Preparation, characterization, and stability of liposome-based formulations of mitoxantrone

The preparation, characterization, and stability of lyophilized liposome-based formulation of mitoxantrone was investigated. Mitoxantrone was entrapped inside small, unilamellar liposomes composed of dioleoylphosphocholine (DOPC), cholesterol, and cardiolipin. The mean vesicle size and drug entrapment efficiency of the liposomes were ~ 150 nm and ~ 99%, respectively. Less than 1% of drug was lost and mean vesicle size remained unchanged after sterile filtration. The pre-lyophilized (pre-lyo) formulations were characterized by a differential scanning calorimetric (DSC) method. Results showed that the glass transition temperatures (Tg') increased as the molar ratios of sucrose:lipid and trehalose:lipid in the formulations were increased. The maximum Tg' of the pre-lyo formulations containing 10:1 sucrose:lipid and trehalose:lipid molar ratios were - 37°C and - 41°C, respectively. After reconstitution of the lyophilized cake of the sucrose-containing formulation, the mean vesicle size was comparable to pre-lyo liposome size. In vitro release studies showed that less than 2% of mitoxantrone was released after an extensive dialysis against phosphate buffered saline (PBS) at 37°C, indicating that the mitoxantrone was highly associated and retained inside the liposomes. Short-term stability studies of the sucrose-containing formulations revealed that the reconstituted and eight-fold diluted formulations were stable for up to 8 hours at room temperature. Long-term stability studies of lyophilized liposomal mitoxantrone showed that the lyophilized formulation was stable for up to 13 months after storage at refrigerated condition.     

Characterising the time-dependant behaviour on the single fibre level of SHCC: Part 2: The rate effects on fibre pull-out tests

This paper is the second part of a two paper series about the time-dependant behaviour of Strain Hardening Cement-based Composite (SHCC) on the single fibre level. Having dealt with mechanisms of creep in SHCC in the first part, this paper reports single fibre pull-out tests that were done to investigate the effect of the pull-out rate on the mechanical response of the interface between the fibre and the matrix. It was found that not only the pull-out resistance increased with an increase of the pull-out rate but the probability of fibre rupture during pull-out as well. Another important finding was that the interfacial shear resistance and slip-hardening coefficient are not only dependant on the pull-out rate, but also the embedment length.     

CO2 laser-assisted preparation of transparent Eu2Ti2O7 thin films

We present a laser-assisted preparation of transparent europium-titanate Eu₂Ti₂O₇ thin films with tailored structural and optical properties. We have evaluated the effects of the irradiation time on the structural and the optical properties of the films. This approach allows the preparation of nanocrystalline crack-free films and micro patterns. The amorphous thin films were prepared by a sol-gel method. The films were annealed by a CO₂ laser beam for various time intervals. The laser irradiation induced a crystallization process that resulted in the formation of Eu₂Ti₂O₇ nanocrystals. The nanocrystals regularly grew with increasing irradiation time reaching the size from 25?nm to 45?nm. A film of a thickness 480?nm exhibited an optical transmission of 91.9% that is close to the maximal theoretical limit. The film's refractive index at 632?nm was 2.26. A micrometric pattern was prepared by a direct laser writing followed by a wet chemical etching. Feasibility of the demonstrated approach, together with the high film's quality, and europium-titanate chemical resistivity open up many opportunities for advanced applications. The approach can be used for a preparation of protective coatings and integrated photonic devices such as planar optical waveguides and couplers.     

Detection of RDX traces at the surface with sonic aerosol flow desorption

The use of a high-speed aerosol flow is proposed for sampling RDX from the surface followed by chromatographic analysis. The aerosol is generated from different solvents by means of a coaxial nebulizer. The effect of the aerosol flow parameters (solvent flowrate, an angle of the nebulizer inclination with respect to the surface) and various solvents (water, acetone, and hexane) on the efficiency of the RDX desorption was investigated. The optimal angle of the nebulizer was found to be 30°, under these conditions, the desorption of RDX from the surfaces of different structure (metal, glass, leather, cotton fabric, and paper) has also been studied. It is shown that under the action of an aerosol created using water and acetone, desorption from a smooth surface occurs most efficiently (1.5 times higher than with hexane). In this case, the sample removes almost completely (about 80%) by the aerosol flow in a few seconds. A relationship between the desorption efficiency and the amount of the solvent sprayed (that is the amount of aerosol particles in desorbing flow) has a characteristic maximum which location depends on the properties of the solvent spray. This effect is associated with a rate of solvent evaporation. Under optimal conditions for desorption of RDX from a smooth surface using an aqueous aerosol, an LOD of ～10?ng can be achieved. For porous and rough surfaces, the efficiency of the analyte desorption decreases (three times for leather and cotton fabric). The results of the experiments conducted allow one to conclude that the RDX solubility in the solvent used does not affect considerably the efficiency of the RDX desorption. It is assumed that small aerosol drops are very active and can capture the particles of the target analyte. This promotes the desorption of RDX molecules from the surface.

© 2018 American Association for Aerosol Research     

Heteroalleles in Common Wheat: Multiple Differences between Allelic Variants of the Gli-B1 Locus

The Gli-B1-encoded γ-gliadins and non-coding γ-gliadin DNA sequences for 15 different alleles of common wheat have been compared using seven tests: electrophoretic mobility (EM) and molecular weight (MW) of the encoded major γ-gliadin, restriction fragment length polymorphism patterns (RFLPs) (three different markers), Gli-B1-γ-gliadin-pseudogene known SNP markers (Single nucleotide polymorphisms) and sequencing the pseudogene GAG56B. It was discovered that encoded γ-gliadins, with contrasting EM, had similar MWs. However, seven allelic variants (designated from I to VII) differed among them in the other six tests: I (alleles Gli-B1i, k, m, o), II (Gli-B1n, q, s), III (Gli-B1b), IV (Gli-B1e, f, g), V (Gli-B1h), VI (Gli-B1d) and VII (Gli-B1a). Allele Gli-B1c (variant VIII) was identical to the alleles from group IV in four of the tests. Some tests might show a fine difference between alleles belonging to the same variant. Our results attest in favor of the independent origin of at least seven variants at the Gli-B1 locus that might originate from deeply diverged genotypes of the donor(s) of the B genome in hexaploid wheat and therefore might be called “heteroallelic”. The donor’s particularities at the Gli-B1 locus might be conserved since that time and decisively contribute to the current high genetic diversity of common wheat.     

Physical Understanding of Active Control of Beam Scanning in Preventing Top Concavity in Electron Beam Welding

Metallurgical and Materials Transactions A - Low-frequency scanning electron beam welding (SEBW) is recently recognized as a possible control method for preventing the top concavity behavior in...     

Influence of addition of nanosize barium cerate on the microstructure and properties of top-seeded melt growth YBCO bulk superconductors

Barium cerate (BaCeO₃) is one of the possible additions to bulk YBa₂Cu₃O₇ single-grain superconductors to suppress the growth of Y₂BaCuO₅ (Y211) particles. This paper investigates the synthesis of barium cerate powder and its use in YBa₂Cu₃O₇ bulk superconductors. Crystalline barium cerate was synthesized by solid-state reaction, by co-precipitation of oxalates and by sol-gel method. Final calcination was held in air or in vacuum. It is shown that the most efficient in refining Y211 is nanocrystalline barium cerate prepared by sol-gel method calcined in vacuum. The effective refinement of Y211 particles occurred over the entire interval of nanocrystalline BaCeO₃ addition from 0.38 to 1.90 wt%. The optimal concentration of nanosize barium cerate was determined, microstructure and superconducting properties were characterized. The effect of Y211 content on trapped field in YBCO bulks with addition of nanocrystalline barium cerate is shown.