Nature-Inspired Effects of Naturally Occurring Trace Element-Doped Hydroxyapatite Combined with Surface Interactions of Mineral-Apatite Single Crystals on Human Fibroblast Behavior

Innovative engineering design for biologically active hydroxyapatites requires enhancing both mechanical and physical properties, along with biocompatibility, by doping with appropriate chemical elements. Herein, the purpose of this investigation was to evaluate and elucidate the model of naturally occurring hydroxyapatite and the effects of doped trace elements on the function of normal human fibroblasts, representing the main cells of connective tissues. The substrates applied (geological apatites with hexagonal prismatic crystal habit originated from Slyudyanka, Lake Baikal, Russia (GAp) and from Imilchil, The Atlas Mountains, Morocco (YAp)) were prepared from mineral natural apatite with a chemical composition consistent with the building blocks of enamel and enriched with a significant F− content. Materials in the form of powders, extracts and single-crystal plates have been investigated. Moreover, the effects on the function of fibroblasts cultured on the analyzed surfaces in the form of changes in metabolic activity, proliferation and cell morphology were evaluated. Apatite plates were also evaluated for cytotoxicity and immune cell activation capacity. The results suggest that a moderate amount of F− has a positive effect on cell proliferation, whereas an inhibitory effect was attributed to the Cl− concentration. It was found that for (100) GAp plate, fibroblast proliferation was significantly increased, whereas for (001) YAp plate, it was significantly reduced, with no cytotoxic effect and no immune response from macrophages exposed to these materials. The study of the interaction of fibroblasts with apatite crystal surfaces provides a characterization relevant to medical applications and may contribute to the design of biomaterials suitable for medical applications and the evaluation of their bioavailability.

Defects of diamond crystal structure as an indicator of crystallogenesis

Based on the study of a representative collections of diamonds from diamondiferous formations of the Urals and deposits of the Arkhangelsk and Yakutian diamond provinces, we established patterns of zonal and sectoral distribution of crystal structure defects in crystals of different morphological types, identified the specifics of crystals formed at different stages of crystallogenesis and performed a comprehensive analysis of constitutional and population diversity of diamonds in different formations. We identified three stages in the crystallogenesis cycle, which correspond to normal and tangential mechanisms of growth and the stage of changing crystal habit shape. At the stage of changing crystal habit shape, insufficient carbon supersaturation obstructs normal growth mechanism, and the facets develop from existing surfaces. Due to the absent stage of growth layer nucleation, formation of new {111} surfaces occurs much faster compared to tangential growth mechanism. This effect allows to explain the absence of cuboids with highly transformed nitrogen defects at the A-B1 stage: they have all been refaceted by a regenerative mechanism. Based on the revealed patterns, a model of diamond crystallogenesis was developed, which takes into account the regularities of growth evolution, thermal history and morphological diversity of the crystals. The model implies the possibility of a multiply repetitive crystallization cycle and the existence of an intermediate chamber; it allows to explain the sequence of changes in morphology and defect-impurity composition of crystals, as well as a combination of constitutional and population diversity of diamonds from different geological formations.

Mesocrystals from Platinum Nanocubes

Platinum nanoparticles are widely known for their numerous electrochemical and catalytic applications. Enhanced or novel properties that may arise when ordering such particles in a highly defined manner, however, are still subject to ongoing research, as superstructure formation on the mesoscale is still a major challenge to be overcome. In this work, we therefore established a reproducible method to fabricate micrometer-sized superstructures from platinum nanocubes. Through small-angle X-ray scattering and electron diffraction methods we demonstrate that the obtained superstructures have a high degree of ordering up to the atomic scale and, therefore, fulfill all criteria of a mesocrystal. By changing the solvent and stabilizer in which the platinum nanocubes were dispersed, we were able to control the resulting crystal habit of the mesocrystals. Aside from mesocrystal fabrication, this method can be further utilized to purify nanoparticle dispersions by recrystallization with respect to narrowing down the particle size distribution and removing contaminations.

Framboid Mineralogy

Framboids are dominantly made of pyrite. The limiting factors for other minerals forming framboids include the requirements of crystal habit, solubility, and natural abundances of the constituent elements for framboid formation. Detailed examination of reports of non-pyritic framboids reveal microcrystalline material within and associated with framboids (e.g., greigite) and sub-spherical crystalline aggregates (e.g., marcasite, chalcocite-digenite, magnetite). Framboids are sometimes observed replaced by other minerals. Pyrite framboids are often formed during the earliest stages of sedimentation or mineralization and therefore are subject to further reactions with later fluids. Minerals such as copper, cobalt, zinc, and lead sulfides often display framboidal forms that have replaced original pyrite framboids. Likewise, oxidation of pyrite under some conditions can produce iron (oxyhydr)oxide and iron sulfate framboids.

An Insight into Chemistry and Structure of Colloidal 2D-WS2 Nanoflakes: Combined XPS and XRD Study

The surface and structural characterization techniques of three atom-thick bi-dimensional 2D-WS2 colloidal nanocrystals cross the limit of bulk investigation, offering the possibility of simultaneous phase identification, structural-to-morphological evaluation, and surface chemical description. In the present study, we report a rational understanding based on X-ray photoelectron spectroscopy (XPS) and structural inspection of two kinds of dimensionally controllable 2D-WS2 colloidal nanoflakes (NFLs) generated with a surfactant assisted non-hydrolytic route. The qualitative and quantitative determination of 1T’ and 2H phases based on W 4f XPS signal components, together with the presence of two kinds of sulfur ions, S22− and S2−, based on S 2p signal and related to the formation of WS2 and WOxSy in a mixed oxygen-sulfur environment, are carefully reported and discussed for both nanocrystals breeds. The XPS results are used as an input for detailed X-ray Diffraction (XRD) analysis allowing for a clear discrimination of NFLs crystal habit, and an estimation of the exact number of atomic monolayers composing the 2D-WS2 nanocrystalline samples.

Simple and Rapid Preparation of MIL-121 with Small Particles for Lithium Adsorption from Brine

A novel method to generate an aluminum-based MOF material named as MIL-121 was investigated. MIL-121, [Al(OH)(H2BTEC)·(H2O)]n is a prototypal aluminum MOF with 1,2,4,5-benzenetetracarboxylic acid (BTEC) linkers, which was normally produced by the hydrothermal method. Different from the hydrothermal method, the developed novel method does not involve high temperature and high pressure, instead the MOF material was produced by the traditional cooling crystallization method at ambient pressure and low temperature below 100 °C. The MIL-121 obtained by the novel method possesses the same lithium adsorption performance as that obtained by hydrothermal method, but with lower energy consumption and more environmentally friendly. Compared with hydrothermal method, this method has more advantage to be scaled up to industrialized production. The formation mechanism of MIL-121 in the novel method including nucleation and growth process of MOF crystal was studied. The results indicated that the size and morphology of MIL-121 crystals were influenced by the temperature and additives, respectively. As the reaction temperature increased to 100 °C, the operation time can be shortened to 2–5 h. The crystal habit that was predicted by Material studio software using BFDH, which is a model for crystal habit prediction proposed by Bravais, Friedel, Donnay, and Harker based on the crystal lattice parameters and crystal symmetry in the Morphology module, the simulated morphology of MIL-121 was in accord with that of the products obtained by cooling crystallization. The thermal stability of MIL-121 obtained by cooling crystallization is better than that obtained by the hydrothermal method.

Co-Crystallization Kinetics of 2:1 Benzoic Acid–Sodium Benzoate Co-Crystal: The Effect of Templating Molecules in a Solution

The addition of dissolved templating molecules in crystallization will create “supramolecular assemblies” within the solution, serving as “anchor points” for the solute molecules to nucleate and grow. In this work, nucleation and crystal growth kinetics of 2:1 benzoic acid (HBz)–sodium benzoate (NaBz) co-crystallization with or without templates in a solution were analyzed by monitoring the concentration of the mother liquor during cooling crystallization. The results showed that the addition of the dissolved 2:1 or 1:1 HBz–NaBz co-crystals as templating molecules could reduce the critical free energy barrier of 2:1 HBz–NaBz co-crystal during its nucleation, but did not significantly affect the order of crystal growth rate. On the other hand, the critical free energy barrier of the nucleation process was increased if dissolved NaBz was used as a templating molecule, while a significant rise in the order of crystal growth rate occurred. The crystal habit obtained from the NaBz-templated system was needle-like, suggesting that sodium–sodium coordination chains of NaBz supramolecular assemblies in the solution phase were responsible for creating elongated crystals. Conversely, a large prismatic crystal habit found in non-templated and 2:1 and 1:1 HBz–NaBz co-crystal-templated systems implied that those templating molecules formed sparsely interconnected supramolecular assemblies in the solution phase.

Study of Different Crystal Habits of Aprepitant: Dissolution and Material Attributes

In the present study, aprepitant (APT) was selected to find its suitable crystal habit, which can improve its existing poor dissolution and manufacturing processability. Solvents were screened out for solubility analysis of APT and further crystal habit modification. Solid-state characterization studies like powder X-ray diffraction (PXRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and Fourier infrared spectroscopy (FTIR) distinguished that tabular crystal habit was generated from acetone (APT-AC) and long tabular crystal habit was generated from ethyl acetate (APT-EA). Kawakita analysis and powder flow property studies showed that APT-EA is cohesive, has poor flow property and low bulk density compared to APT-AC (p < 0.05). Heckel plots reflected that APT-EA shows higher fragmentation and particle rearrangement during the initial stages as indicated by the higher intercept values. Higher slopes in APT-EA and APT-AC confirmed better plasticity but lower yield pressure in APT-AC proved good plastic deformation compared to APT-EA (p < 0.05). The dissolution profile of the APT-EA was found to be better than that of APT-AC. Overall, it can be concluded that APT-AC crystal habit has a better flow rate, tensile strength, and plasticity whereas APT-EA has better dissolution.