Chitosan is a rather abundant material with exquisite properties, which may be processed into a variety of materials including hydrogels, fibres, membranes, etc. The production of chitosan-based nanogels, also known as macromolecular miceles, has been successfully achieved using different techniques
Colloidal Nanoparticles: Functionalization for Biomedical Applications
β Scribed by Jana, Nikhil R
- Publisher
- Chapman and Hall/CRC
- Year
- 2019
- Tongue
- English
- Leaves
- 157
- Category
- Library
No coin nor oath required. For personal study only.
β¦ Table of Contents
Content: Cover
Half Title
Title Page
Copyright Page
Contents
Preface
Acknowledgments
Author
Chapter 1: Application Potential of Nanoparticles and Importance of Functionalization
1.1 INTRODUCTION
1.2 WHY NANOPARTICLES?
1.3 WHY FUNCTIONALIZATION?
1.4 WHY SELECTED NANOPARTICLES AND SELECTED METHODS?
REFERENCES
Chapter 2: Design Considerations of Nanoparticle Functionalization
2.1 INTRODUCTION
2.2 SIZE
2.3 SHAPE
2.4 COMPOSITION AND PHYSICAL PROPERTIES
2.5 BIOCOMPATIBILITY AND BIODEGRADABILITY
2.6 HYBRID AND MULTIFUNCTIONAL NANOPARTICLES
2.7 WATER SOLUBILITY AND COLLOIDAL STABILITY 2.8 SURFACE CHEMISTRY, CHARGE AND LIPOPHILICITY2.9 BIOFUNCTIONALITY
2.10 NONSPECIFIC INTERACTION
2.11 CONTROLLING NANOPARTICLE MULTIVALENCY
REFERENCES
Chapter 3: Chemical Synthetic Methods of Selected Nanoparticles
3.1 INTRODUCTION
3.2 Au NANOPARTICLES
3.2.1 Citrate-Capped Au (3-4 nm)
3.2.2 Citrate-Capped Au (12-20 nm)
3.2.3 Surfactant-Capped Hydrophilic Au Nanoparticles via Seeding Growth (5-50 nm)
3.2.4 Weakly Adsorbed Surfactant-Capped Hydrophobic Au Nanoparticles (2-5 nm)
3.2.5 Thiol-Capped Hydrophobic Au (2-6 nm)
3.3 Au NANORODS 3.3.1 Au Nanorods via Seedless Approach (5-10 nm Γ 20-50 nm)3.3.2 Au Nanorods via Seeding Growth Approach (10-20 nm Γ 20-100 nm)
3.4 Ag NANOPARTICLES
3.4.1 Citrate-Capped Ag (20-30 nm)
3.4.2 Surfactant- and Thiol-Capped Hydrophobic Ag Nanoparticles (2-5 nm)
3.5 Ag-CAPPED Au (Ag@Au) NANOPARTICLES (25-30 nm)
3.6 HYDROPHOBIC CdSe-ZnS QUANTUM DOTS (2-6 nm)
3.7 HYDROPHOBIC Mn-DOPED ZnS AND Mn-DOPED ZnSeS NANOPARTICLES (4-5 nm)
3.8 FLUORESCENT CARBON NANOPARTICLES
3.8.1 Hydrophilic Carbon Nanoparticles (10-Β50 nm) with Blue-Green Emission 3.8.2 Hydrophobic Carbon Nanoparticles with Yellow-Red Emission (3-10 nm)3.9 HYDROPHOBIC IRON OXIDE NANOPARTICLES (5-25 nm)
3.10 HYDROPHOBIC ZnO NANOPARTICLES (5 nm)
3.11 HYDROPHOBIC HYDROXYAPATITE NANORODS/NANOWIRES (2-5 nm Γ 10-1000 nm)
3.12 HYDROPHOBIC TIO. 2. NANORODS (2-3 nm Γ 25-35 nm)
3.13 N, F-CODOPED HYDROPHOBIC TIO. 2. NANOPARTICLES (150-225 nm)
3.14 COLLOIDAL GRAPHENE OXIDE VIA MODIFIED HUMMER'S METHOD
3.15 POLYASPARTIC ACID MICELLES (25-100 nm)
3.16 POLY(LACTIC-CO-GLYCOLIC ACID) NANOPARTICLES AND DRUG-LOADED NANOPARTICLES (100-500 nm)
3.17 LIPOSOME VESICLES (10-25 nm) 3.18 ALBUMIN NANOPARTICLES (100 nm)References
Chapter 4: Selected Coating Chemistry for Water-Soluble, Core-Shell-Type Nanoparticles with Cross-Linked Shells
4.1 INTRODUCTION
4.2 SILICA COATING
4.2.1 Hydrophilic Au Nanoparticles (4-5 nm) with Primary Amine Termination
4.2.2 Hydrophilic Ag Nanoparticles (4-5 nm) with Primary Amine Termination
4.2.3 Hydrophilic Iron Oxide Nanoparticles (5 nm) with Primary Amine Termination
4.2.4 Hydroxyapatite Nanorods with Primary Amine Termination
4.2.5 Primary Amine-Terminated Magnetic Mesoporous Silica Nanoparticles (50-100 nm)
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