Influence of solvents on particle size and luminescence performance of monodisperse spherical lutetium compounds

The aim of this work was to assess the impact of solvent selection on the microfluidic production of liposomes. To achieve this, liposomes were manufactured using small-scale and bench-scale microfluidics systems using three aqueous miscible solvents (methanol, ethanol or isopropanol, alone or in combination). Liposomes composed of different lipid compositions were manufactured using these different solvents and characterised to investigate the influence of solvents on liposome attributes. Our studies demonstrate that solvent selection is a key consideration during the microfluidics manufacturing process, not only when considering lipid solubility but also with regard to the resultant liposome critical quality attributes. In general, reducing the polarity of the solvent (from methanol to isopropanol) increased the liposome particle size without impacting liposome short-term stability or release characteristics. Furthermore, solvent combinations such as methanol/isopropanol mixtures can be used to modify solvent polarity and the resultant liposome particle size. However, the impact of solvent choice on the liposome product is also influenced by the liposome formulation; liposomes containing charged lipids tended to show more sensitivity to solvent selection and formulations containing increased concentrations of cholesterol or pegylated-lipids were less influenced by the choice of solvent. Indeed, incorporation of 14 wt% or more of pegylated-lipid was shown to negate the impact of solvent selection.

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Tunable luminescence and cytotoxicity of Samarium-doped calcium–strontium–hydroxyapatite for cell imaging

Functional Materials Letters ◽

10.1142/s1793604722500059 ◽

2021 ◽

Author(s):

Yinpo Qiao

Keyword(s):

Particle Size ◽

Cell Imaging ◽

Strontium Hydroxyapatite ◽

Radiative Transitions ◽

Dipole Interactions ◽

Energy Transfers ◽

Diffraction Peaks ◽

Orange Color ◽

Luminescence Performance ◽

Color Emission

Samarium (Sm)-doped calcium–strontium–hydroxyapatite (Ca–Sr–HA:Sm) materials were designed and prepared, and the influence of Sr-introduction on the structure, photoluminescence (PL) and cytotoxicity of samples was revealed. The Sr-doping deduces the shift of some diffraction peaks to smaller angles and enlarges the particle size of samples. The typical red– orange emissions and corresponding luminescence quenching of Sm[Formula: see text] were observed, and the optimal luminescence performance appeared when [Formula: see text](Sr) = 7(Sr/Ca = 7/3) and quenching concentration closes to [Formula: see text](Sm) = 0.8 mol.%. The non-radiative transitions and energy transfers due to the dipole–dipole interactions between ions with different symmetry are essential to the luminescence and quenching of Sm[Formula: see text]. Furthermore, the viability values of human HepG2 cells are calculated larger than 90%, and the red–orange color emission was observed when the particles are incubated with cells.

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Microstructural characterization of laser-melted/roller-quenched dicalcium silicate

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100104972 ◽

1988 ◽

Vol 46 ◽

pp. 582-583

Author(s):

C. J. Chan ◽

K. R. Venkatachari ◽

W. M. Kriven ◽

J. F. Young

Keyword(s):

Particle Size ◽

Raw Materials ◽

Shape Change ◽

Microstructural Characterization ◽

Particle Size Effect ◽

Dicalcium Silicate ◽

Laser Melting ◽

Uniform Size ◽

Cell Shape Change ◽

Wide Range

Dicalcium silicate (Ca2SiO4) is a major component of Portland cement. It has also been investigated as a potential transformation toughener alternative to zirconia. It has five polymorphs: α, α'H, α'L, β and γ. Of interest is the β-to-γ transformation on cooling at about 490°C. This transformation, accompanied by a 12% volume increase and a 4.6° unit cell shape change, is analogous to the tetragonal-to-monoclinic transformation in zirconia. Due to the processing methods used, previous studies into the particle size effect were limited by a wide range of particle size distribution. In an attempt to obtain a more uniform size, a fast quench rate involving a laser-melting/roller-quenching technique was investigated.The laser-melting/roller-quenching experiment used precompacted bars of stoichiometric γ-Ca2SiO4 powder, which were synthesized from AR grade CaCO3 and SiO2xH2O. The raw materials were mixed by conventional ceramic processing techniques, and sintered at 1450°C. The dusted γ-Ca2SiO4 powder was uniaxially pressed into 0.4 cm x 0.4 cm x 4 cm bars under 34 MPa and cold isostatically pressed under 172 MPa. The γ-Ca2SiO4 bars were melted by a 10 KW-CO2 laser.

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Analytical Electron Microscopy study of two vehicle-aged automotive exhaust catalysts having dissimilar activities

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100153336 ◽

1989 ◽

Vol 47 ◽

pp. 272-273

Author(s):

Sooho Kim ◽

M. J. D’Aniello

Keyword(s):

Electron Microscopy ◽

Particle Size ◽

Noble Metal ◽

Catalyst Deactivation ◽

Analytical Electron Microscopy ◽

Microscopy Study ◽

Metal Particles ◽

Automotive Exhaust ◽

Exhaust Catalysts ◽

Analytical Electron

Automotive catalysts generally lose-agtivity during vehicle operation due to several well-known deactivation mechanisms. To gain a more fundamental understanding of catalyst deactivation, the microscopic details of fresh and vehicle-aged commercial pelleted automotive exhaust catalysts containing Pt, Pd and Rh were studied by employing Analytical Electron Microscopy (AEM). Two different vehicle-aged samples containing similar poison levels but having different catalytic activities (denoted better and poorer) were selected for this study.The general microstructure of the supports and the noble metal particles of the two catalysts looks similar; the noble metal particles were generally found to be spherical and often faceted. However, the average noble metal particle size on the poorer catalyst (21 nm) was larger than that on the better catalyst (16 nm). These sizes represent a significant increase over that found on the fresh catalyst (8 nm). The activity of these catalysts decreases as the observed particle size increases.

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