by Au Yuk Sin. / Thesis (M.Phil.)--Chinese University of Hong Kong, 1995. / Includes bibliographical references (leaves 100-113). / Chapter Chapter 1 --- Introduction / What is AIDS? --- p.1 / Situation in the World --- p.2 / Situation in Asia --- p.4 / Chapter Chapter 2 --- The AIDS Situation in Hong Kong --- p.8 / Historical Development of the AIDS Programme in Hong Kong --- p.8 / The Hong Kong AIDS Campaign (1987-1994) / Problem Definition Phase --- p.10 / Implementation Phase / Objectives --- p.11 / Targets --- p.12 / Channels --- p.12 / Media Package --- p.15 / Budget --- p.15 / Timing --- p.16 / Evaluation Phase / Non-Government Organisations (NGOs) / The Hong Kong AIDS Foundation --- p.16 / AIDS Concern / Hong Kong Ten Percent Club --- p.17 / The Horizons --- p.17 / The AIDS Trust Fund --- p.17 / Chapter Chapter 3 --- Theoretical Framework / Revised Protection Motivation Theory --- p.19 / Information / Persuasion Model --- p.22 / Review of Relevant Research Findings on Protection Motivation Theory --- p.24 / Chapter Chapter 4 --- Literature Review / Global Research on AIDS / Positive Results --- p.27 / Mixed Results --- p.28 / Minimal Effects --- p.30 / Evaluation of Research Findings --- p.31 / Local Research on AIDS / CNTA Survey (Wave II)(May 1987) --- p.32 / CNTA Survey (Wave III)(March 1988) --- p.32 / KABP Study (February 1992) --- p.33 / HKIPM Survey (February 1992) --- p.34 / Survey on the Effectiveness of the APIs on AIDS (November 1992) --- p.35 / Evaluation of the School Education Programmes on AIDS (September-December 1993) --- p.36 / Evaluation of Local Research --- p.37 / Chapter Chapter 5 --- Methodology / Design --- p.38 / Sample --- p.40 / Hypotheses --- p.41 / Measurement --- p.44 / Chapter Chapter 6 --- Findings --- p.46 / Chapter Chapter 7 --- Discussion --- p.62 / Chapter Chapter 8 --- Conclusion --- p.73 / Appendix 1 Tables --- p.77 / Appendix 2 Organisational Structure of Hong Kong's AIDS Programme1994 --- p.83 / Appendix 3 (a) Questionnaire (English) --- p.84 / Appendix 3 (b) Questionnaire (Chinese) --- p.92 / Appendix 4 Field Report --- p.99 / Bibliography --- p.100

Diss. (sammanfattning) Stockholm : Karolinska institutet, 2002. / Härtill 6 uppsatser.

Diss. (sammanfattning) Stockholm : Karol. inst., 2004. / Härtill 5 uppsatser.

Thesis (M.P.H.M.)--Mahidol University, 2000.

An immunoglobulin-fortified milk replacer and a subcutaneous (SC) injectable solution of immunoglobulins (Ig) were examined as methods of achieving passive immunity in neonatal calves. Bovine Ig, from abattoir blood, were purified by polyphosphate fractionation and ion-exchange chromatography. In experiment 1, carried out at Agriculture Canada Research Station, Agassiz, 37 colostrum-deprived Holstein-Friesian bull calves were allotted to one of four treatments. Col/WM calves were fed colostrum on day 1 and whole milk, days 2 - 42. MR-Nolg calves (control) were fed milk replacer with no Ig, days 1-42. MR-Hi/Lo calves were fed milk replacer with Ig at 50 mg/ml on day 1, and at 10 mg/ml, days 2 -21. MR-Hi/No calves were fed milk replacer with Ig at 50 mg/ml, day 1,'and with no Ig, days 2 - 21. From days 2 2 - 42, MR-Hi/Lo and MR-Hi/No treatment calves received milk replacer with no Ig. In experiment 2, carried out at the University Research Farm at Oyster River, 24 colostrum-deprived Holstein-Friesian bull calves were allotted to one of three treatments. The first two treatments were the same as for experiment 1, Col/WM and MR-Nolg fed for days 1-21. MR-Lo Inj calves were fed milk replacer with Ig at 10 mg/ml, days 1-21, and were also given a SC injection of Ig solution within the first 6 hours of life. For days 2-42, calves were fed WM or MR-Nolg, as per experiment 1. For both experiments, blood samples and calf weights were taken at birth, 24 & 48 hours of age, day 7 and weekly thereafter for six weeks. Diarrhea (scours) levels, rectal temperatures and general health of calves were recorded daily for the first three weeks as well. Experiment 1 survival at 6 weeks of age was 11 out of 11 calves for Col/WM treatment, 8 out of 8 calves for MR-Hi/Lo treatment, 7 out of 8 calves for MR-Hi/No and a significantly lower (P>0.05) 7 out of 9 calves for MR-Nolg. In experiment 2, survival was 7 out of 8 calves for both Col/WM and MR-Lo-Inj treatments and a significantly lower (P>0.05) 4 out of 8 calves for MR-Nolg treatment. Calves on MR-Hi/No had significantly higher diarrhea levels than the other three treatments over weeks one and four in experiment 1. In experiment 2, calves which did not receive any Ig had significantly higher diarrhea levels over weeks three and four than calves which received Ig. Experiment 1 average daily gains (ADG) were significantly higher for calves on Col/WM, MR-Hi/Lo and MR-Hi/No treatments than for calves on MR-Nolg at six weeks of age. In experiment 2, six week ADG were significantly higher for calves on Col/WM and MR-Lo Inj treatments than for MR-Nolg. For both experiments, serum Ig levels of calves on Col/WM were significantly higher than calves on the other treatments at 24 and 48 hours of age. MR-Hi/Lo, MR-Hi/No and MR-Lo Inj calves trended to higher serum Ig levels than MR-Nolg calves but were not significantly different. Calves which received Ig, from colostrum, the Ig-fortified milk replacer or a subcutaneous Ig injection, had higher survival rates, lower diarrhea levels, less antibiotic treatment and higher average daily gains than calves hot receiving any Ig. It was concluded that immunoglobulins, administered either orally or parenterally, are an effective, alternative method, for providing passive immunity in neonatal calves. / Land and Food Systems, Faculty of / Graduate

Bakgrund: Vårdrelaterad pneumoni är en av de vanligaste vårdrelaterade infektionerna inom svensk sjukvård. Att drabbas av vårdrelaterad pneumoni ökar risken för sjuklighet samt dödlighet. Munvård är en basal omvårdnadsåtgärd som sjuksköterskan ansvarar över. I dagsläget är munvård en åtgärd som genomförs för patientens välbefinnande snarare än som en preventiv åtgärd. När munvård inte utförs kan det leda till förändringar i munhålan som i sin tur ger ökad risk för pneumoni. Syfte: Att undersöka effekterna av munvård som prevention mot vårdrelaterad pneumoni hos patienter inlagda på sjukhus. Metod: En litteraturstudie baserad på åtta kvantitativa interventionsstudier. Databassökningen genomfördes i Cinahl och PubMed. Analysen genomfördes med hjälp av Popenoes analysmodell för att sedan sammanställas till ett resultat. Resultat: I sju av åtta studier minskade insjuknandet av vårdrelaterad pneumoni efter implementering av en munvårdsintervention. Konklusion: Det finns ett samband mellan minskat insjuknande i vårdrelaterad pneumoni och munvårdsinterventioner. För att fastställa munvårdens effekt mot vårdrelaterad pneumoni krävs vidare forskning. / Background: Hospital acquired pneumonia is one of the most common healthcare associated infections in Sweden. Suffering from hospital acquired pneumonia increases the risk of morbidity and mortality. Oral care is basic nursing care. Oral care is often considered a comfort arrangement in caring for patients, rather than a preventive one. The risk of pneumonia increases due to changes in the oral cavity which is a cause of not receiving oral care. Aim: To investigate the effects of oral care as prevention of hospital acquired pneumonia in patients admitted to hospitals. Methods: The analysis was conducted using Popenoe's analysis model. Eight quantitative studies were analyzed, which were identified in the databases PubMed and Cinahl. Using Popenoe´s model a result could be concluded. Results: The analysis of the eight studies presented a decreased incidence of hospital acquired pneumonia in seven studies after an implementation of an oral care intervention. Conclusion: It was found to be a relationship between reduction in the incidence of hospital acquired pneumonia and oral care intervention. In order to determine the effect of oral care due to hospital acquired pneumonia, supplementary research is required.

by Lam Tin Lun. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2000. / Includes bibliographical references (leaves 131-151). / Abstracts in English and Chinese. / Acknowledgment --- p.I / Table of content --- p.II / List of Tables --- p.IX / List of Figures --- p.XI / Abbreviation --- p.XIII / Abstract --- p.XIV / 論文摘要 --- p.XVI / Chapter CHAPTER 1 --- INTRODUCTION --- p.1 / Chapter 1.1 --- Acquired immunodeficiency syndrome (AIDS) --- p.1 / Chapter 1.1.1 --- History of AIDS --- p.1 / Chapter 1.1.2 --- Definition of AIDS --- p.2 / Chapter 1.1.3 --- HIV/AIDS Around the World --- p.4 / Chapter 1.1.4 --- HIV/AIDS in Hong Kong --- p.4 / Chapter 1.1.4.1 --- Hong Kong AIDS Update --- p.4 / Chapter 1.1.4.2 --- AIDS Transmission --- p.6 / Chapter 1.1.4.3 --- Main AIDS Complications Occur in Hong Kong --- p.6 / Chapter 1.2 --- Human Immunodeficiency Virus (HIV) --- p.7 / Chapter 1.2.1 --- Classification of HIV --- p.7 / Chapter 1.2.2 --- The Structure of HIV Virion --- p.9 / Chapter 1.2.3 --- The HIV Genome --- p.11 / Chapter 1.2.4 --- The Life Cycle of HIV --- p.12 / Chapter 1.2.4.1 --- Invasion of the Cells --- p.12 / Chapter 1.2.4.2 --- Integration into cell genome --- p.13 / Chapter 1.2.4.3 --- Protease and assembly to the virus --- p.13 / Chapter 1.2.5 --- Three Essential Enzymes for HTV-1 Replication --- p.16 / Chapter 1.2.5.1 --- HIV-1 Reverse Transcriptase (HIV-1 RT) --- p.16 / Chapter 1.2.5.2 --- HIV-1 Integrase (HIV-1 IN) --- p.17 / Chapter 1.2.5.3 --- HIV-1 Protease (HIV-1 PR) --- p.18 / Chapter 1.2.6 --- The Different Stages of HIV Infection --- p.19 / Chapter 1.3 --- AIDS therapy --- p.23 / Chapter 1.3.1 --- Drugs Approved by US Food and Drug Administration (FDA) --- p.23 / Chapter 1.3.2 --- Vaccine --- p.26 / Chapter 1.3.3 --- Chemokine Receptor Inhibitor --- p.27 / Chapter 1.3.4 --- Antisense Oligonucleotides Therpay --- p.28 / Chapter 1.3.5 --- Traditional Chinese Medicine (TCM) --- p.29 / Chapter 1.4 --- Objective of My Project --- p.32 / Chapter CHAPTER 2 --- SCREENING OF TRADITIONAL CHINESE MEDICINAL PLANTS FOR HIV-1 PROTEASE INHIBITION --- p.33 / Chapter 2.1 --- Introduction --- p.33 / Chapter 2.2 --- Materials and Methods --- p.35 / Chapter 2.2.1 --- Materials --- p.35 / Chapter 2.2.2 --- Extraction Methods --- p.36 / Chapter 2.2.2.1 --- Aqueous Extraction --- p.36 / Chapter 2.2.2.2 --- Methanol Extraction --- p.37 / Chapter 2.2.3 --- Preparation of Recombinant HIV-1 Protease --- p.37 / Chapter 2.2.3.1 --- Selection of Appropriate Clone --- p.37 / Chapter 2.2.3.2 --- Large-scale Expression of Recombinant HIV-1 Protease --- p.38 / Chapter 2.2.2.3 --- Purification of Recombinant HIV-1 Protease by DEAE Sepharose CL-6B Chromatography --- p.38 / Chapter 2.2.3.4 --- Purification of Recombinant HIV-1 Protease by Mono-S Cation Chromatography --- p.39 / Chapter 2.2.3.5 --- Refolding of Purified Recombinant HIV-1 Protease --- p.40 / Chapter 2.2.3.6 --- Protein Concentration Determination --- p.41 / Chapter 2.2.3.7 --- Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE) --- p.41 / Chapter 2.2.4 --- Characterization of HTV-1 Protease --- p.42 / Chapter 2.2.4.1 --- HIV-1 PR Fluorogenic Assays --- p.42 / Chapter 2.2.4.2 --- HIV-1 PR Assay by Reverse Phase HPLC Separation of Cleavage Products of the Synthetic Peptide Substrate --- p.43 / Chapter 2.3 --- Results --- p.44 / Chapter 2.3.1 --- Functional Analysis of Recombinant HIV-1 PR Activity --- p.44 / Chapter 2.3.2 --- Screening of Crude Extracts for Inhibition of HIV-1 PR Activity --- p.48 / Chapter 2.4 --- Discussion --- p.53 / Chapter CHAPTER 3 --- ISOLATION AND CHARACTERIZATION OF ACTIVE CONSTITUENTS FROM METHANOL EXTRACTS OF WOODWARDIA UNIGEMMATA AGAINST HIV-1 PROTEASE --- p.56 / Chapter 3.1 --- Introduction --- p.56 / Chapter 3.2 --- Materials and Methods --- p.57 / Chapter 3.2.1 --- Materials --- p.57 / Chapter 3.2.2 --- Methods --- p.58 / Chapter 3.2.2.1 --- Methanol Extraction --- p.58 / Chapter 3.2.2.2 --- Removal of Tannins --- p.60 / Chapter 3.2.2.3 --- Glucosidase Digestion --- p.60 / Chapter 3.2.2.4 --- Analytical Thin Layer Chromatographic (TLC) --- p.61 / Chapter 3.2.2.5 --- A cid Hydrolysis --- p.62 / Chapter 3.2.2.6 --- Electrospray Mass Spectrometry --- p.62 / Chapter 3.2.2.7 --- Dose-response Curve --- p.63 / Chapter 3.2.2.8 --- Kinetic Studies --- p.63 / Chapter 3.2.2.9 --- Activity of the HPLC-purified principle (s) on Other Aspartyl Proteases --- p.63 / Chapter 3.3 --- Results --- p.66 / Chapter 3.3.1 --- Purification of Methanol Extracts of Woocdwardia unigemmata --- p.66 / Chapter 3.2.2 --- Removal of Tannins --- p.70 / Chapter 3.2.3 --- Glucosidase Digestion --- p.73 / Chapter 3.2.4 --- Acid Hydrolysis --- p.73 / Chapter 3.2.5 --- Analytical Thin Layer Chromatography --- p.74 / Chapter 3.2.6 --- Electrospray Mass Spectrometry --- p.80 / Chapter 3.2.7 --- Dose-response Inhibition of HIV-1 Protease --- p.80 / Chapter 3.2.8 --- Kinetic Studies --- p.85 / Chapter 3.2.9 --- Effects of HPLC-purified Active Principle on Other Aspartyl Proteases --- p.87 / Chapter 3.3 --- Discussion --- p.89 / Chapter CHATPER 4 --- IDENTIFICATION OF SELECTIVE RNA APTAMERS AGAINST HIV-1 PROTEASE BY SYSTEMATIC EVOLUTION OF LIGANDS BY EXPONENTIAL ENRICHMENT (SELEX) --- p.95 / Chapter 4.1 --- Introduction --- p.95 / Chapter 4.2 --- Materials and Methods --- p.101 / Chapter 4.2.1 --- Materials --- p.101 / Chapter 4.2.2 --- Methods --- p.102 / Chapter 4.2.2.1 --- PCR Amplification for the Generation of a Double-Stranded DNA Library --- p.103 / Chapter 4.2.2.2 --- Preparation of RNA Pools --- p.104 / Chapter 4.2.2.3 --- In vitro Selection of RNA Ligands --- p.104 / Chapter 4.2.2.4 --- Reverse Transcription Reaction of Selected RNA --- p.108 / Chapter 4.2.2.5 --- Cloning of the Amplified cDNA pools --- p.108 / Chapter 4.2.2.6 --- Subcloning of the digested DNA product into pBluescript® IIKS (-) --- p.108 / Chapter 4.2.2.8 --- RNA Labeling with Digoxigenin (DIG) --- p.109 / Chapter 4.2.2.9 --- Binding Affinity of RNA Ligands for HIV-1 PR --- p.109 / Chapter 4.2.2.10 --- Competition Binding Reactions --- p.111 / Chapter 4.2.2.11 --- HIV-1 PR Inhibitory Activities of the Selected RNA Ligands --- p.112 / Chapter 4.3 --- Results --- p.113 / Chapter 4.3.1 --- In Vitro Selection of RNA Ligands --- p.113 / Chapter 4.3.2 --- Sequences of RNA Ligands --- p.114 / Chapter 4.3.3 --- Binding Affinity of RNA Ligands --- p.114 / Chapter 4.3.4 --- Inhibitory Activity of RNA Ligands --- p.119 / Chapter 4.4 --- Discussion --- p.122 / Chapter CHAPTER 5 --- GENERAL DISCUSSION --- p.128 / REFERENCES --- p.132

Thesis (Ph.D.)--Memorial University of Newfoundland, 2002. / Restricted until October 2003. Bibliography: leaves 148-161.

No description available.

Diss. (sammanfattning) Stockholm : Karolinska institutet, 2006. / Härtill 4 uppsatser.