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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
RAW 264.7 cells (macrophage cell line) leading to cell death through reac-
tive oxygen species (ROS)-induced cellular apoptosis at the concentration
-
the stem cells. Fan and co-researchers examined the cytocompatibility and
-
-

Graphene-based System for Drug Delivery and Biomedical Application
149
in vivo, that is, spleen, kidney, lungs, and liver in mice over 90 days period
Raman intensity, elevated I
D
I
G
∼
∼
FIGURE 5.2 Suggested receptor-mediated phagocytic mechanism and other important
Source

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Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
accumulation in the lungs and liver although in a time and dose-dependent
and spleen, the reticuloendothelial system, and eventually excreted through
5.4 DRUG DELIVERY AND BIOMEDICAL APPLICATIONS
As discussed in the earlier sections that graphene and its derivatives possess
excellent physical, chemical, thermal and optoelectronic properties, thereby,
-
nanomaterials.
5.4.1 DRUG DELIVERY

Graphene-based System for Drug Delivery and Biomedical Application
151
graphene, enabling it to load hydrophobic drugs, genes, peptides, etc. through
-
-
cancer cell lines in concentration and in time-dependent manner (Xu et al.,

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Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
colon cancer cell line) and HepG2 (liver cancer cell line) although nontoxic
delivery system (Bullo et al., 2019).
FIGURE 5.3
Source
Society.
physiological system, prolonged circulation time, and ability to accumulate
-

Graphene-based System for Drug Delivery and Biomedical Application
153
-
cytoskeleton, and membrane-associated genes. Furthermore, in vivo study
depletion, and pathogenicity to vital organs such as the liver and lung in
(GO-NH
2
-
GO (Lu et al., 2012). Other synthetic polymers such as poly--lysine (PLL),
-
nontoxicity and natural abundance. Chitosan, gelatin, sodium alginate,

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Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
FIGURE 5.4
Source:-
cal Society.
-
animal study revealed that as-prepared nanostructure can suppress tumor

Graphene-based System for Drug Delivery and Biomedical Application
155
-
-
-
-
-
-

156
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
2016). On the other side, colorectal cancer, ovarian cancer, prostate cancer,
breast cancer, neuroblastoma cancer, and pancreatic cancers overexpressed
-
-
elevated in the tumor microenvironment compared to the normal cells due
-
Due to its noninvasive nature, light, that is, visible light, ultraviolet

Graphene-based System for Drug Delivery and Biomedical Application
157
nanoparticles (MSN) have been developed. NIR exposure disrupted the
to poly(N,N
5.4.2 GENE DELIVERY
-
tives is used. Chitosan, PEG, and polyethylenimine (PEI) such as polymers
this end. For instance, a research group has developed oleic acid and polyami-
cytotoxicity against MG-63 and HeLa cells. Further study revealed that the
-
-
-
tives is generally done by click chemistry, that is, carbodiimide chemistry.
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