Chapter
1.2.2 Mucoadhesive composites
1.2.3 Hydrogel and inorganic composites
1.2.4 Theranostic composites
2 - Redox-responsive hydrogels
2.2 Preparation of redox-responsive poly(amido amine)s
2.2.1 Synthesis of PEGylated hyperbranched poly(amido amine)s
2.2.2 Synthesis of thermoresponsive hyperbranched poly(amido amine)s
2.3 Redox-responsive hydrogels
2.3.1 Redox-responsive poly(amido amine) hydrogels
2.3.2 Other redox-responsive hydrogels
2.4 Redox-responsive nanogels/microgels
2.4.1 Redox-responsive poly(amido amine) nanogels/microgels from emulsion with surfactants
2.4.2 Redox-responsive poly(amido amine) nanogels/microgels from emulsion without surfactants
2.4.3 Redox-responsive nanogels/microgels from thermoresponsive poly(amido amine)s
2.4.4 Other redox-responsive nanogels/microgels
3 - Stimuli-responsive guar gum composites for colon-specific drug delivery
3.2 Drug delivery applications of guar gum composites
3.2.1 pH-responsive composites
3.2.2 Thermoresponsive guar gum composites
3.2.3 Cross-linked guar gum composites
3.2.4 Graft polymerization
4 - Biopolymer-based nanocomposites for transdermal drug delivery
4.1.1 Metered dose transdermal spray
4.1.2 Historical perspectives
4.1.3 Barriers to transdermal drug delivery: lead from skin pathophysiology
4.1.4 Biopolymers for transdermal drug delivery: formulation prerequisites
4.1.5 Biopolymer-based composites versus synthetic polymers
4.2 Biopolymer-based nanocomposites used in transdermal drug delivery: technologies and applications
4.2.1 Lipidic biopolymer-based nanosystems
4.2.3 Transdermal patches
4.3 Biopolymer-based systems under clinical investigation
4.4 Updates on patents and regulatory aspects of TDD
4.5 Innovations and future prospects in TDD
5 - Composites of hydrogels and nanoparticles: a potential solution to current challenges in buccal drug delivery
5.2 Potential of BDD systems in medicine and dentistry
5.2.1 Anatomy of the oral mucosa
5.2.2 Oral mucosal features involved in buccal drug delivery
5.3 Key factors in formulating BDD systems
5.3.1 Physiological factors
5.3.2 Pharmaceutical factors
5.4 Hydrogel–nanoparticle composites: an overview
5.4.2 Nanoparticles for BDD
5.4.3 Composite hydrogels for BDD
5.5 Nanostructured fillers in hydrogel–NP composites
5.5.1 Polymeric hydrogel–NP composites
5.5.2 Lipid hydrogel–NP composites
5.6 Complementary formulation strategies for BDD
5.6.1 Permeation enhancers
5.7 Conclusions and future perspectives
6 - Biocomposites in ocular drug delivery
6.2 Strategies for ocular drug delivery
6.2.1 Hybrid nanocomposites
6.2.2 In situ forming composite hydrogels
6.2.4 Composite films/inserts
6.2.5 Biopolymer solid lipid nanoparticles
7 - Dendrimers: smart nanoengineered polymers for bioinspired applications in drug delivery
7.1.2 Dendrimers versus polymers
7.2.1 PAMAM (Starburst) dendrimers
7.2.2 Poly(propyleneimine) dendrimers
7.2.3 Amino acid dendrimers
7.2.4 Triazine dendrimers
7.2.5 Phosphorous dendrimers
7.2.6 Carbosilane dendrimers
7.2.8 Polyglycerol dendrimers
7.2.9 Gallic acid–based dendrimers
7.2.11 Miscellaneous dendrimers
7.3 Surface engineering of dendrimers
7.3.2 Conjugation chemistry
7.3.3 Surface engineered dendrimers
7.4 Dendrimers as scaffolds: guest–host relationship
7.4.1 Dendrimers as vesicles: physical encapsulation of drug
7.4.2 Dendrimers as template: chemical conjugation of drug
7.5 Characterization of dendrimers
7.6 Dendrimer hybrids with other nanocarriers
7.6.1 Carbon-based nanomaterials–dendrimers
7.6.2 Lipid–dendrimer hybrids
7.6.3 Quantum dots–dendrimers
7.6.4 Nanoparticles–dendrimers
7.6.5 Miscellaneous nanohybrids based on dendrimers
7.7 Biomedical applications of dendrimers
7.7.1 Combined delivery of drugs
7.7.3 Ability to overcome drug resistance
7.7.4 Topical delivery system
7.7.5 Stimuli-responsive dendrimers
7.7.6 In cardiovascular disorders
7.8 Safety and toxicity issues
7.8.1 Alleviating toxicity of dendrimers
7.9 Conclusion and future considerations
8 - Nanoparticles for tumor targeting
8.2 Malignant tumors and barriers for drug delivery of nanoparticles
8.2.1 Tumors, tumor microenvironment, and potential targets for tumor treatment
8.2.2 The kinetic process and transport barriers in delivering therapeutics to their intended targets
8.3 Nanoparticles for tumor targeting
8.3.1 General principles of tumor-targeting nanoparticles
8.3.2 Current use of nanoparticles for tumor targeting
8.3.2.2 Polymer nanoparticles
8.3.2.5 Solid lipid nanoparticles
8.3.2.6 Dendrimer nanoparticles
8.3.2.7 Inorganic nanoparticles
8.3.2.8 Hybrid nanoparticles
8.3.2.9 Biomimetic nanoparticles
8.3.2.10 Other nanoparticles
8.3.3 Strategies to optimize nanoparticles for tumor targeting
8.3.3.1 Optimization of nanoparticle properties to improve passive tumor targeting
8.3.3.2 Active targeting nanoparticles
8.3.3.3 Smart nanoparticles for tumor targeting
8.3.3.4 Priming the tumor microenvironment to optimize nanoparticle targeting to tumors
8.4 Future perspectives and conclusion
8.4.1 Improve understanding of the pharmacokinetics of nanoparticles
8.4.2 Use of better experimental models
8.4.3 Challenges and opportunities of translating tumor-targeting nanoparticles
9 - Bioinspired nanotheranostics for cancer management
9.2 Theranostics and nanomedicine
9.2.1 Basic components for manufacturing theranostic nanoagents
9.3 Biopolymers as nanotheranostic agents
9.3.3 Peptide/protein-based nanotheranostics
9.4 Lipid-based nanotheranostic agents
9.4.2 Micelles as theranostic agent
9.5 Conclusion and future prospects
10 - Biopolymers for gene delivery applications
10.2 Protein-based nanoparticles
10.2.1 Collagen nanoparticle
10.2.2 Gelatin nanoparticle
10.2.5 Recombinant protein-based polymers
10.3 Polysaccharide nanoparticles
10.3.1.1 Chitosan derivatives
10.4 Biopolymeric smart materials
10.4.1 Internal stimuli responsive
10.4.1.1 Thermoresponsive
10.4.1.3 Redox responsive/glutathione responsive
10.4.1.4 Biological responsive
11 - Biomedical and drug delivery applications of functionalized inorganic nanomaterials
11.1.1 Nanotechnology and nanomedicine
11.1.2 History of gold, silver and silica materials
11.2 Biomedical applications of functionalized inorganic nanoparticles
11.2.1 Anti-cancer activity
11.2.2 Pro-angiogenic property
11.2.3 Anti-angiogenic therapy
11.2.4 Anti-microbial activity
11.2.6 Tissue engineering
11.2.9 Anti-diabetic property
11.2.10 Anti-inflammatory activity
11.2.11 Medicinal applications of bio-synthesized nanoparticles
11.3 Functionalized inorganic nanomaterials as delivery vehicles
11.3.2 Nucleic acid delivery
11.3.3 Antigen/protein delivery
11.4 Pharmacokinetics of functionalized inorganic nanoparticles
11.4.1 Absorption and bio-distribution
11.4.1.1 Gold nanoparticles
11.4.1.2 Silver nanoparticles
11.4.1.3 Silica nanoparticles
11.4.2 Bio-degradation and clearance
11.4.2.1 Gold nanoparticles
11.4.2.2 Silver nanoparticles
11.4.2.3 Silica nanoparticles
11.5 Status of inorganic nanomaterials in clinical study
11.6 Conclusions and future prospects
12 - Chitosan/carbon-based nanomaterials as scaffolds for tissue engineering
12.2 Chitosan as a tissue engineering material
12.3 CNMs in tissue engineering
12.3.4 Reduced graphene oxide
12.4 Chitosan–CNM composite scaffolds
12.4.1 Chitosan–CNM nanofibers
12.4.2 Chitosan–CNM films
12.4.3 Chitosan–CNM scaffolds
12.5 Applications of chitosan–CNM composite scaffolds
12.5.1 Bone tissue engineering
12.5.2 Nerve tissue engineering
12.5.3 Cardiac tissue engineering
12.5.4 Wound healing and skin tissue engineering
12.6 Toxicity associated with CNMs