Novel drug delivery systems in the management of CNS disorders /
Novel Drug Delivery Systems in the Management of CNS Disorders offers a comprehensive source of information on delivering drugs to the central nervous system to treat various diseases and conditions. The book covers a wide range of CNS disorders, including epilepsy, Parkinson's, Alzheimer'...
| Corporate Author: | |
|---|---|
| Other Authors: | , , , , |
| Format: | eBook |
| Language: | English |
| Published: |
London :
Academic Press,
[2025]
|
| Subjects: | |
| Online Access: | Connect to the full text of this electronic book |
Table of Contents:
- Front Cover
- Novel Drug Delivery Systems in the Management of CNS Disorders
- Novel Drug Delivery Systems in the management of CNS Disorders
- Copyright
- Dedication
- Contents
- Contributors
- About editors
- Foreword
- Preface
- Introduction
- I
- Introduction to drug delivery to the CNS
- 1
- General anatomy and physiology of the brain
- 1. Introduction
- 2. Anatomy
- 2.1 Meninges
- 2.2 Ventricular system of the brain
- 2.3 Cerebrospinal fluid
- 2.4 Forebrain
- 2.4.1 Telencephalon
- 2.4.1.1 Cerebrum
- 2.4.1.2 Basal ganglia
- 2.4.1.3 Hippocampus
- 2.4.1.4 Amygdala
- 2.4.2 Diencephalon
- 2.4.2.1 Thalamus
- 2.4.2.2 Hypothalamus
- 2.5 Midbrain (diencephalon)
- 2.6 Hindbrain (rhombencephalon)
- 2.6.1 Pons
- 2.6.2 Medulla oblongata
- 2.6.3 Cerebellum
- 3. Physiology
- 3.1 Neurohumoral transmission
- 3.1.1 Glutamate
- 3.1.2 GABA
- 3.1.3 Glycine
- 3.1.4 Serotonin
- 3.1.5 Dopamine
- 4. Conclusion
- Acknowledgments
- References
- 2
- Drug delivery to brain: Formulation challenges and potential approaches
- 1. Introduction
- 2. Brain barriers
- 2.1 The endothelial blood brain barrier
- 2.2 Glia limitans
- 2.3 Choroid plexus and blood cerebrospinal fluid barrier (BCSFB)
- 2.4 Additional brain barriers
- 3. Nanotechnology-based drug delivery systems
- 3.1 Nanoparticles
- 3.2 Liposomes
- 3.3 Solid lipid nanoparticles (SLNs)
- 3.4 Nanostructured lipid carriers (NLCs)
- 4. Approaches to overcome brain barriers
- 4.1 Convection-enhanced delivery (CED)
- 4.2 Focused ultrasound (FUS)-mediated BBB disruption
- 4.3 Implantable devices
- 4.4 Active targeting
- 4.5 Intranasal delivery
- 5. Challenges for scale-up of nano-formulations
- 6. Conclusion and future prospects
- References
- 3
- Possible targets in the management of various CNS disorders
- 1. Introduction.
- 2.4.5.3 GDEPT/VDEPT
- gene-directed enzyme prodrug therapy/vírus-directed enzyme prodrug therapy
- 2.5 Prodrug advances in different diseases
- 2.5.1 Parkinson disease (PD)
- 2.5.2 Alzheimer's disease
- 2.5.3 Brain tumor
- 3. Conclusion
- References
- 6
- Traditional practices in CNS drug delivery
- 1. Introduction
- 2. Alzheimer's disease
- 3. Parkinson's disease
- 4. Epilepsy
- 5. Types of epilepsy
- 6. Structural components of BBB
- 7. Emphasize on drugs: Improved drug delivery to the brain
- 7.1 Nanocarriers in CNS drug delivery
- 8. Liposomes
- 9. Micelles
- 10. Solid lipid nanoparticles
- 11. Microspheres
- 12. Nasal-to-brain drug administration
- 13. Nanocarriers' neurotoxic properties
- 14. Models for CNS delivery of drug in vivo and in vitro
- 15. In vitro models for CNS delivery of drug
- 16. Primary mono-cell culture
- 17. Co-culture
- 18. Triple cultures
- 19. In vivo models for CNS drug delivery
- 20. Rodent model
- 21. Zebrafish model
- 22. Drosophila model
- 23. Concluding remarks and future exploration
- References
- 7
- Emerging need of novel drug delivery systems in management of CNS disorders
- 1. Introduction
- 1.1 Current challenges in treating CNS disorders
- 1.2 Novel drug delivery systems: A hope for breaching the barriers
- 2. CNS targeting: Approaches using novel formulations
- 2.1 Vesicular drug delivery systems
- 2.2 Polymeric drug delivery system
- 2.3 Lipoidal drug delivery system
- 2.4 Carbon-based drug delivery system
- 3. Nanocarriers for targeting CNS disorders
- 3.1 Alzheimer's disease
- 3.2 Parkinson's disease
- 3.3 Hungtington's disease (HD)
- 3.4 Schizophrenia
- 4. Challenges
- 5. Conclusion
- References
- 8
- Nose to brain drug delivery through advanced drug delivery systems
- 1. Introduction.
- 1.1 Advantages, challenges, and barriers in nose-to-brain drug delivery
- 1.2 Advantages
- 1.3 Challenges
- 1.3.1 Trigeminal pathway
- 1.3.2 Olfactory pathway
- 1.4 Pharmacokinetics of drugs delivered to brain through nasal route
- 2. Potential applications in neurological disorders
- 3. Advanced drug delivery systems for nose-to-brain drug delivery
- 3.1 Nanocarriers
- 3.1.1 Nanoparticles for nose-to-brain drug delivery
- 3.1.2 Nanocarriers for nose-to-brain drug delivery
- 3.2 Mucoadhesion
- 4. Challenges and key considerations for successful translation to clinical practice
- 5. Conclusion
- References
- 9
- Physiologically based pharmacokinetic (PBPK) modeling for CNS delivery
- 1. Introduction
- 2. Modeling of transporter mediated drug absorption, interactions and clearance based on physiological principles
- 3. PBPK model for drug transit to the brain via transferrin receptors
- 4. Drug disposition in the brain: In vitro to in vivo extrapolation linked to physiologically based pharmacokinetic models
- 5. CNS delivery in an anti-Alzheimer medication using a novel anionic polymer as a carrier
- 6. PBPK modeling approach for human CNS drug distribution predictions
- 7. Investigating the CNS transit characteristics using mathematical modeling and simulation
- 8. PBPK model for plasma protein bound drug delivery at brain
- 9. Modifying the pharmacokinetics of medicines that target the central nervous system with lipid nanoparticles
- 10. Nanocarriers for effective CNS delivery
- 11. Magnetic iron oxide nanoparticles for drug releaseand brain imaging
- 12. Mouse brain antibody disposition PBPK model
- 13. In vitro BBB experimental models for CNS drug delivery
- 14. Applications of exosomes as CNS drug delivery devices
- 15. Enhanced CNS drug delivery through nanotechnology for schizophrenia management.
- 16. Transient opening of the BBB by vasoactive peptides to improve CNS drug delivery
- 17. Treatment of brain tumors using drug delivery to the CNS
- 18. Nanoemulsions in CNS drug delivery
- 19. Pharmacokinetics of CNS penetration
- 20. Current strategies for targeted brain drug delivery
- 21. Pharmacokinetic model (physiologically-based) of the brain regional lipid variance
- 22. A translational platform PBPK model for antibody disposition in the brain
- 23. Blood-brain barrier transit and central nervous system effects of drugs
- 24. Development of a frontal cortex pharmacokinetics and zone-specific PBPK brain model to assess hippocampus
- 25. Physiologically based pharmacokinetic modeling of nanoparticle bio-dissemination
- 26. Essential brain PBPK model for antibody therapeutics for CNS syndrome
- 27. Assuming drug concentration-time profiles in several CNS compartments
- 28. Physiologically based pharmacokinetic (PBPK) model for bio-dissemination of radiolabeled peptides in patients along neuroen ...
- 29. PBPK modelling of nanomaterials
- 30. Physiologically based pharmacokinetic (PBPK) modeling of RNAi therapeutics
- 31. PBPK modeling for presuming brain levels of drugs in rat
- 32. PBPK model exploring the blood-milk barrier in lactating breeds to dairy goats and cows
- 33. PBPK model for kids about to reach maturation
- 34. The aspect of the physiologically based pharmacokinetic model (PBPK) in pharmaceuticals and environmental chemical risk ass ...
- 35. PBPK modeling on assuming human CNS pharmacokinetics
- References
- II
- Novel drug delivery systems to specific CNS disorders
- 10
- Superparamagnetic iron oxide nanoparticles and their potential role in the diagnosis and therapeutics of vario ...
- 1. Introduction
- 2. Synthesis and characterization of SPIONs
- 2.1 Routes of synthesis of SPIONs.