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依托氧气低温等离子体方法制备可用于疝修复的β-环糊精改性PP抗菌补片材料

Abstract第5-7页
摘要第8-11页
Acknowledgements第11-18页
List of Abbreviations第18-23页
Chapter 1 Introduction第23-33页
    1.1 Problem of statements第25-26页
    1.2. Goals and objectives第26页
    1.3. Innovation points第26-27页
    1.4. Limitations第27页
    1.5. Outline of the thesis第27-29页
    References第29-33页
Chapter 2 Reviews of literature第33-61页
    2.1 Textile fundamentals第33-35页
    2.2 Currently available implants for hernia repair第35-39页
        2.2.1 Composite implants第35-37页
        2.2.2 Synthetic meshes第37-39页
    2.3 Physical properties of meshes第39-44页
        2.3.1 Mesh weight第39-40页
        2.3.2 Mesh pore shape, pore size and porosity第40-43页
        2.3.3 Mesh shrinkage after implantation第43-44页
    2.4. Mechanical properties第44-45页
        2.4.1 Mesh bursting strength第44页
        2.4.2 Mesh elasticity and strength第44-45页
    2.5 Current methods of mesh implantation第45-46页
    2.6 Mesh infection and its prevention during implantation第46-47页
    2.7 Surface modification of polypropylene meshes to prevent mesh infection第47-48页
    2.8 Surface modification of PP fibers with cold oxygen plasma treatment第48-49页
    2.9 Cyclodextrins and its complexes with triclosan and levofloxacin第49-50页
    References第50-61页
Chapter 3 Surface modifications of polypropylene hernia mesh materials with ?-cyclodextrin and triclosan via cold oxygen plasma: characterization and antibacterial properties第61-88页
    3.1 Introduction第61-63页
    3.2 Experimental第63-64页
        3.2.1 Materials第63页
        3.2.2 Cold plasma surface functionalization第63页
        3.2.3 Incorporation of β- cyclodextrin (CD&HDI)第63-64页
        3.2.4 Loading of triclosan第64页
    3.3 Characterization第64-68页
        3.3.1 SEM, EDX and AFM第64页
        3.3.2 FTIR第64页
        3.3.3 XRD第64页
        3.3.4 Water contact angle第64-65页
        3.3.5 Thermal analysis第65页
        3.3.6 Antibacterial activity assessment第65-66页
        3.3.7 Drug release of triclosan loaded samples.第66页
        3.3.8 Statistical analysis第66-68页
    3.4 Results and discussions第68-82页
        3.4.1 Surface modification of PP meshes第68页
        3.4.2 Surface morphology of PP meshes第68-71页
        3.4.3 Characterization of β-cyclodextrin and triclosan on modified PP meshes.第71-74页
        3.4.4 Water contact angle第74-76页
        3.4.5 Polymer structure and thermal properties第76-78页
        3.4.6 Antibacterial activity第78-80页
        3.4.7 In-vitro drug release from coated PP meshes第80-82页
    3.5 Summary第82页
    References第82-88页
Chapter 4 Preparation of β-cyclodextrin incorporated PP mesh materials: captured levofloxacin HCL for antimicrobial properties第88-103页
    4.1 Introduction第88-89页
    4.2. Experimental第89-92页
        4.2.1 Materials第89页
        4.2.2 Surface functionalization第89-90页
        4.2.3 CD incorporation第90页
        4.2.4 Levofloxacin HCL loading第90页
        4.2.5 Drug release of levofloxacin HCL loaded samples:第90-92页
    4.3 Results and discussions第92-100页
        4.3.1 Surface modification and loading of levofloxacin第92页
        4.3.2 Surface morphology of CD coated and levofloxacin loaded meshes第92-94页
        4.3.3 Element analysis of coated meshes第94-95页
        4.3.4 FTIR analysis of modified meshes第95页
        4.3.5 Antibacterial activity of modified PP meshes第95-98页
        4.3.6 Drug release from levofloxacin loaded meshes第98-100页
    4.4 Summary第100页
    References第100-103页
Chapter 5 Controlled drug release and antibacterial properties of PP mesh materials grafted with β-cyclodextrin and captured triclosan第103-125页
    5.1 Introduction第103-105页
    5.2 Experimental第105-106页
        5.2.1 Materials第105页
        5.2.2 Two- grafting steps (PP-HDI-CD incorporation)第105-106页
        5.2.3 Loading of triclosan第106页
    5.3 Results and discussions第106-120页
        5.3.1 Cyclodextrin grafting and loading of triclosan第106-108页
        5.3.2 Surface morphology of PP meshes第108-111页
        5.3.3 Characterization of HDI, CD, and triclosan on modified PP mesh第111-113页
        5.3.4 Hydrophilicity of PP meshes (Water contact angle)第113-115页
        5.3.5 Structural and thermal properties第115-116页
        5.3.6 Antibacterial activity第116-119页
        5.3.7 Kinetics of drug release第119-120页
    5.4 Summary第120-121页
    References第121-125页
Chapter 6 Controlled levofloxacin HCL release and antibacterial properties of covalently bonded β-cyclodextrin polypropylene mesh materials for hernia repair第125-145页
    6.1 Introduction第125-128页
    6.2 Experimental第128-129页
        6.2.1 Materials第128页
        6.2.2 Two steps grafting HDI -CD onto PP mesh.第128页
        6.2.3 Loading of levofloxacin HCL第128-129页
    6.3 Results and discussions第129-140页
        6.3.1 Cyclodextrin grafting and levofloxacin HCL loading:第129-131页
        6.3.2 Surface morphology and roughness of PP meshes devices第131-132页
        6.3.3 Characterization of modified PP meshes第132-135页
        6.3.4 Antibacterial activity第135-139页
        6.3.5 Release of levofloxacin from CD modified meshes第139-140页
    6.4 Summary第140-141页
    References第141-145页
Chapter 7 Conclusions and future suggestions第145-150页
    7.1 Conclusions第145-147页
        7.1.1 Conclusion 1第145-146页
        7.1.2 Conclusion 2第146页
        7.1.3 Conclusion 3第146页
        7.1.4 Conclusion 4第146-147页
        7.1.5 Conclusion 5第147页
    7.2 Future work第147-149页
        7.2.1 Surface modification of small and medium pore size PP meshes with different shapes第148页
        7.2.2 Mechanical tests第148页
        7.2.3 Cell culture experiments第148页
        7.2.4 In vivo animal tests第148-149页
    References第149-150页
Findings of Publications第150-151页

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