polymeric batteries or smart mirrors and processes and devices under development, such as biocompatible nervous system interfaces, smart membranes, and electron-ion transducers, all of them based on the electrochemical behavior of electrodes that are three dimensional at the molecular level. During the discussion we will emphasize the analogies between these electrochemical systems and analogous biological systems. Our aim is to introduce an electrochemistry for conducting polymers, and by extension, for any electrodic process where the structure of the electrode is taken into account. 

New natural polymers based on synthesis from renewable resources, improved recyclability based on retrosynthesis to reusable precursors, and molecular suicide switches to initiate biodegradation on demand are the exciting areas in polymer science. In the area of biomolecular materials, new materials for implants with improved durability and biocompatibility, light-harvesting materials based on biomimicry of photosynthetic systems, and biosensors for analysis and artificial enzymes for bioremediation will present the breakthrough opportunities. Finally, in the field of electronics and photonics, the new challenges are molecular switches, transistors, and other electronic components molecular photoad-dressable memory devices and ferroelectrics and ferromagnets based on nonmetals. 

Block copolymers, polymer blends, polymers at interfaces, liquid crystalline polymers, polymers with novel optical and electronic properties, cross-linked polymers (including elastomers and thermosets), and biocompatible polymers are all areas of active research that are beyond the scope of this chapter. 

Relevant issues still to be addressed in constructing amperometric enzyme sensors either using the electrical wiring of enzymes with redox polymers or with flexible polymeric electron mediators are sensor efficiency, accuracy, reproducibility, selectivity, insensitivity to partial pressure of oxygen, detectivity (signal-to-noise ratio) as well as sensor hfetime and biocompatibility [47]. Then we can address manufacturability and the cost of use of either in vitro or in vivo sensors. 

The direct electrochemistry of redox proteins has developed significantly in the past few years. Conditions now exist that permit the electrochemistry of all the proteins to be expressed at a range of electrodes, and important information about thermodynamic and kinetic properties of these proteins can be obtained. More recently, direct electron transfer between redox enzymes and electrodes has been achieved due to the more careful control of electrode surfaces. The need for biocompatible surfaces in bioelectrochemistry has stimulated the development of electrode surface engineering techniques, and protein electrochemistry has been reported at conducting polymer electrodes 82) and in membranes 83, 84). Furthermore, combination of direct protein electrochemistry with spectroscopic methods may offer 85) a novel way of investigating structure-function relationships in electron transport proteins. 

A variant of CVD, termed plasma polymerization, has been used to produce polymer coatings. So far, it has been used in a limited number of applications most notably to produce biocompatible coatings for electronic sensors that are implanted in humans. This process is also being investigated for polymer coating applications. As the name implies, an RF generator is used to induce a plasma environment into which the monomer components are introduced. The electrons from the plasma induce the polymerization reaction at the surface of the substrate. The power input to the plasma must be kept low to prevent secondary reactions from destroying the polymer structure. 

Polymer-supported Ag nanoparticles have been widely investigated and provide potential applications as catalysts, photonic and electronic sensors, wound dressings, body wall repairs, augmentation devices, tissue scaffolds, and antimicrobial filters [15-22]. For these applications, Ag nanoparticles have to be supported in a biocompatible polymer system [23-26]. The electrospinning technique has often been adopted for the incorporation of Ag nanoparticles into polymer porous media. In this chapter, we review the preparation methods and properties of Ag nanoparticles incorporated into polymeric nanofibers and their applications in the fields of filtration, catalysis, tissue engineering and wound dressing. 

The Canine Model. While ex vivo models often are considered to be an improvement over in vitro biocompatibility test systems, the problem of describing extremely complex blood—polymer interactions still remains. In this study, we used radioisotope-labeled proteins and platelets and scanning electron microscopy. In other studies, we applied immunolabeling techniques and transmission electron microscopy. The application of these tools to an in vivo or ex vivo system provides more pertinent data than that often obtained in an in vitro system. Through this approach we hope to gain some insights into the complicated interactions of blood with biomaterials. 

Crystal Morphology Crystal morphology determines the mechanical properties, the biodegradability, and the biocompatibility of polymers. Thus, it is necessary to understand the mechanism of polymer crystallization in order to control the polymer microstructure and, thereby, its properties. The crystallinity and cavitation of polymers have been studied using optical and in situ electron microscopy as complementary techniques, among many others. 

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