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...

Full description

Bibliographic Details
Corporate Author: ScienceDirect (Online service)
Other Authors: Dureja, Harish
Format: eBook
Language:English
Published: London : Academic Press, 2024.
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 &amp
  • 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.