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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5882_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

Carbon-Based Nanomaterials: An Overview 25
Fig. 8 Biomedical applications of carbon-based nanomaterials
5.5 Biomedical Applications
Carbon-based nanomaterials have emerged as revolutionary entities in the realm
of biomedical applications, displaying their versatility and exceptional properties.
These materials hold immense promise in various biomedical fields, ranging from
drug delivery and imaging to tissue engineering and biosensing. (Fig. 8) The inherent
ability of carbon-based nanomaterials to interact at the molecular level opens up new
avenues for targeted therapies and diagnostic tools, paving the way for groundbreaking advancements in the field of medicine and healthcare.
5.5.1 Tissue Engineering
The ideal tissue engineering scaffold should provide microenvironment for cells
that closely mimics the natural conditions found in the human body’s tissue. CNbased scaffolds offer notable benefits for promoting cell development, demonstrating
minimal cytotoxicity, facilitating productive nutrient administration in the scaffold

26 S. K. Swain et al.
microenvironment by featuring chemically modified components conducive to cell–
cell communiqué and enhancing cell distribution capability for bone tissue engineering. CNTs exhibit an axial Young’s modulus of about 1 TPa and 150 GPa of
tensile strength value, attributed to the high stiffness of the hexagonal molecular
network formed by the C–C bonds. As a result, CNTs serve as rigid substances
with the ability to undergo deformation either due to the impact of electric force or
under the influence compression. Modifying the surface of CNTs or functionalizing
their surface stands out as an effective approach for improving interactions between
cells and scaffolds, consequently enhancing cell spreading within the proximate
environment of the scaffold region.
Biological scaffolds based on carbon dots (CDs) have been proposed as potential
substances for bone resurgence and the refurbishing of bone imperfections. The findings demonstrated that the optimal biological activity, including osteoblastic affixation, osteogenic differentiation and rapid increase in cells development,was achieved
with a composite comprising 10% by weight gelatin in polymeric CD-peptide.
Fullerene-based scaffolds play a crucial role in diverse bone tissue engineering
applications, offering favourable conditions for bone cell proliferation with minimal
cytotoxicity. Their unique properties contribute to effective stimulation of bone cell
growth.The increased hydrophobicity and surfaceroughness of fullerene-based scaffolds enhance their capacity to regulate cell attachment, leading to improved bone
tissue thickness. This, in turn, facilitates the unique mineralization process associated with CNs. The distinctive structural features of the fullerene molecule allow
for precise organization and regulation of the morphology in the final bone tissue
structure.
NDs, recognized as the sole non-toxic CNs, have recently found application in bone tissue engineering. Unlike other carbon nanomaterials, these NDs
offer distinct advantages, including commendable mechanical strength, effective
osteogenic activity, positive stimulation of mineralization and noteworthy antiinflammatory properties [111]. Parizek et al. conducted a separate study where they
engineered polymers coated with NDs for applications in bone tissue engineering.
The study revealed that PLGA-ND exhibited significant mechanical strength and
demonstrated the ability to bind with human osteoblast-like MG-63 cells, facilitating their proliferation. Notably,this technique stands out for its safety, non-toxicity
and non-inflammatory characteristics [112].CNshavealsoproveneffectiveinovercoming challenges associated with the regeneration of cartilage and cardiac tissue
[113, 114].
5.5.2 Wound Healing
Wound management involves creating a conducive surrounding for the wound to
heal without skin deterioration, encompassing considerations such as size, seriousness, profoundness and region. CNs exhibit unprecedented feasibility in managing

Carbon-Based Nanomaterials: An Overview 27
inveterate wound infections in contrast to conventional avenue. While their biocompatibility remains a subject of controversy, the robust geometry of CNs equips them
to undergo four distinct mechanisms as outlined below:
•
Crack bridging is a mechanism wherein CNs exert stress to counterbalance
applied forces by spanning the two surfaces, thereby impeding and retarding
crack progression.
•
In the pull-out mechanism, CNs are recognized for extracting the matrix and
exerting interstice friction, effectively deaccelerating the propagation of cracks.
•
In the crack deflection mechanism, the crack dissipates great energy as it follows
an intricate route, and the existence of CNs prevents the crack from continuing
along its trajectory.
•
In crack tip shielding, the apex of a rupture is constrained, resulting in an
insufficient magnitude of energy for the debonding of the interfacial region.
CNs have a direct impact on the morphology, virtue of cell membranes and
metabolic pathways of microscopic creatures. The dimension, quantity and exterior
part of these CNs contribute to the effective inactivation of microbes. Fullerene stands
out as an excellent material for preventing bacterial infections. Fullerene possesses
outstanding antioxidant properties, rendering it a promising candidate for application in wound healing. Its capability to detoxify reactive oxygen/nitrogen species
and scavenge them is noteworthy. Additionally, in photodynamic therapy, fullerene
can generate reactive oxygen species upon exposure to light. It has been identified as
a beneficial agent in enhancing wound healing by actively participating during the
modulation of inflammatory and proliferative stages.
Recent studies have highlighted the cell and tissue regeneration-promoting properties of GO. rGO is frequently preferred over GO because of its exceptional electrical conductive nature. In vitro and in vivo investigations have reported the accomplished application of GO and rGO in wound closure and recovery mechanisms,
attributed to their astonishing possession. These materials facilitate the relocation
and proliferation of keratinocyte cells, thereby promoting the closure and recovery
process of wounds. Moreover, GO exhibits angiogenic possessions. These materials
can be incorporated into a wound dressing patch for enabling regulated administration and release of active components essential for the process of wound healing.
Graphene demonstrates a significant attribute of uniform dispersity upon release,
maintaining its antibacterial activities and promoting the migration of human fibroblasts. This makes it highly suitable for application in wound dressings. The investigation demonstrated that graphene preserves its bactericidal actions via wrapping
methods and sharp-edged when enzymatically released. Graphene and its nanohybrids exhibit substantial antibiofilm actions and wide range of bactericidal effects.
The antimicrobial mechanism of GO includes lipid extraction, chemical oxidative
stress, mechanical wrapping and a cutting-edge nanoknife impact. These peculiarities collectively contribute to delaying the development of microbial resistance to
GO.
CNTs are recognized for enhancing the epithelization process by increasing
the wideness of the epithelium in wound recovery process. CNT-based materials

28 S. K. Swain et al.
exhibit a range of properties, including antibacterial, antimicrobial, antioxidant,
adhesive and mechanical attributes, which can collectivelycontribute significantly in
wound closure and recovery mechanism. An investigation involving human dermal
fibroblasts and murine fibroblast cells was conducted to investigate the impact of
MWCNTs. The conclusion drawn was that MWCNTs initiate wound healing action
by suppressing genes associated with adhesion.
ND exhibits outstanding characteristics with the existence of hydrophilic functional groups on its exterior part, enhancing the effective superintendence of moisture
and promoting extend of wicking process during wound dressing. The scaffold also
demonstrated magnificent cellular performances. It was observed that the agglomeration of NDs was influenced by a higher concentration of NDs in nanofibers, leading
to enhanced hydrophilic behaviour without exhibiting cytotoxicity.This study established the antibacterial activity of NDs, revealing that an increment in concentration
of NDs resulted in a decreased binding affinity of Staphylococcus aureus bacteria.
Cell viability, cytotoxicity and cell proliferation assays were conducted to verify
the possessions of NDs in wound closure and repairing pathways. Both in vitro and
in vivostudies substantiated that scaffolds fabricated from ND-dispersed nanofibrous
are highly favourable for managing intricate and deadly wounds.
CQDs demonstrate outstanding catalytic and fluorescence properties, along
with antibacterial capabilities, making them suitable for biomedical applications.
However, uncertainties persist regarding the interaction of CQD with bacteria, the
predicament of defensiveness and the manifestation of bactericidal actions. In one of
latest investigations, the bactericidal possessions of positive charge-carrying CQD
were highlighted, indicating their activeimpact on various types of bacteria, including
Gram-negative, Gram-positive and drug-resistant strains. Their research gets undivided concentration on understanding the mechanism of positive charge-carrying
carbon nanodots. The study revealed that –NH
- and –NH-modified carbon nanodots
2
lead to initiate robust adherence action on t he cell membrane of bacteria [115].
5.5.3 Drug Delivery
Although the four distinct classes of carbon materials those differ in their size, dimensions and shapes, they all share characteristics of nanoengineered materials with
numerous captivating attributes that render them appealing as therapeutic administration vehicles. Primarily, CNs have the ability to disperse in aqueous media. In
addition to straightforward translocation via cellular membranes, CNs also demonstrate the capability to penetrate cells via energy-driven endocytic routes. Secondly,
they can penetrate and amass within tumour tissues due to the enhanced permeability
and retention (EPR) effect. The EPR effect facilitates the preferential transport of
CNs loaded with medication components to tumour locations, enhancing the effectiveness of regulated delivery for antitumor therapeutics. Thirdly, CNs demonstrate
an exceptional capacity for therapeutic accommodation onto their surface through
both covalent and non-chemical associations, attributed to their high aspect ratios
and surface areas [116].

Carbon-Based Nanomaterials: An Overview 29
The ability to create supramolecular substances with polycyclic aromatic
molecules via π–π stacking is one of the distinctive features of CNTs. The surface
of pristine CNTs can adsorb various anticancerous therapeutics as well as huge polymeric anticancer constituents. The binding forces at play in such interactions involve
stacking associations between the water-repulsive parts of the adsorbed molecules
and the lipophobic surface of CNT, characterized by π–π stacking associations. As
numerous anticancer therapeutics possess water-repulsive properties, these forces
play a key role in facilitating the accommodation of such therapeutics onto or
into the CNTs. Furthermore, the likelihood of ionic interactions is high, facilitating
the adsorption of molecules, particularly in instances where the CNTs surface has
undergone chemical modification involving charged functional groups [117].
Due to t he numerous advantages of CDs, including rapid cell extraction, excellent
biological compatibility, robust fluorescence, long-lasting stability and no impact on
therapeutics actions, many scientists utilize CDs as multipurpose systems for therapeutic administration and loading. As an illustration, CDs were incorporated into the
zeolite imidazole framework (ZIF). This 5-FU therapeutic carrier highlighted pHsensitivemedication administration. Since 2008, multiple research groups have dedicated their efforts to the development of medication administration vehicles crafted
from nanographene. Monolayers of GO or rGO can serve as effective platforms for
therapeutic loading owing to their enriched specific exterior region. The electrons
present on the exterior regions of the nanographene can form bonds with diverse
arrays of aromatic therapeutic molecules via π–π associations. Subsequently, the
modified GO or rGO surfaces can be connected with targeting molecules, enabling
the selective administration of medications to specific cells [118]. Meticulously
planned therapeutics those can be loaded onto GO include doxorubicin (DOX) and
camptothecin (CPT).
A diverse array of therapeutics or substances can be readily associated with
the exterior and interior surfaces of fullerenes because of their peculiar structural
features that incorporates sundry conjugated double bonds. This makes them competent substances for clinical applications. However, the hydrophobic characteristics
of fullerenes pose a limitation on their pharmaceutical activities. To address this
issue, chemical modifications have been carried out using organic components such
as amino acids, carboxylic acids, polyhydroxy groups and amphiphilic polymers.
Apart from their outstanding chemical and optical possessions, the facile modifications of NDs’ surface render them quintessential suitors for biomedical and pharmaceutical applications. Moreover, over the past few years, numerous studies have
provided evidence supporting the biocompatibility and non-toxic nature of NDs.
In general, NDs are regarded as the least risky among nanocarbon components.
Hence, researchers have extensively explored their potential applications as therapeutic administration agents, diagnostic equipment and imaging instruments. Further
modification is crucial to prevent the aggregation of NDs and enable their use in
therapeutic applications, which can be categorized into two distinct classes: one is
doping and another one is surface modifications. The doping process resulted with
imperfections inside the materials, caused by extraneous atoms through high-energy
methodology, subsequently leading to generation of optically active components.

30 S. K. Swain et al.
Surface modifications of NDs involved chemical reactions with organic components,
namely, natural polymers, genetic material peptides and amino acids to enhance the
biomedical-related activities and possessions of NDs [119].
5.5.4 Sensing
In recent times, CNs have been subjected either to thorough examination, serving
as discrete molecular-like sensors or as components that can be seamlessly integrated into devices. In addition, the approaches for integrating carbon nanomaterials into biological sensors encompass direct growth on a substrate, drop casting,
integration into polymers, co-deposition with metal nanoparticles and utilization in
field-effecttransistor (FET)-based devices to augment conductivity [120]. Graphenes
and CNTs exhibit distinctive physicochemical properties, including charge carrier
mobility thermal conductivity and specific surface area, which have garnered their
attention in biosensing applications. These materials are frequently employed to
enhance electrode functionality by providing excellent conductivity, high specific
surface area and robust binding affinity for other nanoparticles and probe molecules.
This modification aims to achieve heightened sensitivity in immunosensors [121].
Functionalized fullerenes and electrodes modified with fullerenes have proven effective in detecting a diverse array of molecules, such as fluoride ions, glucose, H
2O2
and various organic vapours [122]. CDs have undergone extensive exploration due
to their tailored optical possessions, resistance to photobleaching, low noxious effect
and remarkable cell-friendly capability. A crucial advantage of CDs stems from the
adjustable fluorescence properties, originating from the quantum confinement consequences and the surface or edge ramification. The fluorescence emission wavelength
of CDs can be modulated across the strong ultraviolet to near-infrared domain by
controlling man-made precursors, circumvents and approaches. This versatility positions them as propitious frameworks for applications in biosensing and bioimaging
[123]. SWCNHs exhibit the characteristic of self-aggregation, leading to the formation of 80–100 nm spherical conglomerates with diverse morphological structural
entities such as dahlia, bud and seed structures, rather than remaining disseminated
individually. These distinctive shapes impart unique properties, including great exterior surface region, abundant interior nanospace, high conductive value and mechanical strength, rendering them best-suited substances for various sensing applications
such as electrochemical, fluorescent and resistive sensing. Initially, SWCNHs have
found extensive use as electrode materials in electrochemical sensing. Additionally,
beyond electrochemical sensing, SWCNHs have been employed in other sensing
modalities, such as resistive sensors, capitalizing on the conductive characteristics
inherent in SWCNHs [124]. SWCNHs extensively implemented in the biosensing
of H
, glucose, etc. [125, 126].
2O2

Carbon-Based Nanomaterials: An Overview 31
6 Challenges and Future Perspectives
Existence of nanostructured carbon-based materials is known since ancient age;
however, their properties towards potential application needs to be further elaborated
as future prospective materials. The nano-dimensional CNMs havemagic property as
compared to their bulk counterparts because of their high aspect ratio. The structure
and morphology of CNMs have major role predicting their application in various
sectors including diversebiomedical applications. Nowadaysresearchers are engaged
to synchronize the properties with application in length and breadth to propose a
future prospective smart material.
7 Concluding Remarks
The surface-to-volume ratios of CNMs are very important for exploring different
unexpected properties inviting various proposed applications. From graphene’s
exceptional conductivity to CNT’s extraordinary strength are the example of the
versatility of CNMs. Going deeper into the intricacies of CNMs, not only their
impressive physical attributes but also the potential for sustainable solutions and
eco-friendly applications of CNMs are uncovered. This chapter has provided a foundation for understanding the diverse nature of CNMs, their synthesis methods and
the crucial role they play in shaping the future of biomedical application to meet the
scope of the present book.
Acknowledgements Authors convey their thanks to the Department of Science and Technology,
Government of India, for providing INSPIRE Fellowship to S. Patra for pursuing her PhD degree.
The University Grant Commission, New Delhi, India, is also acknowledged for awarding SJSGC
doctoral fellowship to K. M. Sahu.
Conflict of Interest The authors declare that there is no conflict of interest in publishing this
article.
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