
Advances in Polymers for Biomedical Applications
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Content
- Intro
- Contents
- Preface
- Acknowledgments
- Chapter 1
- Innovative Biopolymer Nano-Multilayered Films for Biomedical Applications: Fabrication and Physical Properties
- Abstract
- 1. Introduction
- 2. Results
- 2.1. Effect of the Substrate Properties on the PEMs Deposition
- 2.1.1. Degree of Crystallinity
- 2.1.2. Corona Polarity
- 2.1.3. Substrate Porosity
- 2.2. Methods of Deposition
- 2.3. Effect of pH and Ionic Strength on the PEMs Structure
- 2.4. Physical Properties of PEMs, Swelling, Mechanical Properties
- 2.4.1. Adhesion and Surface Free Energy of PEMs
- 2.4.2. Swelling
- 2.4.3. Mechanical Properties
- 2.5. Stability of PEMs at Different Environment Conditions
- 2.5.1. Stability of PEMs at Different Ionic Strength
- 2.5.2. Stability of PEMs at Different pH
- 2.5.3. Stability of PEMs at Different Temperature
- Conclusion
- Acknowledgment
- References
- Chapter 2
- Polymer Grafted Smart Mesoporous Silica Nanoparticles: Challenges and Advances in Controlled Drug Delivery Applications
- Abstract
- 1. Introduction
- 2. Synthesis of Mesoporous Silica Nanoparticles
- 3. Surface Functionalization of Mesoporous Silica Nanoparticles
- 4. Mechanism of Cellular Uptake of MSNs
- 5. Targeting Cancer Cells
- 5.1. Passive Targeting
- 5.2. Active Targeting
- 6. Biocompatibility and Biodegradation of Mesoporous Silica Nanoparticles
- 7. Surface Functionalization of MSNs with Polymers for Drug Delivery Applications
- 7.1. Surface Functionalization of MSNs with Synthetic Polymers for Targeted Drug Delivery
- 7.2. Surface Functionalization of MSNs with Natural Polymers for Targeted Drug Delivery
- 8. Carboxymethyl Cellulose Grafted Mesoporous Silica Nanoparticles (MSN-CMC)
- 8.1. Synthesis of Mesoporous Silica Nanoparticles
- 8.2. Synthesis of Carboxymethyl (CMC) Grafted Mesoporous Silica Nanoparticles (MSNs)
- 8.3. Synthesis of Curcumin Loaded MSN-CMC
- 8.4. In Vitro Cytotoxicity Assay
- 8.5. Intracellular Uptake of MSN Particles
- 8.6. Apoptosis by Annexin V-FITC PI Staining
- Conclusion
- Acknowledgments
- References
- Chapter 3
- Biodegradable Shape Memory Polyurethane and Its Nanocomposites for Biomedical Applications
- Abstract
- 1. Introduction
- 2. Shape Memory Polyurethanes (SMPUs)
- 3. Mechanism of Generation of Thermoresponsive Shape Memory Effects in Segmented Polyurethanes
- 4. Behavior and Performance of Shape Memory POLYURETHANES (SMPUs)
- 5. Shape Memory Polyurethanes Nanocomposites
- 6. Shape Memory Polyurethanes Nanocomposites for Biomedical Applications
- Conclusion
- Acknowledgments
- Références
- Chapter 4
- Advances in Polymers for Drug Delivery and Wound Healing Applications
- Abstract
- 1. Introduction
- 2. Chitosan (CS) Drug Delivery Systems
- 3. Polylactic Acid (PLA) Drug Delivery Systems
- 4. Polyethyleneglycol (PEG) Drug Delivery Systems
- 5. Polylactic-Co-Glycolic Acid (PLGA) Drug Delivery Systems
- 6. Molecularly Imprinted Polymer (MIP) Drug Delivery Systems
- 7. Smart Polymeric Drug Delivery Systems
- 8. DFT Computations on Drug Delivery Systems
- 8.1. Delivery of Anti-Hypertensive Hydrochlorothiazide Drug Using Ethyleneglycol
- 8.1.1. Computational Methods
- 8.1.2. Results and Discussion
- 8.1.2.1. Optimization and Energies of the Structures
- 8.1.2.2. NBO Analysis
- 8.1.2.3. QTAIM Analysis
- 8.1.2.4. NQR Analysis
- 8.1.3. Summary
- 8.2. MIP Drug Delivery Systems
- 9. CS Wound Healing Materials
- 10. PLA Wound Healing Materials
- 11. PEG Wound Healing Materials
- 12. PLGA Healing Materials
- Conclusion
- Acknowledgments
- References
- Chapter 5
- Modified Biopolymers and Its Potential Significance in Targeted Drug Delivery and Disease Diagnosis
- Abstract
- Introduction
- 1.1. Polysaccharide Based Biopolymers
- 1.1.1. Functional Modification: Cross Linking
- 1.1.2. Polyion-Complex
- 2. Chitosan
- 2.1. Modified Chitosan
- 2.2. Chitosan-Based Nano Medicines for Cancer Treatment
- 3. Alginate
- 3.1. Modified Alginates
- 3.2. Hybrid Microparticles
- 3.3. Hybrid Aerogels
- 3.4. Microcapsules
- 3.5. Alginate Hydrogel: Drug Delivery Applications
- 4. Dextran
- 4.1. Dextran Conjugates for Drug Delivery
- 4.2. Dextran as Drug Carrier
- 4.3. Modified Dextran
- 4.4. Dextran as Stimuli-Responsive Drug Carriers
- 4.5. Bioresponsive Drug Delivery System
- 4.6. Dextran Based Nanoparticles
- 4.7. Modified Biopolymers in Disease Diagnosis
- 5. Hyaluronic Acid
- 5.1. Modified Hyaluronic Acid
- 5.2. Functionalized HA Derivatives /Modifications in Hyaluronic Acid
- 5.3. Functional Modifications in Hyaluronic Acid
- 5.4. Smart Nanocarrier Based on PEGylated Hyaluronic Acid for Cancer Therapy
- 6. Heparin
- 6.1. Modified Heparin
- 6.2. Heparin Based Binary Drug Delivery Systems
- 6.3. Modified Heparin in Combination Therapy
- 6.4. Heparin Conjugated Nanoparticles for Drug Delivery
- Conclusion
- Acknowledgments
- References
- Chapter 6
- Validation of Nano Bis-Demethoxy Curcumin Analog (NBDMCA) as Adjuvants for Multidrug Resistant Infections
- Abstract
- 1. Introduction
- 1.1. Multidrug Resistance
- 1.2. Phytochemicals
- 1.3. Turmeric
- 1.3.1. Curcuminoids
- 1.3.2. Bisdemethoxy Curcumin Analog
- 2. Experimental Section
- 2.1. Materials
- 2.2. Measurements
- 2.3. Methods
- 2.3.1. Preparation of NBDMCA
- 2.3.2. Characterization of NBDMCA
- 2.3.2.1. Particle Size and Zeta Potential Measurement
- 2.3.2.2. Microscopic Imaging
- 2.3.2.3. Spectral Studies
- 2.4. Antimicrobial Screening
- 2.4.1. Agar Disc Diffusion Method
- 2.4.1.1. Medium
- 2.4.1.2. Inoculum
- 2.4.1.3. Method
- 2.4.2. Resazurin Based Antibacterial Activity
- 2.4.2.1. Minimal Inhibitory Concentration
- 2.4.2.2. Inoculum Preparation
- 2.4.2.3. Preparation of Resazurin Solution
- 2.4.2.4. Method
- 2.5. Visualization of Bacteria NBDMCA Interaction
- 2.5.1. Medium
- 2.5.2. Inoculum
- 2.5.3. Method
- 3. Results and Discussion
- 3.1. Characterisation of BDMCA
- 3.2. Anti-Bacterial Activity
- 3.3. Resazurin Assay
- 3.4. Visualization of Bacteria NBDMCA Interaction
- Conclusion
- References
- Chapter 7
- Plasma Functionalisation of Polycaprolactone Surface for Biomedical Applications
- Abstract
- 1. Introduction
- 2. Applications of PCL Based Scaffolds
- 2.1. Tissue Engineering
- 2.2. Bioimmobilization
- Conclusion
- References
- Chapter 8
- Advances in Directional Delivery of DNA and siRNA
- Abstract
- Introduction
- Advances in Directional Delivery of DNA and siRNA
- DNA Directional Delivery through Polymers
- Asymmetric Polyplex-Nanocapsules Loaded with Photosensitizer for Light Assisted Gene Transfer [11]
- Chitosan Nanoparticle Based Delivery of Fused NKG2D-IL-21 Gene Suppresses Growth of Colon Cancer in Mice
- PAMAM/DNA Dendriplex Coated with Hyaluronic Acid for Efficient Targeted Gene Delivery to Tumor Cells [25]
- Phenylboronic Acid-Sugar Grafted Polymer Construct as a Dual Stimuli-Responsive Gene Carrier for Targeted Anti-Angiogenic Tumor Therapy [39]
- siRNA Directional Delivery through Polymers
- Arginine Engrafted Biodegradable Polymer for the Systemic Delivery of siRNA for Gene Therapy Purposes
- Methods for Hepatocyte Specific Delivery of siRNA
- Targeted siRNA Delivery to Prevent Nitric Oxide Mediated Cell Death after Spinal Cord Injury
- Targeted siPLK1 Delivery Using Polymerosomes to Treat Lung Cancer
- References
- Chapter 9
- Chitosan Containing Biomaterials for Tissue Engineering Applications
- Abstract
- Abbreviations
- 1. Introduction
- 2. Chitosan Activities and Properties Useful for Applications in Tissue Engineering
- 3. Chitosan-Based Products Used in Tissue Engineering
- 3.1. 3D Chitosan-Based Scaffolds
- 3.1.1. Chitosan Hydrogels
- 3.1.1.1. Chitosan Hydrogels Formed by Physical Association
- 3.1.1.2. Chitosan Coordination Complexes
- 3.1.1.3. Polyelectrolyte Complexes (PEC)
- 3.1.1.4. Chemically Crosslinked Chitosan Hydrogels
- 3.1.1.5. Applications of the Chitosan Hydrogels
- 3.1.2. Chitosan Sponges
- 3.2. 2D Chitosan Scaffolds, Used for Wound Healing
- 3.2.1. Chitosan Films
- 3.2.2. Porous Membranes from Chitosan Nanofibers
- 3.2.3. Chitosan Membranes Used for Coating of the Titanium Surfaces
- 4. Chitosan Applications in Tissue Regeneration
- 4.1. Wound Healing
- 4.1.1. Chitosan Based Systems Used for Wound Healing
- 4.1.2. Chitosan-Based Adhesives for Tissues
- 4.1.3. Effects of the Chitosan Based Products, Evidenced by In Vitro and Preclinic Studies
- 4.1.4. Effects of the Chitosan Based Products Evidenced by Clinical Studies
- 4.1.5. Chitosan Based Dressings as Devices for Drug Release for Improving the Antimicrobial Effect and the Wound Healing Rate
- 4.1.5.1. Chitosan Used For Antimicrobial Drug Carriers
- 4.1.5.2. Chitosan Systems as Carriers of Growth Factors
- 4.1.5.3. Chitosan Systems Used as Carriers of Other Drugs
- 4.1.6. Other Systems Obtained from Chitosan and Hyaluronic Acid
- 4.2. Bone Tissue Engineering
- 4.2.1. Chitosan Scaffolds in Bone Tissue Engineering
- 4.2.2. Scaffolds for Bone Tissue Based on Chitosan Hydrogels
- 4.2.3. Chitosan/CNT Composites
- 4.2.4. Chitosan Blends and Composite Scaffolds
- 4.2.4.1. Physical Blends
- 4.2.4.2. Polyelectrolyte Complexes
- 4.2.4.3. Scaffolds Based on Chitosan-Calcium Phosphate Composites
- 4.2.4.3.1. Chitosan/Hydroxyapatite Composites (CS/HAp)
- 4.2.4.3.2. Chitosan/Calcium Phosphate Composites
- 4.2.4.3.3. Coating of the Chitosan Scaffolds with Calcium Phosphate
- 4.2.4.3.4. Multicomponent Chitosan-Based Scaffolds
- Conclusion
- References
- Chapter 10
- Dressing Materials Using Herbal Drugs for Better Wound Management
- Abstract
- 1. Introduction
- 2. Classification of Wounds
- 3. Phases of Wound Healing
- 3.1. The Inflammatory Phase
- 3.2. Proliferative Phase
- 3.3. Remodeling Phase
- 4. Wound Management
- 4.1. Advancement in Wound Dressing
- 5. Herbal Drugs with Wound Healing Activities
- 5.1. Herbal Drug Loaded Wound Dressings
- Conclusion
- References
- Chapter 11
- Stimuli-Responsive Hydrogels through Gamma Radiation Induced Graft Copolymerization of Hydrophilic Monomers onto Polymeric Films: For Biomedical Applications
- Abstract
- 1. Introduction
- 1.1. Hydrogels
- 2. Classifications of Hydrogels
- 2.1. Based on Physical and Chemical Composition
- 2.1.1. Homopolymeric Hydrogels
- 2.1.2. Copolymeric Hydrogels
- 2.1.3. Interpenetrating Polymer Network (IPN) Hydrogels
- 2.2. Based on the Presence of Ionic Charges on the Monomer
- 2.2.1. Non-Ionic Hydrogels
- 2.2.2. Ionic Hydrogels
- 2.2.2.1. Anionic Hydrogels
- 2.2.2.2. Cationic Hydrogels
- 3. Polyampholytic Hydrogels
- 3.1. Based on Their Physical Nature
- 3.1.1. Hydrogels Network Structures
- 3.1.2. Amorphous Hydrogels Structures
- 3.1.3. Semicrystalline Hydrogels Structures
- 3.1.4. Hydrogen Bonded Hydrogels Structures
- 3.2. Based on Response to the Environmental Factors
- 3.2.1. pH-Sensitive Polymer
- 3.2.2. Temperature-Sensitive Polymer
- 4. Applications of Hydrogels
- 4.1. Biomedical Applications of Hydrogels
- 4.1.1. Hydrogels Useful in Drug Delivery
- 4.1.2. Transdermal Delivery
- 4.1.3. Diffusion-Controlled Delivery Systems
- 4.2. Agricultural Applications
- 4.3. Environmental Applications
- 4.4. Dye Uptake
- 4.5. Other Applications
- 5. Challenges in the Field of Hydrogels
- 5.1. Hydrogels on Polymeric Surfaces
- 5.2. Graft-Copolymerization
- 5.3. Advantages of Grafting Method
- 5.4. Radiation Induced Graft Copolymerization
- 5.4.1. Controlling Factors of Graft Copolymerization
- 6. Methods of Radiation Grafting
- 6.1. Simultaneous Radiation Grafting Method (Direct or Mutual)
- 6.2. Pre-Irradiation Method
- 6.3. Per-Oxidation Grafting Method
- 6.4. Formation of Hydroperoxides
- 7. Applications
- 8. Future Directions
- Conclusion
- References
- Chapter 12
- Therapeutic Applications of Polymeric Hydrogels
- Abstract
- 1. Hydrogels
- 1.1. History of Hydrogels
- 1.2. Classification of Polymeric Hydrogels
- 1.3. Natural Polymer Based Hydrogels
- 1.3.1. Cellulose Based Hydrogels
- 1.3.2. Chitosan Based Hydrogels
- 1.3.3. Hyaluronic Acid Hydrogels
- 1.3.4. Dextran Hydrogels
- 1.3.5. Alginate Hydrogels
- 1.4. Synthetic Polymer Based Hydrogels
- 1.4.1. Poly(ethylene glycol) (PEG) and Poly (ethylene oxide) (PEO) Hydrogels
- 1.4.2. Poloxamer Hydrogels
- 1.4.3. Poly(hydroxyethyl methacrylate) pHEMA Hydrogels
- 1.4.4. Polyacrylamide (PAAm) Hydrogels and Its Derivatives
- 1.4.5. Polyvinyl Alcohol (PVA) Hydrogels
- 2. Polymeric Hydrogels and Therapeutics
- 2.1. Hydrogels in Drug Delivery
- 2.1.1. Polymeric Hydrogels Used for Colon-Targeted Drug Delivery
- 2.1.2. Mucoadhesive Polymeric Hydrogels for Buccal, Nasal and Ocular Drug Delivery
- 2.1.3. Polymeric Hydrogels as Floating Drug Delivery System for Gastric Delivery
- 2.2. Hydrogels for Sustained Delivery
- 2.3. Polymeric Hydrogels for Tissue Engineering
- 2.4. Polymeric Hydrogels Used for the Gene Therapy
- 3. General Mechanism of Drug Release from Polymeric Hydrogel
- Conclusion
- References
- Chapter 13
- Bioinspired Materials for Diagnostic Imaging Applications
- Abstract
- Introduction
- Polymer Nanoparticles
- Block Copolymers
- Liposomes
- References
- Chapter 14
- Recent Advances in Polymeric Drug Delivery Carrier Systems
- Abstract
- 1. Introduction
- 2. Polymers Used in Drug Delivery Carrier Systems
- 3. Poymeric Drug Delivery Carrier Systems
- Polymeric Microspheres
- Polymeric Nanoparticles
- Polymeric Vesicles
- Polymeric Micelles
- Polymer Drug Conjugates
- Dendrimers
- Polymeric Gels and Hydrogels
- Capsosomes
- 4. Responsive Polymeric Drug Delivery Carrier Systems
- 4.1. Responsive Systems Based on Temperature
- 4.2. Responsive Systems Based on pH
- 4.3. Responsive Systems Based on Redox Potential
- 5. General Mechanism of Drug Release from PDDCS
- Conclusion
- References
- Chapter 15
- Value Added Wound Healing Material of Cross Linked PVA-Alginate Network
- Abstract
- 1. Introduction
- 1.1. Wound-Type and Healing
- Hemostasis
- Inflammation
- Migration
- Proliferation
- Maturation or Remodelling
- 1.2. Wound Dressing
- 1.2.1. Traditional Wound Dressing
- 1.2.2. Advanced Wound Dressings
- Hydrogels
- Hydrocolloid Dressings
- Chitosan Dressings
- 1.3. Alginate-The Signature of Seaweed's Cell Wall
- 1.4. Electrospinning Creates Nano-Platform for Wound Healing Applications
- 1.5. Electrospinning of Alginate Is a Challenging Task
- 1.6. A Renowned co-Polymer Candidate - The Poly Vinyl Alcohol (PVA)
- 1.7. Citric Acid Is a Promising Choice of Cross Linker for Alginate
- 1.8. Calcium Alginate Is Advantageous Over Sodium Alginate
- 2. Materials and Methods
- 2.1. Chemicals and Equipments
- 2.2. Preparation of Alginate-PVA Blend
- 2.3. Electrospinning
- 2.4. Physiochemical Characterization of the Fibre Web
- 2.5. Moisture Vapour Transmission Rate
- 2.6. Thermogravimetric Analysis
- 2.7. Antibacterial Activity
- 3. Results and Discussion
- 3.1. The Web Morphology
- 3.2. The FTIR Spectral Peaks
- 3.3. Thermal Degradation Behaviour of Nanofibrous Web
- 3.4. Moisture Vapour Transmission Rate
- 3.5. Antibacterial Attribute of the Cross Linked PVA-Alginate Nanoweb
- 4. Summary
- Conclusion
- References
- About the Editors
- Index
- Blank Page
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