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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5983_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

128
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
Protein
type
Disease Drug Special comment References
disease
(Bashir et al., 2022,
Bashir et al., 2023)
Gelatin
Gallic acid
Gadolinium
magnetic resonance imaging contrast agent.
(Kimura et al., 2021)
Glioblastoma
Paclitaxel Paclitaxel encapsulated in dual stimuli-responsive in situ
(Kang et al., 2021)
Ischemic stroke Estradiol
(Joachim et al., 2020)
Silk
Fibroin
Brain tumor Doxorubicin
and enhance the blood–brain barrier transverses through their
(Pandey et al., 2020a,
Pandey et al., 2020b)
Photothermal
glioblastoma
Indocyanine green
mice
(Xu et al., 2018)
Neurodegenerative
diseases such
disease
Crocin
(Song et al., 2022)
Quercetin
astrocyte marker GFAP.
(Moreno et al., 2017)
TABLE 4.3
(Continued)

Natural Biocarriers for Brain Targeting
129
Protein
type
Disease Drug Special comment References
Glioblastoma Curcumin
nanoparticles.
Casein Glioma Hydroxycamptothecin
(Gao et al., 2019)
Iron overloaded (Adel et al., 2021)
TABLE 4.3
(Continued)

130
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
2019).
-
-
-
technique to overcome the restricted brain permeability and to augment
macrophage-derived exosomes and blood serum-derived exosomes delivery
et al., 2019).

Natural Biocarriers for Brain Targeting
131
-
TABLE 4.4
Exosomes
sources
Drug Disease Special comment References
Blood Dopamine
disease
receptor interaction.
(Qu et al.,
2018)
Macrophages
derived
exosomes
Ginsenoside
Rg1
Rg1 could inhibit the
exosomes-miR-21 release
the brain, enhancing tissue
3 protein expression,
matrix metalloproteinases
proteolysis, and restricting
proteins degradation thus
protecting the blood–brain
barrier integrity.
2021)
Macrophages
derived
exosomes
Baicalin ischemic
stroke
Baicalin-loaded exosomes
revealed better targeting
Baicalin-loaded exosomes
reactive oxygen species.
(Huang et
al., 2021)
Plasma
exosomes
Quercetin
disease
Enhanced brain delivery
quercetin using drug-loaded
symptoms
(Qi et al.,
2020)
Macrophage-
derived
exosomes
Curcumin Ischemia-
Inhibiting reactive oxygen
species-mediated mitochon-
drial apoptosis in a transient
cerebral ischemia rat model.
(He et al.,
2020)

132
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
4.3 CONCLUSIONS AND PERSPECTIVES
carbohydrate and protein-based carriers tailored to target the brain have
KEYWORDS
• biocarriers
• targeting
• Alzheimer's disease
• Parkinson's disease
• exosomes
• polysaccharides based carriers
• protein based carriers
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