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应答型杂化纳米给药系统用于肿瘤诊疗的研究

摘要第3-8页
ABSTRACT第8-9页
Chapter 1 Literature Review第13-39页
    1.1 Nanotheranostics第13-22页
        1.1.1 Introduction of nanotheranostics第14-15页
        1.1.2 Nanotheranostics in therapy第15-18页
        1.1.3 Nanotheranostics in imaging第18-22页
    1.2 Stimulate Responsive Nanocarriers第22-29页
        1.2.1 Exogenous and endogenous stimulus responsive nanocarriers第22-27页
        1.2.2 Organic pH responsive nanocarriers第27-28页
        1.2.3 Inorganic pH responsive nanocarriers第28-29页
    1.3 MRI Guided Nanocarrier System第29-31页
        1.3.1 T_1 contrast agents第29-30页
        1.3.2 T_2 contrast agents第30页
        1.3.3 Progress of MRI contrast agents第30-31页
    1.4 Drug and Imaging Agent Loading Methods of Nanotheranostics第31-36页
        1.4.1 Covalent drug and imaging agent delivery systems第32-33页
        1.4.2 Non-covalent drug and imaging agent delivery systems第33-34页
        1.4.3 Hybrid drug and imaging agent delivery systems第34页
        1.4.4 Imaging agent as drug carrier第34-36页
    1.5 Novelty and Significance of This Project第36-39页
Chapter 2 Synthesis of Camptothecin Phosphonates第39-51页
    2.1 Introduction of camptothecin第39-40页
    2.2 Materials and Instruments第40-42页
        2.2.1 Materials第40-41页
        2.2.2 Instruments第41-42页
    2.3 Synthesis and Characterization of Camptothecin Phosphonate第42-47页
        2.3.1 Synthesis of camptothecin phosphonate(CPT-P)第42-43页
        2.3.2 Characterization of camptothecin phosphonate第43-45页
        2.3.3 Results and discussion第45-47页
    2.4 Synthesis and Characterization of Camptothecin Diphosphonate第47-51页
        2.4.1 Synthesis of camptothecin diphosphonate(CPT-2P)第47-48页
        2.4.2 Characterization of camptothecin diphosphonate第48页
        2.4.3 Results and discussion第48-51页
Chapter 3 Preparation and Characterization of Hybrid Nanocarriers第51-81页
    3.1 Materials and Instruments第52-54页
        3.1.1 Materials第52-53页
        3.1.2 Instruments第53-54页
    3.2 Preparation of Hybrid Nanocarriers第54-55页
    3.3 The Optimization of Hybrid Nanocarriers第55-64页
        3.3.1 The measurement of drug loading content第55-59页
        3.3.2 The hydrodynamic diameters of different hybrid nanocarriers第59-61页
        3.3.3 The serum stability of different types of hybrid nanocarriers第61-63页
        3.3.4 Results and discussion第63-64页
    3.4 Characterization of Hybrid Nanocarrier第64-68页
        3.4.1 The storage stability of hybrid nanocarrier第64-65页
        3.4.2 The morphology of hybrid nanocarriers第65-66页
        3.4.3 Determination of Mn~(2+) content in hybrid nanocarriers第66-68页
        3.4.4 Results and discussion第68页
    3.5 In Vitro CPT-2P and Mn~(2+) Release第68-74页
        3.5.1 In vitro CPT-2P release第68-70页
        3.5.2 In vitro Mn~(2+) release第70-72页
        3.5.3 Results and discussion第72-74页
    3.6 In Vitro MRI Analysis第74-76页
        3.6.1 In vitro MR relaxivity measurements第74-75页
        3.6.2 Results and discussion第75-76页
    3.7 Determination of ICG Loading in Hybrid Nanocarriers第76-81页
        3.7.1 The preparation of LMnP/ICG-CPT-2P hybrid nanocarriers第76页
        3.7.2 The fluorescent sensor(ICG)loading content第76-81页
Chapter 4 In Vitro Study of Hybrid Nanocarriers第81-91页
    4.1 Materials and Instruments第81-82页
        4.1.1 Materials第81-82页
        4.1.2 Instruments第82页
    4.2 In Vitro Cytotoxicity第82-86页
        4.2.1 The preparation of sample solution第83-84页
        4.2.2 Results and discussion第84-86页
    4.3 Cellular Uptake第86-88页
        4.3.1 The procedure of cellular uptake test第86-87页
        4.3.2 Results and discussion第87-88页
    4.4 Hemocompatibility Analysis第88-91页
        4.4.1 The procedure of hemocompatibility analysis第88-89页
        4.4.2 Results and discussion第89-91页
Chapter 5 In Vivo Study of Hybrid Nanocarriers第91-103页
    5.1 Materials and Instruments第91-92页
        5.1.1 Materials第91-92页
        5.1.2 Instruments第92页
    5.2 In Vivo MRI Measurements第92-95页
        5.2.1 Establishment of mouse breast cancer model第92-93页
        5.2.2 The procedure of in vivo MRI analysis第93页
        5.2.3 Results and discussion第93-95页
    5.3 Biodistribution and Pharmacokinetics第95-97页
        5.3.1 The experiment of biodistribution and pharmacokinetics第95-96页
        5.3.2 Results and discussion第96-97页
    5.4 In Vivo Antitumor Efficacy第97-103页
        5.4.1 In vivo antitumor efficacy study第97-99页
        5.4.2 Histopathological and apoptosis analysis第99-101页
        5.4.3 Results and discussion第101-103页
Chapter6 Conclusion and Prospect第103-107页
    6.1 Conclusion第103-105页
    6.2 Prospect第105-107页
Reference第107-117页
Notes on publications and participation in scientific research第117-119页
Acknowledgements第119-120页

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