In the simplest case, appropriately adding
nanoparticulates to a polymer matrix can enhance its performance, often dramatically, by simply capitalizing on the nature and properties of the nanoscale filler (these materials are better described by the term
nanofilled polymer composites carbon nanotubes, molybdenum disulfide and tungsten disulfide are being used as reinforcing agents to fabricate mechanically strong biodegradable polymeric nanocomposites for bone tissue engineering applications. The addition of these nanoparticles in the polymer matrix at low concentrations (~0.2 weight %) cause significant improvements in the compressive and flexural mechanical properties of polymeric nanocomposites. Potentially, these nanocomposites may be used as a novel, mechanically strong, light weight composite as bone implants. The results suggest that mechanical reinforcement is dependent on the nanostructure morphology, defects, dispersion of nanomaterials in the polymer matrix, and the cross-linking density of the polymer. In general, two-dimensional nanostructures can reinforce the polymer better than one-dimensional nanostructures, and inorganic nanomaterials are better reinforcing agents than carbon based nanomaterials. In addition to mechanical properties, polymer nanocomposites based on carbon nanotubes or graphene have been used to enhance a wide range of properties, giving rise to functional materials for a wide range of high added value applications in fields such as energy conversion and storage, sensing and biomedical tissue engineering. For example, multi-walled carbon nanotubes based polymer nanocomposites have been used for the enhancement of the electrical conductivity. An alternative route to synthesis of nanocomposites is
sequential infiltration synthesis, in which inorganic nanomaterials are grown within polymeric substrates using vapor-phase precursors that diffuse into the matrix. Furthermore, nanocomposites can be prepared via
in situ generation of nanoparticles on and within polymeric materials, an approach that relies on the chemical transformation of suitable precursors to targeted nanoparticles synchronous with the build-up of the nanohybrid systems. The
in situ-generated nanoparticles tend to nucleate and grow on the active sites of the macromolecular chains, showing strong adhesion on the polymeric host. Nanoscale dispersion of filler or controlled nanostructures in the composite can introduce new physical properties and novel behaviors that are absent in the unfilled matrices. This effectively changes the nature of the original matrix and accelerated
biodegradability. A range of polymeric nanocomposites are used for biomedical applications such as tissue engineering, drug delivery, cellular therapies. Due to unique interactions between polymer and nanoparticles, a range of property combinations can be engineered to mimic native tissue structure and properties. A range of natural and synthetic polymers are used to design polymeric nanocomposites for biomedical applications including starch, cellulose, alginate, chitosan, collagen, gelatin, and fibrin, poly(vinyl alcohol) (PVA), poly(ethylene glycol) (PEG), poly(caprolactone) (PCL), poly(lactic-co-glycolic acid) (PLGA), and poly(glycerol sebacate) (PGS). A range of nanoparticles including ceramic, polymeric, metal oxide and carbon-based nanomaterials are incorporated within polymeric network to obtain desired property combinations. ==Magnetic nanocomposites==