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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5463_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •About the Editor
- •Contents
- •Contributors
- •1.1.4 Components of niosome
- •1.1.5 Factors affecting niosomes
- •Preface
- •Abstract
- •1.1 Introduction
- •1.1.1 Why niosome?
- •1.1.2 Advantages of niosome
- •1.1.3 Structure of niosome
- •1.2 Applications of niosome
- •1.2.2 Niosomes for the delivery of therapeutics
- •1.2.3 Niosomes in biomedical applications
- •1.3 Conclusions and future prospects
- •Keywords
- •References
- •Abstract
- •2.1 Introduction
- •2.2 Conclusions
- •Acknowledgments
- •Keywords
- •References
- •Abstract
- •3.1 Introduction
- •3.2.1 Parameters involved in electrospinning process
- •3.2.2 Biomaterials for electrospinning
- •3.3 Electrospun nanofibers as drug delivery systems
- •3.3.1 Blending electrospinning
- •3.3.2 Emulsion electrospinning
- •3.3.3 Coaxial electrospinning
- •3.3.4 Surface modifications
- •3.4 Electrospun nanofibers for tissue engineering
- •3.4.1 Electrospun nanofibers for hard tissue engineering
- •3.5 Cancer diagnosis and therapy
- •3.6 Concluding remarks and future perspectives
- •Keywords
- •References
- •4. Natural Biocarriers for Brain Targeting
- •Abstract
- •4.1 Introduction
- •4.1.1 Central nervous system
- •4.2 Biocarriers
- •4.2.1 Carbohydrates carriers
- •4.2.2 Protein carriers
- •4.2.3 Exosomes
- •4.3 Conclusions and perspectives
- •Keywords
- •References
- •Abstract
- •5.1 Introduction
- •5.2 Synthesis of graphene family nanomaterials
- •5.2.1 Graphene synthesis
- •5.2.2 GO and rGO Syntheses
- •5.2.3 GQd synthesis
- •5.4 Drug delivery and biomedical applications
- •5.4.1 Drug delivery
- •5.4.2 Gene delivery
- •5.4.3 Bioimaging
- •5.4.4 Photothermal therapy
- •5.4.5 Tissue engineering
- •5.5 Summary and future prospect
- •Keywords
- •References
- •6. Nanotechnology in Gene Delivery
- •Abstract
- •6.1 Introduction
- •6.2 Gene delivery
- •6.3 Nanotechnology in gene delivery
- •Keywords
- •References
- •Abstract
- •7.1 Introduction
- •7.2 Additive manufacturing in pharmacology
- •7.2.1 Extrusion-based 3D printing techniques
- •7.2.2 Stereolithography
- •7.2.3 Selective laser sintering
- •7.2.4 Binder jet printing
- •7.3 Most common polymers
- •7.3.1 Natural polymers
- •7.3.2 Synthetic polymers
- •7.3.2.5 Polyvinylpyrrolidone
- •7.4 Common 3D-printed dosage forms
- •7.4.1 Scaffolds
- •7.4.2 Tablets
- •Keywords
- •References
- •7.4.3 Microneedles
- •7.4.4 Capsule
- •7.4.5 Films
- •7.5 Main factors in drug delivery
- •7.5.1 Nature of polymers
- •7.5.2 Matrix permeability
- •7.5.3 Polymer blends
- •7.5.4 Specific surface area
- •7.5.5 Infill density and patterns
- •7.5.6 Pores
- •7.5.7 Cross-linking
- •7.5.8 Coating
- •7.5.9 Core/shell and multicompartment
- •7.6 Final considerations and future perspectives
- •Abstract
- •8.1 Introduction
- •8.2.1 Polymer solution concentration and viscosity
- •8.2.2 Molecular weight of polymer
- •8.2.3 Surface tension
- •8.2.4 Electrical conductivity
- •8.2.5 Applied voltage
- •8.2.6 Feed rate/flow rate
- •8.2.7 Temperature and humidity
- •8.3 Method of preparation for nanofibers
- •8.3.1 Electrospinning
- •8.3.2 Self-assembly
- •8.3.3 Phase separation
- •8.3.4 Drawing of nanofibers
- •8.3.5 Template synthesis
- •8.4 Biomedical applications of nanofibers
- •8.4.1 Wound dressing
- •8.4.2 Tissue engineering
- •8.4.3 In cancer therapy
- •8.4.4 Miscellaneous
- •8.5 Drug delivery application
- •8.5.1 Antihypertensive drug
- •8.5.2 Antimicrobial drug
- •8.5.3 Growth hormone
- •8.5.4 Miscellaneous
- •8.6 Conclusion
- •Keywords
- •References
- •Abstract
- •9.1 Introduction
- •9.2 Tissue engineering
- •9.3 Nanotechnology
- •9.4 Polymeric scaffolds in tissue engineering
- •9.5 Challenges
- •Keywords
- •References
- •Abstract
- •10.1 Introduction
- •10.2 Ideal properties of bioceramics
- •10.2.1 Mechanical property
- •10.2.2 Porosity, pore size, and shape
- •10.2.3 Biocompatibility and biodegradability
- •10.2.4 Osteoconductivity and osseointegrity
- •10.3 Bioceramics in orthopedic applications
- •10.4 Bioceramics in maxillofacial surgery
- •10.5 Bioceramic in drug delivery applications
- •10.6 Doped bioceramic in biomedical application
- •10.7 Conclusions
- •10.8 Future direction
- •Acknowledgments
- •Keywords
- •References
- •Index

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Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
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Advances in Pharmaceutical T echnology for Drug Delivery Systems (PTDDS), Volume 2: Recent Progress
in Biomedical Applications. Sougata Jana (Ed.)
© 2025 Apple Academic Press, Inc. Co-published with CRC Press (Taylor & Francis)
Natural Biocarriers for Brain Targeting
RAWIDH ALSAIDALANI
1
and HEBA A. GAD
1,2
1
2
CHAPTER 4
ABSTRACT
issue that requires a tailored delivery system. Nanotechnology represents a
protein-based carriers. Finally, special attention is given to exosomes as
4.1 INTRODUCTION
4.1.1 CENTRAL NERVOUS SYSTEM

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Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
-
includes brain tumors, stroke, and trauma. Figure 4.1 reveals the various
-
FIGURE 4.1

Natural Biocarriers for Brain Targeting
103
involved in this process is the blood barriers, including the blood–brain
nervous system, either using an invasive route or a noninvasive technique.
target site, such as into the cerebrum, ventricles, and spinal cord. Nonin-
transporters, (3) blood–brain barrier disruption using chemical, physical, or
et al., 2015).
4.1.2 NANOTECHNOLOGY TO OVERCOME THE BLOOD–BRAIN
BARRIER
ability to attach a targeting legend, biocompatibility, and biodegradability
polymers (natural or synthetic), lipids, proteins, polysaccharides, metals, and
inorganic compounds (Barbu et al., 2009).
4.2 BIOCARRIERS
such as cell structure, cell division, communications, substance transport,

104
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
outstanding advantages that permit their use, such as being biocompatible,
FIGURE 4.2
4.2.1 CARBOHYDRATES CARRIERS
are condensed together by glycosidic linkages to produce polysaccharides.
-
epithelium and mucous membranes because they contain hydrophilic groups
such as hydroxyl, carboxyl, and amino groups (Peptu et al., 2014).

Natural Biocarriers for Brain Targeting
105
Using carbohydrate polymers, it is possible to improve the pharmacoki-
brain (Ansari et al., 2020).
Chitosan is considered the second most prevalent naturally derived poly-
absorption and enhancing bioavailability (Sinha et al., 2004, Rehman et al.,
-
minergic neurons in the substantia nigra pars compacta, accompanied by
-
-
al., 2020). A second strategy involves using chitosan nanocarriers to deliver

106
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
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ability. On the contrary, the developed rotigotine-loaded chitosan nanopar-
neurons through an endocytic mechanism (Bhattamisra et al., 2020). Another
-
dramatically increase bioavailability in the brain (Mittal et al., 2016). In
addition, chitosan-coated-poly(lactic-co-glycolic acid)-nanoparticles can
-
(Ahmad, 2017).
-
loaded in chitosan nanoparticles and evaluated in an aluminum chloride-
transporting the cargo to the brain, as demonstrated by improved behavior
-
designed chitosan nanovehicles that serve as early therapeutic and diagnostic

Natural Biocarriers for Brain Targeting
107
agents. Magnetic resonance imaging contrast agents or single photon emis-
Furthermore, the nanovehicles contained either immunosuppressants (e.g.,
2014).
demonstrating that a mucoadhesive microemulsion containing chitosan
et al., 2018).
-
-
tions (Liu et al., 2018).
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