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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

328
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Index
A
Administrative routes
intramuscular (IM), 10–11
intravenous, 9–10
nasal administration, 15–16
ocular delivery, 13–14
oral delivery, 12–13
pulmonary route, 14–15
subcutaneous, 11
transdermal, 11–12
transmucosal drug delivery, 16
Albumin, 116–119
Alginates, 114–115, 205–206
Antihypertensive, 261–262
Antimicrobial, 262–263
B
Biocarriers, 103–104
carbohydrates, 104–105
exosomes, 116–131
protein, 115–116
Bioceramics system
biomedical application, 291, 294
biodegradability, 296–297
doped, 310–312
drug delivery, 308–310
mechanical, 294–295
orthopedic, 298–304
osteoconductivity, 297–298
porosity, 295–296
Brain targeting, 22, 101
alginates, 114–115
biocarriers, 103–104
carbohydrates, 104–105
exosomes, 116–131
protein, 115–116
carbohydrates, 114
chitosan, 105–111
hyaluronic acid, 111–114
cyclodextrin, 115
dextran, 115
protein
albumin, 116–119
casein, 125–126
collagen, 119–121
gelatin, 121–123
Breast cancer
and cardiotoxicity, applications, 35
advances, 51–56
nutritional, 46–51
physical exercise, 42–46
C
Cancer diagnosis, 82–88
Cancer therapy, 257–258
Carbohydrates
chitosan, 105–111
hyaluronic acid, 111–114
Cardiotoxicity
breast cancer, 35
advances, 51–56
nutritional, 46–51
physical exercise, 42–46
Casein, 125–126
Cellulose, 205
Charge-inducing molecules, 6
Chitosan, 206–207
Cholesterol, 6
Coating, 225
Critical packing parameter (CPP), 7–8
Cyclodextrin, 115
D
3D printed devices, 197
common polymers

334 Index
alginate, 205–206
cellulose, 205
chitosan, 206–207
synthetic, 207
dosage, 211
capsule, 220
microneedles, 218–220
tablets, 217–218
extrusion
semisolid, 202–203
blends, 222–223
coating, 225
cross-linking, 224–225
matrix, 222
multicompartment, 225–226
pores, 224
extrusion, 201
selective laser, 204
stereolithography, 203
synthetic
eudragit, 210–211
gelatin methacrylate (GelMA), 210
polycaprolactone, 207–208
polyethylene glycol, 208–209
polylactic acid, 208
polyvinyl alcohol, 209
polyvinylpyrrolidone (PVP), 209–210
Dextran, 115
Diagnostic imaging, 20–21
Drug delivery, 308–310
E
Electrospinning, 70–71, 250
biomaterials, 73
parameters, 71–73
Electrospun technology, 67
biomaterials
composite, 75
natural, 73–74
synthetic, 74–75
cancer diagnosis, 82–88
electrospinning, 70–71
biomaterials, 73
parameters, 71–73
blending, 76–77
coaxial, 78
emulsion, 77–78
tissue engineering, 79
hard, 79–81
Eudragit, 210–211
Extrusion, 201
F
Fused deposition, 201–202
G
Gelatin, 121–123
Gelatin methacrylate (GelMA), 210
Gene delivery, 175
carbon-based, 186–188
dendrimer, 184–185
intracellular, 177–178
metallic, 189–191
polymer, 180–184
preclinical studies, 179–180, 180
properties, 178–179
silica, 188–189
solid–lipid nanoparticles (LNPs), 185–186
Graphene quantum dots (GQd)
bottom–up, 146–147
Graphene-based system, 139
applications
bioimaging, 159–161
drug delivery, 150–157
gene, 157–159
photothermal, 161–164
tissue engineering, 164–167
cytocompatibility, 147–150
graphene quantum dots (GQd)
bottom–up, 146–147

Index 335
synthesis, 141
GQd, 145
graphene, 141–143
reduced graphene oxide (rGO), 143–145
H
Hyaluronic acid, 111–114
Hydrophilic-lipophilic balance (HLB), 6
I
Intramuscular (IM), 10–11
M
N
application, 259–260, 264–265
antihypertensive, 261–262
antimicrobial, 262–263
cosmetics, 258
parameters, 247
electrical, 248–249
molecular, 248
polymer, 248
temperature, 249
voltage, 249
preparation
applications, 253–254
cancer therapy, 257–258
electrospinning, 250
miscellaneous, 258
phase separation, 251–252
synthesis, 253
tissue engineering, 256–257
blending, 76–77
coaxial, 78
emulsion, 77–78
Nanotechnology
in gene delivery, 175
carbon-based, 186–188
dendrimer, 184–185
intracellular, 177–178
metallic, 189–191
polymer, 180–184
preclinical studies, 179–180, 180
properties, 178–179
silica, 188–189
solid–lipid nanoparticles (LNPs),
185–186
273
engineering, 280–284
nanotechnology, 278–280
tissue, 275–278
Nasal administration, 15–16
Niosomes
administrative routes
intramuscular (IM), 10–11
intravenous, 9–10
nasal administration, 15–16
ocular delivery, 13–14
oral delivery, 12–13
pulmonary route, 14–15
subcutaneous, 11
transdermal, 11–12
transmucosal drug delivery, 16
advantages, 3–4
biomedical applications
brain targeting, 22
diagnostic imaging, 20–21
nonviral gene delivery, 24–25
targeted drug delivery, 22–23
vaccine delivery, 21–22
components
charge-inducing molecules, 6
cholesterol, 6
hydrophilic-lipophilic balance (HLB), 6
drug delivery, 2
critical packing parameter (CPP), 7–8

336 Index
HLB value, 7
phase transition temperature, 8–9
structure, 4
therapeutics
anticancer drugs, 17–18
clinical trial, 19–20
hemoglobin, 19
natural products, 18–19
protein and peptide, 16–17
Nonviral gene delivery, 24–25
O
Ocular delivery, 13–14
Oral delivery, 12–13
Osteoconductivity, 297–298
P
Phase separation, 251–252
Phase transition temperature, 8–9
Polyethylene glycol, 208–209
Polylactic acid, 208
Polyvinyl alcohol, 209
Polyvinylpyrrolidone (PVP), 209–210
Porosity, 295–296
Protein
albumin, 116–119
casein, 125–126
collagen, 119–121
gelatin, 121–123
Pulmonary route, 14–15
R
Reduced graphene oxide (rGO), 143–145
S
Selective laser, 204
Semisolid, 202–203
Solid–lipid nanoparticles (LNPs), 185–186
Stereolithography, 203
T
anticancer drugs, 17–18
clinical trial, 19–20
hemoglobin, 19
natural products, 18–19
protein and peptide, 16–17
hard, 79–81
V
Vaccine delivery, 21–22
W
Wound dressing, 255–256
Z
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