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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

158
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
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observed that hydrothermally prepared system (RGPP) had higher gene trans-
processesendorse covalent nucleophilic interaction among the epoxy moieties
-
∼
2
∼
FIGURE 5.5
Nanocomposites.
Source
Society.

Graphene-based System for Drug Delivery and Biomedical Application
159
5.4.3 BIOIMAGING
-
ment, and prognosis compared to the normal physiological condition. In the
-
cability in this sector.
Despite various limitations such as background scoring, and photo-
-
2010).

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Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
-
-
FIGURE 5.6 In vivo
Source
Chemical Society.

Graphene-based System for Drug Delivery and Biomedical Application
161
While the other noninvasive, hybrid imaging technique, photoacoustic
-
2012). Other group developed graphene-tied poly(vinyl alcohol) microbub-
5.4.4 PHOTOTHERMAL THERAPY
-
-
peutic strategies. Photothermal therapy is one such novel approach. In
-

162
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
irradiation, thereby, killing both Staphylococcus aureus (Gram-positive)
and Escherichia coli
graphene nanomaterials plays a critical role in its applications. In a study ,
-
-
cidal activity through photothermal therapy compared to the negatively
E. coli
al., 2017).
-
study exposed the BSA-rGO and DOX-BSA-rGO-treated U87MG cells
2
-
and enhanced photothermal properties. Such nanopatch exhibited a higher

Graphene-based System for Drug Delivery and Biomedical Application
163
FIGURE 5.7
2
culture medium, (B) BSA-rGO, and (C) DOX-BSA-rGO nanosheets. NIR irradiation groups:
Source
Chemical Society.

164
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
compared to uncoated rGO and gold-coated GO (Lim et al., 2013). Due to
-
context, a research group developed tripeptide -arginyl-glycyl--aspartic
5.4.5 TISSUE ENGINEERING
-
-
-
-
graphene and its derivatives in various tissue engineering applications.
and obesity demand bone tissue engineering. Due to the extraordinary

Graphene-based System for Drug Delivery and Biomedical Application
165
et al., 2022). In another study, researchers have developed hydroxyapatite
3
) and tensile strength (105
MPa) compared to the hydroxyapatite-PLA matrix. Such mechanically
tough matrix promotes bone regeneration (Chen et al., 2018). Furthermore,
-
-

166
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
FIGURE 5.8 Specimen
Chemical Society.
collagen, glycosaminoalycan, proteoglycans, and non-collagenous proteins,
-
not regenerate upon damage. In this regard, cartilage tissue engineering
murine chondrocyte cells, and SW1353 cells. In vivo results depicted the
-
tions (Lyu et al., 2022).

Graphene-based System for Drug Delivery and Biomedical Application
167
In this scenario, several cardiac tissue constructs have developed to mimic the
ECM in the cardiac tissue through tissue engineering approaches. Graphene
-
-
very close electrical conductivity and mechanical property compared to
is, Nkx 2.5and Connexin-43 could be observed (Pilato et al., 2023). Besides
engineering applications such as skin, muscle, and neural tissue engineering
due to their unique properties.
5.5 SUMMARY AND FUTURE PROSPECT
-
-
the end product. Furthermore, more in vivo
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