Food-borne delivery systems of functional substances for precision nutrition /

Food-Borne Delivery Systems of Functional Substances for Precision Nutrition, Volume 112 highlights new advances in the field, with this new volume presenting interesting chapters on a range of topics, including Biological activity, limitations, and steady-state delivery of functional substances for...

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Bibliographic Details
Corporate Author: ScienceDirect (Online service)
Other Authors: Tan, Mingqian (Editor)
Format: eBook
Language:English
Published: [San Diego, CA] : Academic Press, 2024.
Series:Advances in food and nutrition research ; v. 112.
Subjects:
Online Access:Connect to the full text of this electronic book
Table of Contents:
  • Front Cover
  • Series Page
  • Advances in Food and Nutrition Research
  • Copyright
  • Contents
  • Contributors
  • Preface
  • Chapter One: Biological activity, limitations and steady-state delivery of functional substances for precision nutrition
  • 1 Introduction and classification of functional substances
  • 2 Challenges of functional substances in precision nutrition
  • 2.1 Factors impacting the stability of functional substances
  • 2.1.1 Light
  • 2.1.2 Oxygen
  • 2.1.3 Temperature
  • 2.1.4 pH
  • 2.1.5 Metal ions
  • 2.1.6 Solubility
  • 2.2 Bioavailability
  • 2.2.1 Strong acidic environment in the gastric cavity
  • 2.2.2 Enzyme metabolism in the gastrointestinal tract
  • 2.2.3 Food matrix
  • 2.2.4 Changes in the structure and permeability of delivery systems
  • 2.2.5 Physiological barrier of mucous layer
  • 3 Current status of delivery systems of functional substances
  • 3.1 Design of stability encapsulation methods and construction of delivery system for functional substances
  • 3.2 Targeted controlled release of functional substances
  • 3.2.1 pH-responsive drug delivery system
  • 3.2.2 Enzyme responsive release delivery system
  • 3.2.3 Redox response release delivery system
  • 3.2.4 Targeted delivery system
  • 4 Desirable characteristics of functional substance delivery systems
  • 4.1 Food grade status
  • 4.2 High loading capacity
  • 4.3 Targeting
  • 4.4 Controlled release capacity
  • 4.4.1 pH-response release
  • 4.4.2 ROS-response release
  • 4.4.3 GSH-response release
  • 5 Applications of food-borne delivery systems for precise nutrient delivery
  • 5.1 Passive targeting
  • 5.2 Active targeting
  • 5.2.1 Receptor targeting
  • 5.2.2 Stimulus responsive targeted
  • 5.2.3 Gastrointestinal tract cell targeting
  • 5.2.4 Other tissue and organ targeting
  • 5.2.5 Targeting specific organelles
  • Acknowledgements
  • References.
  • Chapter Two: Nanoparticle delivery systems of functional substances for precision nutrition
  • 1 Introduction
  • 2 Design and preparation of nanoparticle delivery systems for functional substances
  • 2.1 Bioactive polysaccharides
  • 2.2 Bioactive proteins and peptides
  • 2.3 Polyunsaturated fatty acid
  • 2.4 Vitamins
  • 2.5 Probiotics
  • 2.6 Enzymes
  • 2.7 Phytochemicals
  • 3 Application of nanoparticle delivery systems in nutritional intervention
  • 3.1 Environmental stimuli-responsive delivery systems
  • 3.1.1 pH-responsive delivery systems
  • 3.1.1.1 Enzyme-responsive delivery systems
  • 3.1.1.2 Mucoadhesive and mucus-penetrating delivery systems
  • 3.2 Site-specific delivery systems
  • 3.3 Delivery systems for diseases intervention
  • 3.3.1 Obesity
  • 3.3.2 Inflammatory bowel disease
  • 3.3.3 Liver disease
  • 3.3.4 Tumors and cancer
  • 4 Conclusions
  • References
  • Chapter Three: Micellar delivery systems of bioactive compounds for precision nutrition
  • 1 Introduction
  • 2 Background of micelles
  • 2.1 Preparation methods of micelles
  • 2.1.1 Dialysis method
  • 2.1.2 Direct dissolution method
  • 2.1.3 Solvent evaporation method
  • 2.1.4 Thin-film hydration method
  • 2.1.5 Ultrasonication
  • 2.1.6 pH cycling method
  • 2.1.7 Other methods
  • 2.2 Fundamental characteristics of polymeric micelles
  • 2.2.1 Particle size and shape of polymeric micelles
  • 2.2.2 Surface charge of polymeric micelles
  • 3 Major polymeric micelles and customized strategies for improving their properties
  • 3.1 Polymeric micellar delivery systems
  • 3.1.1 Protein-based micelles
  • 3.1.1.1 Casein-based micelles
  • 3.1.1.2 Whey protein-based micelles
  • 3.1.2 Polysaccharide-based micelles
  • 3.1.2.1 Chitosan-based micelles
  • 3.1.2.2 Starch-based micelles
  • 3.1.2.3 Dextran-based micelles
  • 3.1.2.4 Curdlan-based micelles
  • 3.1.2.5 Other polysaccharides-based micelles.
  • 3.1.3 Other polymeric-basic micelles
  • 3.2 Customized strategies for modifying polymeric micelle properties
  • 3.2.1 Changing internal properties
  • 3.2.1.1 Enzyme cross-linking
  • 3.2.1.2 Glycosylation modification
  • 3.2.1.3 Moderate enzymolysis
  • 3.2.1.4 Octenyl succinic anhydride (OSA) modification
  • 3.2.2 Changing medium environment
  • 3.2.2.1 pH variations
  • 3.2.2.2 Temperature variations
  • 3.2.2.3 Ultrasonication
  • 3.2.2.4 High hydrostatic pressure (HHP) treatment
  • 4 Polymeric micelles for delivering bioactives
  • 4.1 Polymeric micellar carriers for carotenoids
  • 4.2 Polymeric micellar carriers for polyphenols
  • 4.3 Polymeric micellar carriers for vitamins
  • 4.4 Polymeric micellar carriers for other bioactives
  • 5 Micellar carriers for precision nutrition
  • 5.1 Targeted-release of bioactives
  • 5.2 Organ-targeted ability of bioactives
  • 5.3 Cell uptake promotion of bioactives
  • 5.4 Application in nutritional intervention of chronic diseases
  • 5.4.1 Inflammatory bowel disease
  • 5.4.2 Obesity
  • 5.4.3 Cancer
  • 5.4.4 Liver diseases
  • 6 Conclusions
  • References
  • Chapter Four: Microgel delivery systems of functional substances for precision nutrition
  • 1 Introduction
  • 2 Biopolymers for the preparation of microgel
  • 2.1 Polysaccharide
  • 2.2 Protein
  • 3 Microgel fabrication strategies and methods
  • 3.1 The "top-down" route
  • 3.2 The "bottom-top" route
  • 3.3 Other preparation routes
  • 4 Characteristics and functions of microgel delivery system
  • 4.1 Characteristics of microgel delivery system
  • 4.2 High encapsulation of microgel delivery system
  • 4.3 Responsive-release function of microgel delivery system
  • 4.4 Targeting function of microgel delivery system
  • 4.5 Good bioaccessibility and absorption of microgel delivery system
  • 5 Microgel delivery system for precision nutrition.
  • 4.1 Controlling gastrointestinal fate of bioactive components
  • 4.1.1 Mouth
  • 4.1.2 Stomach
  • 4.1.3 Small intestine
  • 4.1.4 Colon
  • 4.2 Application of microcapsule delivery systems in chronic disease intervention
  • 4.2.1 Nutritional intervention on inflammatory bowel disease
  • 4.2.2 Nutritional intervention on alcoholic/nonalcoholic fatty liver disease
  • 4.2.3 Nutritional intervention on diabetes
  • 4.2.4 Nutritional intervention on cancer
  • 5 Conclusions
  • References
  • Chapter Seven: Liposomes delivery systems of functional substances for precision nutrition
  • 1 Introduction
  • 2 Designing and modification of liposomes
  • 2.1 Natural and synthetic liposomes
  • 2.2 Surface modification of liposomes
  • 2.2.1 The evolution of liposomes
  • 2.2.2 PEG-modified liposomes
  • 2.2.3 Targeted liposomes
  • 2.3 Specific modalities of liposome surface modification
  • 2.3.1 Liposomes modified by polymers
  • 2.3.2 Liposomes modified with nanoparticles
  • 2.3.3 Liposomes modified with functional groups
  • 3 Application status of liposomes in functional substances
  • 3.1 Preparation method of food-grade liposomes
  • 3.1.1 Conventional preparation methods of food-grade liposomes
  • 3.1.1.1 Mechanical dispersion method
  • 3.1.1.2 Thin film dispersion method
  • 3.1.1.3 Detergent removal method
  • 3.1.1.4 Solvent injection method
  • 3.1.1.5 Reverse phase evaporation method
  • 3.1.1.6 Calcium fusion method
  • 3.1.2 Novel methods
  • 3.1.2.1 Supercritical fluid method
  • 3.1.2.2 Dynamic high pressure microfluidization method
  • 3.1.2.3 Membrane contactor-based method
  • 3.1.2.4 Freeze-drying double emulsions
  • 3.1.2.5 Other methods
  • 3.2 Loading and encapsulation of nutrients
  • 3.2.1 Passive loading
  • 3.2.2 Active loading
  • 3.3 Applications of nutrient-loaded liposomes in the food industry
  • 3.3.1 Loading enzyme preparations.