Synthetic Method for Preparing High-Performance Europium-Doped Up-Conversion Ceramic Material Precursor

2019 ◽  
Vol 953 ◽  
pp. 101-112
Author(s):  
Zhi Zhang ◽  
Yi Wang Chen ◽  
Xu Liang Lv ◽  
Pin Zhang ◽  
Guang Zhen Cui ◽  
...  
Keyword(s):  
Calcium Fluoride ◽  
High Performance ◽  
Control Variable ◽  
Reaction Medium ◽  
Average Diameter ◽  
Test Methods ◽  
Precipitation Method ◽  
Powder Materials ◽  
Lanthanum Doping ◽  
Reaction Concentration

In this paper, a direct co-precipitation method was used to prepare antimony-doped calcium fluoride nanopowders (NPs). The effects of reaction concentration, reaction medium and lanthanum doping on the properties of calcium fluoride NPs were investigatedviaa control variable method and the best preparation conditions was identified. The structural analysis of the powder materials prepared in this work were carried out by XRD, SEM, ICP and other test methods. By analyzing the experimental data, we found that the best performance of Eu-doped CaF2NPs can be acquired under the reaction concentration of 1 mol/L in aqueous solution. In the same time, the NPs possess a high degree of dispersion with an average diameter of 22 nm, which is beneficial to the preparation of transparent Eu3+: CaF2ceramics with excellent up-conversion luminescence. The results show that the grain size, the crystallinity of the NPs and the amount of Eu infiltration have a decreasing tendency with the increasing reaction concentration, while the degree of agglomeration of the NPs can be enhanced by increasing the reaction concentration.

scholarly journals Large-scale fabrication of porous YBO 3 hollow microspheres with tunable photoluminescence

2018 ◽  
Vol 5 (4) ◽  
pp. 172186 ◽  
Author(s):  
Zhenhe Xu ◽  
He Yu ◽  
Feixue Ai ◽  
Guiyan Zhao ◽  
Yanfeng Bi ◽  
...  
Keyword(s):  
High Performance ◽  
Large Scale ◽  
Low Cost ◽  
Exchange Process ◽  
Hollow Spheres ◽  
Average Diameter ◽  
Hollow Microspheres ◽  
Precipitation Method ◽  
Polystyrene Spheres ◽  
Ion Exchange Process

Hollow lanthanide-doped compounds are some of the most popular materials for high-performance luminescent devices. However, it is challenging to find an approach that can fabricate large-scale and well-crystallized lanthanide-doped hollow structures and that is facile, efficient and of low cost. In this study, YBO 3 : Eu 3+ /Tb 3+ hollow microspheres were fabricated by using a novel multi-step transformation synthetic route for the first time with polystyrene spheres as the template, followed by the combination of a facile homogeneous precipitation method, an ion-exchange process and a calcination process. The results show that the as-obtained YBO 3 : Eu 3+ /Tb 3+ hollow spheres have a uniform morphology with an average diameter of 1.65 µm and shell thickness of about 160 nm. When used as luminescent materials, the emission colours of YBO 3 : Eu 3+ /Tb 3+ samples can be tuned from red, through orange, yellow and green-yellow, to green by simply adjusting the relative doping concentrations of the activator ions under the excitation of ultraviolet light, which might have potential applications in fields such as light display systems and optoelectronic devices.

scholarly journals A Novel Fluoride Anion Modified Gelatin Nanogel System

2008 ◽  
Vol 11 (4) ◽  
pp. 32 ◽  
Author(s):  
Daocheng Wu ◽  
Mingxi Wan
Keyword(s):  
Drug Release ◽  
High Performance ◽  
Average Diameter ◽  
Controlled Drug Release ◽  
Correlation Spectroscopy ◽  
Precipitation Method ◽  
Fluoride Anion ◽  
Size Change ◽  
Triggered Drug Release ◽  
Ultrasound Generator

Purpose. Controlled drug release, especially tumor-targeted drug release, remains a great challenge. Here, we prepare a novel fluoride anion-modified gelatin nanogel system and investigate its characteristics of ultrasound-triggered drug release. Methods. Adriamycin gelatin nanogel modified with fluoride anion (ADM-GNMF) was prepared by a modified co-precipitation method with fluoride anion and sodium sulfate. The loading and encapsulation efficiency of the anti-neoplastic agent adriamycin (ADM) were measured by high performance liquid chromatography (HPLC). The size and shape of ADM-GNMF were determined by electron microscopy and photo-correlation spectroscopy. The size distribution and drug release efficiency of ADM-GNMF, before and after sonication, were measured by two designed measuring devices that consisted of either a submicron particle size analyzer and an ultrasound generator as well as an ultrasound generator, automatic sampler, and HPLC. Results. The ADM-GNMF was stable in solution with an average diameter of 46±12 nm; the encapsulation and loading efficiency of adriamycin were 87.2% and 6.38%, respectively. The ultrasound-triggered drug release and size change were most efficient at a frequency of 20 kHz, power density of 0.4w/cm2, and a 1~2 min duration. Under this ultrasound-triggered condition, 51.5% of drug in ADM-GNMF was released within 1~2 min, while the size of ADM-GNMF changed from 46 ± 12 nm to 1212 ± 35 nm within 1~2 min of sonication and restored to its previous size in 2~3 min after the ultrasound stopped. In contrast, 8.2% of drug in ADM-GNMF was released within 2~3 min without sonication, and only negligible size changes were found. Conclusions. The ADM-GNMF system efficiently released the encompassed drug in response to ultrasound, offering a novel and promising controlled drug release system for targeted therapy for cancer or other diseases.

Development and Characterization Colchicine-Loaded PEGylated Gelatin Nanoparticles for Targeted Delivery to Tumor

2013 ◽  
Vol 6 (2) ◽  
pp. 2058-2063
Author(s):  
G D Chandrethiya ◽  
P K Shelat ◽  
M N Zaveri
Keyword(s):  
Drug Delivery ◽  
Targeted Delivery ◽  
High Performance ◽  
Entrapment Efficiency ◽  
Stability Study ◽  
Spherical Particles ◽  
Precipitation Method ◽  
Antitumoral Activity ◽  
Gelatin Nanoparticles

PEGylated gelatin nanoparticles loaded with colchicine were prepared by ethanol precipitation method. Poly-(ethylene glycol)-5000-monomethylether (MPEG 5000), a hydrophilic polymer, was used to pegylate gelatin.  Gluteraldehyde was used as cross-linking agent. To obtain a high quality product, major formulation parameters were optimized.  Spherical particles with mean particles of 193 nm were measured by a Malvern particle size analyzer. Entrapment efficiency was found to be 71.7 ± 1.4% and determined with reverse phase high performance liquid charomatography (RP-HPLC). The in vitro drug release study was performed by dialysis bag method for a period of 168 hours. Lyophilizaton study showed sucrose at lower concentrations proved the best cryoprotectant for this formulation.  Stability study revealed that lyophilized nanoparticles were equally effective (p < 0.05) after one year of storage at 2-8°C with ambient humidity. In vitro antitumoral activity was accessed using the MCF-7 cell line by MTT assay.  The IC50 value was found to be 0.034 μg/ml for the prepared formulation. The results indicate that PEGylated gelatin nanoparticles could be utilized as a potential drug delivery for targeted drug delivery of tumors.  

Development and validation of a LC-MS/MS method for quantification of mobocertinib (TAK-788) in plasma and its application to pharmacokinetic study in rats

2020 ◽  
Vol 23 ◽  
Author(s):  
Bo Li ◽  
Jin Wang ◽  
Xinyao Dou ◽  
Xinjie Zhang ◽  
Xianbei Xue ◽  
...  
Keyword(s):  
Oral Administration ◽  
Pharmacokinetic Study ◽  
High Performance ◽  
Kinase Inhibitor ◽  
Internal Standard ◽  
Selected Reaction Monitoring ◽  
Precipitation Method ◽  
Plasma Samples ◽  
Bioanalytical Method Validation ◽  
Extraction Recovery

Aim and Objective:: An analytical method for the determination of mobocertinib, an investigational tyrosine kinase inhibitor, was developed and optimized by high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) in rat plasma. Materials and Methods:: Plasma samples were pretreated by the protein precipitation method with a methanol solution of osimertinib as the internal standard (IS). Chromatographic separation was performed using an Inertsil ODS-3 column (50 mm × 4.6 mm, I.D. 5 μm) column with the temperature maintained at 40 °C. The mobile phase consisted of water (containing 0.1% formic acid) and methanol in a gradient mode at a flow rate of 0.5 mL/min. Mass spectrometric detection was carried out in the selected reaction monitoring (SRM) mode with positive electrospray ionization, and the mass transitions of mobocertinib and osimertinib were m/z 587.01 → 71.88 and m/z 499.80 → 71.94, respectively. The method was validated in terms of selectivity, linearity, accuracy and precision, extraction recovery and matrix effect, stability and carryover as per the guidelines for bioanalytical method validation (FDA, 2018). The method was applied to the pharmacokinetic study of mobocertinib in rats by oral gavage at the doses of 2, 6, and 18 mg/kg. A total of 216 plasma samples from 18 rats were analyzed. Results:: It showed good linearity over the range of 1-1000 ng/mL (R2 = 0.9957). The intra-batch accuracy was within 94.65-102.59% and the precision was within 5.49-10.46%. The inter-batch accuracy was within 97.08-102.25% with a precision of 7.54-10.13%. The extraction recovery and matrix factor were acceptable for the bioanalysis of mobocertinib. Additionally, mobocertinib was found to be stable under the detected conditions. Mobocertinib showed linear pharmacokinetic characteristics following oral administration to rats at 2.0-18.0 mg/kg. Conclusion:: The developed and validated method was successfully employed in the pharmacokinetic study in rats following oral administration of mobocertinib at the doses of 2, 6, and 18 mg/kg.

Deproteinizing methods evaluated for determination of uric acid in serum by reversed-phase liquid chromatography with ultraviolet detection.

1987 ◽  
Vol 33 (8) ◽  
pp. 1427-1430 ◽  
Author(s):  
R Sakuma ◽  
T Nishina ◽  
M Kitamura
Keyword(s):  
Uric Acid ◽  
Liquid Chromatography ◽  
Perchloric Acid ◽  
High Performance ◽  
Reversed Phase ◽  
Precipitation Method ◽  
Zinc Hydroxide ◽  
Good Precision ◽  
Ultraviolet Detection

Abstract We evaluated six deproteinizing methods for determination of uric acid in serum by "high-performance" liquid chromatography with ultraviolet detection: those involving zinc hydroxide, sodium tungstate, trichloroacetic acid, perchloric acid, acetonitrile, and centrifugal ultrafiltration (with Amicon MPS-1 devices). We used a Toyosoda ODS-120A reversed-phase column. The mobile phase was sodium phosphate buffer (40 mmol/L, pH 2.2) containing 20 mL of methanol per liter. Absorbance of the eluate was monitored at 284 nm. The precipitation method with perchloric acid gave high recoveries of uric acid and good precision, and results agreed with those by the uricase-catalase method of Kageyama (Clin Chim Acta 1971;31:421-6).

Novel Fe3O4/HNT@rGO composite via a facile co-precipitation method for the removal of contaminants from aqueous system

RSC Advances ◽  
2016 ◽  
Vol 6 (54) ◽  
pp. 49228-49235 ◽  
Author(s):  
Chengwei Gao ◽  
Baojun Li ◽  
Ning Chen ◽  
Jie Ding ◽  
Qiang Cai ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Water Treatment ◽  
Potential Application ◽  
High Performance ◽  
Aqueous System ◽  
Precipitation Method ◽  
Precipitation Process ◽  
System P ◽  
Removal Of Contaminants ◽  
Co Precipitation

Fe3O4/HNT@rGO composite (FHGC) was fabricated via a facile co-precipitation process, followed by heat treatment. For RhB and As5+removal, the high performance and easy separation of FHGC highlight its potential application in water treatment.

Effect of the Synthesis Method on the Properties of Ultrafine YAG Powder

2018 ◽  
Vol 281 ◽  
pp. 40-45
Author(s):  
Jie Guang Song ◽  
Lin Chen ◽  
Cai Liang Pang ◽  
Jia Zhang ◽  
Xian Zhong Wang ◽  
...  
Keyword(s):  
Particle Size ◽  
Calcination Temperature ◽  
Hydrothermal Reaction ◽  
Synthesis Method ◽  
Particle Morphology ◽  
Precipitation Method ◽  
Molar Ratio ◽  
Synthesis Process ◽  
Powder Materials ◽  
Co Precipitation

YAG materials has a number of unique properties, the application is very extensive. In this paper, the superfine YAG powder materials were prepared by co-precipitation method and hydrothermal precipitation method. The influence of synthesis process on the morphology of the powder was investigated. The results showed that the precursor powder prepared via the co-precipitation method is mainly from amorphous to crystalline transition with the increasing calcination temperature, the precursor agglomeration is more serious, In the process of increasing the calcination temperature, the dispersibility of the roasted powder is greatly improved, which is favorable for the growth of the crystal grains, so that the particle size of the powder is gradually increased, the YAG precursor prepared by the co-precipitation method is transformed into YAG crystals, the phase transition occurs mainly between 900 and 1100°C. When the molar ratio of salt to alkali is Y3+: OH-=1: 8 via the hydrothermal reaction, the YAG particles with homogeneous morphology can be obtained. When the molar ratio of salt and alkali is increased continuously, the morphology of YAG particles is not obviously changed. The co-precipitation method is easy to control the particle size, the hydrothermal method is easy to control the particle morphology.

A Novel Approach to Nanoscale Materials Synthesis Using Industrial Laser Processing of Organosilazane Liquid Precursors

1990 ◽  
Vol 206 ◽  
Author(s):  
Tongsan D. Xiao ◽  
Peter R. Strutt ◽  
Kenneth E. Gonsalves
Keyword(s):  
Ceramic Powder ◽  
Average Diameter ◽  
Current Approach ◽  
Powder Materials ◽  
Materials Synthesis ◽  
Laser Plume ◽  
New Approach ◽  
Novel Approach ◽  
Liquid Precursors ◽  
Short Time

ABSTRACTA new approach has been developed for the synthesis of nanoscale ceramic powder materials from liquid organosilazane precursors. This technique, by exploiting fast kinetic chemical and physical reactions, makes it possible to synthesize significant quantities of material in a relatively short time. In the current approach aerosols of a silazane monomer, (CH3SiHNH)n, (n = 3 or 4), of mol. wt. 280–320, are injected into the beam of a cw industrial CO2 laser to obtain nanoscale ceramic powders. Injection of the aerosol into the laser-beam results in a high-temperature plume. Rapid condensation of the molecular precursor species emerging from the laser plume results in the formation of preceramic polymer particles, with an average diameter of 62 nm. One attractive feature of this process is that 70 wt.% of the liquid precursor is converted into nanoscale powders. Another feature is that only a further 10 wt.% loss occurs during post thermal treatment to form the end-product.

Monodisperse Fe3O4/Fe Core/Shell Nanoparticles with Enhanced Magnetic Property

2011 ◽  
Vol 306-307 ◽  
pp. 410-415
Author(s):  
Li Sun ◽  
Fu Tian Liu ◽  
Qi Hui Jiang ◽  
Xiu Xiu Chen ◽  
Ping Yang
Keyword(s):  
Average Diameter ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
Core Shell ◽  
X Ray Diffraction ◽  
Shell Nanoparticles ◽  
X Ray ◽  
Transmission Electron ◽  
Shell Particles ◽  
Core Shell Nanoparticles

Core/shell type nanoparticles with an average diameter of 20nm were synthesized by chemical precipitation method. Firstly, Monodisperse Fe3O4 nanoparticles were synthesized by solvethermal method. FeSO4ž7H2O and NaBH4 were respectively dissolved in distilled water, then moderated Fe3O4 particles and surfactant(PVP) were ultrasonic dispersed into the FeSO4ž7H2O solution. The resulting solution was stirred 2 h at room temperature. Fe could be deposited on the surface of monodispersed Fe3O4 nanoparticles to form core-shell particles. The particles were characterized by using various experimental techniques, such as transmission electron microscopy (TEM), X-ray diffraction (XRD), AGM and DTA. The results suggest that the saturation magnetization of the nanocomposites is 100 emu/g. The composition of the samples show monodisperse and the sides of the core/shell nanoparticles are 20-30nm. It is noted that the formation of Fe3O4/Fe nanocomposites magnetite nanoparticles possess superparamagnetic property.

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