Handbook of immunoassay technologies : approaches, performances, and applications /
Handbook of Immunoassay Technologies: Approaches, Performances, and Applications, Second Edition unravels the role of immunoassays in the biochemical sciences.During the last four decades, a wide range of immunoassays has been developed, ranging from the conventional enzyme-linked immunosorbent assa...
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| Other Authors: | , |
| Format: | eBook |
| Language: | English |
| Published: |
London, United Kingdom :
Academic Press,
2025.
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| Edition: | Second edition. |
| Subjects: | |
| Online Access: | Connect to the full text of this electronic book |
Table of Contents:
- Front Cover
- Handbook of Immunoassay Technologies
- Copyright Page
- Contents
- List of contributors
- Preface
- Objectives
- Scope
- Target audience
- Book organization
- 1 Immunoassays: an overview
- 1 Overview of immunoassays
- 2 Antibody structure
- 3 Need for immunoassays
- 3.1 Clinical
- 3.2 Industrial
- 3.3 Environment and security
- 3.4 Food
- 3.5 Personalized healthcare
- 4 Immunoassay formats
- 5 Conclusions and future trends
- References
- 2 Antibody immobilization and surface functionalization chemistries for immunodiagnostics
- 1 Introduction
- 2 Surface functionalization chemistries
- 2.1 Hydroxyl groups
- 2.2 Amino groups
- 2.3 Carboxyl groups
- 2.4 Sulfhydryl groups
- 2.5 Epoxy groups
- 3 Antibody immobilization chemistries
- 3.1 Covalent
- 3.2 Oriented
- 3.3 Noncovalent
- Adsorption
- 3.3.1 Affinity
- 3.4 Site-specific
- 3.5 Peptide nucleic acid and deoxyribonucleic acid-directed
- 3.6 Recombinant antibody
- 4 Surface characterization
- 5 Conclusions, challenges, and future trends
- References
- 3 Monoclonal antibody generation by phage display: history, state-of-the-art, and future
- 1 Introduction
- 1.1 History of the development of antibody phage display
- 1.2 Antibody formats used for phage display
- 1.3 Further recombinant antibody formats
- 2 Phage display selection
- 2.1 Advantages of recombinant antibody selection
- 2.2 Guided selection
- 2.3 Affinity improvement
- 2.4 Other selection technologies
- 3 Antibody libraries
- 3.1 Immune libraries
- 3.2 Naive natural libraries
- 3.3 Naive semisynthetic libraries
- 3.4 Naive synthetic libraries
- 3.5 Special library designs
- 3.6 Synthetic libraries from non-human species
- 4 In vitro selection of antibodies for specific applications
- 4.1 Tissue panning for immunohistochemistry antibodies.
- 4.2 Sandwich pair selection, complex-specific antibodies, and drug monitoring
- 4.3 Sophisticated guided selection strategies
- 4.4 Fully human controls in diagnostic immunoassays
- 5 Site-specific conjugation and modification of antibody functionality
- 6 Conclusion and outlook
- 6.1 Future
- References
- 4 Bioanalytical requirements and regulatory guidelines for immunoassays
- 1 Introduction
- 2 Bioanalytical requirements for an immunoassay
- 2.1 Accuracy
- 2.2 Precision
- 2.3 Selectivity
- 2.4 Sensitivity
- 2.5 Reproducibility
- 2.6 Stability
- 2.7 Recovery
- 2.8 Calibration curve
- 2.9 Bioanalytical performance parameters
- 2.9.1 Limit of blank
- 2.9.2 Limit of detection
- 2.9.3 Limit of quantification
- 2.9.4 Lower limit of the linear interval
- 2.9.5 Lower limit of the measuring interval
- 2.9.6 Errors
- 2.9.7 Carryover
- 2.9.8 Interference
- 2.9.9 Quality controls
- 2.9.10 Linear range
- 2.9.11 Analytical measurement range
- 2.9.12 Clinically reportable range
- 2.9.13 Bias
- 2.9.14 Hook effect
- 2.9.15 Method comparison
- 2.9.16 Cross-reactivity
- 3 Critiques and outlook
- 4 Conclusions
- References
- 5 Enzyme-linked immunoassays
- 1 Introduction
- 2 Conventional enzyme-linked immunoassays
- 2.1 Enzyme-linked immunosorbent assay
- 2.1.1 Direct ELISA
- 2.1.2 Indirect ELISA
- 2.1.3 Sandwich ELISA
- 2.2 Competitive enzyme-linked immunoassay
- 3 Emerging enzyme-linked immunoassays
- 3.1 High-sensitivity sandwich EIA
- 3.2 Highly simplified rapid sandwich EIA
- 3.3 Wash-free immunoassays
- 3.4 Multiplex immunoassays
- 3.5 Nano-/micro-material-based EIA
- 3.6 Paper-based EIA
- 3.7 Microfluidics-based EIA
- 3.7.1 Optimizer ELISA
- 3.7.2 Centrifugal microfluidics-based IA
- 3.8 Smartphone-based EIA
- 4 Portable analyzer-based immunoassays
- 5 Critiques and outlook
- 6 Conclusions
- References.
- 6 Chemiluminescent immunoassays (CLIA)
- 1 Introduction
- 2 Chemiluminescent immunoassay mechanisms
- 2.1 Glow chemiluminescence
- 2.2 Flash chemiluminescence
- 2.3 Electrochemiluminescence
- 3 Commercial chemiluminescence immunoassay analyzers
- 3.1 Closed system
- 3.2 Open system
- 4 Commercial and potential aspects of CLIA
- 5 Conclusions
- References
- 7 Lateral flow immunoassays
- 1 Introduction
- 1.1 Lateral flow immunoassays
- 1.1.1 History of the technology
- 1.1.2 Basic technology
- 1.1.3 Recognition elements
- 1.1.4 Signal labels
- 1.1.5 Storage of lateral flow devices
- 2 Advances in lateral flow immunoassays
- 2.1 Coupling to a range of detection principles
- 2.2 Combination with amplification procedures
- 2.3 Multianalyte lateral flow immunoassays
- 2.4 Reading and quantifying multispot lateral flow assays
- 2.4.1 Lateral flow reader for microarrays-a real-time video reader
- 2.4.2 Reading arrays by smartphone and other applications
- 2.5 Integration of lateral flow immunoassays with paper diagnostics
- 3 Challenges and future directions
- 3.1 Updated SWOT analysis
- 3.2 Bibliographic and commercial data
- 4 Conclusions
- Acknowledgments
- References
- 8 Paper-based immunoassays
- 1 Introduction
- 2 Paper-based immunoassays: strategies and detection principles
- 2.1 Colorimetric method
- 2.1.1 AuNPs
- 2.1.2 Enzymes
- 2.1.3 Carbon nanoparticles
- 2.1.4 Magnetic nanoparticles
- 2.2 Thermal method
- 2.3 Electrochemical method
- 2.4 Magnetic method
- 3 Development of the paper-based immunoassays devices
- 3.1 Sensitivity improvement
- 3.2 Automatic detections
- 3.3 Semiquantification detection and quantification detection
- 4 Conclusions
- References
- 9 Acoustic wave-based immunoassays
- 1 Introduction
- 2 Clinical diagnostics
- 2.1 Quartz crystal microbalance immunosensors.
- 2.1.1 Direct immunosensors
- 2.1.2 Indirect immunosensors
- 2.1.3 Sandwich-amplified immunosensors
- 2.2 Surface acoustic wave immunosensors
- 2.2.1 Direct immunosensors
- 3 Detection of microbial pathogens and toxins
- 3.1 Quartz crystal microbalance immunosensors
- 3.1.1 Direct immunosensors
- 3.1.2 Indirect immunosensors
- 3.1.3 Sandwich-amplified immunosensors
- 3.2 Surface acoustic wave immunosensors
- 3.2.1 Direct immunosensors
- 3.2.2 Sandwich-amplified immunosensors
- 4 Detection of parasites
- 4.1 Quartz crystal microbalance immunosensors
- 4.1.1 Direct immunosensors
- 4.1.2 Indirect immunosensors
- 4.1.3 Sandwich-amplified immunosensors
- 5 Detection of viruses
- 5.1 Quartz crystal microbalance immunosensors
- 5.1.1 Direct immunosensors
- 5.1.2 Indirect immunosensors
- 5.1.3 Sandwich-amplified immunosensors
- 5.2 Surface acoustic wave immunosensors
- 6 Quartz crystal microbalance and surface acoustic wave-based electronic noses
- 7 Quartz crystal microbalance and surface acoustic wave immunoassays in environmental monitoring and allergens detection
- 8 Integrated acoustic wave immunosensors for point of care
- 9 Commercial acoustic wave immunosensors
- 10 Market potential and conclusions
- Acknowledgments
- References
- 10 Interferometry-based immunoassays
- 1 Introduction-general context
- 2 Principles of operation
- 2.1 Label-free optical sensing
- 2.2 Interferometric sensors
- 3 Sensor surface functionalization
- 3.1 Chemical activation of transducers
- 3.2 Immobilization of recognition molecules
- 3.3 Elimination of nonspecific binding
- 3.4 Application of interferometric immunosensors
- 3.5 Mach-Zehnder interferometers
- 3.6 Young interferometers
- 3.7 Bimodal interferometers
- 4 Conclusions and future perspectives
- References
- 11 Nanomaterial- and micromaterial-based immunoassays.
- 1 Introduction
- 2 Micromaterial-based immunoassay
- 2.1 Fluorescent polystyrene microsphere
- 2.2 Magnetic microbeads
- 2.3 Nanomaterial-based immunoassay
- 3 Colorimetric immunoassay
- 3.1 Lateral flow assay
- 3.2 Plate-based colorimetric immunoassay
- 4 Electrochemical immunoassay
- 5 Fluorescent immunoassay
- 5.1 Heterogeneous immunoassay
- 5.2 Fluorescence resonance energy transfer assay
- 6 Conclusion
- References
- 12 Microcantilever-based sensors
- 1 Introduction
- 2 Microcantilevers and their modes of operation
- 2.1 Operating modes for cantilever mass sensors
- 3 Detection methods
- 3.1 Optical
- 3.2 Piezoresistive
- 3.3 Capacitive
- 3.4 Piezoelectric
- 3.5 Interferometry
- 3.6 Optical diffraction grating
- 3.7 Charge-coupled device
- 4 Bending behavior of microcantilevers
- 5 Fabrication of microcantilevers
- 6 Microcantilever-based sensors
- 6.1 Detection of biomolecules
- 6.1.1 DNA
- 6.1.2 Prostate-specific antigen
- 6.1.3 Myoglobin
- 6.1.4 Lipoproteins
- 6.1.5 Glucose
- 6.1.6 Tributyrin
- 6.2 Detection of gaseous analytes
- 6.3 Detection of chemicals and metal ions
- 6.4 Detection of humidity and pH
- 6.5 Detection of explosives and monitoring of ammunition
- 7 Electronic nose
- 8 Nanocantilevers
- 9 Commercial availability
- 10 Conclusions and future trends
- References
- 13 Quartz crystal microbalance-based sensors
- 1 Introduction
- 2 Detection of biomolecules
- 3 Detection of bacteria
- 4 Detection of volatile organic compounds
- 5 Detection of chemical analytes
- 6 Detection of gaseous analytes
- 7 Special analytical applications
- 8 Other analytical applications
- 9 Conclusions and future trends
- References
- Further reading
- 14 Electrochemical immunosensors fundamentals and applications in clinical diagnostics
- 1 Introduction.