scholarly journals Production, Optimization and Characterization of Polylactic Acid Microparticles Using Electrospray with Porous Structure

2021 ◽  
Vol 11 (11) ◽  
pp. 5090
Author(s):  
Muhammed Enes Tasci ◽  
Berna Dede ◽  
Eray Tabak ◽  
Aybuke Gur ◽  
Rabia Betul Sulutas ◽  
...  
Keyword(s):  
Polylactic Acid ◽  
Spherical Shape ◽  
Particle Morphology ◽  
Average Diameter ◽  
Solution Concentration ◽  
Single Step ◽  
Production Optimization ◽  
Sem Images ◽  
Micron Size ◽  
Polymeric Microparticles

Polymeric microparticles with controlled morphologies and sizes are being studied by researchers in many applications, such as for drug release, healthcare and cosmetics. Herein, spherical and porous polymeric microparticles of different sizes and morphologies by electrospray technique have been developed as a viable alternative. In this work, polylactic acid (PLA) microparticles with a spherical shape and porous morphology were successfully produced via an electrospray technique in a single step. Molecular interactions between the components and the effect of parameters, such as varying solvent compositions, flow rates and voltage on microparticle morphology, were investigated over the particle formation. It was observed that the type of solvents used is the most effective parameter in terms of particle morphology, size and distribution. When the optical microscopy and SEM images of the microparticles were examined, 3 wt.% PLA in dichloromethane (DCM) solution concentration with an applied voltage of 18 kV and a flow rate of 20 µL/min was found to be the optimum parameter combination to achieve the desired spherical and porous micron-size particles. The average diameter of the particles achieved was 3.01 ± 0.58 µm. DCM was found to be a more suitable solvent for obtaining microparticles compared to the other solvents used. Finally, particles that are obtained by electrospraying of PLA–DCM solution are porous and monodisperse. They might have excellent potential as a carrier of drugs to the targeted sides and can be used in different biomedical applications.

scholarly journals Production and characterization of lipid microparticles produced by spray cooling encapsulating a low molar mass hydrophilic compound

2010 ◽  
Vol 30 (1) ◽  
pp. 276-281 ◽  
Author(s):  
Alda Jusceline Leonel ◽  
Hulda Noemi Mamani Chambi ◽  
Daniel Barrera-Arellano ◽  
Heloise Oliveira Pastore ◽  
Carlos Raimundo Ferreira Grosso
Keyword(s):  
Glucose Solution ◽  
Spherical Shape ◽  
Average Diameter ◽  
Solution Concentration ◽  
Spray Cooling ◽  
The Core ◽  
Lipid Mixtures ◽  
Continuous Surface ◽  
Lipid Microparticles

The objective of this research was to produce and characterize lipid particles (MpLs) that may be used as carriers of high amounts of hydrophilic core and evaluate the influence of the core amount on the performance of lipid microparticles. The MpLs were produced by spray cooling from solid and liquid lipid mixtures (stearic and oleic fatty acids and partly hydrogenated vegetable fat) containing glucose solution as core and soy lecithin as surfactant. The performance of MpLs was evaluated by means of the effective amount of encapsulated core, the core amount present on the surface of MpLs (superficial glucose) and the core release profile in aqueous solution. Morphological observations showed that MpLs presented spherical shape and a rugged and continuous surface, and an average diameter between 25 and 32 µm. The effective amount of encapsulated core was greater than 78% for all formulations evaluated. Larger amounts of superficial glucose were found in formulations in which more concentrated glucose solutions were used, regardless of the glucose lipid-solution ratio. The release results showed that core retention was significantly influenced by the glucose solution concentration, whereas release modulation was influenced by the glucose lipid-solution ratio.

scholarly journals Inkjet Printable and Self-Curable Disperse Dyes/P(St-BA-MAA) Nanosphere Inks for Both Hydrophilic and Hydrophobic Fabrics

Polymers ◽  
2018 ◽  
Vol 10 (12) ◽  
pp. 1402 ◽  
Author(s):  
Yawei Song ◽  
Kuanjun Fang ◽  
Yanfei Ren ◽  
Zhiyuan Tang ◽  
Rongqing Wang ◽  
...  
Keyword(s):  
Fiber Surface ◽  
Spherical Shape ◽  
Average Diameter ◽  
Film Coating ◽  
Water Soluble ◽  
Disperse Dyes ◽  
Scanning Calorimetry ◽  
Sem Images ◽  
Long Term Stability ◽  
Dsc Measurements

Low-water-soluble disperse dyes possess a broad color gamut and good durability, but they need chemical or physical modification before being used in inks and can only be applied to several kinds of hydrophobic fabrics. In this work, disperse dyes/P(St-BA-MAA) nanospheres (known as DPN) absorbed by sodium nitrilotriacetate (known as NTA@DPN) were prepared and applied into ink formulations, which exhibited high dye fixation, long-term stability and self-curable ability without addition of any binder. Transmission electron microscopy (TEM) images showed the nanospheres have homogeneous core-shell spherical shape and the average diameter increased by 20.6 nm after coloration. X-ray diffraction (XRD), Fourier transform infrared spectrum (FTIR), and differential scanning calorimetry (DSC) measurements illustrated the interaction between dyes and nanospheres and indicated that the colored nanospheres contained both dye molecules and crystalline dyes. The Zeta potential and particle size measurements demonstrated that the dispersion stability was improved when sodium nitrilotriacetate (NTA) was absorbed onto DPN. The rheological behavior of the NTA@DPN inks was Newtonian and desired droplet formation was achieved at the viscosity of 4.23 mPa·s. Both hydrophilic cotton and hydrophobic polyester fabrics were cationic modified before used, which had an excellent image quality and desired rubbing fastness after inkjet printing. Scanning electron microscope (SEM) images showed NTA@DPN formed stable deposits on the surface of modified fibers and could self-cure to form continuous film coating on the fiber surface after being baked at 150 °C without addition of any binder.

scholarly journals Plasma-Assisted Synthesis of Multicomponent Nanoparticles Containing Carbon, Tungsten Carbide and Silver as Multifunctional Filler for Polylactic Acid Composite Films

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 991
Author(s):  
Nichapat Boonyeun ◽  
Ratana Rujiravanit ◽  
Nagahiro Saito
Keyword(s):  
Tungsten Carbide ◽  
Polylactic Acid ◽  
Ag Nanoparticles ◽  
Composite Films ◽  
Spherical Shape ◽  
Antibacterial Activities ◽  
Atomic Ratio ◽  
Average Particle ◽  
Particle Sizes ◽  
Sem Images

Multicomponent nanoparticles containing carbon, tungsten carbide and silver (carbon-WC-Ag nanoparticles) were simply synthesized via in-liquid electrical discharge plasma, the so-called solution plasma process, by using tungsten electrodes immersed in palm oil containing droplets of AgNO3 solution as carbon and silver precursors, respectively. The atomic ratio of carbon:W:Ag in carbon-WC-Ag nanoparticles was 20:1:3. FE-SEM images revealed that the synthesized carbon-WC-Ag nanoparticles with particle sizes in the range of 20–400 nm had a spherical shape with a bumpy surface. TEM images of carbon-WC-Ag nanoparticles showed that tungsten carbide nanoparticles (WCNPs) and silver nanoparticles (AgNPs) with average particle sizes of 3.46 nm and 72.74 nm, respectively, were dispersed in amorphous carbon. The carbon-WC-Ag nanoparticles were used as multifunctional fillers for the preparation of polylactic acid (PLA) composite films, i.e., PLA/carbon-WC-Ag, by solution casting. Interestingly, the coexistence of WCNPs and AgNPs in carbon-WC-Ag nanoparticles provided a benefit for the co-nucleation ability of WCNPs and AgNPs, resulting in enhanced crystallization of PLA, as evidenced by the reduction in the cold crystallization temperature of PLA. At the low content of 1.23 wt% carbon-WC-Ag nanoparticles, the Young’s modulus and tensile strength of PLA/carbon-WC-Ag composite films were increased to 25.12% and 46.08%, respectively. Moreover, the PLA/carbon-WC-Ag composite films possessed antibacterial activities.

Characterization of Precipitated Calcium Carbonate from Eggshell Powder

2011 ◽  
Vol 410 ◽  
pp. 228-231
Author(s):  
Wimonlak Sutapun ◽  
Yupaporn Ruksakulpiwat ◽  
Nitinat Suppakarn ◽  
Rachasit Jeencham ◽  
Ajcharaporn Aontee
Keyword(s):  
Particle Size ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Average Particle Size ◽  
Spherical Shape ◽  
Average Diameter ◽  
Single Step ◽  
Average Particle ◽  
Precipitated Calcium Carbonate

In this work, PCC was prepared from chicken eggshell powder (ESP) by dissolving 100 g ESP in 1 M hydrochloric acid at room temperature. Under vigorous stirring, PCC was precipitated from the ESP-dissolved solution using 1 M sodium carbonate solution. The dried PESP (precipitated eggshell powder) was then characterized by particle size analyzer, X-ray diffractometer, Brunauer-Emmett-Teller surface analyzer and thermogravimetric analyzer. The particle shape of the PESP was revealed using scanning electron microscope. It was found that PESP was a binary mixer of calcite and vaterite. The particles were in cubic and spherical shape. In addition, PESP had a volume average diameter of 8.16 μm, D[V, 0.5] of 7.22 μm, D[V,0.9] of 16.57 μm, and the specific surface area of 4.38 m2/g. The average particle size was lower than and the specific surface area was higher than that of ESP. The decomposition process of PESP occured in a single step between 610 and 770 °C, with 44.43% weight loss.

Nanostructured Polymetallic Powders to Create New Functional Materials on its Base

2015 ◽  
Vol 670 ◽  
pp. 49-54 ◽  
Author(s):  
Yuriy A. Zaharov ◽  
Valeriy M. Pugachev ◽  
Kseniya A. Datiy ◽  
Anna N. Popova ◽  
Anastasiya S. Valnyukova ◽  
...  
Keyword(s):  
Particle Size ◽  
Phase Diagrams ◽  
Spatial Organization ◽  
Functional Materials ◽  
Particle Morphology ◽  
Cloud Type ◽  
Synthesis Conditions ◽  
Micron Size ◽  
Common Nature ◽  
20 Nm

In the paper, the particle morphology is considered and the slices of phase diagrams of nanosystems agreeable to the synthesis conditions are constructed according to the data obtained earlier by authors, as well as new results of the study of nanostructured Fe-Co, Fe-Ni, Co-Ni, Fe-Co-Ni, Fe-Pt, Cu-Ni and Ni-Cd powders. It is found that all considered polymetallic systems have common nature of the particle size spatial organization, i.e., 7-20 nm nanocrystals (for different systems) form highly compact aggregates (40-100 nm) which put together into loose porous agglomerates (up to 200-250 nm) and then into unconsolidated micron size formation of cloud type. It is classified uncovered features of nanostructured polymetallic phase diagrams in comparison with phase diagrams of bulk systems. Magnetic properties of nanosystems are studied.

scholarly journals Fast Dissolving Electrospun Nanofibers Fabricated from Jelly Fig Polysaccharide/Pullulan for Drug Delivery Applications

Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 241
Author(s):  
Thangavel Ponrasu ◽  
Bei-Hsin Chen ◽  
Tzung-Han Chou ◽  
Jia-Jiuan Wu ◽  
Yu-Shen Cheng
Keyword(s):  
Drug Delivery ◽  
Water Vapor Permeability ◽  
Electrospun Nanofibers ◽  
Average Diameter ◽  
Xrd Analysis ◽  
Water Soluble ◽  
Vapor Permeability ◽  
Uv Spectrum ◽  
Sem Images ◽  
Triton X

The fast-dissolving drug delivery systems (FDDDSs) are developed as nanofibers using food-grade water-soluble hydrophilic biopolymers that can disintegrate fast in the oral cavity and deliver drugs. Jelly fig polysaccharide (JFP) and pullulan were blended to prepare fast-dissolving nanofiber by electrospinning. The continuous and uniform nanofibers were produced from the solution of 1% (w/w) JFP, 12% (w/w) pullulan, and 1 wt% Triton X-305. The SEM images confirmed that the prepared nanofibers exhibited uniform morphology with an average diameter of 144 ± 19 nm. The inclusion of JFP in pullulan was confirmed by TGA and FTIR studies. XRD analysis revealed that the increased crystallinity of JFP/pullulan nanofiber was observed due to the formation of intermolecular hydrogen bonds. The tensile strength and water vapor permeability of the JFP/pullulan nanofiber membrane were also enhanced considerably compared to pullulan nanofiber. The JFP/pullulan nanofibers loaded with hydrophobic model drugs like ampicillin and dexamethasone were rapidly dissolved in water within 60 s and release the encapsulants dispersive into the surrounding. The antibacterial activity, fast disintegration properties of the JFP/pullulan nanofiber were also confirmed by the zone of inhibition and UV spectrum studies. Hence, JFP/pullulan nanofibers could be a promising carrier to encapsulate hydrophobic drugs for fast-dissolving/disintegrating delivery applications.

Preparation of CuO Nanopowder in Aqueous Solution by Applying Ultrasonic and its CO Gas Sensitivity

2007 ◽  
Vol 544-545 ◽  
pp. 901-904 ◽  
Author(s):  
Ji Bum Yang ◽  
Tae Gyung Ko ◽  
Sang Jin Jung ◽  
Jae Hee Oh
Keyword(s):  
Aqueous Solution ◽  
Gas Sensing ◽  
Spherical Shape ◽  
Particle Morphology ◽  
High Yield ◽  
Ambient Conditions ◽  
Gas Sensitivity ◽  
Molar Ratios ◽  
Naoh Solution ◽  
Co Gas

We report on a process in which CuO nanopowder was produced in a high yield by adopting ultrasonic in aqueous solution. In our experiment, CuCl2 solution was reacted with NaOH solution and NaNO2, at ambient conditions applying ultrasonic for 5 min. Precipitation was performed by varying the molar ratios of NaOH/CuCl2 and NaNO2/CuCl2. CuO nanoparticles of ~ 5 nm and spherical shape were obtained at the NaOH/CuCl2 of 2.0 and the NaNO2/CuCl2 of 0.097. Without ultrasonication, an amorphous phase was formed at these conditions. This indicates that sonochemical reaction facilitates direct formation of the nanosized CuO particles. In addition, the particle morphology varied from sphere through ellipsoid to needle forms depending on pH. In thick films prepared with the CuO powder for gas sensing, the maximum CO gas sensitivity reached 93 % at the temperature of 250 °C and depended linearly on CO concentration in log scale over the range of 10 ~ 104 ppm.

Optimization of the Preparation Process of Nano-TiO2/Micro-Cu Composite Particles

2010 ◽  
Vol 105-106 ◽  
pp. 492-494 ◽  
Author(s):  
Bin Wang ◽  
Hai Ping Cui ◽  
Jun Yan ◽  
Shi Guo Du
Keyword(s):  
Particle Morphology ◽  
Oxide Semiconductor ◽  
Photon Absorption ◽  
Composite Particles ◽  
Preparation Process ◽  
Nano Tio2 ◽  
Surface Design ◽  
Acidic Aqueous Solution ◽  
Micron Size ◽  
Hydrolysis Of

Nano-TiO2/micro-Cu composite particles were prepared by hydrolysis of Ti(OBu)4 in abundant acidic aqueous solution and subsequent reflux in the presence of micron size Cu powders. The preparation process was optimized using response surface design with the degradation of TiO2/Cu particles to Methyl orange as target. The particle morphology and composition were characterized by FE-SEM, XPS and XRD. The photon absorption properties of composite particles was investigated by the UV-VIS DRS experiments, and the results show the photoabsorption property of composite particles is intermediate between TiO2 particles and Cu powders, showing cooperative effect by the combination of oxide semiconductor particles with metal substrate.

scholarly journals Characterisation of Particulate Matter Emitted from Cofiring of Lignite and Agricultural Residues in a Fixed-Bed Combustor

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Nattasut Mantananont ◽  
Savitri Garivait ◽  
Suthum Patumsawad
Keyword(s):  
Particle Size ◽  
Particulate Matter ◽  
Rice Husk ◽  
Fixed Bed ◽  
Spherical Shape ◽  
Particle Morphology ◽  
Fuel Mixture ◽  
Agricultural Residues ◽  
Particulate Matter Emission ◽  
Air Supply

This study is focused on the emission of fixed bed combustor batch operated. Real-time analyser ELPI (electrical low-pressure impactor) system was used to size-segregated particulate matter emission ranging from 40 nm to 10 μm. The results show that total number concentration were3.4×103,1.6×104, and1.5×105 particles/cm3⋅kgfuel, while total mass of particles were 12.2, 8.0, and 6.5 mg/Nm3⋅kgfuelfor combustion of lignite, rice husk and bagasse, respectively. But it can be noticed that cofiring released more particulate matter. Meanwhile it was found that the effect of ratio of over-fired air to total air supply is more pronounced, since decrease in this ratio, the amount of particles are decreased significantly. For particle size distribution, it can be observed that submicron-sized particles dominate and the most prevailing size is in the range: 50 nm<Dp<100 nm, for lignite and agricultural residues. However, during cofiring of fuel mixture at 70% rice husk mass concentration, it is found that there are two major fractions of particle size; 40 nm<Dp<70 nm and 0.2 μm<Dp<0.5 μm. The analysis of particle morphology showed that the isolate shape of submicron particle produced during lignite combustion is characterised by different geometries such as round, capsule, rod, flake-like, whereas the spherical shape is obtained with combustion of rice husk.

scholarly journals Use of Electrosprayed Agave Fructans as Nanoencapsulating Hydrocolloids for Bioactives

Nanomaterials ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 868 ◽  
Author(s):  
Jorge Ramos-Hernández ◽  
Juan Ragazzo-Sánchez ◽  
Montserrat Calderón-Santoyo ◽  
Rosa Ortiz-Basurto ◽  
Cristina Prieto ◽  
...  
Keyword(s):  
Uv Light ◽  
Particle Morphology ◽  
Bioactive Compound ◽  
Processing Parameters ◽  
Degree Of Polymerization ◽  
Spherical Particles ◽  
Sem Images ◽  
High Degree ◽  
Thermal Stability Of ◽  
Β Carotene

High degree of polymerization Agave fructans (HDPAF) are presented as a novel encapsulating material. Electrospraying coating (EC) was selected as the encapsulation technique and β-carotene as the model bioactive compound. For direct electrospraying, two encapsulation methodologies (solution and emulsion) were proposed to find the formulation which provided a suitable particle morphology and an adequate concentration of β-carotene encapsulated in the particles to provide a protective effect of β-carotene by the nanocapsules. Scanning electron microscopy (SEM) images showed spherical particles with sizes ranging from 440 nm to 880 nm depending on the concentration of HDPAF and processing parameters. FTIR analysis confirmed the interaction and encapsulation of β-carotene with HDPAF. The thermal stability of β-carotene encapsulated in HDPAF was evidenced by thermogravimetric analysis (TGA). The study showed that β-carotene encapsulated in HDPAF by the EC method remained stable for up to 50 h of exposure to ultraviolet (UV) light. Therefore, HDPAF is a viable option to formulate nanocapsules as a new encapsulating material. In addition, EC allowed for increases in the ratio of β-carotene:polymer, as well as its photostability.

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