Some of the most relevant finite-size and surface effects in the magnetic and transport properties of magnetic fine particles and granular solids are reviewed. The stability of the particle magnetization, superparamagnetic regime and the magnetic relaxation are discussed. New phenomena appearing due to interparticle interactions, such as the collective state and non-equilibrium dynamics, are presented. Surface anisotropy and disorder, spin-wave excitations, as well as the enhancements of the coercive field and particle magnetization are also reviewed. The competition of surface and finite-size effects to settle the magnetic behaviour is addressed. Finally, two of the most relevant phenomena in the transport properties of granular solids are summarized namely, giant magnetoresistance in granular heterogeneous alloys and Coulomb gap in insulating granular solids.

Monodisperse magnetite Fe 3 O 4 nanoparticles of controlled size within 6 and 20 nm in diameter were synthesized by thermal decomposition of an iron organic precursor in an organic medium. Particles were coated with oleic acid. For all samples studied, saturation magnetization M s reaches the expected value for bulk magnetite, in contrast to results in small particle systems for which M s is usually much smaller due to surface spin disorder. The coercive field for the 6 nm particles is also similar to that of bulk magnetite. Both results suggest that the oleic acid molecules covalently bonded to the nanoparticle surface yield a strong reduction in the surface spin disorder. However, although the saturated state may be similar, the approach to saturation is different and, in particular, the high-field differential susceptibility is one order of magnitude larger than in bulk materials. The relevance of these results in biomedical applications is discussed.

The local heat delivered by metallic nanoparticles selectively attached to their target can be used as a molecular surgery to safely remove toxic and clogging aggregates. We apply this principle to protein aggregates, in particular to the amyloid beta protein (Abeta) involved in Alzheimer's disease (AD), a neurodegenerative disease where unnaturally folded Abeta proteins self-assemble and deposit forming amyloid fibrils and plaques. We show the possibility to remotely redissolve these deposits and to interfere with their growth, using the local heat dissipated by gold nanoparticles (AuNP) selectively attached to the aggregates and irradiated with low gigahertz electromagnetic fields. Simultaneous tagging and manipulation by AuNP of Abeta at different stages of aggregation allow both, noninvasive exploration and dissolution of molecular aggregates.