Advances in Food and Nutrition Research /

Advances in Food and Nutrition Research, Volume 111 provides the latest on highly timely topics, including Understanding the Heterocyclic Aromatic Amine Research: An Overview and Recent Findings, Recent advances and challenges in the analysis of natural toxins, High Pressure Processing Plus Technolo...

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Bibliographic Details
Corporate Author: ScienceDirect (Online service)
Other Authors: Toldrá, Fidel (Editor)
Format: eBook
Language:English
Published: San Diego, CA : Academic Press, [2024]
Edition:First edition.
Series:Advances in food and nutrition research ; Volume 110.
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: Understanding the heterocyclic aromatic amines: An overview and recent findings
  • 1 Fundamentals of heterocyclic aromatic amines (HAAs)
  • 2 Formation of heterocyclic aromatic amines
  • 2.1 Chemical structure, properties, and classification of HAAs
  • 2.2 Precursors and mechanisms of HAAs formation during cooking processes
  • 2.3 Environmental and dietary occurrence
  • 2.4 Estimation of HAAs exposure and risk assessment
  • 3 Mitigation strategies and risk reduction
  • 3.1 Factors influencing HAAs formation, including temperature, cooking methods, and food composition
  • 3.2 Approaches and technologies to minimize HAAs formation during cooking
  • 4 Analysis and detection methods
  • 4.1 Overview of analytical techniques used for HAAs separation, detection and quantification
  • 4.2 Advances in sample preparation methods for HAAs analysis
  • 5 Toxicology and health effects
  • 5.1 Carcinogenicity of HAAs
  • 5.2 Mechanisms of HAA-induced carcinogenesis and genotoxicity
  • 5.3 Other potential health effects associated with HAAs exposure
  • 6 Conclusion and future perspectives
  • 6.1 Summary of the review's key points and findings
  • 6.2 Recommendations for future research directions
  • References
  • Chapter Two: Recent advances and challenges in the analysis of natural toxins
  • 1 Introduction
  • 2 Production, metabolism, and legislation of natural toxins
  • 2.1 Production and producers of natural toxins
  • 2.2 Metabolism and conversion of natural toxins
  • 2.2.1 Metabolism prior to human consumption
  • 2.2.2 Non-metabolic conversion
  • 2.2.3 Human metabolism after consumption
  • 2.3 Occurrence and legislation of NTs in food and feed
  • 2.4 (Legislative) Requirements for the analysis of natural toxins.
  • 3 Analysis of natural toxins
  • 3.1 On-site screening of natural toxins
  • 3.1.1 On-site sample preparation
  • 3.1.2 Detection level 1: predictive modeling
  • 3.1.2.1 Predictive modeling (PM)
  • 3.1.2.2 Application of detection level 1: predictive modeling
  • 3.1.3 Detection level 2: indirect screening
  • 3.1.3.1 Spectral screening methods
  • 3.1.3.2 NIR and MIR spectroscopy
  • 3.1.3.3 Hyperspectral imaging
  • 3.1.3.4 Application of spectral screening methods
  • 3.1.3.5 Indirect electrochemical screening
  • 3.1.3.6 Application of indirect electrochemical screening
  • 3.1.3.7 Nucleic acid amplification-based screening
  • 3.1.3.8 Application of nucleic acid amplification-based screening
  • 3.1.4 Detection level 3: recognition-based direct screening
  • 3.1.4.1 Immunochemical detection
  • 3.1.4.2 Aptamer-based detection
  • 3.1.4.3 MIP-based detection
  • 3.1.4.4 Application of level 3: recognition-based screening
  • 3.1.5 Detection level 4: direct instrumental screening
  • 3.1.5.1 Portable mass spectrometry
  • 3.1.5.2 Portable ion-mobility spectrometry
  • 3.1.5.3 Application of level 4: direct instrumental screening
  • 3.2 Lab-based analysis of natural toxins
  • 3.2.1 Detection level 5: targeted analysis
  • 3.2.1.1 Sample preparation
  • 3.2.1.2 Detection
  • 3.2.2 Detection level 6: multiclass (targeted) analysis
  • 3.2.2.1 Sample preparation
  • 3.2.2.2 Detection
  • 3.2.3 Non-targeted analysis
  • 3.2.3.1 Nuclear magnetic resonance spectroscopy
  • 3.2.3.2 HRMS
  • 3.2.4 Detection level 7: non-targeted identification of known toxins
  • 3.2.5 Detection level 8: (tentative) identification of unknown compounds
  • 3.2.5.1 Prioritization of data
  • 3.2.5.2 Effect-directed assays
  • 3.2.5.3 Classic annotation
  • 3.2.5.4 Molecular networking
  • 3.2.5.5 NT metabolites
  • 4 Challenges and perspectives
  • Author contributions
  • Declaration of competing interest.
  • 2 The main source of bioactive peptides preventing alcoholic liver injury
  • 3 Production of bioactive peptides for the prevention of alcoholic liver injury
  • 3.1 Enzymatic hydrolysis
  • 3.2 Simulated gastrointestinal digestion
  • 3.3 Modification of protein hydrolysates
  • 3.4 Fermentation
  • 3.5 In silico hydrolysis and screening
  • 4 How bioactive peptides prevent alcoholic liver injury: underlying mechanisms of action
  • 4.1 Facilitation of alcohol metabolism
  • 4.2 Reducing oxidative stress
  • 4.3 Regulation of fatty acid metabolism
  • 4.4 Anti-inflammation
  • 4.5 Regulation of gut microbiota and barrier function
  • 5 Structure-activity relationship of peptides preventing alcoholic liver injury
  • 6 Summary
  • References
  • Chapter Six: Hempseed protein-derived short- and medium-chain peptides and their multifunctional properties
  • 1 Introduction
  • 2 Hempseed proteins and their functional properties
  • 2.1 Hempseed proteins
  • 2.2 Hempseed concentrates and isolates
  • 2.3 Techniques for hemp protein extraction
  • 2.3.1 Defatting process
  • 2.3.2 Alkaline extraction-isoelectric precipitation
  • 2.3.3 Salt extraction
  • 2.3.4 Other isolation methods
  • 2.4 Nutritional properties of hempseed proteins
  • 2.5 Functionality of hempseed proteins
  • 2.5.1 Hempseed proteins solubility
  • 2.5.2 Water-holding, oil-holding and gelation properties of hempseed protein
  • 2.5.3 Emulsifying properties
  • 2.5.4 Foaming properties
  • 2.5.5 Film formation capacity
  • 3 Peptide production by enzymatic digestion
  • 3.1 In silico strategies for improving the hydrolysis process
  • 4 Biological activities of hempseed protein hydrolysates
  • 4.1 Antioxidant activity
  • 4.2 Antidiabetic activity
  • 4.3 Anticancer activity
  • 4.4 Antihypertensive activity
  • 4.5 Hypocholesterolemic activity
  • 4.6 Anti-inflammatory and neuroprotective properties.
  • 5 Methodologies for extraction and separation of bioactive peptides
  • 5.1 Short-chain bioactive peptides
  • 5.2 Medium-sized peptides
  • 6 Trans-epithelial transport of hemp seed protein and peptides
  • 7 Conclusions and future perspectives
  • References
  • Chapter Seven: Condensed tannins-Their content in plant foods, changes during processing, antioxidant and biological activities
  • 1 Introduction
  • 2 Chemical structure of condensed tannins
  • 3 Methods of extraction of tannins from plant material
  • 4 Methods of determination
  • 5 Sources of condensed tannins
  • 6 Effect of processing on the content of condensed tannins in plant foods
  • 7 Antioxidant activity of condensed tannins
  • 8 Biological activity of condensed tannins
  • 8.1 Antimicrobial activity
  • 8.2 Anti-inflammatory activity
  • 8.3 Anticancer activity
  • 8.4 Anti-diabetes activity
  • 8.5 Anti-obesity activity
  • 9 Interaction of condensed tannins with proteins
  • 10 Condensed tannins and astringency
  • 11 Concluding remarkes
  • References
  • Chapter Eight: Food applications of bioactive biomaterials based on gelatin and chitosan
  • 1 Introduction
  • 2 Gelatin extraction
  • 3 Chitosan extraction
  • 4 Preparation methods of gelatin and chitosan edible films
  • 4.1 Casting
  • 4.2 Extrusion and molding
  • 5 Enhanced gelatin films properties with additives
  • 6 Enhanced chitosan films properties with additives
  • 7 Investigating release kinetics
  • 8 Development of smart films
  • 9 Utilization of gelatin and chitosan for food coatings and films
  • 9.1 Evaluation of mechanical and permeability properties
  • 9.2 Food applications
  • 10 Conclusion and future advancements
  • Acknowledgment
  • References
  • Back Cover.