Encapsulation of radioactive metals inside multilayered polyhedral shells of carbon as a barrier to radionuclide release

A carbon nanoencapsulate has a polyhedral outer shell of nested, concentric layers of carbon. The shell defines an internal cavity where a metal is encapsulated. Although the rare-earth carbides readily hydrolyze in moist air, the carbides in these carbon shells did not degrade after exposure to air for considerable lengths of time. This means that the carbide particle is physically enclosed within the carbon cavity completely, and the cavity protects it perfectly against attack of water molecules. Considering intrinsic chemical stability of carbon under oxygen free condition, this structure may be a perfect barrier to extremely long-term release of radionuclides. Because encapsulation of LaC₂ within carbon nanoparticles increased drastically from by-product to major product, it would be possible to find the optimized condition that complete encapsulation is achieved. Intrinsic stability of carbon and carbon coated waste nanoparticles may provide an improved barrier to radionuclide release by groundwater.     

Synthesis and Characterization of Nanocapsules of a-Fe(NiCoAl) Solid-solution

α-Fe(NiCoAl) solid-solution nanocapsules were prepared with pure powders of Fe, Ni, Co and Al by the plasma arc-discharging using a copper crucible. The shapes of the nanocapsules are in polyhedrons with the core/shell structure. The body centered cubic (BCC) phase is formed in the core. The size of the nanocapsules is in the range of 10~120 nm and the thickness of the shell is 4~11 nm. Saturation magnetization Js=150 Am2/kg and coercivity iHC=24.3 kA/m are achieved for the nanocapsules.     

Process Optimization,Physical Properties,and Environmental Stability of an α-Tocopherol Nanocapsule Preparation Using Complex Coacervation Method and Full Factorial Design

α-Tocopherol (α-Toc) has valuable biological activity, but its activity is limited when exposed to environmental factors. Nanocapsules can be used to overcome this problem. Using nanocapsules in the range of 100–200 nm is more beneficial. A 2⁴ full factorial design was carried out to optimize the size of nanocapsules using the complex coacervation method. The four factors were the amount of the wall material, the ratio of core material to wall material, the pH of the solution, and the speed of the homogenizer. The smallest nanocapsules (176 nm) were obtained at a wall content (gelatine and pectin) of 0.8 mg, a percentage of core material (α-Toc) to wall material of 20%, a pH = 4.5, and a homogenizer speed of 12,000 rpm. The encapsulation efficiency was 90.6 ± 1.1%, and the encapsulation yield was 83.4 ± 1.6%. Assessment of the stability of α-Toc after 1 month showed that encapsulation could improve its stability in the presence of three influential factors: humidity, light, and temperature.     

Thermosensitive poly(N-isopropylacrylamide) nanocapsules with controlled permeability

In this paper, novel thermosensitive poly(N-isopropylacrylamide) (PNIPAM) nanocapsules with temperature-tunable diameter and permeability are reported. Firstly, the core-shell composite microparticles were synthesized by precipitation polymerization with isothiocyanate fluorescein (FITC) entrapped SiO₂ as core and cross-linked PNIPAM as shell. Then, the SiO₂ core was etched by hydrofluoric acid at certain condition and the pre-trapped FITC molecules remained within the inner cavity. The FITC release profile and TEM studies clearly indicate that the release behavior of FITC could be controlled effectively by the external temperature. Above the LCST of PNIPAM (32 °C), the dehydrated PNIPAM shell inhibited the release of FITC from the internal cavity while below its LCST, the fluorophore could permeate the swollen shell easily.     

Optimization of nanocapsules preparation by the emulsion-diffusion method for food applications

The aim of this work was to establish the conditions to obtain polymeric nanocapsules containing food ingredients by the emulsification-diffusion method. The Response Surface Methodology was used to optimize the process. The variables studied were shear rate (3070-18,920 s⁻¹), polymer-wall concentration: poly-?-caprolactone (PCL, 100-300 mg), and stabilizer concentration: polyvinyl alcohol (PVAL, 25-100 g/L). The analyzed responses were particle size (PS), polydispersion index (PDI), density (ρ_nc), and zeta potential (ζ). The results of ρ_nc and micrographs confirmed the presence of capsular structures. The most efficient conditions to obtain nanocapsules were 10,917 s⁻¹, 50 g/L of PVAL and 256 mg of PCL, predicting a response of PS = 250 nm, ρ_nc = 1.021 g/cm³, PDI = 0.045, and ζ = −20.02. It was concluded that keeping the same preparation conditions, the formation of nanocapsules is also possible from other food oily materials with similar characteristics (predicting values PS ≈ 300 nm and ζ ≈ −25). The proposed nanocapsules may have application in food preservation and storage.     

Temperature‐Sensitive Nanocapsules for Controlled Drug Release Caused by Magnetically Triggered Structural Disruption

Self‐assembled nanocapsules containing a hydrophilic core and a crosslinked yet thermosensitive shell are successfully prepared using poly(ethylene‐oxide)‐poly(propylene‐oxide)‐poly(ethylene‐oxide) block copolymers, 4‐nitrophenyl chloroformate, gelatin, and 1‐ethyl‐3‐(3‐dimethylaminopropyl) carbodiimide. The core is further rendered magnetic by incorporating iron oxide nanoparticles via internal precipitation to enable externally controlled actuation under magnetic induction. The spherical nanocapsules exhibit a hydrophilic‐to‐hydrophobic transition at a characteristic but tunable temperature reaching 40 °C, triggering a size contraction and shrinkage of the core. The core content experiences very little leakage at 25 °C, has a half life about 5 h at 45 °C, but bursts out within a few minutes under magnetic heating due to iron oxide coarsening and core/shell disruption. Such burst‐like response may be utilized for controlled drug release as illustrated here using a model drug Vitamin B12.     

Selective synthesis of carbon nanotubes and nanocapsules using naphthalene pyrolysis assisted with ferrocene

Selective synthesis of well aligned multi-walled carbon nanotubes (MW-CNT) and multi-shelled carbon nanocapsule (MS-CNC) using pyrolysis of naphthalene with the presence of ferrocene was experimentally examined. With higher mole fraction of naphthalene to ferrocene, more MW-CNTs could be synthesized due to higher concentration of carbonaceous precursors emerging from the decomposed naphthalene. Based on kinetic analysis, at lower temperature, MW-CNTs could preferably be synthesized due to the controlled supply of carbonaceous clusters to get onto the surface of Fe clusters. On the other hand, at temperature higher than 900 °C the Fe clusters become more active to catalyze carbonaceous precursors to undergo self assembling process of MS-CNCs. With cheaper cost of naphthalene compared with other high-value hydrocarbons, usage of naphthalene would provide an advantage of reasonably economical synthesis of MW-CNT or MS-CNC.     

Project,Design, and Use of a Pilot Plant for Nanocapsule Production

The aim of this study was to find the scale-up parameters necessary for the preparation of nanocapsules (NCs) for pharmaceutical purposes. Starting from the laboratory scale (0.06 L), we designed and assembled a pilot plant (2 L) to produce NCs with the so-called emulsification-diffusion technique. We wanted to check if classical tools adequate for the pharmaceutical industry and for industrial scale-up purposes according to well-known chemical engineering technique could be used to perform the NC preparation. Experiments were carried out by varying some operative parameters, such as the impeller speed, the agitation duration for the emulsion preparation, and the reagent concentrations. As expected, good accordance between the NC produced at the laboratory scale and at the pilot plant scale was obtained. We conclude that the pilot plant can be used to perform a scale-up study of the industrial production of NC.