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Characteristics of Artemether Loaded PLGA Microparticles Fabricated by the Coaxial Electrospray:Validation of Enhanced Encapsulation Efficiency and Bioavailability

ABSTRACT第7页
CHAPTER 1 INTRODUCTION第15-29页
    1.1 MALARIA第15-23页
        1.1.1 DESCRIPTION第15-16页
        1.1.2 HISTORY & ETIOLOGY第16-17页
        1.1.3 MODE OF TRANSMISSION第17-18页
        1.1.4 LIFE CYCLE OF PLASMODIUM PARASITES第18-19页
        1.1.5 SYMPTOMS第19页
        1.1.6 DIAGNOSIS第19-21页
        1.1.7 CONVENTIONAL TREATMENT AND NANOMEDICINE FOR MALARIATREATMENT第21-23页
    1.2 ARTEMETHER第23-26页
        1.2.1 CHEMISTRY & STRUCTURE第24页
        1.2.2 MECHANISM OF ACTION第24-25页
        1.2.3 PHARMACOKINETIC第25页
        1.2.4 CLINICAL USES/THERAPEUTIC INDICATIONS第25页
        1.2.5 DOSAGE第25页
        1.2.6 AVAILABLE FORMS/FORMULATIONS第25-26页
        1.2.7 ADVERSE EFFECTS第26页
        1.2.8 CAUTIONS & CONTRAINDICATIONS第26页
        1.2.9 INTERACTIONS第26页
        1.2.10 LIMITATIONS/DRAWBACKS第26页
    1.3 POLY LACTIC-CO-GLYCOLIC ACID(PLGA)第26-29页
CHAPTER 2 ELECTROSPRAY METHOD第29-39页
    2.1 SINGLE-AXIAL ELECTROSPRAY第29-31页
        2.1.1 CHARGED DROPLETS THEORY第30-31页
        2.1.2 EQUIPMENT USED FOR SINGLE-AXIAL ELECTROSPRAY SYSTEM第31页
    2.2 COAXIAL ELECTROSPRAY METHOD第31-39页
        2.2.1 MODES OF COAXIAL ELECTROSPRAY第33页
        2.2.2 THE STABLE CONE-JET MODE第33-34页
        2.2.3 PROCESS PARAMETERS第34-39页
            2.2.3.1 INFLUENCE OF LIQUID FLOW RATE ON CONE-JET MODE第34-35页
            2.2.3.2 INFLUENCE OF VOLTAGE APPLIED ON CONE-JET MODE第35页
            2.2.3.3 LIQUID PROPERTIES第35页
            2.2.3.4 SURFACE TENSION第35-36页
            2.2.3.5 VISCOSITY第36页
            2.2.3.6 ELECTRICAL CONDUCTIVITY第36-37页
            2.2.3.7 RELATIVE PERMITIVITY第37页
            2.2.3.8 DENSITY第37页
            2.2.3.9 NEEDLE SIZE AND ELETRODE CONFIGURATION第37-38页
            2.2.3.10 SCALING LAWS第38-39页
CHAPTER 3 CHARACTERISTICS OF ARTEMETHER LOADED PLGAMICROPARTICLES FABRICATED BY COAXIAL ELECTROSPRAY:VALIDATION OF ENHANCED ENCAPSULATION EFFICIENCY ANDBIOAVAILABILITY第39-55页
    3.1 CES EXPERIMENTAL SETUP AND FABRICATION OFMICROPARTICLES第40-42页
    3.2 MATERIALS AND METHODS第42-46页
        3.2.1 MATERIAL第42页
        3.2.2 METHODS第42页
        3.2.3 MORPHOLOGICAL CHARACTERIZATION第42-46页
            3.2.3.1 SCANNING ELETRON MICROSCOPY第42页
            3.2.3.2 CON FOCAL LASER SCANNING MICROSCOPY第42页
            3.2.3.3 MEASUREMENT AND SIZE DISTRIBUTION第42-43页
            3.2.3.4 DIFFERLNTIAL SCANNING CALORIMETRY第43页
            3.2.3.5 DEERMINATION OF LOADING RATE AND ENCAPSULATION EFFICIENY第43页
            3.2.3.6 IN VITRO DRUG RELEASE第43-44页
            3.2.3.7 LIQUIAD CHROMATOGRAPIIY-MASS SPECTROSCOPY第44页
            3.2.3.8 CELL CULTURE AND MAINTENANCE第44页
            3.2.3.9 CYTOTOXICITY第44-45页
            3.2.3.10 IN VIVO PHARMACOKINETICS STUDY OF ARTEMETHER LOADED PLGA MPsBY LC-MS第45-46页
            3.2.3.11 STATISTICAL ANALYSIS第46页
    3.3 RESULT AND DISCUSSION第46-55页
        3.3.1 FABRICATION OF ARTEMETHER LOADED PLGA MICROPARTICLES第46-47页
        3.3.2 CHARACTERIZATION OF ARTEMETHER LOADED PLGA MICROPARTICLES第47-48页
        3.3.3 FORMATION OF CORE-SHELL STRUCTURE第48-49页
        3.3.4 DIFFERENTIAL SCANNING CALORIMETRY (DSC)第49-50页
        3.3.5 ENCAPSULATION EFFICIENCY AND CYTOTOXICITY第50-51页
        3.3.6 IN VITRO RELEASE PROFILE OF ARTEMETHER IN ARTEMETHER LOADEDPLGA MICROPARTICLES第51页
        3.3.7 PHARMACOKINETIC STUDY OF ARTEMETHER LOADED PLGA-MPS INADULT WISTAR RATS第51-53页
        3.3.8 CONCLUSION第53-55页
CONCLUSIONS AND FUTURE WORK第55-57页
REFERENCES第57-64页
ACKNOWLEDGEMENTS第64-65页
ACADEMIC PAPERS第65页

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