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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5362_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Carbon Based Nanomaterials for Drug Delivery
- •Preface
- •Acknowledgements
- •Contents
- •Editor and Contributors
- •Abbreviations
- •1.2 Market Statistics
- •Carbon-Based Nanomaterials: An Overview
- •1. Introduction
- •1.1 Evolution of Carbon-Based Nanomaterials
- •2. Carbon-Based Nanostructures
- •2.1 Fullerene
- •2.2 Carbon Nanotubes (CNTs)
- •2.4 Graphene
- •2.5 Nanodiamonds (NDs)
- •2.6 Nano-Onions (CNOs)
- •2.7 Nanohorns (CNHs)
- •2.8 Carbon Dots (CDs)
- •2.9 Nanoporous Activated Carbon
- •3. Synthesis Techniques
- •4. Properties of Carbon-Based Nanomaterials
- •4.1 Physicochemical Properties
- •4.2 Thermal Properties
- •4.3 Mechanical Properties
- •4.4 Optoelectronic Properties
- •4.5 Antimicrobial Properties
- •4.6 Biological Properties
- •5. Applications of Carbon-Based Nanomaterials
- •5.1 Environmental Remediation
- •5.2 Agriculture
- •5.3 Biofuel
- •5.4 Energy Storage
- •5.5 Biomedical Applications
- •6. Challenges and Future Perspectives
- •7. Concluding Remarks
- •References
- •Carbon-Based Nanostructured Materials: Designing, Properties and Applications
- •1. Introduction
- •2.1 Zero-Dimensional Carbon-Based Nanostructures (0D)
- •2.2 One-Dimensional Carbon-Based Nanostructures
- •2.3 Two-Dimensional (2D) Carbon-Based Nanostructures
- •2.4 Three-Dimensional (3D) Carbon-Based Nanostructures
- •3.1 Chemical Vapor Deposition
- •3.2 Hydrothermal and Solvothermal Techniques
- •3.3 Microwave-Assisted Technique
- •3.4 Chemical Oxidation Synthesis
- •4. Properties of Carbon-Based Nanostructured Materials
- •4.1 Thermal Properties
- •4.2 Mechanical Properties
- •4.3 Optoelectronic Properties
- •4.4 Antimicrobial Properties
- •4.5 Biological Properties
- •5. Applications of Carbon-Based Nanostructured Materials
- •5.2 Antibacterial and Antiviral Applications
- •5.3 Theragnostic
- •5.4 Wound Healing
- •5.5 Tissue Engineering
- •5.6 Drug Delivery
- •5.7 Biosensing
- •6. Challenges and Future Perspectives
- •7. Concluding Remarks
- •References
- •Drug Delivery System and Technologies
- •1. Introduction
- •2. Drug Delivery System
- •2.1 Conventional Drug Delivery System
- •2.2 Advanced Drug Delivery System
- •2.3 Controlled and Sustainable Drug Delivery System
- •3. Drug Delivery Technologies
- •3.1 Active and Passive Drug Delivery
- •3.2 Smart Drug Delivery
- •3.3 Intravenous and Extravaneous Drug Delivery
- •3.4 Various Types of Delivery Technologies
- •4. Challenges and Future Perspectives
- •5. Conclusion
- •References
- •Carbon-Based Nanomaterials for Drug Delivery: Past, Present, Future Directions
- •1. Introduction
- •3. Current Status in Drug Delivery by CNMs
- •3.1 Graphene-Based Nanomaterials in Drug Delivery
- •3.4 Nanodiamond Based Drug Delivery Systems
- •3.5 Nano-Onions in Drug Delivery
- •3.6 Nanohorns in Drug Delivery
- •3.7 Fullerene in Drug Delivery
- •4. Challenges and Future Perspective
- •5. Conclusions
- •References
- •Carbon Nanomaterial-Incorporated Supramolecular Drug Delivery
- •1. Introduction
- •2. Different Carbon Nanomaterials in Drug Delivery
- •2.1 Carbon Nanotubes (CNTs)
- •2.3 Graphene
- •2.4 Carbon Quantum Dots
- •2.5 Fullerene
- •2.6 Carbon Nanohorns
- •2.7 Carbon Nano-Onions
- •2.8 Nano-Diamond
- •3. Supramolecular Chemistry in Drug Delivery
- •3.1 Principles of Supramolecular Chemistry
- •3.3 Applications of Supramolecular Biomaterials
- •4. Carbon Nanomaterial-Incorporated Supramolecular Drug Delivery
- •5.1 Cyclodextrins
- •5.2 Calixarenes
- •5.3 Cucurbituril
- •5.4 Pillarenes
- •5.5 Crown Ether
- •6. Toxicity Concerns of Carbon Nanomaterials
- •7. Improving the Effectiveness of Nanoparticle Systems
- •8. Future of Nanomedicine
- •9.1 Challenges
- •9.2 Future Perspectives and Opportunities
- •9.3 Conclusions
- •References
- •Carbon Nanomaterial-Based Polymeric Nanocomposites for Drug Delivery
- •1. Introduction
- •2.1 Carbon Quantum Dot-Based Polymer Nanocomposite
- •2.2 Carbon Nanotube-Based Polymer Nanocomposite
- •2.3 Graphene Quantum Dot-Based Polymer Nanocomposite
- •2.5 Fullerene-Based Polymer Nanocomposite
- •2.6 Nanodiamond-Based Polymer Nanocomposite
- •3. Drug Delivery Systems Using Carbon Nanomaterial
- •3.1 Anticancer Drug Delivery
- •3.3 Infectious Disease Drug Delivery
- •3.4 Topical Drug Delivery
- •3.5 Brain Drug Delivery
- •3.6 Oral Drug Delivery
- •4. Challenge and Future Perspectives
- •5. Conclusion
- •References
- •Carbon Nanomaterial-Incorporated Polysaccharide-Based Nanocomposite for Drug Delivery
- •1. Introduction
- •1.1 Drug Delivery
- •1.2 Carbon Nanomaterials
- •1.3 Polysaccharide-Based Nanocomposite
- •2.1 CN-Incorporated Alginate-Based Nanocomposite
- •2.2 CN-Incorporated Cellulose-Based Nanocomposite
- •2.3 CN-Incorporated Chitosan-Based Nanocomposite
- •2.4 CN-Incorporated Dextran-Based Nanocomposite
- •2.5 CN-Incorporated Hyaluronic Acid-Based Nanocomposite
- •2.6 CN-Incorporated Starch-Based Nanocomposite
- •2.7 CN-Incorporated Pectin-Based Nanocomposite
- •2.8 CN-Incorporated Guar Gum-Based Nanocomposite
- •2.9 CN-Incorporated Agarose-Based Nanocomposite
- •2.10 CN-Incorporated Carrageenan-Based Nanocomposite
- •2.11 CN-Incorporated Glucomannan-Based Nanocomposite
- •3. Challenges and Future Prospective
- •4. Concluding Remarks
- •References
- •Graphene-Based Nanomaterials for Drug Delivery
- •1. Introduction
- •1.1 Challenges in Conventional Drug Delivery Systems
- •1.2 Overview of Nanomaterials for Drug Delivery
- •1.3 Role of Graphene-Based Nanomaterials in Drug Delivery
- •2. Synthesis of Graphene
- •2.1 Chemical Reduction Method
- •2.2 Thermal Reduction
- •2.3 Electrochemical Reduction
- •2.4 Chemical Vapor Deposition Method
- •2.5 Mechanical Exfoliation
- •2.6 Epitaxial Growth Method
- •2.7 Growth in Solvothermal and Hydrothermal Systems
- •2.8 Electrochemical Deposition
- •3. Types of Graphene-Based Materials
- •3.1 Graphene Quantum Dots, (GQDs)
- •3.2 Graphene Oxide (GO)
- •3.3 Graphene Nanoribbons (GNRs)
- •3.4 Oxidized Graphene Nanoribbons
- •4. Graphene Functionalized Materials for Drug Delivery
- •4.1 In Bone Tissue Regeneration
- •4.2 In Neural Regeneration
- •4.3 In Photodynamic and Photothermal Therapy
- •4.4 In Enhancing Cellular and Humoral Immunity
- •4.6 Miscellaneous
- •5. Challenges and Future Perspective
- •6. Conclusion
- •References
- •Carbon Quantum Dots Based Materials for Drug Delivery
- •1. Introduction
- •2. Synthesis Process of Carbon Quantum Dots
- •2.1 Top-Down Approaches
- •2.2 Bottom-Up Approaches
- •2.3 Microwave-Assisted Method
- •2.4 Electrochemical Method
- •2.5 Laser Ablation Method
- •2.6 Pyrolysis Method
- •2.7 Template-Assisted Method
- •4. Challenges and Future Perspective
- •5. Concluding Remarks
- •References
- •Carbon-based Nanocarriers for Sustained Drug Release in Dentistry
- •1. Introduction
- •2.1 Oral Mucosa Structure
- •2.2 Sites for Drug Delivery
- •2.3 Permeability
- •3. Local Drug Delivery for Dental Diseases
- •3.1 Odontogenic Infection
- •3.2 Non-odontogenic Infection
- •4. Bio-adhesive Nanoparticles: Novel Treatment Modality
- •4.1 Bio-adhesive Nanoparticles
- •4.2 Mechanism of Bioadhesion
- •5.1 Carbon Nanotubes
- •5.2 Graphene
- •5.3 Nanodiamonds
- •5.4 Fullerenes
- •5.5 Porous Carbon
- •5.6 Carbon Dots
- •6. Drug Delivery Systems Based on CBNs
- •6.2 Immediate Drug Delivery System (IDDS)
- •6.3 Sustained-release Drug Delivery Systems
- •6.4 Controlled Drug Delivery System (CDDs)
- •8. Conclusion
- •References
- •Fullerene Based Materials for Drug Delivery
- •1. Introduction
- •2. Types of Fullerene Derivatives
- •2.1 Exohedral Fullerene Derivatives
- •2.2 Endohedral Fullerene Derivatives
- •2.3 Surface Derivatized Fullerenes
- •3. Interaction of Fullerene Derivatives for Drug Delivery
- •4. Fullerene Based Materials for Drug Delivery
- •4.1 Nucleic Acid Delivery
- •4.2 Peptide Delivery
- •4.3 Topical Drug Delivery
- •4.4 Infectious Diseases Drug Delivery
- •4.5 Anticancer Drug Delivery
- •4.7 Brain Drug Delivery
- •4.8 Ocular Drug Delivery
- •5. Challenges and Future Perspectives
- •6. Concluding Remarks
- •6.1 Abbreviations
- •References
- •Graphene Quantum Dots-based Nanomaterials for Drug Delivery
- •1. Introduction
- •2. Synthesis of GQDs
- •3. GQD’s Properties for Drug Delivery
- •3.1 Optical Properties
- •3.2 Physicochemical Properties
- •3.3 Mechanical Properties
- •3.4 Biocompatibility and Cytotoxicity
- •4. Characterization of GQDs-Based Nanomaterials
- •4.1 Characterization of Multifunctional GQDs-Based Nanomaterials
- •5.1 Strategies for Developing Medication Delivery Systems Based on GQD
- •5.2 PH-responsive Drug Delivery Systems (GQD-DDSs)
- •5.3 Targeted Drug Delivery Using Ligand-Based GQDs as a Mediator
- •5.4 Improvement of Medicines’ Pharmacological Properties Using GQDs
- •5.5 Enhancing Cytotoxicity with GQD-DDS
- •7. Applications of Chiral GQDs
- •10. Challenges and Future Perspectives
- •11. Conclusions
- •References
- •Carbon Nano-onions for Drug Delivery
- •1. Introduction
- •2. Carbon Nano-Onion: A Multi-Layered Nanocarrier
- •3. Synthesis of Carbon Nano-Onions
- •3.1 Annealing Method
- •3.2 Carbon Ion Implantation Method
- •3.3 Arc Discharge Method
- •3.4 Carbon Vapour Deposition Method
- •3.5 Pyrolysis Method
- •6. Carbon Nano-Onions in Drug Delivery
- •6.1 Delivery of Therapeutic Agents
- •6.2 Delivery of Targeting Agents
- •6.3 Delivery of Imaging Agents
- •7. Challenges and Future Perspectives
- •8. Concluding Remarks
- •References
- •Chitosan/Carbon Nanocomposites in Drug Delivery and Cardiovascular Diseases
- •1. Introduction
- •1.1 Drug Delivery
- •1.2 Cardiovascular Diseases
- •1.3 Chitosan and Its Properties
- •1.4 Chitosan/Carbon Nanocomposites
- •2. Chitosan/Carbon Nanocomposites in Drug Delivery
- •3. Chitosan/Carbon Nanocomposites in CVDs
- •3.1 Chitosan-Based Scaffolds
- •3.2 Chitosan in Cardiac Tissue Engineering
- •3.3 Chitosan-Based Cell Therapy
- •3.4 Chitosan-Based Gene Delivery
- •3.5 Chitosan-Protein Interaction
- •4. Challenges and Future Perspective
- •5. Concluding Remarks
- •References
- •Graphene Reinforced Chitosan Nanocomposites for Drug Delivery
- •1. Introduction
- •2. Chitosan: Structure and Properties
- •3. Graphene: Structure, Types and Properties
- •4.1 Electrospinning Method
- •4.2 Sol–gel Method
- •4.3 Solution Mixing Method
- •4.4 In-situ Polymerization Method
- •5.2 Chitosan/Graphene Aerogels
- •5.3 Chitosan/Graphene Hydrogels
- •5.4 Chitosan/Graphene Thin Films
- •6.1 Oral Drug Delivery
- •6.2 Mucosal Drug Delivery
- •6.3 Transdermal Drug Delivery
- •6.4 Parenteral Drug Delivery
- •7. Challenges and Future Perspectives
- •8. Concluding Remarks
- •References
- •1. Introduction
- •2. Functionalization of CNFs
- •2.1 The Need for Functionalization

Graphene-Based Nanomaterials for Drug Delivery 245
allowing for regulated release in reaction to environmental stimuli, thanks to their
special electrical features [75].
3.5 Nanoflakes of Graphene
Small, thin, and irregularly shaped graphene structures with lateral dimensions
ranging from a few nanometers to micrometers are known as graphene nanoflakes.
They can be created using bottom-up synthesis techniques or top-down procedures
like mechanical exfoliation. Due to their large surface area, simplicity of functionalization, and biocompatibility, graphene nanoflakes have demonstrated potential
as drug carriers. These nanoflakes are attractive candidates for intracellular drug
delivery because of their irregular structure, which may enhance cellular uptake and
drug release. For effective drug delivery, additional research is needed to maximize
their drug-loading capability and enhance their biodegradability.
Promising prospects for drug delivery applications include graphene-based nanomaterials such as GQDs, GO, graphene nanoribbons, oxidized graphene nanoribbons,
and graphene nanoflakes. They are adaptable platforms for drug delivery s ystems
thanks to their special qualities, which include a wide surface area, functionalization
potential, and customizable electrical and optical properties. Utilizing these unique
characteristics, scientists can create focused and regulated drug delivery systems
that have the potential to completely change therapeutic approaches across a range
of biological sectors [76]. To successfully translate these findings into practical applications, more study is necessary to fully understand their biocompatibility, in vivo
behavior, and long-term safety profiles.
4 Graphene Functionalized Materials for Drug Delivery
Over time, the discipline of medication administration has made incredible strides,
changing how modern medicine is practiced. Graphene functionalized materials
have become a viable platform with distinct features and a wide range of applications among the many developments (Fig. 6). With a focus on their uses in bone
tissue regeneration, neural regeneration, photodynamic and photothermal therapy,
enhancing cellular and humoral immunity, antibacterial action against Gram-Positive
and Gram-Negative bacteria, and other applications, this chapter examines the multifaceted role of graphene functionalized materials in drug delivery. Targeting particular tissues, organs, or cells while limiting negative effects on healthy tissues is the
goal of drug delivery systems, which attempt to increase the therapeutic efficacy of
drugs. Due to its outstanding biological, mechanical, electrical, and optical qualities,
graphene, a single layer of carbon atoms organized in a two-dimensional lattice,
has attracted a lot of interest. Researchers have modified graphene’s properties to fit

246 A. Mohamed Noor et al.
Fig. 6 Different applications of graphene functionalized for drug delivery
different drug delivery applications by functionalizing it with bioactive chemicals,
peptides, or nanoparticles, unleashing its potential to transform medical treatments.
4.1 In Bone Tissue Regeneration
A crucial component of regenerative medicine is bone tissue regeneration, which
has the potential to significantly improve the lives of millions of people with
bone illnesses and injuries. Traditional methods of bone grafting have drawbacks,
such as inadequate host tissue integration and possible immunological reactions.
Graphene, graphene functionalized materials, and its derivatives offer a creative
answer to these problems. Graphene derivatives have the capability to form composites with diverse structures, thereby enhancing their properties. This, in turn, directly
enhances the functionality of bone-related cells or indirectly promotes them through
external stimuli. Graphene derivatives can facilitate the growth and proliferation of
osteoblasts, induce osteogenic differentiation of stem cells by activating specific
signal pathways, and up-regulate the expression of specific factors in macrophages,
hence ultimately leading to bone regeneration. The remarkable mechanical strength
and biocompatibility of graphene make it a prime choice for applications involving
bone tissue regeneration. Researchers have added bioactive chemicals and growth
factors to graphene to functionalize it, promoting osteogenesis and improving the
integration of grafts with host tissue. These modified graphene scaffolds serve

Graphene-Based Nanomaterials for Drug Delivery 247
as precise drug delivery devices, dispensing growth hormones and osteogenic
substances just where damage has occurred. As a result, bone regeneration is sped up,
improving healing outcomes. Additionally, because of graphene’s electrical conductivity, electroactive scaffolds can be created to promote bone tissue growth and nerve
regeneration alongside bone healing [77, 78].
4.2 In Neural Regeneration
The intricate process of neural regeneration offers individuals with neurological
diseases and traumas great hope [79]. The promotion of significant neuronal regeneration and functional recovery is frequently difficult with conventional therapy.
Graphene functionalized materials have become a fascinating approach to overcome these challenges. Because of graphene’s special qualities such as its electrical
conductivity and capacity to promote brain cell growth, it is a desirable option for
use in applications involving neural regeneration [80]. Researchers have successfully
functionalized graphene with medicinal medicines and neurotrophic factors to help
with neuronal regeneration and repair. In 2021, Qian et al. reported that graphenebased nanomaterials have little toxicity and can repair massive nerve damage in the
central and peripheral nervous systems through dual control of Schwann cells and
astroglia. By using 4% of graphene-based nanomaterials in the PCL matrix, it exerts
low toxicity and displays a long-term effect of reparation. The toxicity still concerns
researchers which may harm organs hence ensuing renal and hepatic failure, however,
it is found that axon and myelin were repaired after the application of graphenebased scaffold implantation [81]. On the other hand, targeted medication delivery
to injured brain tissues is made possible by these functionalized graphene carriers,
which speeds up regeneration and promotes functional recovery. The restoration of
sensory and motor functions in individuals with spinal cord injuries and other neurological disorders has also shown promise for graphene-based neural interfaces and
neuroprosthetic devices [82].
4.3 In Photodynamic and Photothermal Therapy
Non-invasive therapeutic techniques including photodynamic therapy (PDT) and
photothermal t herapy (PTT) have drawn a lot of attention in the fight against cancer.
These treatments rely on light-activated chemicals to selectively kill cancer cells
while protecting healthy tissues. Materials with graphene functionalization have
shown considerable promise for improving PDT and PTT effectiveness. Graphene
is a prime candidate for photothermal therapy due to its outstanding light absorption and photothermal conversion capabilities. In 2023, Lee et al. have reported
that both reduced graphene oxide quantum dots (RGQDs) and hyaluronic acid

248 A. Mohamed Noor et al.
Fig. 7 Visible confocal fluorescence microscopy image of reduced graphene quantum dots and
Hyaluronic acid graphene quantum dots within HeLa cells demonstrating both extracellular and
intracellular photothermal therapy potential. Reproduced with permission from MDPI [83]
graphene quantum dots (HGQDs) display synergistic effect of promising biocompatible image-guided photothermal agents and drug delivery capabilities which further
expand Graphene Quantum Dots applications into highly desired drug/PTT combo
treatment methods. As shown in Fig. 7a, d, the green fluorescence of the 535 nm
observed within HeLa cells using a lamp illumination at 460 ± 20 nm and Fig. 7b,
e shows NIR imaging with 808 nm laser excitation. Figure 7c, f demonstrates the
1080 nm fluorescence spectra obtained within the cellular structures by RGQDs and
HGQDs respectively, validating the intracellular presence of GQDs with less visibleoverlapping and background-free measurement [83]. Graphene-based drug delivery
systems can assemble in tumor tissues when functionalized with photosensitizers
and targeting ligands. These functionalized graphene materials produce localized
heat when exposed to near-infrared light, which causes cancer cells to be selectively destroyed [84]. Functionalized graphene can work as an effective photosensitizer carrier in photodynamic treatment. Reactive oxygen species are released by the
functionalized graphene upon light activation, effectively eliminating cancer cells.
The synergistic advantages of combining PDT and PTT in a single graphene-based
nanocomposite have been astounding, increasing treatment efficacy while reducing
side effects [ 85].
4.4 In Enhancing Cellular and Humoral Immunity
A potential strategy for treating a number of illnesses, including cancer and autoimmune disorders, is immunotherapy. Exciting possibilities exist for improving cellular

Graphene-Based Nanomaterials for Drug Delivery 249
and humoral immunity thanks to graphene functionalized materials. With the use
of immunomodulatory substances like cytokines or immunomodulatory peptides,
researchers have functionalized graphene [86, 87]. As a result of these functionalized graphene carriers’ potent immune response modulation, the body’s protection
against infections is improved, and tissue regeneration is encouraged. Additionally,
using functionalized graphene as a platform, immunomodulators can be precisely
delivered to the troubled locations for treatment.
4.5 In Antibacterial Action Against Gram-Positive
and Gram-Negative Bacteria
An important global health concern is the emergence of antibiotic-resistant microorganisms. Graphene functionalized materials offer a potential remedy for efficiently
battling viruses that are resistant to medication. Researchers have created antibacterial nanostructured graphene composites by functionalizing graphene with antimicrobial peptides and nanoparticles. These modified graphene materials have the ability to
damage bacterial membranes, which results in bacterial death. Antimicrobial medications can be delivered to specific areas of the body utilizing graphene carriers,
which limits harm to healthy tissues and lowers the chance of systemic toxicity [88].
Additionally, graphene’s special qualities, namely, its expansive surface area and
high loading capacity, make it a desirable choice for antibacterial applications.
4.6 Miscellaneous
Graphene functionalized materials have demonstrated potential in numerous other
drug delivery fields outside of the aforementioned applications. For instance, in
order to effectively treat chronic inflammatory illnesses, researchers have looked
into graphene-based carriers for the targeted delivery of anti-inflammatory pharmaceuticals. A potential advancement in the treatment of genetic problems is the
delivery of small interfering RNA (siRNA) using functionalized graphene for use
in gene therapy applications [89]. In addition, the problem of multidrug resistance
in cancer treatment has been addressed by research into graphene functionalized
materials to increase the effectiveness of conventional chemotherapy medications
[90]. In the area of drug delivery, graphene functionalized materials have become a
game-changing platform, transforming the management of numerous medical disorders. The special qualities and adaptability of graphene have opened up a wide
range of potential for medical applications, including bone tissue regeneration, brain
repair, cancer therapy, and immunomodulation. The development of graphene-based
drug delivery systems is encouraging, but before they are widely used in clinical
settings, significant issues with biocompatibility, long-term safety, and scalability

250 A. Mohamed Noor et al.
must be resolved. Table 1 summarizes graphene and graphene-based materials with
their unique application and features. As research advances, graphene functionalized materials have the potential to transform contemporary medicine and usher in
a brand-new age of precise and effective medication delivery.
5 Challenges and Future Perspective
Due to their distinct and unrivaled structure and properties, graphene has recently
attracted substantial attention in the field of medicine and gene delivery. These biomaterials have made great strides in previous research, which highlights their enormous
potential for biomedical applications. To fully explore their potential, additional
preclinical research is still required. There is still a paucity of knowledge on what
happens inside the body after loading graphene carriers with drugs, despite the focus
on drug-carrying capability and bio-properties characterization in cell lines. More
research is required on the interactions of graphene with cells and the efficacy of
these carriers in vivo in animals, including studies on clearance processes, long-term
cytotoxicity, tissue biodistribution, and intracellular uptake patterns. Understanding
the behavior of graphene-based materials inside the body requires in-depth knowledge of their many characteristics and surface functions. Through the development
of advanced graphene-based nanomaterials, gene transfection may be more effective.
Although AIDS, neurological illnesses, and cardiovascular diseases are also important to pay attention to and investigate, the current trend in therapeutics research
mostly focuses on cancer therapies. The goal of this assessment is to open the door
for more in-depth investigation in this area.
The use of graphene and products based on it still entails inherent hazards despite
efforts to lessen its toxicity. The European Scientific Committee on Emerging and
Newly Identified Health Risks (SCENIHR) has designated these substances as
hazardous agents. Critical elements like form, size, exposure type and duration,
aggregation state, and concentration must be taken into account while researching
nanomaterials for biomedical research in order to determine their safety. The toxicity of the interaction between graphene nanoparticles and cells/tissues is still a
major worry. For instance, the long-term interaction with tissues should be carefully addressed when graphene-based devices are utilized as scaffolds in tissue engineering, demanding effective synthesis and purifying processes. Contaminants found
in the samples can also be blamed for toxicity, emphasizing the value of meticulous cleaning procedures throughout production. Toxicology is also influenced by
the morphological features of graphene, such as form and size. For determining
graphene’s biocompatibility, one should consider factors such as its size, agglomeration, and surface chemistry. Less toxicity has been observed in smaller flakes,
highlighting the importance of graphene size in target cell internalization.
In conclusion, investigating graphene-based materials necessitates taking into
account a variety of elements and traits, such as size, shape, functionalization,
and functionalizing groups, as well as in-vivo concentration, pharmacokinetics,

Graphene-Based Nanomaterials for Drug Delivery 251
Ta bl e 1 Example of Graphene and graphene oxide-based materials with their promising advantages and properties. Reproduced with permission from WILEY Online Library [90]
Materials Applications Important features
Multifunctionalized GO Targeted cancer
Carboxymethyl cellulose-GO Targeted and sustained
GO Cancer therapy and
GO-hyaluronic acid-Arg-Gly-Asp peptide Targeted cancer
Magnetic
GO-chitosan-PEG-N-Hydroxysuccinimide
polyvinylpyrrolidoneand β-cyclodextrin-modified GO
GO@soy phosphatidylcholine-folic acid
nanohybrid
therapy and drug
delivery
drug delivery
drug delivery system
therapy and anticancer
drug delivery
Anticancer drug
delivery system
Targeted anticancer
drug delivery
Antitumor therapy and
targeted drug delivery
· No noticeable toxic
effects
· Higher drug stacking
capability
· pH-responsive drug
discharge features
· Particular target
transport and effectual
cell inhibition
· No noticeable toxicity
with sustained and
prolonged release of
doxorubicin
· Incorporation of GO
nanosheets highly
improved the swelling
capacity of hydrogels
· Sustained-release
nanoformulation
· Improved suppression
of cancer cell growth
· Low toxicity
· High drug loading
· Improved specificity
and efficiency of
anticancer drug delivery
· Good biocompatibility
· Low cytotoxicity
· pH-responsive
controllable drug release
behavior
· High drug loading
potentials
· Low toxicity
· pH-dependent drug
release
· No noticeable toxicity
· pH-dependable drug
release
· Improved steadiness
and good
biocompatibility
(continued)

252 A. Mohamed Noor et al.
Ta bl e 1 (continued)
Materials Applications Important features
· Higher drug packing
ability
· Effectual cellular
uptake
· Regulated drug
discharge
Chitosan-grafted-poly(methacrylic acid)/GOAnticancer drug
GO/chitosan oligosaccharide/
γ-polyglutamic acid
Superparamagnetic iron oxide-GO Smart nanotheranostics
Chitosan-carboxylated GO Gene delivery · High gene transferring
Modified GO Gene delivery · Low toxicity
GO/ethylene glycol-polycaprolactone Anticancer drug
GO-nanoscale hydroxyapatite Cancer therapy
delivery
Anticancer drug
delivery
platform
delivery; tumor therapy
(chemotherapy and
photothermal therapy)
· No detectable toxicity
· Significant
biocompatibility
· High drug packing
capacity
· pH-dependent drug
delivery performance
· No detectable toxicity
· Simple delivery and
controllable anticancer
drug release behavior
· Good biocompatibility
· pH-dependable drug
release
properties
· Improved release of
DNA
· Suitable interaction
with DNA and
hydrophobic immune
adjuvant
· Low cytotoxicity
· Improved
biocompatibility and
biodegradability
· High drug release and
inhibition of tumor
growth
· High biocompatibility
· High photothermal
therapy activity
· Improved drug release
behavior
(continued)

Graphene-Based Nanomaterials for Drug Delivery 253
Ta bl e 1 (continued)
Materials Applications Important features
· High drug loading
capacity
Polymer G nano-aerogels Anticancer drug
Starch-G nanosheets Anticancer drug
Reduced-GO nanostructures Cancer therapy and
Reduced-GO nanostructures Anticancer drug
Nanoscale GO loaded with HN-1 (a
tumor-targeted peptide)
D-mannose-mediated
chitosan-functionalized GO nanosystems
delivery
delivery
anti-inflammatory
effects
delivery
Anticancer drug
delivery
Anticancer drug
delivery
· High anticancer
drug-releasing with
pH-dependable behavior
· High anticancer drug
loading capacity
· Sustained-release
behavior
· Good biocompatibility
· Low toxicity with
improved therapeutic
efficacy
· Anti-proliferative
activity with high
efficacy
· Sustained pH-sensitive
drug release
· Improved therapeutic
efficacy
· High drug loading
capacity
· High hemolytic toxicity
to rabbit red blood cells
· High stability to the
biological solution
· High tumor-targeting
behavior
· pH-responsive drug
release
· High cellular uptakes
and cytotoxicity toward
tumor cells
· Good biocompatibility
· Targeted and controlled
delivery
· Intracellular discharge
of marine
algae-mediated
anticancer drugs versus
glioblastoma cancers
(e.g., ulvan)
(continued)

254 A. Mohamed Noor et al.
Ta bl e 1 (continued)
Materials Applications Important features
5-Fluorouracil and curcumin loaded
chitosan/reduced GO nanocomposites
Anticancer drug
delivery
· Synergistic inhibitory
effects against the
growth of HT-29 colon
cancerous cells
· Dual-drug loading
properties
and pharmacodynamics. To ascertain the security and possible uses of graphenebased nanomaterials in medication delivery and other biomedical domains, thorough
investigation and comprehension of these issues are required.
6 Conclusion
The book chapter offers a succinct summary of the many processes utilized to create
graphene. Chemical reduction, CVD, mechanical and chemical exfoliation, epitaxial
growth, and layer-by-layer assembly are a few of these techniques those utilized in
the preparation of graphene and its derivatives. Regarding scalability, quality, and
control over graphene characteristics, each process has specific benefits and drawbacks. Understanding these synthesis methods is essential for streamlining graphene
production and modifying its characteristics for particular uses across a range of
industries. The importance of examining various synthesis techniques is emphasized
in this book chapter in order to fully harness the potential of graphene in advanced
technologies, it is essential to explore its capabilities and applications.
Additionally, the major categories of graphene-based nanomaterials have been
emphasized. These include graphene nanoflakes, graphene nanoribbons, GO, GQDs,
and graphene nanoribbons. Each substance has unique qualities and production
techniques that make them each strong contenders for applications in medication
delivery. The properties of GQDs include fluorescence and quantum confinement
effects, making them very relevant for many applications such as bioimaging and
drug delivery. Controlled drug release systems can be easily functionalized using
GO, which is generated from graphene. Targeted drug delivery may be possible
with graphene nanoribbons and oxidized graphene nanoribbons with distinctive edge
effects. Unusual-shaped graphene nanoflakes have potential for intracellular drug
delivery. Understanding these materials makes it easier to use them as effectively as
possible in various technological developments.
A brief summary of the uses of materials with graphene functionalized for drug
delivery is also included in the book chapter. Researchers are looking into the effects
of these chemicals in a variety of settings, including their potential use in photodynamic and photothermal therapy, in promoting cellular and humoral immunity, and
in inhibiting the growth of Gram-positive and Gram-negative bacteria. Graphene’s
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