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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5705_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 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)
Graphene-based System for Drug
Delivery and Biomedical Application
SANTANU GHOSH
1
, SOUMYARUP DUTTA
2
, and MOUMITA KUNDU
2
1
2
CHAPTER 5
ABSTRACT
(2D) nanomaterial, in 2004, it gained mammoth research interest in various
sp
2
been developed including graphene oxide (GO), reduced graphene oxide
-
drug delivery , gene delivery , bioimaging, photothermal therapy, and tissue
engineering.

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Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
5.1 INTRODUCTION
-
sp
2
that is, graphene oxide (GO), reduced graphene oxide (rGO), and graphene
-
elevated electron transport capacity at ambient conditions, desirable thermal
sensing, electronics, energy, and biomedical applications (Ghosh and Chat-
drug delivery, gene delivery, sensing, tissue engineering, etc. (Ghosal and
Sarkar, 2018).

Graphene-based System for Drug Delivery and Biomedical Application
141
including drug delivery, gene delivery, bioimaging, photothermal therapy,
and tissue engineering.
5.2 SYNTHESIS OF GRAPHENE FAMILY NANOMATERIALS
nanosheets, GO, rGO, and GQd. From bulk graphite, graphene sheets are
5.2.1 GRAPHENE SYNTHESIS
-
-

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Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
Ni (Reina et al., 2009). CVD technique has been also employed to develop
larger graphene sheets (in centimeters) using methane as the carbon source
attachment to the underlying silicon atoms. Here, the silicon layer serves as
an insulator and does not exert electronic properties like graphene. Note-
the solution processable technique to prepare graphene has been recently

Graphene-based System for Drug Delivery and Biomedical Application
143
-tyrosine (Shams et al., 2015).
5.2.2 GO AND RGO SYNTHESES
-
also employed to produce GO.
to produce graphite oxide through oxidation (Brodie, 1860). Staudenmaier

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Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
acid reacts to potassium permanganate to produce dimanganeseheptaoxide,
FIGURE 5.1
Source
Chemical Society.

Graphene-based System for Drug Delivery and Biomedical Application
145
researchers used several reducing agents including potassium hydroxide,
-
tive agent, sodium borohydride decreases the electrical resistance less than
5.2.3 GQD SYNTHESIS
Several processes are included under chemical ablation, that is, solvo-

146
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
-
°
3+
metal

Graphene-based System for Drug Delivery and Biomedical Application
147
60
60
5.3 CYTOCOMPATIBILITY AND BIOCOMPATIBILITY OF GRAPHENE
AND ITS DERIVATIVES
-
-
ones and hydrophilic is more cytocompatible than the hydrophobic graphene
high stability in biological medium thereby reducing the cytotoxicity. For
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