Ethyl cellulose nanoparticles as stabilizers for Pickering emulsions

Pickering emulsions stabilized by ethyl cellulose nanoparticles have recently received –great attention for their remarkable stability and numerous industrial applications. De- spite this, the exact stabilization mechanism of such Pickering emulsions is still not fully understood. Both the stabilization of the emulsion by particle adsorption at the inter- face and through network formation in the continuous phase (leading to a yield stress) have been suggested. In this work we study soybean oil-in-water emulsions stabilized by ethyl cellulose nanoparticles and find, by the use of confocal microscopy and interfa- cial tension measurements, that the main stabilization mechanism of this nanoparticle- stabilized emulsions is the adsorption of the particles at the interface, instead of forming a network in the continuous phase. At the same time, oscillatory rheology measurements reveal that the emulsions exhibit a yield stress well below the random close-packing limit for hard spheres, suggesting short-range interactions between the droplets caused by the presence of the particles at the interface. The presence of the particles at the interface in combination with the observed rheological behavior of an attractive emulsion gives a strong indication for a particle-bridged stabilized emulsions

Is there a difference between surfactant-stabilised and Pickering emulsions?

What measurable physical properties allow one to distinguish surfactant-stabilised from Pickering emulsions? Whereas surfactants influence oil/water interfaces by lowering the oil/water interfacial tension, particles are assumed to have little effect on the interfacial tension. Here we perform interfacial tension (IFT) measurements on three different systems: (1) soybean oil and water with ethyl cellulose nanoparticles (ECNPs), (2) silicone oil and water with the globular protein bovine serum albumin (BSA), and (3) sodium dodecyl sulfate (SDS) solutions and air. The first two systems contain particles, while the third system contains surfactant molecules. We observe a significant decrease in interfacial tension with increasing particle/molecule concentration in all three systems. We analyse the surface tension data using the Gibbs adsorption isotherm and the Langmuir equation of state for the surface, resulting in surprisingly high adsorption densities for the particle-based systems. These seem to behave very much like the surfactant system: the decrease in tension is due to the presence of many particles at the interface, each with an adsorption energy of a few kBT. Dynamic interfacial tension measurements show that the systems are in equilibrium, and that the characteristic time scale for adsorption is much longer for particle-based systems than for surfactants, in line with their size difference. In addition, the particle-based emulsion is shown to be less stable against coalescence than the surfactant-stabilised emulsion. This leaves us with the conclusion that we are not able to make a clear distinction between the surfactant-stabilised and Pickering emulsions

Fully-biobased UV-absorbing nanoparticles from ethyl cellulose and zein for environmentally friendly photoprotection

Effective photoprotection is a vital consumer issue. However, there are many concerns regarding the adverse environmental and health impacts associated with current organic and inorganic UV filters. Here, we prepare fully-biobased UV-absorbing nanoparticles from ethyl cellulose (ECNPs) and zein (ZNPs) with encapsulated biobased photoprotectants obtainable from plants and foods (quercetin, retinol, and p-coumaric acid), which have the potential to satisfy both environmental and health issues in photoprotection. We show the ability of ECNPs and ZNPs to be easily tuned compositionally to obtain uniform, broadband UV spectrum absorbance profiles, and prepare transparent UV-absorbing coatings from the ECNPs. We find that the maximum loadings for retinol, quercetin, and p-coumaric acid into the ECNPs are 31 wt%, 14 wt%, and 13 wt% respectively. The ECNP size remains constant (except for the largest loading of retinol, 31 wt%) and the absolute zeta potential increases upon increasing the loading of quercetin and retinol, whereas increasing the loading of p-coumaric acid results in increasing the particle size and a lower absolute zeta potential. We find that quercetin and retinol are effectively retained inside the ECNPs at 64-70% after 72 hours. These results have significant implications for the development of novel photoprotection technologies and functional nanoparticles

Size and Optically Tunable Ethyl Cellulose Nanoparticles as Carriers for Organic UV Filters

Optically active nanoparticles (NPs) are potential building blocks for bottom-up functional technology in applications such as displays, sensors, and sunscreens. For sunscreens in particular, NPs can be used as delivery systems for organic UV filters in order to minimise skin exposure to these molecules. Here, we investigate the synthesis of size-tunable ethyl cellulose NPs (ECNPs) and their application as carriers for multiple organic UV filters. We prepared ECNPs with sizes of 50 to 165 nm via an antisolvent precipitation technique and investigate the incorporation of three commonplace organic UV filters – oxybenzone, avobenzone, and octinoxate – into the ECNPs. We found the particle loading varied greatly with each UV filter. Photodegradation of the UV filters remained unchanged upon incorporation into ECNPs and was not affected by co-encapsulating the antioxidant α-tocopherol. These results can significantly advance the development of environmentally friendly functionalized nanoparticles and UV-protective coatings

Fully-biobased UV-absorbing nanoparticles from ethyl cellulose and zein for environmentally friendly photoprotection

Effective photoprotection is a vital consumer issue. However, there are many concerns regarding the adverse environmental and health impacts associated with current organic and inorganic UV filters. Here, we prepare fully-biobased UV-absorbing nanoparticles from ethyl cellulose (ECNPs) and zein (ZNPs) with encapsulated biobased photoprotectants obtainable from plants and foods (quercetin, retinol, and p-coumaric acid), which have the potential to satisfy both environmental and health issues in photoprotection. We show the ability of ECNPs and ZNPs to be easily tuned compositionally to obtain uniform, broadband UV spectrum absorbance profiles, and prepare transparent UV-absorbing coatings from the ECNPs. We find that the maximum loadings for retinol, quercetin, and p-coumaric acid into the ECNPs are 31 wt%, 14 wt%, and 13 wt% respectively. The ECNP size remains constant (except for the largest loading of retinol, 31 wt%) and the absolute zeta potential increases upon increasing the loading of quercetin and retinol, whereas increasing the loading of p-coumaric acid results in increasing the particle size and a lower absolute zeta potential. We find that quercetin and retinol are effectively retained inside the ECNPs at 64-70% after 72 hours. These results have significant implications for the development of novel photoprotection technologies and functional nanoparticles

Fully-biobased UV-absorbing nanoparticles from ethyl cellulose and zein for environmentally friendly photoprotection

Effective photoprotection is a vital consumer issue. However, there are many concerns regarding the adverse environmental and health impacts associated with current organic and inorganic UV filters. Here, we prepare fully-biobased UV-absorbing nanoparticles from ethyl cellulose (ECNPs) and zein (ZNPs) with encapsulated biobased photoprotectants obtainable from plants and foods (quercetin, retinol, and p-coumaric acid), which have the potential to satisfy both environmental and health issues in photoprotection. We show the ability of ECNPs and ZNPs to be easily tuned compositionally to obtain uniform, broadband UV spectrum absorbance profiles, and prepare transparent UV-absorbing coatings from the ECNPs. We find that the maximum loadings for retinol, quercetin, and p-coumaric acid into the ECNPs are 31 wt%, 14 wt%, and 13 wt% respectively. The ECNP size remains constant (except for the largest loading of retinol, 31 wt%) and the absolute zeta potential increases upon increasing the loading of quercetin and retinol, whereas increasing the loading of p-coumaric acid results in increasing the particle size and a lower absolute zeta potential. We find that quercetin and retinol are effectively retained inside the ECNPs at 64-70% after 72 hours. These results have significant implications for the development of novel photoprotection technologies and functional nanoparticles

Ethyl cellulose nanoparticles as stabilizers for Pickering emulsions

Pickering emulsions stabilized by ethyl cellulose nanoparticles have recently received –great attention for their remarkable stability and numerous industrial applications. De- spite this, the exact stabilization mechanism of such Pickering emulsions is still not fully understood. Both the stabilization of the emulsion by particle adsorption at the inter- face and through network formation in the continuous phase (leading to a yield stress) have been suggested. In this work we study soybean oil-in-water emulsions stabilized by ethyl cellulose nanoparticles and find, by the use of confocal microscopy and interfa- cial tension measurements, that the main stabilization mechanism of this nanoparticle- stabilized emulsions is the adsorption of the particles at the interface, instead of forming a network in the continuous phase. At the same time, oscillatory rheology measurements reveal that the emulsions exhibit a yield stress well below the random close-packing limit for hard spheres, suggesting short-range interactions between the droplets caused by the presence of the particles at the interface. The presence of the particles at the interface in combination with the observed rheological behavior of an attractive emulsion gives a strong indication for a particle-bridged stabilized emulsions