Empirical search for factors affecting mean particle size of PLGA microspheres containing macromolecular drugs

2016 ◽  
Vol 134 ◽  
pp. 137-147 ◽  
Author(s):  
Jakub Szlęk ◽  
Adam Pacławski ◽  
Raymond Lau ◽  
Renata Jachowicz ◽  
Pezhman Kazemi ◽  
...  
Author(s):  
Nisha Patel ◽  
Hitesh A Patel

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.


Author(s):  
Anjali Pandya ◽  
Rajani Athawale ◽  
Durga Puro ◽  
Geeta Bhagwat

Background: The research work involves development of PLGA biodegradable microspheres loaded with dexamethasome for intraocular delivery. Objective: To design and evaluate long acting PLGA microspheres for ocular delivery of dexamethasone. Method: Present formulation involves the development of long acting dexamethasone loaded microspheres composed of a biodegradable controlled release polymer, Poly(D, L- lactide-co-glycolide) (PLGA), for the treatment of posterior segment eye disorders intravitreally. PLGA with monomer ratio of 50:50 of lactic acid to glycolic acid was used to achieve a drug release up to 45 days. Quality by Design approach was utilized for designing the experiments. Single emulsion solvent evaporation technique along with high pressure homogenization was used to facilitate formation of microspheres. Results: Particle size evaluation, drug content and drug entrapment efficiency were determined for the microspheres. Particle size and morphology was observed using Field Emission Gun-Scanning Electron Microscopy (FEG-SEM) and microspheres were in the size range of 1-5 μm. Assessment of drug release was done using in vitro studies and transretinal permeation was observed by ex vivo studies using goat retinal tissues. Conclusion: Considering the dire need for prolonged therapeutic effect in diseases of the posterior eye, an intravitreal long acting formulation was designed. Use of biodegradable polymer with biocompatible degradation products was a rational approach to achieve this aim. Outcome from present research shows that developed microspheres would provide a long acting drug profile and reduce the frequency of administration thereby improving patient compliance.


2021 ◽  
Vol 13 (5) ◽  
pp. 168781402110178
Author(s):  
Zhengang Liu ◽  
Weinan Diao ◽  
Zhenxia Liu ◽  
Fei Zhang

Particle deposition could decrease the aerodynamic performance and cooling efficiency of turbine vanes and blades. The particle motion in the flow and its temperature are two important factors affecting its deposition. The size of the particle influences both its motion and temperature. In this study, the motion of particles with the sizes from 1 to 20 μm in the first stage of a turbine are firstly numerically simulated with the steady method, then the particle deposition on the vanes and blades are numerically simulated with the unsteady method based on the critical viscosity model. It is discovered that the particle deposition on vanes mainly formed near the leading and trailing edge on the pressure surface, and the deposition area expands slowly to the whole pressure surface with the particle size increasing. For the particle deposition on blades, the deposition area moves from the entire pressure surface toward the tip with the particle size increasing due to the effect of rotation. For vanes, the particle capture efficiency increases with the particle size increasing since Stokes number and temperature of the particle both increase with its size. For blades, the particle capture efficiency increases firstly and then decreases with the particle size increasing.


Author(s):  
Longzhe Jin ◽  
Jianguo Liu ◽  
Jingzhong Guo ◽  
Jiaying Wang ◽  
Tianyang Wang

AbstractTo investigate the factors affecting the wettability of copper mine blasting dust, the primary blasting dust was collected from an open-pit copper mine and separated into hydrophilic blasting dust (HLBD) and hydrophobic blasting dust (HBBD) using water flotation method. The physicochemical properties of HLBD and HBBD were measured and compared with each other. The properties included particle size distributions (PSDs), micromorphologies, pore structures, mineral components and surface organic carbon functional groups. The results show that particle size and pore structure of the blasting dust are the main factors affecting its wettability. Specifically, particle size of HBBD is smaller than that of HLBD, and their respiratory dust (less than 10 µm) accounts for 61.74 vol% and 53.00 vol%, respectively. The pore structure of HBBD is more developed, and the total pore volume of HBBD is 1.66 times larger than that of HLBD. The identical mineral compositions were detected in HLBD and HBBD by X-rays diffraction (XRD); however, the surface organic hydrophobic component of HBBD is slightly larger than that of HLBD, this may be the reason for the poor wettability of HBBD. This study is significant to understand the effects of physicochemical properties of copper mine blasting dust on its wettability.


RSC Advances ◽  
2016 ◽  
Vol 6 (24) ◽  
pp. 19657-19661 ◽  
Author(s):  
C. Ashok raja ◽  
S. Balakumar ◽  
D. Durgalakshmi ◽  
R. P. George ◽  
B. Anandkumar ◽  
...  

45S5 Bioglass with a mean particle size in the nano regime was synthesized and fabricated with rGO sheets using three different strategies.


1991 ◽  
Vol 48 (10) ◽  
pp. 1882-1886 ◽  
Author(s):  
Michael K. Young ◽  
Wayne A. Hubert ◽  
Thomas A. Wesche

We compared samples collected from 10 substrates of various compositions with a single-probe freeze-core sampler, a triple-probe freeze-core sampler, a McNeil sampler, and a shovel. The accuracy with which these devices sampled particles larger than 50 mm in diameter varied; they were oversampled by the freeze-core devices, sampled in proportion to their availability by a shovel, and sampled inconsistently by the McNeil sampler. The geometric mean particle size and variance of single-probe freeze-core samples consistently exceeded those of samples collected with the other devices. Most sample means also exceeded the test substrate means. By excluding the proportions of particles larger than 50 mm in diameter in our analyses, we found that proportions of several particles sizes in samples collected by different methods differed significantly from the actual proportions in test substrates. There were few differences between the single- and triple-probe freeze-core samples or between McNeil and shovel samples. All four samplers were biased, but the McNeil sampler most frequently produced samples that approximated the true substrate composition.


Author(s):  
Vaishak Ramesh Sagar ◽  
Samuel Lorin ◽  
Johan Göhl ◽  
Johannes Quist ◽  
Christoffer Cromvik ◽  
...  

Abstract Selective laser melting (SLM) process is a powder bed fusion additive manufacturing process that finds applications in aerospace and medical industries for its ability to produce complex geometry parts. As the raw material used is in powder form, particle size distribution (PSD) is a significant characteristic that influences the build quality in turn affecting the functionality and aesthetics aspects of the product. This paper investigates the effect of PSD on the printed geometry for 316L stainless steel powder, where three coupled in-house simulation tools based on Discrete Element Method (DEM), Computational Fluid Dynamics (CFD), and Structural Mechanics are employed. DEM is used for simulating the powder bed distribution based on the different powder PSD. The CFD is used as a virtual testbed to determine thermal parameters such as heat capacity and thermal conductivity of the powder bed viewed as a continuum. The values found as a stochastic function of the powder distribution is used to analyse the effect on the melted zone and deformation using Structural Mechanics. Results showed that mean particle size and PSD had a significant effect on the packing density, melt pool layer thickness, and the final layer thickness after deformation. Specifically, a narrow particle size distribution with smaller mean particle size and standard deviation produced solidified final layer thickness closest to nominal layer thickness. The proposed simulation approach and the results will catalyze in development of geometry assurance strategies to minimize the effect of particle size distribution on the geometric quality of the printed part.


Author(s):  
Seema Kohli ◽  
Abhisek Pal ◽  
Suchit Jain

Objective: The purpose of this research work was to develop and evaluate microspheres appropriate for controlled release of zidovudine (AZT).Methods: The AZT loaded polylactide-co-glycolide (PLGA) microspheres were prepared by W/O/O double emulsion solvent diffusion method. Compatibility of drug and polymer was studied by Fourier-transform infrared spectroscopy (FTIR). The influence of formulation factors (drug: polymer ratio, stirring speed, the concentration of surfactant) on particle size encapsulation efficiency and in vitro release characteristics of the microspheres was investigated. Release kinetics was studied and stability study was performed as per ICH guidelines.Results: Scanning electron microscopy (SEM) images show good reproducibility of microspheres from different batches. The average particle size was in the range of 216-306 μm. The drug-loaded microspheres showed 74.42±5.08% entrapment efficiency. The cumulative percentage released in phosphate Buffer solution (PBS) buffer was found to be 55.32±5.89 to 74.42±5.08 %. The highest regressions (0.981) were obtained for zero order kinetics followed by Higuchi (0.968) and first order (0.803).Conclusion: Microsphere prepared by double emulsion solvent diffusion method was investigated and the results revealed that 216-306 μm microsphere was successfully encapsulated in a polymer. FT-IR analysis, entrapment efficiency and SEM Studies revealed the good reproducibility from batch to batch. The microspheres were of an appropriate size and suitable for oral administration. Thus the current investigation show promising results of PLGA microspheres as a matrix for drug delivery and merit for In vivo studies for scale up the technology.


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