scholarly journals The Effect of Carboxymethyl Glucomannan Concentration on the Properties of Glucomannan-Chitosan Hydrogel for Lactobacillus acidophilus FNCC 0051 Encapsulation

2021 ◽  
Vol 18 (16) ◽  
Author(s):  
Veriani APRILIA ◽  
Agnes MURDIATI ◽  
Pudji HASTUTI ◽  
Eni HARMAYANI
Keyword(s):  
Particle Size ◽  
Cold Storage ◽  
Lactobacillus Acidophilus ◽  
Self Assembly ◽  
Spherical Shape ◽  
Physical Barrier ◽  
Chitosan Hydrogel ◽  
Uniform Particles ◽  
Viability Study ◽  
Continuous Surface

The effect of porang (Amorphophallus oncophyllus) glucomannan concentration on the properties of glucomannan-chitosan hydrogel was investigated for Lactobacillus acidophilus FNCC 0051 encapsulation. The spherical shape with a continuous surface of the particle was self-assembly formed. The increase of glucomannan concentration from 0.3 to 0.9 % smoothly increased their small particle size from 1.08 ± 0.02 µm to 2.12 ± 0.00 µm and no significant change on the positive zeta potential values. The polydispersity indexes with the value between 0.4 to 0.5 were categorized as uniform particles. However, these values were higher compared to other studies which used konjac glucomannan-chitosan as the hydrogel materials. The encapsulation study with Lactobacillus acidophilus FNCC 0051 showed that the highest value was achieved when the same ratio of glucomannan and chitosan was applied (0.5 %). The viability study proved the perfect protection of hydrogel during 56 days of cold storage and pasteurization treatment with the cell viabilities of 100 % and 58.13 ± 18.5 %, respectively. HIGHLIGHTS Glucomannan concentration influenced particle size and encapsulation efficiency of hydrogel Hydrogel was potential as acidophilus carrier in the gut due to its pH sensitivity Hydrogel had continuous surface to provide a stronger physical barrier for the acidophilus against harsh environment Hydrogel proved well protection of acidophilus during pasteurization and cold storage GRAPHICAL ABSTRACT

Application of Plakett-Burman Screening Design in Optimization of Process Parameters for Formulation of Canaglifozin Nanosuspension

2020 ◽  
Vol 13 (6) ◽  
pp. 5208-5216
Author(s):  
Nisha Patel ◽  
Hitesh A Patel
Keyword(s):  
Particle Size ◽  
Particle Diameter ◽  
Spherical Shape ◽  
Water Soluble ◽  
Pareto Chart ◽  
Independent Variables ◽  
Mean Particle Size ◽  
Screening Design ◽  
Stirring Time ◽  
Response Variables

In this study, we sought to improve the dissolution characteristics of a poorly water-soluble BCS class IV drug canaglifozin, by preparing nanosuspension using media milling method. A Plackett–Burman screening design was employed to screen the significant formulation and process variables. A total of 12 experiment were generated by design expert trial version 12 for screening 5 independent variables namely the amount of stabilizer in mg (X1), stirring time in hr (X2), amt of Zirconium oxide beads in gm (X3), amount of drug in mg (X4) and stirring speed in rpm (X5) while mean particle size in nm (Y1) and drug release in 10 min. were selected as the response variables. All the regression models yielded a good fit with high determination coefficient and F value. The Pareto chart depicted that all the independent variables except the amount of canaglifozin had a significant effect (p<0.001) on the response variables. The mathematical model for mean particle size generated from the regression analysis was given by mean particle size = +636.48889 -1.28267 amt of stabilizer(X1) -4.20417 stirring time (X2) -7.58333 amt of ZrO2 beads(X3) -0.105556 amt of drug(X4) -0.245167 stirring speed(X5) (R2=0.9484, F ratio=22.07, p<0.001). Prepared canaglifozin nanosuspension exemplified a significant improvement (p<0.05) in the release as compared to pure canaglifozin and marketed tablet with the optimum formulation releasing almost 80% drug within first 10min. Optimized nanosuspension showed spherical shape with surface oriented stabilizer molecules and a mean particle diameter of 120.5 nm. There was no change in crystalline nature after formulation and it was found to be chemically stable with high drug content.

scholarly journals Surface Activity of Humic Acid and Its Sub-Fractions from Forest Soil

2021 ◽  
Vol 13 (15) ◽  
pp. 8122
Author(s):  
Shijie Tian ◽  
Weiqiang Tan ◽  
Xinyuan Wang ◽  
Tingting Li ◽  
Fanhao Song ◽  
...  
Keyword(s):  
Surface Tension ◽  
Particle Size ◽  
Humic Acid ◽  
Forest Soil ◽  
Surface Activity ◽  
Self Assembly ◽  
Average Particle Size ◽  
Gaussian Model ◽  
Exponential Model ◽  
Average Particle

Surface activity of humic acid (HA) and its six sub-fractions isolated from forest soil were characterized by surface tension measurements, dynamic light scattering, and laser doppler electrophoresis. The surface tension of HA and its sub-fractions reduced from 72.4 mN·m−1 to 36.8 mN·m−1 in exponential model with the increasing concentration from 0 to 2000 mg·L−1. The critical micelle concentration (CMC) and Z-average particle size ranged from 216–1024 mg·L−1 and 108.2–186.9 nm for HA and its sub-fractions, respectively. The CMC have related with alkyl C, O-alkyl C, aromatic C, and carbonyl C (p < 0.05), respectively, and could be predicted with the multiple linear regression equation of CMC, CMC = 18896 − 6.9 × C-296 × alkyl C-331 × aromatic C-17019 × H/C + 4054 × HB/HI (p < 0.05). The maximum particle size was 5000 nm after filtered by a membrane with pore size of 450 nm, indicating HA and its sub-fractions could progressed self-assembly at pH 6.86. The aggregate sizes of number-base particle size distributions were mainly in six clusters including 2 ± 1 nm, 5 ± 2 nm, 10 ± 3 nm, 21 ± 8 nm, 40 ± 10 nm, and >50 nm analyzed by Gaussian model that maybe due to the inconsistency of the components and structures of the HA sub-fractions, requiring further study. It is significance to explore the surface activity of HA and its sub-fractions, which is helpful to clarify the environmental behavior of HA.

A ‘Building Block’ Approach To Mixed-Colloid Systems Through Electrostatic Self-Organization

2001 ◽  
Vol 676 ◽  
Author(s):  
Trent H. Galow ◽  
Andrew K. Boal ◽  
Vincent M. Rotello
Keyword(s):  
Particle Size ◽  
Self Assembly ◽  
Building Block ◽  
Acid Base ◽  
Electrostatic Assembly ◽  
Polymer Colloid ◽  
Colloid Systems ◽  
Carboxylic Acid Derivative ◽  
Block Approach ◽  
Shape And Size

ABSTRACTWe have developed a highly modular electrostatically-mediated approach to colloid-colloid and polymer-colloid networks using ‘building block’ and ‘bricks and mortar’ self-assembly methodologies, respectively. The former approach involved functionalization of one type of nanoparticle building block with a primary amine and a counterpart building block with a carboxylic acid derivative. After combining these two systems, acid-base chemistry followed by immediate charge-pairing resulted in the spontaneous formation of electrostatically-bound mixed-nanoparticle constructs. The shape and size of these ensembles were controlled via variation of particle size and stoichiometries. In the ‘bricks and mortar’ approach, a functionalized polymer is combined with complementary nanoparticles to provide mixed polymer-nanoparticle networked structures. A notable feature is the inherent porosity resulting from the electrostatic assembly. The shape and size of these ensembles were controlled via variation of particle size, stoichiometries and the order in which they were added.

Preparation ZnO nanoparticles with Different Concentration by Laser Ablation in Liquid

2021 ◽  
Vol 39 (1B) ◽  
pp. 197-202
Author(s):  
Ghufran S. Jaber ◽  
Khawla S. Khashan ◽  
Maha J. Abbas
Keyword(s):  
Particle Size ◽  
Laser Ablation ◽  
Laser Pulse ◽  
Laser Energy ◽  
Average Particle Size ◽  
Spherical Shape ◽  
Pulse Number ◽  
Average Particle ◽  
Zno Nps ◽  
Laser Ablation In Liquid

The effects of varying laser pulse numbers on the fabricated of ZnONPs by pulsed laser ablation in deionized water of Zn-metal are investigated. The Nd: YAG laser at energy 600mJ prepared three samples by change the laser pulse number (100, 150, and 200). The results were collected and examined using an electron scanning microscope, XRD – diffraction, and transmission electron microscope. The result revealed the colloidal spherical shape and the homogeneous composition of the ZnO NPs. The nanoparticles resulted in different concentrations and sized distributions by changing the pulse number of a laser. The average particle size and the mass concentration of particle size increase with an increasing number of laser pulses by fixed the laser energy.

Microstructure and Properties of TiC-CrNiMo SHS Spray Powder and Thermally Sprayed Coating

2000 ◽  
Author(s):  
M. Väisänen ◽  
P. Vuoristo ◽  
T. Mäntylä ◽  
V. Maunu ◽  
P. Lintunen ◽  
...  
Keyword(s):  
Particle Size ◽  
Corrosion Behaviour ◽  
Metallic Matrix ◽  
Electrochemical Corrosion ◽  
Wear Test ◽  
Spherical Shape ◽  
Open Circuit ◽  
Hvof Spraying ◽  
Particle Size Range ◽  
Abrasion Wear

Abstract Titanium carbide cermet spray powder was produced by the SHS process (Self-propagating High-temperature Synthesis) using elemental Ti, C, Mo and prealloyed CrNiMo powders as starting materials. The powder was characterised (particle size distribution, phase structure, morphology) and the internal structure of each cermet particle was found out to be dense consisting of fine distribution of carbides embedded in a metallic matrix. The particle size range suitable for thermal spraying was obtained by sieving and air classifying. The coatings were prepared by HVOF spraying (DJH2600 and DJH2700). The dry abrasion wear resistance was evaluated by the rubber wheel abrasion wear test and electrochemical corrosion behaviour by open circuit potential measurements. According to the XRD analysis the amount of retained carbides in the coatings is high and the carbide phase has a spherical shape also in the coatings. The microstructure of coatings obtained is dense and the coatings possess good properties in wear and corrosion tests. WC-Co-Cr and Cr3C2-NiCr powders were used for comparison.

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 Effect of the polymeric coating over Fe3O4 particles used for magnetic separation

2010 ◽  
Vol 8 (5) ◽  
pp. 1041-1046 ◽  
Author(s):  
Raúl Reza ◽  
Carlos Martínez Pérez ◽  
Claudia Rodríguez González ◽  
Humberto Romero ◽  
Perla García Casillas
Keyword(s):  
Particle Size ◽  
Magnetite Nanoparticles ◽  
Average Particle Size ◽  
Spherical Shape ◽  
Polymeric Coating ◽  
Average Particle ◽  
Synthesis Conditions ◽  
Aging Conditions ◽  
Magnetite Particles ◽  
Average Size

AbstractIn this work, the synthesis of magnetite nanoparticles by two variant chemical coprecipitation methods that involve reflux and aging conditions was investigated. The influence of the synthesis conditions on particle size, morphology, magnetic properties and protein adsorption were studied. The synthesized magnetite nanoparticles showed a spherical shape with an average particle size directly influenced by the synthesis technique. Particles of average size 27 nm and 200 nm were obtained. When the coprecipitation method was used without reflux and aging, the smallest particles were obtained. Magnetite nanoparticles obtained from both methods exhibited a superparamagnetic behavior and their saturation magnetization was particle size dependent. Values of 67 and 78 emu g−1 were obtained for the 27 nm and 200 nm magnetite particles, respectively. The nanoparticles were coated with silica, aminosilane, and silica-aminosilane shell. The influence of the coating on protein absorption was studied using Bovine Serum Albumin (BSA) protein.

Effect of Several Factors on the Synthesis of Calcium Hydroxide Prepared by Spray Drying Method Using Limestone

2007 ◽  
Vol 544-545 ◽  
pp. 733-736
Author(s):  
Moon Kwan Choi ◽  
Jin Sang Cho ◽  
Sung Min Joo ◽  
Jin Koo Park ◽  
Ji Whan Ahn ◽  
...  
Keyword(s):  
Particle Size ◽  
Calcium Carbonate ◽  
Spray Drying ◽  
Feeding Rate ◽  
Spherical Shape ◽  
Initial Reaction ◽  
Outlet Temperature ◽  
Drying Method ◽  
Precipitated Calcium Carbonate ◽  
Carbonation Process

The purpose of this work is to influence of CaO concentrations of 5.0 wt.% and 10.0 wt.%, slurry feeding rate of 200~400 /min, rotating rate of drum of 5,000 and 10,000 rpm, inlet and outlet temperature on the synthesis of Ca(OH)2 powder, and the synthesis of precipitated calcium carbonate by carbonation process using Ca(OH)2 prepared by spray drying method. As the feeding rate of slurry was increased, the particle size of Ca(OH)2 was decreased. Regardless of rotating rate of drum, when the concentration of CaO was 5.0 wt.% and 10.0 wt.%, the morphology of Ca(OH)2 showed spherical shape of 10~30 μm and 20~60 μm, respectively. The specific surface area of synthesized Ca(OH)2 was 27~30 m2/g. When the initial reaction temperature was 11 °C and 30 °C, the shape and particle size of precipitated calcium carbonate synthesized in the carbonation process showed the rectangular shape of 0.1~0.4 μm and the spindle shape of 0.5~1.0 μm, respectively.

scholarly journals DEVELOPMENT OF SODIUM ALGINATE COATED NANOPARTICLES OF METRONIDAZOLE FOR THE TREATMENT OF PERIODONTITIS

2019 ◽  
pp. 105-110 ◽  
Author(s):  
MUKUL SINGH ◽  
GAURAV JAIN
Keyword(s):  
Particle Size ◽  
Sodium Alginate ◽  
Biological Membrane ◽  
Spherical Shape ◽  
Prolonged Treatment ◽  
Prolonged Action ◽  
Sem Images ◽  
Mean Particle Size ◽  
Coated Nanoparticles ◽  
Acceptable Range

Objective: The present study was aimed to develop metronidazole (MNZ) loaded poly lactic-co-glycolic acid (PLGA) based mucoadhesive nanoparticles (NPs) in prolonged treatment in periodontitis. Methods: Nanoparticles were prepared by using single (SE) and double (DE) emulsion method to determine the suitability of methods. Prepared NPs were evaluated for surface morpholgy, mean particle size, polydispersity index, zeta potential, mucoadhesion ability and invitro-drug release, Results: SEM images confirmed that NPs were of spherical shape and smooth surface. Mean particle size, of MNZ loaded NPs were found 583.28±18.22 and 872.72±63.18 prepared by SE and DE method. Similarly, polidispersity index (0.68±0.1 and 0.83±0.06) and zeta potention (-33.29±0.7 and-31.28.0.6) was found in acceptable range. Prepared NPs were surface treated with Sodium alginate (SA) to increase mucoadhesive property. It was observe that particles remain adhere till 24 hr with biological membrane. Prepared NPs allow release of MNZ upto 24 h in sustained manner. Conclusion: This study confirms that the prepared MNZ loaded NPs may be used as an better alternate with addition application such as prolonged action thus improved patient compliance.

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