Liu Hua. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2002. / Includes bibliographical references (leaves 139-143). / Abstracts in English and Chinese. / Table of Contents --- p.I / Acknowledgement --- p.VII / Abstract --- p.VIII / Abstract (Chinese) --- p.X / List of Tables --- p.XV / List of Figures --- p.XXIV / List Symbols and Abbreviations / Chapter Chapter One --- Introduction / Chapter 1.1. --- Rationale of study --- p.2 / Chapter 1.2. --- Drug Delivery to the lungs --- p.5 / Chapter 1.3. --- Particle transport and deposition mechanisms --- p.8 / Chapter 1.4. --- Factors affecting particulate interactions --- p.9 / Chapter 1.4.1. --- Particle size --- p.9 / Chapter 1.4.2. --- Particle shape --- p.10 / Chapter 1.4.3. --- Surface texture --- p.10 / Chapter 1.4.4. --- Surface energy --- p.11 / Chapter 1.4.5. --- Contact area --- p.12 / Chapter 1.4.6. --- Relative humidity --- p.12 / Chapter 1.4.7. --- Electrical properties --- p.13 / Chapter 1.5. --- Fine powder production technologies applicable to dry powder inhalation formulations --- p.13 / Chapter 1.5.1. --- Batch crystallization and micronization --- p.14 / Chapter 1.5.2. --- Spray drying --- p.15 / Chapter 1.5.3. --- Supercritical fluid crystallization --- p.17 / Chapter 1.6. --- Physical characterization of aerosol powders --- p.18 / Chapter 1.6.1. --- Microscopy and particle size analysis --- p.19 / Chapter 1.6.2. --- Powder X-ray diffractometry --- p.19 / Chapter 1.6.3. --- Thermal analysis --- p.20 / Chapter 1.6.4. --- In-vitro deposition assessment --- p.20 / Chapter 1.6.5. --- Surface energy measurement by inverse gas chromatography (IGC) --- p.21 / Chapter 1.7. --- Scope of study --- p.22 / Chapter Chapter Two --- Materials and Methods / Chapter 2.1. --- Materials --- p.25 / Chapter 2.2. --- Equipment --- p.25 / Chapter 2.3. --- Methods --- p.27 / Chapter 2.3.1. --- Determination of aqueous solubility of salbutamol sulphate in water --- p.27 / Chapter 2.3.2. --- Preparation of spray-dried salbutamol sulphate powders under different operating conditions --- p.27 / Chapter 2.3.3. --- Preparation of spray-dried salbutamol sulphate powders at various lecithin concentrations --- p.30 / Chapter 2.3.4. --- Preparation of spray-dried salbutamol sulphate powders at various oleic acid concentrations --- p.32 / Chapter 2.3.5. --- Physical characterization of spray-dried salbutamol sulphate powders --- p.34 / Chapter 2.3.5.1. --- Scanning electron microscopy --- p.34 / Chapter 2.3.5.2. --- Specific surface area determination --- p.34 / Chapter 2.3.5.3. --- Particle size distribution measurements --- p.35 / Chapter 2.3.5.4. --- Water content determination --- p.36 / Chapter 2.3.5.5. --- Isothermal water vapour sorption studies --- p.37 / Chapter 2.3.5.6. --- Powder X-ray diffraction --- p.37 / Chapter 2.3.5.7. --- Thermal analysis --- p.38 / Chapter 2.3.5.8. --- Surface energy measurement by inverse gas chromatography --- p.39 / Chapter 2.3.5.8.1. --- Calculation of surface thermodynamic parameters --- p.40 / Chapter 2.3.5.8.1.1. --- Standard Free Energy of Adsorption and Related Thermodynamic Parameters --- p.40 / Chapter 2.3.5.8.1.2. --- Dispersive Component of Surface Free Energy and Related Thermodynamic Parameters --- p.41 / Chapter 2.3.5.8.1.3. --- Specific Interactions and Associated Acid-Base Properties --- p.42 / Chapter 2.3.5.9. --- In-vitro deposition measurement by multi-stage liquid impinger --- p.43 / Chapter Chapter Three --- Results and discussion / Chapter 3.1. --- Influence of spray drying operating parameters --- p.46 / Chapter 3.1.1. --- Drying temperature --- p.46 / Chapter 3.1.1.1. --- "Particle size, particle morphology, and specific surface area" --- p.46 / Chapter 3.1.1.2. --- "Crystallinity, moisture sorption and thermal behaviour" --- p.53 / Chapter 3.1.1.3. --- Surface thermodynamic properties --- p.60 / Chapter 3.1.1.4. --- Aerodynamic properties and in-vitro deposition --- p.64 / Chapter 3.1.2. --- Feed solution concentration --- p.67 / Chapter 3.1.2.1. --- "Particle size, particle morphology and specific surface area" --- p.69 / Chapter 3.1.2.2. --- "Crystallinity, moisture sorption and thermal behaviour" --- p.69 / Chapter 3.1.2.3. --- Surfacethermodynamicproperties --- p.70 / Chapter 3.1.2.4. --- Aerodynamic properties and in-vitro deposition --- p.70 / Chapter 3.1.3. --- Feed speed --- p.72 / Chapter 3.1.3.1. --- "Particle size, particle morphology, and specific surface area" --- p.72 / Chapter 3.1.3.2. --- "Crystallinity, moisture sorption and thermal behaviour" --- p.73 / Chapter 3.1.3.3. --- Surfacethermodynamicproperties --- p.73 / Chapter 3.1.3.4. --- Aerodynamic properties and in-vitro deposition --- p.73 / Chapter 3.2. --- Influence of formulation additives --- p.78 / Chapter 3.2.1. --- Influence of lecithin as additive --- p.78 / Chapter 3.2.1.1. --- "Particle morphology, particle size and specific surface area" --- p.79 / Chapter 3.2.1.2. --- "Crystallinity, moisture sorption and thermal behaviour" --- p.84 / Chapter 3.2.1.3. --- Surfacethermodynamicproperties --- p.90 / Chapter 3.2.1.4. --- Aerodynamic properties and in-vitro deposition --- p.94 / Chapter 3.2.2. --- Influence of oleic acid as additive --- p.101 / Chapter 3.2.2.1. --- "Particle morphology, particle size and specific surface area" --- p.101 / Chapter 3.2.2.2. --- "Crystallinity, moisture sorption and thermal behaviour" --- p.106 / Chapter 3.2.2.3. --- Surfacethermodynamicproperties --- p.123 / Chapter 3.2.2.4. --- Aerodynamic properties and in-vitro deposition --- p.127 / Chapter Chapter Four --- Conclusion and Future Work / Chapter 4.1. --- Conclusion --- p.134 / Chapter 4.1.1. --- Influence of spray drying operating parameters --- p.134 / Chapter 4.1.2. --- Influence of formulation additives --- p.135 / Chapter 4.2. --- Future Work --- p.137 / References --- p.139

by Tai Fai Fok. / Thesis (Ph.D.)--Chinese University of Hong Kong, 1997. / Includes bibliographical references (p. 211-215). / Microfiche. Ann Arbor, Mich. UMI, 1998. 3 microfiches ; 11 x 15 cm.

Fusafungine is an antibiotic of fungal origin with a potent local anti-inflammatory action (German-Fattal, 1995; German-Fattal, 1996). It is administered locally to the nasal and pharyngeal mucosa by spray. It can be hypothesised that the anti-inflammatory action of fusafungine may decrease the development of mucosa! inflammation in such a manner that the incidence of symptoms of upper respiratory tract infection may be reduced if it is administered before, during and after completion of an ultramarathon. Furthermore, fusafungine could also reduce the risk of secondary bacterial infection. The potential value of fusafungine in reducing the symptoms of upper respiratory tract infections or the development of bacterial upper respiratory infection is the focus of this thesis.

by Lam Kuo. / Year shown on spine: 1997. / Thesis (M.Phil.)--Chinese University of Hong Kong, 1996. / Includes bibliographical references (leaves 107-121). / Acknowledgments / List of Abbreviations / Summary / List of Contents / List of Tables / List of Figures / Chapter Chapter 1 --- Introduction and the objectives of the study --- p.1-6 / Chapter Chapter 2 --- Overviews of Bronchopulmonary Dysplasia (BPD) and bronchodilator therapy -- a literature review --- p.7-29 / Chapter 2.1 --- Overview of Bronchopulmonary Dysplasia (BPD) --- p.7-9 / Chapter 2.2. --- Bronchodilator therapy --- p.10-18 / Chapter 2.2.1 --- Therapeutic value on infants with Bronchiolitis / Chapter 2.2.2. --- Therapeutic value on infants with Bronchopulmonary Dysplasia (BPD) / Chapter 2.3. --- "Three modes of aerosol delivery devices --jet nebuliser , ultrasonic nebuliser and metered dose inhaler" --- p.18-29 / Chapter 2.3.1. --- Jet nebuliser / Chapter 2.3.2. --- Ultrasonic nebuliser / Chapter 2.3.3. --- Metered dose inhaler / Chapter 2.3.4. --- Comparison of the therapeutic efficiency between jet nebuliser， ultrasonic nebuliser and Metered dose inhaler / Chapter 2.3.4.a. --- Comparison of particle size / Chapter 2.3.4.b. --- Comparison of aerosol deposition / Chapter 2.3.4.c. --- Comparison of pulmonary function / Chapter Chapter 3 --- Pulmonary function test in neonates --a literature review --- p.30-40 / Chapter 3.1. --- Overview of pulmonary function test in neonates --- p.30 / Chapter 3.2. --- Assessment of pulmonary function test in neonates --- p.31-40 / Chapter 3.2.1. --- Pulmonary mechanics / Chapter 3.2.1.a. --- Lung compliance / Chapter 3.2.1.b. --- Airway resistance / Chapter 3.2.1.c. --- Functional residual capacity (FRC) / Chapter Chapter 4 --- Subjects and methods --- p.41-48 / Chapter 4.1. --- Subjects --- p.41-42 / Chapter 4.2. --- Methods --- p.42-48 / Chapter 4.2.1. --- Delivery of Salbutamol aerosol / Chapter 4.2.1.1. --- Spontaneously breathing non-ventilated infants (group 1) / Chapter 4.2.1.2. --- Ventilator-dependent infants (group 2) / Chapter 4.2.2. --- Monitoring the clinical parameters / Chapter 4.2.3. --- Measurement of pulmonary function / Chapter 4.2.4. --- Statistics / Chapter Chapter 5 --- Results --- p.49-53 / Chapter 5.1. --- Clinical parameters --- p.50-51 / Chapter 5.2. --- Pulmonary function tests --- p.51-53 / Chapter Chapter 6 --- Discussion --- p.54-61 / Chapter 6.1. --- Non-ventilated group --- p.55-58 / Chapter 6.2. --- Ventilated group --- p.58-61 / Chapter Chapter 7 --- Conclusion --- p.62-63 / Tables and Figures / References

Chan, Pui. / "November, 2009." / Thesis (M.Phil.)--Chinese University of Hong Kong, 2010. / Includes bibliographical references (leaves 108-114). / Abstracts in English and Chinese. / Table of Contents --- p.i / Acknowledgement --- p.vi / Abstract --- p.vii / Abstract (Chinese) --- p.ix / Chapter Chapter One --- Introduction / Chapter 1.1. --- Pulmonary Route for Drug Delivery --- p.2 / Chapter 1.2. --- Factors Affecting the Performance of Inhaled Formulations --- p.3 / Chapter 1.2.1. --- Particle Aerodynamic Diameter --- p.4 / Chapter 1.2.2. --- Dispersibility of Particles --- p.5 / Chapter 1.2.3. --- Clearance Mechanism in Lung and Dissolution of Particles --- p.6 / Chapter 1.3. --- Production of Dry Powder Inhalation by Spray Drying --- p.7 / Chapter 1.4. --- Approaches to Enhance Aerosol Performance of Spray Dried Particles --- p.8 / Chapter 1.4.1 --- Porous/Hollow Particles --- p.9 / Chapter 1.4.2 --- Non-Porous Corrugated Particles --- p.10 / Chapter 1.4.3 --- Blends and Ternary Systems --- p.10 / Chapter 1.4.4 --- Surface Energy and Crystallinity Modification --- p.11 / Chapter 1.4.5 --- Other Approaches to Enhancing Aerosol Performance --- p.12 / Chapter 1.5 --- Objectives and Rationale of the Present Study --- p.13 / Chapter 1.6 --- Scope of Present Study and Particle Characterization Techniques Employed --- p.14 / Chapter 1.6.1 --- Microscopy and Particle Density Measurements --- p.14 / Chapter 1.6.2 --- Particle Size Analysis and Particle Dispersibility --- p.15 / Chapter 1.6.3 --- Thermal Analysis and Particle Crystallinity --- p.15 / Chapter 1.6.4 --- Particle Surface Characterization --- p.16 / Chapter 1.6.5 --- Inverse Gas Chromatography --- p.18 / Chapter 1.6.6 --- Fractal Analysis --- p.19 / Chapter 1.6.6.1 --- Background and Origin of Fractal Analysis --- p.19 / Chapter 1.6.6.2 --- Use of Fractal Analysis in Pharmaceutical Research --- p.20 / Chapter 1.6.6.3 --- Methods for fractal analysis --- p.21 / Chapter 1.6.7 --- Atomic Force Microscopy --- p.23 / Chapter 1.6.7.1 --- Background of Atomic Force Microscopy --- p.23 / Chapter 1.6.7.2 --- Characterization of Surface Topography by Atomic Force Microscopy --- p.23 / Chapter 1.6.7.3 --- Measurement of Interaction Forces by Colloid Probe 226}0Ø Microscopy --- p.25 / Chapter 1.6.7.4 --- Use of Atomic Force Microscopy in Pharmaceutical Research --- p.27 / Chapter Chapter Two --- Materials and Methods / Chapter 2.1. --- Materials --- p.30 / Chapter 2.2. --- Equipment --- p.31 / Chapter 2.3. --- Methods --- p.33 / Chapter 2.3.1. --- Powder Preparation --- p.33 / Chapter 2.3.1.1 --- Preparation of Salbutamol Sulphate Samples --- p.33 / Chapter 2.3.1.2 --- Preparation of Disodium Cromoglycate Samples --- p.33 / Chapter 2.3.1.3 --- Preparation of ß-Galactosidase (BG) Samples --- p.34 / Chapter 2.3.2. --- Determination of Aerosol Performance --- p.35 / Chapter 2.3.3. --- Determination of Protein Activity for BG Samples --- p.36 / Chapter 2.3.3.1. --- Enzyme Assay Procedure --- p.37 / Chapter 2.3.3.2. --- Calculation of Enzyme Activity --- p.38 / Chapter 2.3.3.3. --- Determination of Enzyme Activity Retained in Spray-dried Samples --- p.38 / Chapter 2.3.4. --- Physicochemical Characterization of Particles --- p.39 / Chapter 2.3.4.1. --- Scanning Electron Microscopy --- p.39 / Chapter 2.3.4.2. --- Particle Density Determination --- p.39 / Chapter 2.3.4.3. --- Particle Size Analysis --- p.40 / Chapter 2.3.4.4. --- Thermal analysis --- p.41 / Chapter 2.3.4.5. --- Powder X-ray Diffraction --- p.42 / Chapter 2.3.4.6. --- Surface Area Determination --- p.42 / Chapter 2.3.4.7. --- Surface Composition Characterization --- p.43 / Chapter 2.3.4.8. --- Surface Tension Measurement --- p.44 / Chapter 2.3.4.9. --- Inverse Gas Chromatography --- p.45 / Chapter 2.3.4.9.1. --- Calculation of Standard Free Energy of Adsorption --- p.46 / Chapter 2.3.4.9.2. --- Calculation of Dispersive Component of Surface Free Energy --- p.47 / Chapter 2.3.4.9.3. --- Determination of Specific Interactions and Associated Acid-Base Properties --- p.48 / Chapter 2.3.4.10. --- Fractal Analysis --- p.49 / Chapter 2.3.4.11. --- Atomic Force Microscopy --- p.49 / Chapter Chapter Three --- Results / Chapter 3.1. --- In vitro Aerosol Performance --- p.52 / Chapter 3.2. --- Enzyme Activity Retained in BG Samples --- p.55 / Chapter 3.3. --- Scanning Electron Microscopy (SEM) --- p.56 / Chapter 3.3.1. --- SEM of Salbutamol Sulphate Formulations --- p.56 / Chapter 3.3.2. --- SEM of DSCG Formulations --- p.59 / Chapter 3.3.3. --- SEM of BG Formulations --- p.61 / Chapter 3.4. --- Density Measurements --- p.65 / Chapter 3.4.1. --- Densities of Salbutamol Sulphate Formulations --- p.65 / Chapter 3.4.2. --- Densities of DSCG Formulations --- p.66 / Chapter 3.4.3. --- Densities of BG Formulations --- p.67 / Chapter 3.5. --- Particle Size Analysis by Laser Diffraction --- p.68 / Chapter 3.5.1. --- Volume Mean Diameter Measurements --- p.68 / Chapter 3.5.2. --- Particle Size Distributions and Dispersion Patterns of Formulations --- p.70 / Chapter 3.6. --- Thermal Analysis --- p.75 / Chapter 3.7. --- Powder X-ray Diffraction --- p.80 / Chapter 3.8. --- Surface Area Measurements --- p.84 / Chapter 3.9. --- Surface Composition Characterization --- p.85 / Chapter 3.9.1. --- Surface Composition of Salbutamol Sulphate Formulations --- p.85 / Chapter 3.9.2. --- Surface Composition of DSCG Formulations --- p.88 / Chapter 3.9.3. --- Surface Composition of BG/BSA Formulations --- p.89 / Chapter 3.10. --- Surface Tension Measurements --- p.91 / Chapter 3.11. --- Inverse Gas Chromatography --- p.92 / Chapter 3.12. --- Fractal Analysis --- p.93 / Chapter 3.13. --- Atomic Force Microscopy --- p.94 / Chapter Chapter Four --- Discussion / Chapter 4.1. --- Influence of BSA on Aerosol Performance and Protein Integrity --- p.98 / Chapter 4.2. --- Influence of BSA on Physicochemical Properties of Particles --- p.98 / Chapter 4.2.1. --- Influence of BSA on surface corrugation --- p.98 / Chapter 4.2.2. --- Influence of BSA on particle size and dispersion behavior --- p.99 / Chapter 4.2.3. --- Influence of BSA on crystallinity and thermal properties of particles --- p.100 / Chapter 4.2.4. --- Influence of BSA on surface energetics of particles --- p.100 / Chapter 4.3. --- Relationship between Surface Corrugation and Aerosol Performance --- p.101 / Chapter 4.4. --- Mechanism of Surface Modification for BSA on Spray-dried Particles --- p.103 / Chapter Chapter Five --- Conclusions and Future Work / Chapter 5.1. --- Conclusions --- p.106 / Chapter 5.1.1. --- General Aerosolization-Enhancing Effect of BSA --- p.106 / Chapter 5.1.2. --- Surface Modifying Effect of BSA --- p.106 / Chapter 5.1.3. --- Relationship between Surface Corrugation and Aerosol Performance --- p.106 / Chapter 5.2. --- Future Work --- p.107 / References --- p.108