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Experimental and theoretical studies on the particle formation process of particles for the improvement of pulmonary drug delivery Open Access

Descriptions

Other title
Subject/Keyword
Particle Engineering
Crystallization process
Spray drying
Piezoceramic dispenser
Time to reach saturation
Type of item
Thesis
Degree grantor
University of Alberta
Author or creator
Baldelli, Alberto
Supervisor and department
Reinhard Vehring
Examining committee member and department
Martin, Andrew (Mechanical Engineering)
Kostiuk, Larry, W. (Mechanical Engineering)
Olfert, Jason (Mechanical Engineering)
Vehring, Reinhard (Mechanical Engineering)
Traini, Daniela (School of Medical Science, University of Sydney)
Department
Department of Mechanical Engineering
Specialization

Date accepted
2016-07-07T11:27:53Z
Graduation date
2016-06:Fall 2016
Degree
Doctor of Philosophy
Degree level
Doctoral
Abstract
The formation of dry microparticles from evaporating solution droplets was investigated and analyzed. The particle formation involved the creation and production of spray dried microparticles used for the delivery of drugs to treat pulmonary diseases. Studies of particle formation were conducted using a monodisperse droplet chain, which was created using a piezoceramic dispenser with an inner diameter of 30 µm for all the cases analyzed. The initial droplets ranged from 70 to 100 µm, and the final dried microparticles ranged from 0.3 µm to 25 µm, a range relevant to pulmonary drug delivery. The distance between two consecutive droplets was recorded; from these parameters, the main properties of the particle formation process, such as density, mass, aerodynamic diameter, volume equivalent diameter and velocity, were obtained. Studies varied from crystallizing to non-crystallizing systems. For the first group, cellulose acetate butyrate (CAB) in acetone was chosen for its high molecular weight. Such a substance generates high Peclet numbers, a phenomenon previously not analyzed in a monodisperse droplet chain. Initial concentrations of 0.37 and 10 mg/ml were chosen. External temperatures of 30, 40, and 55 °C were selected. For crystallizing systems, the material chosen for particle formation studies was sodium nitrate (NaNO3). The reasons for this choice were the properties of NaNO3: its crystallinity, its chemical structure and its high solubility in water. The use of NaNO3 as a solute allowed investigations of the time for crystallization, data unobtainable in prior experimental approaches. Systematic investigations of particle formation in the NaNO3 system were conducted using an appropriate selection of independent variables and analytical techniques suitable to the evaluation of evaporation and particle properties,. The independent variables and levels were the concentrations of the initial solution, which ranged from 5×10-5 mg/ml to 5 mg/ml, and the temperature of the drying gas, which ranged from 25 to 150 °C. The properties of the final dried particles most closely analyzed were density, void fraction, shell thickness, morphology and surface roughness. The analysis of morphology and roughness were correlated with cohesion forces between two microparticles. Cohesion forces varied from 1 to 100 nN depending on size, roughness and asperities, and peak-to-peak distances of the microparticles. The microparticles selected ranged between 15 and 1 μm, in diameter, between 1710 and 1 nm in roughness, and between 7000 nm and 50 nm in asperities. The experimental results were compared with theoretical results in the literature and the Rabinovich model chosen as the best theoretical method of determining cohesion forces between two rough microparticles. A multicomponent particle formation process involved the formation of microparticles from more than one solute. The multicomponent particle formation has previously been poorly studied, despite its impact on the quality of respiratory drug delivery. Potassium nitrate (KNO3), chosen for its similarities in molecular weight and solubility, was added to the evaporation of NaNO3 droplets. Initial conditions of environmental temperatures of 50 and 100ºC, concentrations of 1 to 10 mg/ml, and molar percentages of NaNO3 and KNO3 of 30:70, 50:50, and 70:30 influenced the time to reach saturation and, therefore, the distribution of chemical components on the shell of the final dried microparticles. The influence of the time to reach saturation on the distribution of final dried microparticles was verified. The solute with a shorter time to reach saturation composed the surface of the shell of final dried microparticles.
Language
English
DOI
doi:10.7939/R3028PQ3Q
Rights
This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for the purpose of private, scholarly or scientific research. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.
Citation for previous publication
Alberto Baldelli, Mohammed A. Boraey, David S. Nobes, Reinhard Vehring, “Analysis of the Particle Formation Process of Structured Microparticles”, Molecular Pharmaceutics, 2015, 12 (8), pp 2562-2573Alberto Baldelli, Rachael Miles, Rory M. Power, Jonathan Reid, Reinhard Vehring, “Effect of the Crystallization Kinetics on the Properties of Spray Dried Microparticles”, Journal of Aerosol Science and Technology, 2016, 50 (7), pp 693-704Alberto Baldelli, Reinhard Vehring, “Analysis of Cohesion Forces of Spray Dried Microparticles”, Journal of Colloids and Surfaces a: Physiochemical and Engineering aspects, published, 2016Alberto Baldelli, Reinhard Vehring, “Control of the distribution of chemical components in spray dried microparticles”, Journal of Aerosol Science and Technology, published, 2016

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