Advanced drug delivery systems for colonic disorders /
Advanced Drug Delivery Systems for Colonic Disorders present the current state of the art methods for targeted drug delivery to the colon. These methods can prolong drug half-lives, improve bioavailability, optimize pharmacokinetics, and reduce medication dosing frequency.Chapters are written in a w...
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| Format: | eBook |
| Language: | English |
| Published: |
London :
Academic Press,
2024.
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| Subjects: | |
| Online Access: | Connect to the full text of this electronic book |
Table of Contents:
- Front Cover
- Advanced Drug Delivery Systems for Colonic Disorders
- Copyright Page
- Contents
- List of contributors
- 1 Introduction to colonic disorders
- 1.1 Introduction
- 1.1.1 Anatomy
- 1.1.2 Transport time
- 1.1.3 Circulatory network
- 1.1.4 Microvilli
- 1.1.5 Intestinal fluid
- 1.1.6 Microbial environment
- 1.2 Classification of colon disorders
- 1.3 Inflammatory bowel disease
- 1.3.1 Crohn's disease
- 1.3.2 Ulcerative colitis
- 1.4 Diverticulosis
- 1.5 Colon cancer
- 1.6 Formulation approaches for targeting colon
- 1.6.1 pH-dependent drug delivery systems
- 1.6.2 Polymer-based nano-/microparticles
- 1.6.3 Lipid-based formulations
- 1.6.4 Tablets and capsules
- 1.6.5 Enzyme-sensitive drug delivery systems
- 1.6.5.1 Polysaccharide-based systems
- 1.6.5.2 Phloral technology
- 1.6.6 Ligand/receptor-mediated drug delivery system
- 1.6.6.1 Antibodies
- 1.6.6.2 Folic acid
- 1.6.7 Magnetically driven drug delivery system
- 1.6.8 Rectal drug delivery
- 1.7 Conclusion
- References
- 2 Cellular and molecular mechanisms involved in colonic disorders
- 2.1 Introduction
- 2.2 Molecular mechanisms involved in colonic disorders
- 2.2.1 Role of inflammatory cytokines in colonic disorders
- 2.2.2 Altered neurotransmitter signaling in colonic disorders
- 2.2.3 Role of eicosanoids
- 2.2.4 Role of nitric oxide
- 2.2.5 Oxidative stress in colonic disorders
- 2.2.6 Role of bidirectional neural-gut connection in Colonic disorders
- 2.2.7 Apoptosis in Colonic disorders
- 2.2.8 Role of neuroendocrine peptides in colonic disorders
- 2.2.9 Genetic mutations in colonic disorders
- 2.3 Conclusion
- References
- 3 Current approaches for treatment of colonic disorder
- 3.1 Introduction
- 3.2 Different type of colonic disorder and their treatment
- 3.2.1 Diverticular disease.
- 3.2.1.1 Medical treatment of diverticular disease
- 3.2.1.1.1 5-ASA in diverticular disease
- 3.2.1.1.2 Probiotics in diverticular disease
- 3.2.1.1.3 Surgery
- 3.2.2 Inflammatory bowel disease
- 3.2.2.1 Current therapeutic
- 3.2.2.2 Antibiotics, prebiotics, and probiotics
- 3.2.2.3 Biologics
- 3.3 Alternative and complementary approaches
- 3.4 Neurokinin antagonists and &
- Kappa
- opioid agonists
- 3.4.1 Colorectal cancer
- 3.4.1.1 Medication and hormones regular
- 3.4.1.2 Preventive strategies
- 3.4.1.3 Primary prevention
- 3.4.1.4 Secondary prevention
- 3.4.1.5 Treatment strategies
- 3.4.1.6 Targeted therapy
- 3.4.1.7 Gene therapy
- 3.4.1.8 Immunotherapy
- 3.4.1.9 Monoclonal antibody therapy
- 3.4.1.10 Cancer vaccines
- 3.4.1.11 OncoVAX
- 3.4.1.12 Adoptive T-cell therapy
- 3.5 Ischemic colitis
- 3.6 Constipation
- 3.6.1 Osmotic laxatives
- 3.6.2 Prokinetic agents
- 3.6.3 Probiotics
- 3.7 Conclusion and future perspective
- References
- 4 Polysaccharides based drug delivery systems for the treatment of colon diseases
- 4.1 Introduction
- 4.2 Types of polysaccharides
- 4.2.1 Chitosan
- 4.2.2 Alginate
- 4.2.3 Pectin
- 4.2.4 Guar gum
- 4.2.5 Dextran
- 4.2.6 Starch
- 4.2.7 Locust bean gum
- 4.2.8 Hyaluronic acid
- 4.2.9 Inulin
- 4.2.10 Cyclodextrins
- 4.2.11 Arabinoxylans
- 4.2.12 Chondroitin sulfate
- 4.3 Tempering in structural arrangement of polysaccharides
- 4.3.1 Physical interaction
- 4.3.2 Chemical interaction
- 4.4 Physicochemical properties of polysaccharides
- 4.5 Biotolerance properties
- 4.6 Development of theranostics
- 4.7 Polysaccharide-based devivery systems
- 4.7.1 Polysaccharide containing microbeads
- 4.7.2 Microspheres made of polysaccharide
- 4.7.3 Nanoparticles derived from polysaccharides
- 4.7.4 Nano-sized spheres of polysaccharide.
- 4.7.5 A nano gel based on polysaccharides
- 4.7.6 Polysaccharide-based quantum dots
- 4.7.7 Polysaccharide derived liposomes
- 4.7.8 Microcapsules developed from polysaccharides
- 4.8 Analyses of colon-specific carriers in vitro and in vivo
- 4.8.1 In vitro evaluation
- 4.8.2 In vivo evaluation
- 4.9 Conclusion
- References
- 5 Synthetic polymers as biomaterials for the treatment of colon diseases
- 5.1 Introduction
- 5.2 Colon diseases
- 5.2.1 Inflammatory bowel diseases
- 5.2.1.1 Colorectal cancer
- 5.3 Colon delivery: physiology and biopharmaceutical considerations
- 5.4 Synthetic polymers as biomaterials for colon drug delivery system
- 5.4.1 pH-dependent polymers
- 5.4.2 Erodible or swellable or time-dependent polymers
- 5.4.2.1 Hydroxypropyl methylcellulose
- 5.4.2.2 Hydroxypropyl cellulose and hydroxyethyl cellulose
- 5.4.3 Water-insoluble polymers (ethyl cellulose)
- 5.4.4 Bacterially triggered polymers (pectin, chitosan, cyclodextrin)
- 5.4.4.1 Polysaccharide modification
- 5.4.4.1.1 Guar gum
- 5.4.4.1.2 Pectin
- 5.4.4.1.3 Chitosan
- 5.4.4.1.4 Dextran
- 5.4.5 Bioresorbable polymers
- 5.5 Industrial patents and marketed preparations
- 5.6 Conclusion
- References
- 6 Mucoadhesive polymers as biomaterials for the treatment of colon disorders
- 6.1 Introduction
- 6.1.1 Mucoadhesion
- 6.1.1.1 Theories of mucoadhesion
- 6.1.1.1.1 Wetting theory
- 6.1.1.1.2 Adsorption theory
- 6.1.1.1.3 Diffusion theory
- 6.1.1.1.4 Fracture theory
- 6.1.1.1.5 Electronic theory
- 6.1.2 Mechanism of mucoadhesion
- 6.1.3 Factors affecting the mechanism of mucoadhesion
- 6.2 Mucoadhesive drug delivery systems
- 6.2.1 Characteristics of ideal mucoadhesive polymer
- 6.2.2 Classification of the mucoadhesive polymers
- 6.3 Mucoadhesive polymers in drug delivery system.
- 6.3.1 Mucoadhesive polymers in the treatment of colon disorders
- 6.3.1.1 Hydrophilic polymers
- 6.3.1.2 Hydrogels
- 6.3.1.3 Thiolated polymers
- 6.3.1.4 Lectin-based polymers
- 6.3.2 Delivery sites of mucoadhesive polymers
- 6.3.2.1 Buccal cavity
- 6.3.2.2 Vaginal and rectal lumen
- 6.3.2.3 Gastrointestinal tract
- 6.3.3 Commercial mucoadhesive drug delivery system
- 6.3.4 Advantages of mucoadhesive-based drug delivery system in the treatment of colon disorders
- 6.4 Recent advances in mucoadhesive polymers for colon disorders
- 6.4.1 Mucoadhesive microspheres
- 6.4.2 Mucoadhesive nanoparticles
- 6.4.3 Dual-drug-loaded mucoadhesive nanoparticles
- 6.4.4 Mucoadhesive chitosan-based nanoparticles
- 6.4.5 Naturally occurring biopolymers
- 6.4.5.1 Amino acid/protein-based mucoadhesive polymers
- 6.4.5.2 Snail-produced mucin proteins
- 6.4.5.3 Zwiterrionic polymeric nanoparticles as mucoadhesive agents
- 6.5 Limitations of mucoadhesive polymers-based drug delivery approaches for the treatment of colon disorders
- 6.6 Future perspectives
- 6.7 Conclusion
- References
- 7 Colon-responsive oral drug delivery for combating colonic disorders
- 7.1 Introduction
- 7.2 Fundamentals of encapsulation technologies for oral delivery for colon diseases
- 7.3 Recent literature in colon-responsive drug delivery
- 7.3.1 pH-sensitive colon-responsive drug delivery
- 7.3.2 Prodrug
- 7.3.3 Time-dependent colon-responsive drug delivery
- 7.3.4 Nanotools for colon-responsive drug delivery
- 7.3.5 Other approaches for colon-responsive drug delivery
- 7.4 Conclusion
- References
- 8 Colon-responsive targeted drug delivery for treating colonic disorder
- 8.1 Introduction
- 8.2 Physiology of the gastrointestinal tract
- 8.3 Physicochemical properties of drugs influencing CDDS.
- 8.4 Different approaches to colon-targeted drug delivery systems
- 8.4.1 Multistimuli systems for colonic drug delivery via the oral route
- 8.4.2 Superporous hydrogels as CDDS
- 8.4.3 pH-Dependent drug delivery systems
- 8.4.4 Lipid-based formulations
- 8.4.5 Bacterial enzymes-based drug delivery system
- 8.4.6 Polysaccharide-based systems
- 8.4.6.1 Polymeric micelles
- 8.4.7 Liposomes in colon-targeted drug delivery systems
- 8.4.8 Microspheres for controlled release of drug molecules
- 8.4.9 Magnetic nanoparticles for colon-targeted drug delivery systems
- 8.5 Challenges and conclusion
- References
- 9 Advancement in targeted drug delivery systems in managing colonic disorders
- 9.1 Introduction
- 9.2 Colon-responsive targeted drug delivery approaches
- 9.2.1 Prodrug
- 9.2.2 pH-sensitive system
- 9.2.3 Bacterial-enzyme activated
- 9.2.3.1 Osmotically controlled
- 9.2.4 Coated tablets and capsules-based approaches
- 9.2.5 Nanotechnology-based targeting
- 9.2.6 Theranostic approach
- 9.2.7 Bioelectronic devices for colon targeting
- 9.2.8 Computer-assisted formulation design development for targeting colon
- 9.3 Conclusion
- References
- 10 Nutraceuticals and phytoceuticals in the treatment of colon disorders
- 10.1 Introduction
- 10.2 Nutraceuticals as drug delivery systems for colonic disorders
- 10.2.1 Functional colonic disorders
- 10.2.2 Constipation
- 10.2.3 Irritable bowel syndrome
- 10.2.4 Functional dyspepsia
- 10.2.5 Gastroesophaegeal reflux disease
- 10.2.6 Various structural colonic disorders
- 10.2.7 Inflammatory bowel disease
- 10.2.8 Gastrointestinal cancer
- 10.2.9 Diverticular disease
- 10.2.10 Colorectal cancer
- 10.3 Plant materials as DDS for colonic disorders
- 10.3.1 Curcumin
- 10.3.2 Phenolic compounds
- 10.3.3 Halocynthiaxanthin
- 10.3.4 Glycyrrhizin glycyrrhizin
- 10.3.5 Saponins.