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Pharmaceutical analysis and in-vitro aerodynamic characterisation of inhaled theophylline formulations containing drug particles prepared by supercritical fluid processing : chromatographic, spectroscopic, and thermal analysis of micron-sized theophylline particles prepared by supercritical fluid technology and in-vitro evaluation of their performance as inhaled dry powder formulationsMohamed, Noha Nahedj Atia January 2009 (has links)
The aim of this work is to study the in-vitro aerodynamic performance of a new inhaled theophylline formulation prepared by supercritical fluids technique. For the analysis of the output from the in-vitro tests (and further in-vivo tests) a new, fast, sensitive high performance liquid chromatographic (HPLC) method was developed and validated for the determination of theophylline and other related derivatives in aqueous and urine samples using new packing materials (monolithic columns). These columns achieve efficient separation under lower backpressure and shorter time comparing to other traditionally or newly introduced C18 columns. Solution enhanced dispersion by supercritical fluid (SEDS) process has been applied for the production of anhydrous theophylline as pure crystals in the range 2-5 μm to be used as new inhaled dry powder formulation for asthma. Fifteen theophylline samples have been prepared under different experimental conditions. The drug produced by this method has been subject to a number of solid-phase analytical procedures designed to establish the crystal structure [X-ray powder diffraction (XRPD)], the structure and conformation [(FTIR), Fourier-transform Raman spectroscopy (FT-Raman)], and the morphology and particle size [scanning electron microscope (SEM)]. While, thermal gravimetric analysis (TGA), and differential scanning calorimetry (DSC) have been used to monitor any phase transition or polymorphic changes after processing. All these analytical techniques gave a satisfactory indication of the solid-state chemistry of the processed particles and assess the development of new inhalation product. The performance of inhaled SEDS theophylline with or without a carrier was evaluated using the developed HPLC method. Three samples having different particle sizes were selected out of the prepared powders by SEDS technique to be tested. The dose sampling unit and the Anderson Cascade Impactor were used to determine the in-vitro emitted dose and the deposition profiles of SEDS samples, respectively. The effect of different inhalation flows was studied using two different flows 28.3, and 60 L min-1 with 4 L inhalation volume. Different DPI devices were investigated in this study; Easyhaler® and Spinhaler®. The particle size has an important effect on the aerodynamic behaviour and deposition profile of inhaled drug, the smaller the particles the greater the total lung deposition. The presence of a carrier improves the respirable fraction for all the tested formulations.
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Pharmaceutical analysis and in-vitro aerodynamic characterisation of inhaled theophylline formulations containing drug particles prepared by supercritical fluid processing. Chromatographic, spectroscopic, and thermal analysis of micron-sized theophylline particles prepared by supercritical fluid technology and in-vitro evaluation of their performance as inhaled dry powder formulations.Mohamed, Noha N.A. January 2009 (has links)
The aim of this work is to study the in-vitro aerodynamic performance of a new inhaled theophylline formulation prepared by supercritical fluids technique.
For the analysis of the output from the in-vitro tests (and further in-vivo tests) a new, fast, sensitive high performance liquid chromatographic (HPLC) method was developed and validated for the determination of theophylline and other related derivatives in aqueous and urine samples using new packing materials (monolithic columns). These columns achieve efficient separation under lower backpressure and shorter time comparing to other traditionally or newly introduced C18 columns.
Solution enhanced dispersion by supercritical fluid (SEDS) process has been applied for the production of anhydrous theophylline as pure crystals in the range 2-5 ¿m to be used as new inhaled dry powder formulation for asthma. Fifteen theophylline samples have been prepared under different experimental conditions.
The drug produced by this method has been subject to a number of solid-phase analytical procedures designed to establish the crystal structure [X-ray powder diffraction (XRPD)], the structure and conformation [(FTIR), Fourier-transform Raman spectroscopy (FT-Raman)], and the morphology and particle size [scanning electron microscope (SEM)]. While, thermal gravimetric analysis (TGA), and differential scanning calorimetry (DSC) have been used to monitor any phase transition or polymorphic changes after processing. All these analytical techniques gave a satisfactory indication of the solid-state chemistry of the processed particles and assess the development of new inhalation product.
The performance of inhaled SEDS theophylline with or without a carrier was evaluated using the developed HPLC method. Three samples having different particle sizes were selected out of the prepared powders by SEDS technique to be tested. The dose sampling unit and the Anderson Cascade Impactor were used to determine the in-vitro emitted dose and the deposition profiles of SEDS samples, respectively. The effect of different inhalation flows was studied using two different flows 28.3, and 60 L min-1 with 4 L inhalation volume. Different DPI devices were investigated in this study; Easyhaler® and Spinhaler®. The particle size has an important effect on the aerodynamic behaviour and deposition profile of inhaled drug, the smaller the particles the greater the total lung deposition. The presence of a carrier improves the respirable fraction for all the tested formulations. / Egyptian Ministry of Higher Education
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Rychlá separace výbušnin vysokoúčinnou kapalinovou chromatografií / Fast separation of explosives by high performance liquid chromatographyŠesták, Jozef January 2011 (has links)
The topic of the diploma thesis is fast separation of explosives by HPLC and development of miniaturized liquid chromatograph for application in a handheld explosives detection device. In this work the retention of some nitrated explosives and selectivity in reversed phase system as a function of mobile phase composition is studied while methanol, acetonitrile and acetone as an organic solvent is used. Best selectivity and good retention can be observed in methanol mobile phase. Acetonitrile and acetone are not suitable for fast isocratic separation of mixture containing pentaerythritol tetranitrate because of its strong retention. Efficiency and permeability of monolithic column (Chromolith CapRod RP-18e) and columns filled with superficially porous particles are compared (Kinetex 2,6 µm C-18, Poroshell 120 SB-C18). Monolithic column with satisfying efficiency and high column permeability is the most suitable solution for fast separation of explosives. Assuming use of explosives detection device in different conditions the separation was optimized on temperature 50 °C. Under these conditions the 35% v/v methanol gives good retention and selectivity. For very fast scan analysis of pentaerythritol tetranitrate or other nitroaromatics use of 70% v/v acetone mobile phase is suitable. Construction of miniaturized liquid chromatograph that enables preconcentration of explosives from aqueous solutions and fast separation in less than 1 minute is described. This concept will be incorporated into the handheld explosives detection device where the explosives vapor will be absorbed into the water and after the separation detected by chemiluminescence.
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Monolitická železobetonová konstrukce víceúčelové budovy / Cast-in-situ reinforced concrete structure of multi-functional buildingMravec, Jakub January 2012 (has links)
The work deals with the static solution of monolithic reinforced concrete multi-purpose building, which includes a design point - supported panel, columns, flaps, underground wall and base band. Assessment of these structures in terms od first critical state -carrying capacity.
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