Engineering of multifunctional drug nanocarriers combining stability and good release properties remains a great challenge. In this work, natural polymers κ-carrageenan (κ-CAR) and chitosan (CS) were deposited onto olive oil nanoemulsion droplets (NE) via layer-by-layer (LbL) self-assembly to study the release mechanisms of the anti-inflammatory diflunisal (DF) as a lipophilic drug model. The nano-systems were characterized by dynamic light scattering (DLS), zeta potential (ζ-potential) measurements, transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray energy dispersive spectroscopy (XEDS) and Fourier transform infrared spectroscopy (FTIR) to confirm the NE-coating with polymer layers. In addition, kinetic release studies of DF were developed by the dialysis diffusion bag technique. Mathematical models were applied to investigate the release mechanisms. The results showed that stable and suitably sized nanocapsules (~300 nm) were formed. Also, the consecutive adsorption of polyelectrolytes by charge reversal was evidenced. More interestingly, the drug release mechanism varied depending on the number of layers deposited. The nanosized systems containing up to two layers showed anomalous transport and first order kinetics. Formulations with three and four layers exhibited Case II transport releasing diflunisal with zero order kinetics. Hence, our results suggest that these polyelectrolyte nanocapsules have great potential as a multifunctional nanocarrier for drug delivery applications.

In recent years, innovative drug nanocarriers have been developed to enhance stability, bioavailability, and provide sustained release. In this chapter, systems based on natural macromolecules, lipids, or polymeric/polyelectrolyte nanocapsules and their principal chemical and functional characteristics are described. Nano-vesicular systems are especially relevant in different fields. Particularly, a promising potential is offered by systems based on colloidal nanocapsules, that exhibit a typical core-shell structure in which the drug can be confined into the cavity or in the polymeric coating that surrounds it. Both the cavity and the active substance can be lipophilic or hydrophilic and in solid or liquid form depending on the materials and methods used, making these nanocapsules attractive carriers for drug delivery. In addition, a compilation of different methods and materials employed in the preparation of these nanosystems and a recent review of applications of lipid and polymeric nanocapsules have been made, focussing on the encapsulation of drugs.

The growing global population has resulted in a higher demand for energy, leading researchers to prioritize the development of alternative energy sources and the improvement of current technologies. Nanofluids (NFs) are a promising method for enhancing heat transfer and efficiently utilizing solar thermal energy. This study describes the preparation of four NFs: two mono NFs of SiC and HfC containing nanoparticle concentrations ranging from 0.10–1.0 wt.%. Moreover, two hybrid NFs were synthesized within the same concentration range (0.10–1.0 wt.%) of SiC-HfC nanocomposites in proportions of 60 wt.% SiC-40 wt.% HfC and 40 wt.% SiC-60 wt.% HfC, all dispersed in a mixture of ethylene glycol (EG) and distilled water (50EG-50H₂O). The materials were synthesized by carbothermal reduction, and the NFs were prepared using the two-step method. The NFs showed stable dispersion, with HfC and 40SiC-60HfC systems exhibiting the higher zeta potential (ζ) values. Viscosity remained largely unaffected by particle addition. The thermal diffusivity of the NFs was measured by the thermal lens spectroscopy (TLS) technique using 1:20 diluted samples. The hybrid nanofluid 40SiC-60HfC improved diffusivity by 66.93%, presenting a synergistic effect in its performance, highlighting its potential in clean energy systems.