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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| Format: | eBook |
| Language: | English |
| Published: |
[San Diego, CA] :
Academic Press,
2024.
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| 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.