دسترسی نامحدود
برای کاربرانی که ثبت نام کرده اند
برای ارتباط با ما می توانید از طریق شماره موبایل زیر از طریق تماس و پیامک با ما در ارتباط باشید
در صورت عدم پاسخ گویی از طریق پیامک با پشتیبان در ارتباط باشید
برای کاربرانی که ثبت نام کرده اند
درصورت عدم همخوانی توضیحات با کتاب
از ساعت 7 صبح تا 10 شب
ویرایش: 1st ed. 2023
نویسندگان: Keerti Jain (editor). N. K. Jain (editor)
سری:
ISBN (شابک) : 9819905370, 9789819905379
ناشر: Springer
سال نشر: 2023
تعداد صفحات: 417
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 11 مگابایت
در صورت تبدیل فایل کتاب Multifunctional And Targeted Theranostic Nanomedicines: Formulation, Design And Applications به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب نانومیدیکین های ترونوستیک چند منظوره و هدفمند: فرمولاسیون ، طراحی و برنامه ها نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
Preface Contents 1: Functionalized Targeted Theranostic Nanomedicines 1.1 Introduction 1.2 Design of Nanotheranostic 1.3 Therapy in Nanotheranostic 1.3.1 Drug Therapy 1.3.2 Gene Delivery 1.3.3 Photodynamic Therapy 1.3.4 Photothermal Therapy 1.4 Nanotheranostic for Imaging 1.4.1 Optical Imaging 1.4.2 Magnetic Resonance Imaging 1.4.3 Computed Tomography 1.4.4 Ultrasound Imaging 1.5 Different Types of Nanotheranostics 1.5.1 Superparamagnetic Iron Oxide Nanoparticles 1.5.2 Gold 1.5.3 Carbon Nanomaterials 1.5.4 Graphene Oxide 1.5.5 Polymeric Nanoparticles 1.5.6 Polymeric Micelles 1.5.7 Liposome 1.6 Regulatory Aspects 1.7 Conclusion References 2: Designing of Smartly Functionalized Theranostic Nanomedicines 2.1 Introduction 2.2 Approaches for Functionalization of Theranostic Nanoparticles 2.2.1 Functionalization of Nanoparticles Using Small Molecule Ligands 2.2.2 Bio-functionalization of Nanoparticles 2.2.2.1 Nucleic Acids 2.2.2.2 Enzymes 2.2.2.3 Peptides 2.2.2.4 Carbohydrates 2.2.2.5 Antibodies 2.3 Methods for Functionalization of Nanoparticles 2.3.1 Covalent Strategies 2.3.1.1 Click-Chemistry Reaction 2.3.1.2 EDC Coupling Reaction 2.3.1.3 Maleimide Coupling 2.3.2 Non-covalent Strategies 2.3.2.1 Ionic Interaction 2.3.2.2 Hydrophobic Coupling 2.4 Conclusion and Future Perspectives References 3: Theranostic Applications of Functionalized Vesicular Carriers 3.1 Introduction 3.2 Functionalized Nanovesicular Carriers 3.3 Liposomes 3.4 Niosomes 3.5 Exosomes 3.6 Disease-Based Study of Theranostic Vesicular Carriers 3.7 Vesicular Carrier System as Imaging Agents 3.8 Toxicity Concerns Related to Nanovesicular Carrier Systems 3.9 Conclusion and Future Perspective References 4: Theranostic Applications of Functionalized Polymeric Nanoparticles 4.1 Introduction 4.2 Composition 4.3 Types of Theranostic Polymers 4.3.1 Internal Stimuli 4.3.2 External Stimuli 4.4 Theranostic Applications of Functionalized Polymeric Nanoparticles 4.4.1 Application in Bioimaging 4.4.2 Optical Imaging 4.4.3 Ultrasound Imaging 4.4.4 Magnetic Resonance Imaging 4.4.5 Photoacoustic Imaging 4.4.6 X-Ray Computed Tomography 4.4.7 Radionuclide Imaging 4.4.8 Radioactive Polymeric Nanoparticles for Imaging and Therapy 4.4.9 Application in Infectious Diseases 4.5 Conclusion References 5: Functionalized Metallic Nanoparticles: Theranostic Applications 5.1 Introduction 5.2 Metal Nanoparticles 5.2.1 Magnetic Nanoparticles 5.2.2 Gold Nanoparticles 5.2.3 Silver Nanoparticles 5.2.4 Up-conversion Nanoparticles 5.3 Functionalization of Metal Nanoparticles 5.3.1 Surface Coating with Mesoporous Silica Nanoparticles 5.3.2 Functionalization with Stimuli-Responsive Polymer 5.4 Properties of Metal Nanoparticles 5.4.1 Physical Properties 5.4.2 Chemical Properties 5.5 Theranostic Applications of Metal Nanoparticles 5.5.1 Drug Delivery 5.5.2 Imaging 5.6 Conclusions References 6: Functionalized Lipidic Nanoparticles: Smartly Engineered Lipidic Theragnostic Nanomedicines 6.1 Introduction 6.1.1 Overview on Smartly Engineered Nanolipid-Based Theranostics 6.1.2 Surface Functionalization Approaches for Programmed Theranostics 6.1.2.1 PEGylation 6.1.2.2 Ligand Functionalized Nanolipidic Theranostics 6.2 Nanolipidic Carriers as Theranostic Systems 6.2.1 Liposomes 6.2.2 Solid Lipid Nanoparticles (SLN) 6.2.3 Lipid Nanoparticles (LNPs) or Lipid-Drug Conjugates 6.2.4 Nanostructured Lipid Carriers (NLCs) 6.3 Biofate of Functionalized Nanolipidic Theranostics 6.3.1 Impact of Particle Size 6.3.2 Impact of Surface Charge 6.3.3 Impact of Hydrophobicity 6.4 Limitations and Challenges of Nanolipidic Theranostics 6.5 Conclusion and Future Prospects References 7: Functionalized Nanoemulsions: Could Be a Promising Approach for Theranostic Applications 7.1 Introduction 7.2 Functionalized Nanoemulsion: Recent Development and Drug Delivery Opportunity 7.3 Functionalized Nanoemulsions Utilized for Theranostic Applications: Contemporary Research 7.3.1 Utilization of Theranostic Nanoemulsion in Different Conditions of Cancers 7.3.2 Utilization of Theranostic Nanoemulsion in Inflammatory Conditions of Disease 7.4 Author Opinion and Future Directions References 8: Functionalized Dendrimers: Promising Nanocarriers for Theranostic Applications 8.1 Introduction 8.2 Dendrimer-Based Molecular Imaging 8.2.1 Dendrimer-Based MRI 8.2.2 Dendrimer-Based CT 8.2.3 Dendrimer-Based SPECT/PET 8.2.4 Dendrimer-Based FOI 8.3 Application of Dendrimer-Based Theranostic System 8.3.1 Nanotheranostic-Assisted Chemotherapy 8.3.2 Nanotheranostic-Assisted Photothermal Therapy 8.3.3 Nanotheranostic-Assisted Gene Therapy 8.3.4 Nanotheranostic-Assisted Photodynamic Therapy 8.4 Conclusion References 9: Functionalized Carbon Nanotubes, Graphene Oxide, Fullerenes, and Nanodiamonds: Emerging Theranostic Nanomedicines 9.1 Introduction 9.2 Carbon-Based Nanomaterials and Theragnosis 9.3 Synthesis and Functionalization of Carbon Nanomaterials 9.3.1 Carbon Nanotubes 9.3.1.1 Single-Walled Carbon Nanotubes (SWCNTs) 9.3.1.2 Multiple-Walled Carbon Nanotubes (MWCNTs) 9.3.2 Synthesis of Carbon Nanotubes (CNTs) 9.3.2.1 Arc Discharge Techniques 9.3.2.2 Laser Ablation Method 9.3.2.3 Chemical Vapor Deposition 9.3.2.4 Synthesis of CNTs by Thermal Decomposition Method 9.3.3 Functionalization of Carbon Nanotubes 9.3.4 Synthesis and Functionalization of Graphene Oxide 9.3.5 Synthesis and Functionalization of Fullerene 9.3.6 Synthesis and Functionalization of Carbon Nanodiamond 9.4 Theranostic Application of Carbon-Based Nanocarriers 9.4.1 Carbon Nanotubes 9.4.2 Graphene 9.4.3 Fullerenes 9.4.4 Carbon Nanodiamonds 9.5 Future Outlook References 10: Quantum Dots: Functionalization and Theranostic Applications 10.1 Introduction 10.2 Properties of Quantum Dots 10.3 Methods of Preparation 10.3.1 Top-Down Approaches 10.3.1.1 Electrochemical/Chemical Oxidation 10.3.1.2 Laser Ablation 10.3.1.3 Ultrasonic Treatment 10.3.1.4 Arc Discharge (ACD) 10.3.2 Bottom-up Approaches 10.3.2.1 Hydrothermal/Solvothermal Synthesis 10.3.2.2 Microwave-Assisted Synthesis 10.3.2.3 Thermal Decomposition 10.3.2.4 Pyrolysis 10.4 Functionalization of Quantum Dots 10.4.1 Non-covalent Binding 10.4.2 Covalent Binding 10.4.2.1 Conjugation with Carboxyl-Containing QDs 10.4.2.2 Conjugation with Amine-Containing QDs 10.4.2.3 Conjugation with Hydroxyl- or Aldehyde-Containing QDs 10.4.2.4 Conjugation with Thiol-Containing QDs 10.5 Role of Quantum Dots in Drug Delivery 10.5.1 Cancer 10.5.2 Neurodegenerative Disorders 10.5.2.1 Alzheimer´s Disease (AD) 10.5.2.2 Parkinson´s Disease 10.5.3 Infectious Diseases 10.5.4 Gene Delivery 10.6 Safety and Toxicity Perspectives of Quantum Dots 10.7 Clinical Status of Quantum Dots 10.8 Current Challenges and Future Aspects 10.9 Conclusion References 11: Functional Nanogels and Hydrogels: A Multipronged Nanotherapy in Drug Delivery and Imaging 11.1 Introduction 11.2 Hydrogels 11.2.1 Hydrogel Classification 11.2.1.1 Source 11.2.1.2 Configuration 11.2.1.3 Depending on the Cross-Linking Type 11.2.1.4 Based on the Electrical Charge 11.2.1.5 Based on the Method of Preparations 11.2.2 Technologies Adopted in Hydrogel Synthesis 11.2.2.1 Inverse-Suspension Polymerization 11.2.2.2 Graft Polymerization 11.2.2.3 Bulk Polymerization 11.2.2.4 Solution Polymerization or Cross-Linking 11.2.2.5 Suspension Polymerization or Inverse-Suspension Polymerization 11.2.2.6 Grafting to a Support 11.2.2.7 Polymerization by Irradiation 11.2.3 Properties of Hydrogel 11.2.4 Theranostic Applications of Hydrogels 11.2.4.1 Active and Passive Drug Delivery 11.2.4.2 Elimination of Dyes and Heavy Metal Ions (Chelating Agent) 11.2.4.3 Scaffolds in Tissue Engineering 11.2.4.4 Contact Lenses 11.2.4.5 Sensors for pH 11.2.4.6 Biosensors 11.2.4.7 Spinal Cord Damage Treated with Injectable Hydrogel 11.2.4.8 Supercapacitor Hydrogels 11.3 Nanogels 11.3.1 Nanogel Synthesis Methodologies 11.3.2 Nanogels´ Properties 11.3.2.1 Biocompatibility and Degradability 11.3.2.2 Elevated Drug Encapsulation Potential 11.3.2.3 Particle Size 11.3.2.4 Solubility 11.3.2.5 Electromobility 11.3.2.6 Colloidal Consistency 11.3.2.7 Non-immunologic Response 11.3.2.8 Others 11.3.3 Categories of Nanogel 11.3.3.1 On the Basis of Response Nonresponsive Nanogels Stimuli-Responsive Nanogel 11.3.3.2 On the Basis of Linkage Physically Cross-Linked Nanogel Liposome-Modified Nanogels Micellar Nanogels Hybrid Nanogel Chemically Cross-Linked Nanogel 11.3.4 Nanogel Uses in Theranostics 11.3.4.1 Nanogel as Therapeutic Drug Transporter 11.3.4.2 Nanogel as Imaging and Diagnosing Tool 11.4 Conclusion References 12: Theranostic Applications of Functionalized Exosomes 12.1 Introduction 12.2 Origin of Exosomes 12.2.1 Macrophage Derived 12.2.2 Tumor Derived 12.2.3 Mesenchymal Stem Cell (MSC) Derived 12.3 Isolation of Exosomes 12.3.1 Ultracentrifugation 12.3.2 Size-Based Filtration 12.3.3 Polymer Precipitation 12.3.4 Immunoaffinity Capture-Based Isolation 12.3.5 Microfluidic-Based Separation 12.3.6 Isolation Using Commercial Kits 12.4 Characterization of Exosomes 12.4.1 Transmission Electron Microscopy (TEM) 12.4.2 Nanoparticle Tracking Analysis (NTA) 12.4.3 Atomic Force Microscopy (AFM) 12.4.4 Dynamic Light Scattering (DLS) 12.4.5 Resistive Pulse Sensing (RPS) 12.4.6 Flow Cytometry 12.5 Functionalization 12.5.1 Click Chemistry/Covalent Modification 12.5.2 Genetic Engineering 12.6 Applications 12.6.1 Theranostic in Brain Disorders 12.6.2 Theranostic in Cancer 12.6.3 Theranostic in CVS 12.6.4 Exosomes in Skin 12.7 Conclusion References 13: Theranostic Applications of Functionalized Polymeric Micelles 13.1 Introduction 13.1.1 Hydrophilic Block 13.1.2 Core Shell 13.2 Micelle Stability and Critical Micelle Concentration (CMC) 13.3 Advantages of Micelles 13.4 Primary Classification of Micelles 13.4.1 Lipid-Based Micelles 13.4.2 The Reverse Micelles 13.4.3 Polymer-Based Micelles 13.5 Polysaccharide-Based Drug Delivery System of Polymeric Micelles 13.6 Features of Polymeric Micelles 13.6.1 Applications of Polymeric Micelles 13.6.2 Enhancement of Bioavailability of Polymeric Micelles 13.6.2.1 Protection of Drugs from GIT 13.6.2.2 Controlled Release of Drug 13.6.2.3 Increasing the Drug Residence Time in GIT 13.6.3 Use of Polymeric Micelles 13.6.3.1 Targeted Drug Delivery 13.6.3.2 Colonic Drug Delivery 13.6.3.3 Ocular Targeted Drug Delivery 13.6.3.4 Targeted Cancer Treatment 13.6.3.5 Diagnostics of Polymeric Micelles 13.7 Theranostics 13.8 Theranostic Use of Polymeric Micelles in Various Diseases 13.8.1 Cancer Theranostics 13.8.1.1 Passive Targeting Enhanced Permeability and Retention (EPR) Effect 13.8.1.2 Active Targeting 13.8.2 Theranostic Applications of Polymeric Micelles in Cancer 13.8.2.1 In Hepatocellular Carcinoma 13.8.2.2 In Breast Cancer 13.8.2.3 In Colorectal Cancer 13.8.2.4 Lung Carcinoma 13.8.3 Biodegradable Polymeric Micelles in Cancer Theranostic 13.8.4 Multifunctional Micelles in Cancer Theranostic 13.8.5 Theranostic Applications of Polymeric Micelles in Diabetes 13.8.6 Theranostic Applications of Polymeric Micelles in Neurodegenerative Disorder 13.8.7 Theranostic Application of Polymeric Micelles in AIDS 13.8.8 Theranostic Application of Polymeric Micelles in Atherosclerosis 13.8.9 Theranostic Application of Polymeric Micelles in Arthritis 13.9 Diagnostic and Imaging Application of Micelles 13.9.1 Optical Imaging 13.9.2 Fluorescent Imaging 13.9.3 The Magnetic Resonance Contrast Agent 13.9.4 X-Ray Computed Tomography 13.9.5 Imaging and Radionuclide-Based Therapy Agents 13.10 Polymeric Micelles as a Prodrug Theranostic 13.11 Polymeric Micelles in Clinical Trial till 05/04/2022 13.12 Conclusion and Future Perspectives References 14: Functionalized Nanocrystals and Theranostic Applications 14.1 Introduction 14.2 Types of Nanocrystals 14.2.1 Chitin and Chitosan 14.2.2 Quantum Dot 14.2.3 Colloidal Nanocrystals 14.2.4 Cellulose Nanocrystal and Nanofibres 14.3 Preparation of Nanocrystals 14.3.1 Top-Down Techniques 14.3.1.1 Media Milling (Nanocrystals) 14.3.1.2 High-Pressure Homogenization (IDD-Ps, DissoCubess, and Nanopure) 14.3.2 Bottom-up Techniques 14.4 Stability 14.4.1 Functionalization of Nanocrystals 14.5 Theranostic Applications of Nanocrystals in Various Diseases. 14.5.1 Cancer 14.5.2 Cardiovascular Disease 14.5.2.1 Atherosclerosis 14.5.2.2 Thrombosis 14.5.2.3 Myocardial Infarction 14.5.2.4 Vascular Injury and Restenosis 14.5.3 Neurodegenerative Disorders 14.5.3.1 Alzheimer´s Disease (AD) 14.5.3.2 Parkinson´s Disease (PD) 14.5.3.3 Prion Disease 14.6 Advantages of Theranostic Nanocrystals 14.7 Challenges and Future Goals References 15: Theranostics Applications of Functionalized Magnetic Nanoparticles 15.1 Introduction 15.2 Synthesis and Functionalization of MNPs 15.2.1 Superparamagnetic Iron Oxide Nanoparticles (SPIONs) 15.2.2 Coated MNPs 15.2.3 MNPs with Improved Magnetic Response 15.2.4 Combination of Magnetic and Au NPs 15.2.5 Monodisperse MNPs 15.2.6 Controlling Surface Functionality Via Surface-Initiated Polymerization 15.3 Applications of Theragnostic Nanoparticles 15.3.1 Applications in Cancer 15.3.2 Theranostics Applications of Magnetic Nanoparticles in Neurodegenerative Disorders 15.3.3 Treatment of Secondary Interventions and Infectious Diseases 15.3.4 MNPs and Targeted Drug Delivery 15.3.4.1 Modification for Tumor Targeting 15.3.4.2 Therapeutic Viruses 15.3.4.3 Nucleic Acid and Protein Delivery 15.3.4.4 Cell-Based Therapies 15.3.5 Targeted Magnetic Nanoparticle for Multimodal Diagnostics 15.3.6 Imaging 15.3.6.1 Photoacoustic Imaging 15.3.6.2 Fluorescence Imaging 15.4 Recent Medicinal Applications of Gold-Coated Iron Oxide Nanoparticles 15.5 Conclusion References 16: Functionalized Mesoporous Silica-Based Nanoparticles for Theranostic Applications 16.1 Introduction 16.2 Basic Structure and Properties 16.3 Introduction of Mesoporous Families 16.3.1 M41S Family 16.3.1.1 MCM-41 16.3.1.2 MCM-48 16.3.1.3 SBA-15 16.3.1.4 SBA-16 16.3.2 PMO Family 16.3.3 ORMOSIL Family 16.3.4 Hollow Family (H-MSN) 16.4 Composition and Method of Preparation 16.4.1 Sol-Gel Method 16.4.2 Microwave-Assisted Technique 16.4.3 Chemical Etching Technique 16.4.4 Template-Assisted Technique 16.4.4.1 Hard Templating Method 16.4.4.2 Soft Templating Method 16.4.5 Effect of Physical Parameters on the Formation of MSNs 16.5 Surface Modification of MSNs 16.5.1 Co-Condensation Method 16.5.2 Post-Grafting Method 16.5.3 Imprint Coating Strategy 16.5.3.1 Physical Targeting or Passive Targeting Composition and Surface Charge Size and Shape 16.5.3.2 Functionalization of MSNs for Active Targeting Functionalized MSNs with Antibodies Functionalized MSNs with Peptides and Transferrins Functionalized MSNs with Aptamers Functionalized MSNs with Vitamins Functionalized MSNs for Stimuli-Sensitive Drug Delivery 16.6 Stimuli-Responsive Drug Release 16.6.1 Internal Stimuli-Responsive Drug Delivery 16.6.1.1 pH as Endogenous Stimuli 16.6.1.2 Redox Potential as Internal Stimuli 16.6.1.3 Enzymatic Degradation as Internal Stimuli 16.6.2 External Stimuli-Responsive Drug Delivery 16.6.2.1 Thermoresponsive as Stimuli 16.6.2.2 ATP-Responsive Drug Delivery 16.6.2.3 H2O2-Responsive Drug Delivery 16.6.2.4 Magnetic Field-Responsive Drug Delivery 16.7 Therapeutic Applications of MSNs 16.7.1 Neurodegenerative Disorder 16.7.2 Cancer Therapy 16.7.3 MSN-Mediated Nanofiber Scaffolds 16.8 Theranostic Applications 16.8.1 Diagnostic Application of MSNs 16.8.2 Magnetic Resonance Imaging 16.8.3 Optical Imaging 16.8.4 Other Imaging Modalities 16.9 Conclusions and Future Outlook References