Nanomaterials 12 01676

nanomaterials
Review
Nanomaterials in Dentistry: Current Applications and
Future Scope
Pavan Kumar Pavagada Sreenivasalu 1 , Chander Parkash Dora 2 , Rajan Swami 2, *, Veeriah Chowdary Jasthi 3 ,
Predeepkumar Narayanappa Shiroorkar 4 , Sreeharsha Nagaraja 5,6, * , Syed Mohammed Basheeruddin Asdaq 7
and Md. Khalid Anwer 8
1 Department of Restorative Dentistry and Endodontics, College of Dentistry, King Faisal University,
Al-Ahsa 31982, Saudi Arabia; [email protected]
2 Department of Pharmaceutics, Maharshi Markendeshwar College of Pharmacy, Maharishi Markandeshwar
Univerisity, Mullana, Ambala 133207, Haryana, India; [email protected]
3 Department of Oral and Maxillofacial Surgery and Diagnostic Sciences, College of Dentistry, King Faisal
University, Al-Ahsa 31982, Saudi Arabia; [email protected]
4 Department of Basic Medical Sciences, College of Medicine, King Faisal University,
Al-Ahsa 31982, Saudi Arabia; [email protected]
5 Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University,
Al-Ahsa 31982, Saudi Arabia
6 Department of Pharmaceutics, VidyaSiri College of Pharmacy, Off Sarjapura Road,
Bangalore 560035, Karnataka, India
7 Department of Pharmacy Practice, College of Pharmacy, AlMaarefa University, Dariyah,
Riyadh 13713, Saudi Arabia; [email protected]
8 Department of Pharmaceutics, College of Pharmacy, Prince Sattam Bin Abdulaziz University,
Al-Kharj 11942, Saudi Arabia; [email protected]
* Correspondence: [email protected] (R.S.); [email protected] (S.N.)
Citation: Sreenivasalu, P.K.P.; Dora,
C.P.; Swami, R.; Jasthi, V.C.; Abstract: Nanotechnology utilizes the mechanics to control the size and morphology of the particles
Shiroorkar, P.N.; Nagaraja, S.; Asdaq, in the required nano range for accomplishing the intended purposes. There was a time when it
S.M.B.; Anwer, M.K. Nanomaterials was predominantly applied only to the fields of matter physics or chemical engineering, but with
in Dentistry: Current Applications
time, biological scientists recognized its vast benefits and explored the advantages in their respective
and Future Scope. Nanomaterials 2022,
fields. This extension of nanotechnology in the field of dentistry is termed ‘Nanodentistry.’ It
12, 1676. https://doi.org/10.3390/
is revolutionizing every aspect of dentistry. It consists of therapeutic and diagnostic tools and
nano12101676
supportive aids to maintain oral hygiene with the help of nanomaterials. Research in nanodentistry is
Academic Editors: Sanjukta Deb, evolving holistically but slowly with the advanced finding of symbiotic use of novel polymers, natural
Sherif Elsharkawy and polymers, metals, minerals, and drugs. These materials, in association with nanotechnology, further
Daniela Iannazzo
assist in exploring the usage of nano dental adducts in prosthodontic, regeneration, orthodontic,
Received: 28 February 2022 etc. Moreover, drug release cargo abilities of the nano dental adduct provide an extra edge to
Accepted: 12 May 2022 dentistry over their conventional counterparts. Nano dentistry has expanded to every single branch
Published: 14 May 2022 of dentistry. In the present review, we will present a holistic view of the recent advances in the field
of nanodentistry. The later part of the review compiled the ethical and regulatory challenges in the
Publisher’s Note: MDPI stays neutral
with regard to jurisdictional claims in
commercialization of the nanodentistry. This review tracks the advancement in nano dentistry in
published maps and institutional affil- different but important domains of dentistry.
iations.
Keywords: nanoparticle; nanodentistry; nano-implant; dental
Copyright: © 2022 by the authors.

Licensee MDPI, Basel, Switzerland. 1. Introduction
This article is an open access article
Nanotechnology has traveled a long way from a mere theoretical concept presented
distributed under the terms and
by Richard Feynman to the incorporation of nanotechnology in every aspect of life, such as
conditions of the Creative Commons
dentistry [1]. Conventional dental technology has been enriched by the revolutionized prin-
Attribution (CC BY) license (https://
creativecommons.org/licenses/by/
ciples of nanotechnology [2]. These principles drive a paradigm shift in the research outlook
4.0/).
of nanotechnologists working in different dentistry domains, such as prosthodontics and
Nanomaterials 2022, 12, 1676. https://doi.org/10.3390/nano12101676 https://www.mdpi.com/journal/nanomaterials

Nanomaterials 2022, 12, 1676 2 of 20
orthodontics. Primarily, dental practitioners focus on the prophylactic treatment of dental

caries and periodontal disease. Though at the time when tooth or periodontium suffer from
infectious disease, the foremost aim of the treatment is to eradicate the pathogens, remove
decayed tissues and restore them, providing long-lasting functionality in the oral cavity.
Different approaches like top-down, bottoms-up, biomimetic, and functional approaches
were explored for each aspect.
Exquisite oral health implicates proper nutrition, which is associated with better
quality of life. Undoubtedly teeth are a perpetual part of oral health [3]. Developing
biocompatible nano products requires a sharp assessment of the anatomy and physiology
of the target site, i.e., teeth and oral cavity. The close contact of nanomaterials with nanopar-
ticles dictates the nanomaterial’s fate in the body. The anatomy, structure, and chemical
composition of human tooth tissues are diversified and the understanding of each part
and individual characteristic abundance of material in each layer provide insight into how
the nanomaterial should be formed specifically as per the requirement of the target layer.
From outside to inside, the tooth can be divided majorly into Enamel, Dentin and Pulp,
Cementum, and Periodontal ligament [4]. Tooth enamel is the most mineralized and hard
solid crystalline structure of hydroxyapatite (HA) with immensely strong intermolecular
forces. Composition vise it is 96 wt.% inorganic material and 4 wt.% organic material and
water. Whereas around 70% of the inorganic material is evident in dentin. It consists of HA
biocomposites that encircle the collagen fibers, the reason why HA is the most widely used
material for dental products, especially in nanoproducts [5].
A tectonic shift in the aim of nano dentistry was recorded with the advancements of
the vast scientific research in the field of nanotechnology. The aim has now shifted from de-
veloping just a supportive nanocomposite to developing a highly efficacious bio-mimicking
biomaterial for restorative dentistry. It was observed from the research data extracted
from the Pubmed search platform that for a very long-time dental research was focused
on nanocomposite only; however, with time, the research trend shifted towards other and
more novel topics (Table 1), such as nanozymes. Meta-analysis of the previously published
research abetted us to analyze the disadvantages and advantages of nanodentistry that
were responsible for restrictive growth and relatively higher research trend in recent times,
respectively. Figure 1 summarizes the advantages and disadvantages of nanodentistry.
Table 1. Research topic click number in PubMed.
Nanotechnology Nanoparticle Nano Nano

Year Nanodentistry Nanorobot
in Dental in Dentistry Implant Composites
2022 3 1 6 2 0 24
2021 182 5 513 84 1 2300
2020 154 5 475 74 0 2266
2019 99 0 385 61 2 1934
2018 108 5 343 68 3 1901
2017 102 0 297 63 0 1810
2016 97 5 277 57 0 1822
2015 89 3 251 60 3 1822
2014 84 5 210 42 2 1705
2013 52 3 148 35 1 1679
2012 49 3 127 32 0 1638
2011 64 3 91 31 2 1451
2010 42 1 73 21 1 1359
2009 42 0 62 23 0 1301
2008 25 1 58 11 0 1301
2007 40 0 44 6 0 1247
2006 35 0 12 4 1 1189
Nanomaterials 2022, 12, x FOR PEER REVIEW 3 of 21
Table 1. Cont.
2007 40
Nanotechnology 0 44
Nanoparticle 6 0 Nano1247
Year Nanodentistry Nano Implant Nanorobot
2006 in Dental
35 0 in Dentistry
12 4 1 Composites
1189
20052005 24 24 0 11 11 7 7 0 0 1109 1109
20042004 22 22 00 5 5 2 2 0 0 998 998
2003 18 0 2 0 0 914
20032002 18 5 00 2 2 1 0 0 0 838 914
2002 5 0 2 1 0 838
Figure1.1.Visual
Figure Visualpresentation
presentationto to demonstrate
demonstrate how how advantages
advantages givegive thrust
thrust to nano
to nano dentistry
dentistry research
research
by tilting the balance towards the pro’s side.
by tilting the balance towards the pro’s side.
ItItisisalready
alreadymentioned
mentioned earlier
earlierthat constructing
that constructinga nano dental
a nano product
dental is anisintricate
product an intricate
technique
techniquerequiring
requiringmatter
matter andandsynthesis
synthesis approach knowledge.
approach These
knowledge. approaches
These approacheswerewere
used to generate novel nanomaterials to synthesize regenerative material,
used to generate novel nanomaterials to synthesize regenerative material, implants, implants, and and
drug enclosing nanoparticles (NPs), etc., [6]. Nanodentistry can be utilized
drug enclosing nanoparticles (NPs), etc., [6]. Nanodentistry can be utilized to generate to generate
practically
practicallyany anyproduct
product using
usingany of of
any thethementioned
mentioned approaches. The The
approaches. never-ending
never-ending tally tally
of the nano-dentistry product includes nanocomposites, nanoimpressions, anti-infective
mouth rinse, or the very commonly used nanofillers. Figure 2 illustrates the synthesis
mouth rinse, or the very commonly used nanofillers. Figure 2 illustrates the synthesis ap-
approach used in nanotechnology and how these approaches can be explored for manufac-
proach used in nanotechnology and how these approaches can be explored for manufac-
turing a tally of nano dental products. Where bottom-up and top-down approaches are
turing
the mostacommonly
tally of nano
useddental
practiceproducts. Where nanodentistry
for constructing bottom-up and top-down
products, approaches are
the biomimetic
the most commonly used practice for constructing nanodentistry products,
approach is still in the research phase. Hence, in the present review, only those approaches the biomi-
metic approach is still in the research phase. Hence,
that followed either the bottom-up or top-down approach were cited. in the present review, only those ap-
proaches that followed
It is already mentioned either the bottom-upthe
that understanding or biomatters
top-down helps
approach were
to make cited.
biomimicking
NPs. This usage of biocompatible material leads to non-toxic NPs that can be retained at the
physiological site for longer periods of time. Moreover, the material used in the construction
of the dental product is different from other NPs due to changes in dental physiology, which
is already being presented in detail in the previous section. Figure 3 demonstrates the
different ways of usage of nanomaterial in nanodentistry. Dental biomaterials have been
studied for decades. These can be classified primarily into four groups such as metals,
ceramics (carbons, ceramic lenses, and glasses), metals, and polymers [7]. Polymers can
further be divided into synthetic or natural products (both plant and animal products) [8].
With the emergence of eco-friendly and green chemistry, increased demand for natural
polymers has been witnessed. Nanotechnology has broadened the holistic view of the
usage of biomaterials in dentistry. Through the current review, we will present an intricate
Figure 2. Various synthesis approaches implemented in nanodentistry.

drug enclosing nanoparticles (NPs), etc., [6]. Nanodentistry can be utilized to generate
practically any product using any of the mentioned approaches. The never-ending tally
mouth rinse, or the very commonly used nanofillers. Figure 2 illustrates the synthesis ap-
Nanomaterials 2022, 12, 1676 proach used in nanotechnology and how these approaches can be explored for 4manufac- of 20
turing a tally of nano dental products. Where bottom-up and top-down approaches are
the most commonly used practice for constructing nanodentistry products, 4the
Nanomaterials 2022, 12, x FOR PEER REVIEW
biomi-
of 21
insight into how is
metic approach nanotechnology assistsphase.
still in the research in designing
Hence, newer and novel
in the present alternatives
review, for ap-
only those
different
proachesbranches of dentistry
that followed either(Figure 4).
the bottom-up or top-down approach were cited.
It is already mentioned that understanding the biomatters helps to make biomimick-

ing NPs. This usage of biocompatible material leads to non-toxic NPs that can be retained
at the physiological site for longer periods of time. Moreover, the material used in the
construction of the dental product is different from other NPs due to changes in dental
physiology, which is already being presented in detail in the previous section. Figure 3
demonstrates the different ways of usage of nanomaterial in nanodentistry. Dental bio-
materials have been studied for decades. These can be classified primarily into four
groups such as metals, ceramics (carbons, ceramic lenses, and glasses), metals, and poly-
mers [7]. Polymers can further be divided into synthetic or natural products (both plant
and animal products) [8]. With the emergence of eco-friendly and green chemistry, in-
creased demand for natural polymers has been witnessed. Nanotechnology has broad-
ened the holistic view of the usage of biomaterials in dentistry. Through the current re-
view, we will present an intricate insight into how nanotechnology assists in designing
Figure
Figure2.
newer 2.Various
and novelsynthesis
Various approaches
alternatives
synthesis implemented
for different
approaches in nanodentistry.
branches
implemented of nanodentistry.
in dentistry (Figure 4).
Material used in Nano-dentistry

Metal Oxide
Zr, Al Based, Ca hydraulic Aluminium Gold
Glass infiltrated silicate
ceramics
High
Silver
Strength Metals
Core Zinc etc.
Lithium Disilicate Inorganic

Glasses Ceramics Material
Iron Oxide
Leucite
Inorganic Titanium Dioxide
adducts
Traditional
Silica Calcium Phosphate

Hydroxyapatite
Polymers Unconventional
Carbon nanotubes
Polymethyl
Synthetic Natural Alginate Graphene oxide
methacrylate
Nanodiamonds
Pectin
Polyamidoamine
PLGA Chitosan Hyaluronic Acid
IPN
Figure 3. Diagrammatic illustration to provide basic material classes used in dentistry.

Figure 3. Diagrammatic illustration to provide basic material classes used in dentistry.
terials 2022,Nanomaterials 2022,
12, x FOR PEER 12, 1676
REVIEW 5 of 21 5 of 20
Application of Nanomaterials in dentistry

Preventive Dentistry Prosthodontic
Metal nanoparticles, inorganic Implants should be microbial
salts resistant as well as hardy enough
to hold roots/teeth.
Teeth Restoration
Amalgams, composites, Orthodontic
resins containing The metallic or polymeric
quaternary ammonium material having antibiofilm
compounds, metal alloys. properties.
Periodontology and bone

Endodontic regeneration
Composites, odontoblast Nanoparticles assists in
stimulation, Drug eluting NPs, regeneration of pulp and
polymeric matrix etc. removal of microbes.
Figure 4. Pictorial representation

Figure 4. Pictorialofrepresentation
applications ofofnanomaterial
applications in
of dentistry.
nanomaterial in dentistry.
2. Application 2.
of Application
the Nano Dentistry
of the Nano Dentistry
2.1. Preventive
2.1. Preventive Dentistry Dentistry
Preventive
Preventive dentistry appliesdentistry applies
a functional a functional
approach approach
to treatment, to treatment,
where where the root cause
the root cause
of the symptoms is treated. Many metal NPs documented in past literature have shown have shown
of the symptoms is treated. Many metal NPs documented in past literature
enormous
enormous potential potential asinantimicrobial
as antimicrobial treating tooth indecay
treatingor tooth decay or
other dental other dental
ailments [8]. ailments [8].
Dental experts also emphasize preventing tooth decay by inhibiting caries through con- through con-
Dental experts also emphasize preventing tooth decay by inhibiting caries
trolling biofilm,trolling biofilm,
enhancing enhancing remineralization,
remineralization, or providing
or providing antibacterial antibacterial
prevention prevention to the
to the
oral cavity [9,10]. Hence, nanotechnologists also working
oral cavity [9,10]. Hence, nanotechnologists also working on toes to provide novel and on toes to provide novel and
efficacious alternatives. Dental preventive products work
efficacious alternatives. Dental preventive products work by two means either by reduc- by two means either by reducing
the biofilm production or by restoring the damaged
ing the biofilm production or by restoring the damaged tooth by remineralization tech- tooth by remineralization techniques
to inhibit the further damage to the pulp and arresting the decline. Tooth decay begins with
niques to inhibit the further damage to the pulp and arresting the decline. Tooth decay
demineralization of the enamel owing to environmental changes. Changes in the microbial
begins with demineralization of the enamel owing to environmental changes. Changes in
homeostasis in the buccal cavity lead to fermentation of the regular intake of sugars lead-
the microbial homeostasis in the buccal cavity lead to fermentation of the regular intake
ing to acidification of the microenvironment, leading to the generation of biofilm, which
of sugars leading to acidification of the microenvironment, leading to the generation of
through an intricate interaction with microbes, gradually dissolves the enamel, followed by
biofilm, which through an intricate interaction with microbes, gradually dissolves the
the production of carries. If ignored further, that may infect the inner organic part of the
enamel, followed by the production of carries. If ignored further, that may infect the inner
tooth and lead to dentine and pulp decay, eventually the loss of teeth [11]. Preliminarily
organic part of the tooth and lead to dentine and pulp decay, eventually the loss of teeth
focus was to remove the deposited biofilm or inhibit the synthesis of biofilm by maintaining
[11]. Preliminarily focus was to remove the deposited biofilm or inhibit the synthesis of
the lower oral pH level [12]. NPs high surface-area-to-volume ratios enable robust drug- or
biofilm by maintaining the lower oral pH level [12]. NPs high surface-area-to-volume ra-
drug-combination loading that may result in synergistic antibiofilm efficacy [13]. However,
tios enable robust drug- or drug-combination loading that may result in synergistic anti-
smaller particle sizes, desirable charge, and hydrophilic/hydrophobic characters favor the
biofilm efficacy [13]. However,
protective smaller
film adhesion overparticle
the teethsizes, desirable
surface. charge, and
Fluoropolymer hydro-
matrix coating layers are
philic/hydrophobic characters favor the protective film adhesion over the teeth
popular for their easy-to-clean purposes [14]. Being a theta surface (lower surface free surface.
Fluoropolymerenergy),
matrix coating layersallow
they easily are popular
detachment for their easy-to-clean
of microbial bilayerpurposes
from the [14]. Be- surface under
tooth
ing a theta surface (lower surface free energy), they easily allow detachment of
the influence of physiological shear. These coatings are particularly advised for patients microbial
bilayer from the tooth
with surface
higher under
carries thei.e.,
risk, influence of physiological
xerostomia. It is evident shear.
that These
effectivecoatings
interaction between
are particularlybiomineral
advised forand patients with higher carries risk, i.e., xerostomia. It is evident
bacteria is only possible if nano-sized particles that are smaller than the
that effective interaction
microorganismsbetween arebiomineral
used [15]. and bacteria is only possible if nano-sized
particles that are smaller than the microorganisms
The casein phosphor-peptides stabilize are usedcalcium
[15]. and phosphate ions through the forma-
The caseintion
phosphor-peptides stabilize calcium and phosphate
of amorphous calcium phosphates employed as biomimetic ions through the for- that diminish
composites
mation of amorphous calcium phosphates employed as biomimetic
microbial adherence by attaching to the surfaces of microbial cells. Furthercomposites that di- antimicrobial
minish microbialuseadherence
of metalsby attaching
has also been to the surfaces
explored forofcenturies.
microbial Zinc cells. oxide
Further antimi-
(ZnO) has been used in
crobial use of metals
many has also been products
conventional explored forfor its
centuries. Zinc oxide
antimicrobial (ZnO)[16].
properties has Many
been usedkinds of toothpaste
in many conventional products for
also incorporate Zn its antimicrobial
acetate and citrate properties
to control [16].
theMany kindsof
formation ofplaque
tooth- [17]. Previous
paste also incorporate Zn acetate and citrate to control the formation of
literature demonstrated that particle size is inversely related to antimicrobial plaque [17]. Pre- activity. Sim-
vious literatureilarly,
demonstrated that particle size is inversely related to antimicrobial
HA of the NPs also influences the microbial interaction with NPs [18]. Moreover, activ-
the literature suggests that bacteria are more likely to acquire resistance to conventional
antibiotics viz a viz. NPs. [19]. Therefore, nanoparticulate metals were considered a better
choice for exploration in antimicrobial activity. Nanosilver (Ag NPs) and copper have
received a lot of attention due to their antimicrobial activity [20]. Recently, Ahmed et al.
beautifully reviewed much recent research on the plant-based synthesis of Ag NPs [21].
Similarly, other green chemistry was also reported and reviewed by many researchers
in different metallic NPs such as Zinc (Zn) and Nickle (Ni). [22,23]. Besides, plenty of
other metals were found to play a dynamic role in preventive nanodentistry, such as cop-
per and titanium. Ag salt NPs were precipitated to synthesize composites that release
bactericidal Ag + ions in the case of Ag salt. Zhang et al. reported that the addition of
nanoparticulate silver in quaternary ammonium dimethacrylate markedly reduced the
microbial biofilm viability required for achieving better antibacterial activity [24]. Simi-
larly, Chang et al. [24] also illustrated the use of Nano Ag with quaternary ammonium
dimethacrylate in the ‘Scotch bond Multi-Purpose’ primer. The association provided the
best outcomes, with augmented antimicrobial effect and attenuated lactic acid production.
The same group also substantiated their previous findings by providing the combinational
effect of Ag NPs, NPs of amorphous calcium phosphate (NACP), and quaternary ammo-
nium methacrylates in controlling the biofilm [25]. Whereas Dias et al. investigated the
effect of modification of Ag NPs with titanium dioxide on microbial biofilm and demon-
strated a reduction in the microbial flora generation and attachment. Magalhães et al.
compared the performance of three different marketing cementing, i.e., Sealapex, RelyX
ARC, and Vitrebond, after incorporating Ag NPs. Inhibition halo was evident in siver
NPs groups viz a viz naïve group where Ag NPs are not incorporated, indicating better
antibacterial properties due to Ag NPs [26]. Gold is a conventional varnish material for
protecting the teeth because of its excellent biocompatibility [27]. Zhang et al. investigated
the role of antibacterial 4,6-diamino-2-pyrimidinethiol-modified gold NP-coated aligners
on the bactericidal and antibiofilm efficacy against P. gingivalis. Results presented gold
NP-associated aligners as an alternate treatment against such infections than the already
present conventional periodontal treatment [28]. Recently, Kamath et al. developed gold
NPs varnish for tooth remineralization and found positive outcomes [29]. There are many
oral rinse products, such as mouthwashes and gargles, which are equipped with NPs for
better efficacy. Similarly, in accordance with this, Kovtan et al. developed a paste or a
rinsing solution containing calcium phosphate NPs, functionalized with the antibacterial
agent chlorhexidine. Calcium carbonate, a natural physiological substance in the tooth,
helps in the remineralization of the enamel loss due to microbes and serves as the second
line of defense in controlling the decay. Moreover, chlorhexidine provides an antimicrobial
effect in the oral microenvironment. There are plenty of mouthwashes available on the
market that uses chlorhexidine as active pharmaceutical. However, scientists have offered
a lucrative way to present chlorhexidine-loaded calcium salt NPs for its advanced benefits.
These NPs, on the one hand, provide an antimicrobial/antibiofilm effect; on the other
hand, calcium salt helps to close the open dentin tubules at the root surface, providing a
remineralization effect to damaged teeth [30]. Similarly, Sun et al. developed a nano-CaF2
spray dried powder that is apparently an effective anticaries agent in increasing the labile F
concentration in oral fluid and thus enhancing tooth remineralization. Iron is associated as
the essential element for the formation of dentin. Moreover, it has a role in the discoloration
of dentin. Liu et al. presented the theranostic potential of ferumoxytol iron oxide NPs
against biofilms harboring Streptococcus mutans [31].
Enamel loss induces dentin to explore, making it hypersensitive to cold and heat.
Modified silica NPs are used to treat dental hypersensitivity through remineralization to
cease expanding decay. Other than HA, hydraulic calcium silicate (hCSCs) re-mineralizes
demineralized dentin is another type of ‘bioceramic’ gaining popularity among dentists
due to their higher strength, superior biologics, and good physiochemical properties [32].
Moreover, hCSCs can re-mineralize demineralized dentin hence aiding in cementing the
tooth and arresting spreading infection to pulp. Zhang et al. presented nano-HA toothpaste
for remineralization of teeth to arrest carries formation using an artificial carries model [33].
Similarly, Huang et al. illustrated a comparative study between nano-HA and sodium
fluoride and substantiated the higher potential of nano-HA in remineralization [34]. Un-
fortunately, the product can penetrate only up to a small depth into the dentin tubules
resulting in partial protection. Dendrimer type versatile and novel nanotherapeutics were
also established for remineralization. Liang et al. investigated the remineralization effects
of poly (amidoamine) (PAMAM) dendrimer plus a bonding agent with NACP in a cyclic
artificial saliva/lactic acid environment. After 20 days, a significant increase in the dentin
layer supported the raised hypothesis [35]. Liposomes have been vastly researched in the
area of biofilm; Nguyen et al. demonstrated that polysaccharide (hyaluronic acids)-coated
liposomes have a better ability to adhere to the tooth than the uncoated liposomes [36].
Infect, the cationic charged liposomes membrane (via attachment of pectin, Hyaluronic
acid, etc.) assist in better adherence to tooth HA and thus retain enamel for longer periods
of time [37]. Moreover, the hydrophilic coating further provides better stability of biofilms
in the salivary microenvironment.
Besides, there are other drug delivery systems that have been vastly being explored
for the same purpose. Table 2 illustrates previous literature reporting advanced drug
delivery systems that have been considered prominent in controlling caries or helping in
the restoration of the teeth.
Table 2. Previous reports on various prominent advanced drug delivery systems show significant
contributions to nanodentistry.
Drug Delivery System Characteristic Action Reference

Nitric oxide-releasing alkyl-modified poly (amidoamine)
Antibiofilm against Streptococcus mutans [38]
dendrimers
poly (amidoamine) containing amorphous calcium
Dendrimer Remineralization [39]
phosphate NPs
Chlorhexidine encapsulated PAMAM dendrimer Remineralization in etched human dentin in vitro [40]
PAMAM dendrimer containing nitric oxide Antibacterial antibiofilm effect [41]
Alendronate conjugated dendrimer targeting Alendronate targeted the PAMAM to HA and
[42]
hydroxyapatide (HA). cooh-PAMAM induced HA crystallization.
De-mineralized human enamel is mineralized in
Anionic PAMAM dendrimer in remineralization [42]
perfectly arranged rod-like crystals.
Solid Lipid NPs Mentha spp. Essential oil encapsulated solid lipid NPs Antimicrobial potential helps in reducing the carries [43]
Anticaries action using antibacterial effect against
Miswak, chitosan NPs, and propolis as varnishes [44]
Streptococcus mutans (S. mutans)
Chitosan NPs Antimicrobial effect against Bacillus pumilus and
Rutin (a flavonoid) encapsulated chitosan NPs Enterococcus faecalis, [45]
Anticariogenic potential
Hybrid copper-chitosan NPs (Core of Copper with
Beneficial to controlling dental plaque formation [46]
chitosan envelope)
Works as a binding agent and provides a remedy for
CuO NPs capped with chitosan [47]
secondary caries.
Improved the mechanical properties of composite and
Combination of ethyl methacrylate with Ag
efficacy of the product increased in terms of reduced [48]
ethylhexanoate
biofilm production
Ag NPs Antimicrobial effect was seen over teeth using an in vivo
Ag NPs [49]
experiment
Synthesis of Ag NPs using locust bean gum (LBG)
Effect of pH was noticed on the size and stability of NPs [50]
polysaccharide plant extract.
Synthesis of Ag NPs using fungal By modulating the temperature [51]
One-pot biosynthesis using marine sponge (Haliclona Significant antiproliferative activity and antibacterial
[52]
exigua) for the synthesis of flower-like Ag NPs activity evident in biofilm bacteria
The product represented long-term stability, superficial
Characterize and evaluate the stability and toxicity with
and in-depth remineralizing capacity with antimicrobial
re-mineralizing effects of silver NPs and fluoride [53]
potential and biocompatibility and did not stain the
anticaries agent (AgF) on staining dental enamel.
enamel.
Implant survival rate has been increased by Ag NPs adsorption on the surface causes the surface to
incorporating Ag porous NPs in polymer matrices of have a porous structure. And provide better [54]
polycaprolactone/polyvinyl alcohol on titanium implant biocompatibility, antimicrobial activity, etc.
Functional remineralization of dentin effect of Zn-doped Clinical outcomes as remineralization of teeth with
Zinc (Zn) [55]
polymeric NPs antimicrobial properties as anti-biofilm.
Impact of phyto-synthesized Zn Oxide NPs (ZnO NPs) The NPs show anti-bacterial properties and can be used
[56]
using Murraya paniculata leaf extracts. for dental composite, etc.
Field Emission Scanning Electron Microscopic images
Fabrication of composites cellulose/polypyrrole demonstrated that bacterial cellulose structure was
preserved with the addition of other agents and the [57]
composed with ZnO NPs
resultant composites showed good antibacterial
properties.
Uniform Zn doped mesoporous NPs were evaluated for The mechanical property of composite is increased with
[58]
antibacterial effects is its bacterial effect.
ZnO NPs with HA NPs have shown increased
ZnO NPs were evaluated for their antibacterial coating
antibacterial activity with osteogenic activity. Thus [59]
over implants
favoring tissue regeneration
Table 2. Cont.
Drug Delivery System Characteristic Action Reference

Effects of incorporation of Zr oxide NPs on antibiofilm
The addition of 0.5% Zr oxide NPs made the dentures
Zirconium (Zr) activity, glucose sorption, weight change, and surface [60]
softer and provided significant anti-biofilm activity.
roughness of two different types of denture liners
Preparation of Zr NPs using NPs using Punica granatum
Antibacterial and antioxidant effect was evident, which
(pomegranate) peel extract and evaluated for their [61]
can be explored for dentistry.
antibacterial effect.
Studied effect of zirconia NPs on mechanical properties NPs of ~50 nm shown adhesive layer or in primer
[62]
of adhesive systems increased tensile strength and promoted mineralization
A simple chemical method was used for the formulation
Results were conclusive in giving better outcomes in
of bimetallic Copper–Nickle (Cu-Ni) NPs and were
Miscellaneous antibacterial activity against Staphylococcus aureus [63]
evaluated for their antibacterial activity on human
(gram-negative) and Escherichia coli (gram-positive).
pathogens
Cu in Zn phosphate cement showed significantly
Mechanophysical and biological characteristics of
augmented odontoblastic differentiation using dental [64]
therapeutic cement after addition of Cu NPs
pulp human cells.
2.2. Tooth Restoration

Following carries management, tooth restoration is the second most impeccable part
of dentistry. Restoration is generally done by many methods starting from fillings, crowns,
implants, bridges, and implants. From the nanotechnological point of view, fillers and
implants are the most popular, as shown in Table 1. Nanofillers present a better adherence
to teeth than the larger size fillers. Restorative filler materials used for remineralization
of the tooth architecture can be classified according to their matrix component (ceramic,
metal, polymer). However, these composites have their advantages and disadvantages.
For example, ceramics composites are very brittle and polymeric composites are prone to
high wear and tear. Literature reviews advocate the use of biological polymer/ biomimetic
polymers to synthesize dental composites.
HA is the main inorganic mineral component of teeth. Many scientific groups are
working to synthesize different adducts of HA to form newer and novel nanocomposites,
which may mimic the physiological elemental composition of teeth. For example, Chung
et al. were successful in preparing a physiological component mixture by mixing NPs of HA
(inorganic component: 75% w) with chitosan (25% w) to behave as an organic component
of nanocomposites [65]. Sharifi et al. prepared HP–gelatin/curcumin nanocomposites
and evaluated their antimicrobial effects against Escherichia coli, Staphylococcus aureus, and
Streptococcus mutans [66]. There are various reports where the group has used different
natural polymers for changing the properties of the organic component of the nanocom-
posites [67]. Consecutively, other scientific groups presented HA nanocomposites coupled
with the antimicrobial effect of metallic NPs such as silver (Ag), gold, iron, silica, and Zn
(Zn). There are literature where multiple metal usage augmented the efficacy of the product.
Imani et al. developed HA/CuO/TiO2 nanocomposites with the highest antibacterial
properties. Development was manifested with the assistance of the robust Quality By
Design principle [68]. Recently, Balu et al. took a challenging task to accommodate Ag
NPs, graphene oxide (GO), multi-walled carbon nanotubes (MWCNTs), and graphene
oxide nano-ribbons (GONRs) in HA nanocomposites. The group studied the effect of
the proportion of carbon on the final hardness of the nanocomposites. Moreover, the Ag
NPs activity was evaluated using biostrain (E. coli and S. aureus bacteria). The developed
nanocomposite provided a model drug release (lidocaine) that may benefit the patient [69].
Other synthetic polymers have been explored as an adjunct in nanocomposites preparation.
Improvement of the mechanical properties of Poly Methyl Methacrylate Nanocomposites
as nanocomposites [70] and compared with HA nanocomposites. Moreover, the drug
(theobromine) eluting character of these nanocomposites was also examined [71].
Although, the research focus has shifted from analyzing the proportion to identifying
and calibrating newer techniques to form nanocomposites. Hou et al. presented three se-
quential one port synthesis methods, where Ag ions are absorbed on the HA nanorods. The
process is simple and validated using an array of pot synthesis methods of the nanocom-
posites. Whereas, Mallakpour et al. developed multiple component nanocomposites
(Polyvinylpyrrolidone/L-leucine Amino Acid, Functionalized Mg-Substituted Fluorapatite
Nanocomposites) employing ultrasonic waves as an energy source [72]. While various

scientific groups used numerous other sources of energy, such as microwaves [73–75],
photons [76] or their combination [77].
2.3. Endodontic
Due to higher vascularity, the pulp of the tooth is considered the most vital, funda-
mental life of the tooth. Hence it is very much important to restore it. Endodontics is the
branch of dentistry that deals with the dental pulp and the area surrounding the dental
pulp. It is needed when the infection crosses the upper part of the teeth, i.e., carriers
and reaches to innermost part, i.e., the pulp. It deals with a specialized antimicrobial as
well as constructive aids to provide long-lasting stability to teeth. However, pulpitis is
a painful and irreversible process, requiring the removal of the entire pulp with a root
canal and replacing the tissue with an inner polymeric material. However, in case invasion
of the inflammation is just superficial, pulp regeneration is also possible. However, pulp
regeneration is difficult and variable with respect to age. Dentin Odontoblast (present at the
periphery of the pulp) stem cells have also been explored for the aforementioned purpose
but illustrated a futile response in the clinical setup [78,79]. Hanafy et al. explored two
commonly used dental biomaterials, i.e., mineral trioxide aggregate (MTA) and nano-HA,
as odontogenic differentiation promotor results demonstrated significantly higher and
upregulated expression of the characteristic genes for odontotomy differentiation, i.e., OPN,
RUNX2, OCN, and Collagen1, in the case of treatment group than the control [80]. Pulp
capping is another method to preserve the vitality of the pulp and contain the infection
outside the vascular region. Li et al. proposed biocompatible, osteogenesis-sensitizing
properties and a combination of micro-nano bioactive glasses. Ca-Zn-Si-based (Zn doped)
bioglasses micro nanospheres for dental pulp capping. Results were encouraging to show
higher antibacterial effects and higher stimulation of macrophages to reduce the proin-
flammatory markers, followed by remineralization of dentin via sensitization of dental
pulp cells [81]. Sinjari et al. proposed a very advanced nanotechnological approach using
drug encapsulated liposomes to reconstruct the homeostasis of dental pulp stem cells. The
treatment was able to restore cell proliferation and attenuate the inflammation markers
hence aiding in tooth restoration regarding 2-hydroxyethyl methacrylate [82]. Similarly,
Kim et al. proposed an RGD peptide conjugated dendrimer-based drug delivery system for
dental pulp differentiation after a traumatic dental injury. Results were very encouraging,
with higher mineralization and odontogenic potential [83]. Elgendy et al. explored natural
scaffolds, i.e., propolis, chitosan, for tooth restoration with a very limited set of experiments
and provided their potential for endodontic treatment due to elevated biocompatibility and
tissue restoration ability [84]. In the same line, Tondnevis et al. proposed the development
of a dental tissue scaffold containing nano-HA or Nano fluoro HA /Chitosan scaffold
using polymers using the freeze-drying technique. Results illustrated that the addition of
chitosan assisted in significant increases in cell proliferation [85] These studies illustrated
the potential of chitosan NPs in dental endodontics. Recently a laboratory study was
reported by Bhaskar et al. dictating the role of eggshell-derived porous nano-HA and CMC
(Carboxy Methylcellulose) composite and showing their effect on dental bioactivity and cell
proliferation using the significant elevation of VEGF and dentine sialophosphoprotein [86].
Amoxicillin-loaded nanodiamond Guttapercha composite (NDGP-AMC) was developed
and tested for its use in root canal treatments with promising results [87]. Other than these
other natural fibers and polymers, i.e., gelatin [88–90], collagen [91,92], and silk [90] have
been explored in nanodentistry.
2.4. Prosthodontic
With the advent of technology, living standards have drastically improved attitudes
towards oral health. Therefore, interest in prosthodontics for advancing research on
artificial restorative materials has been shifted to the upside [93]. Classically, these materials
are broadly categorized into ceramics, resins, polymers, and metals [94]. However, a few
issues are still unsolved to cater to the need for prosthodontics. Here, nanotechnology
played a vital role and different nanomaterials have been synthesized/utilized to cover the
untapped areas of prosthodontics. Nanotechnology has also significantly improved the
properties of existing materials, such as ceramics, impression materials, denture bases, and
types of cement used in prosthodontics.
Prosthodontics are mainly classified into removal or fixed type (tooth-supported or
implant-supported)
2.4.1. Removable Type

In this category, Polymethylmethacrylate (PMMA) polymers and silicone elastomers
are mainly used for denture and maxillofacial prostheses, respectively. However, dimen-
sional changes with PMMA polymers and poor tensile and tearing strength of silicone
elastomers pave the way for using nanotechnology in these types of restorative materi-
als [95]. Firstly, carbon nanotubes lead to a bond formation with PMMA resins/polymers
by weak van der Waal force to improve its dimensional stability for better fit and ten-
sile strength [96]. Secondly, metal-based NPs (Ag, TiO2 , etc.) reinforce PMMA polymers
to improve their tensile strength and antimicrobial activity [97]. Moreover, polyhedral
oligomeric silsesquioxanes (POS), a nano (1.5 nm) silica cage, and metal NPs support
silicone elastomers to improve their tensile strength and physical properties [98,99]. More-
over, nanotechnology improved the pathological states like denture stomatitis induced by
adherence of biofilm of Candida albicans over the denture base materials [100]. Moreover,
Alumina NPs were synthesized and evaluated for improving osseointegrity and curative
process when the dental implant was installed [101].
2.4.2. Fixed Type

In this category, tooth and implant-supported nanomaterials, nanocomposites, and
nanocoatings are primarily used as fixed prostheses. The issue of dimensional unfolding
persisted in the conventional fixed types of restorative materials. Conventional materials
also showed cytotoxic effects by leaching organic monomers into surrounding gum tis-
sues [102]. Nanocomposites based on nanofiller technology solve these issues [103]. Silica or
Zirconia-silica NPs were synthesized by treating silica particles with 3-methacryloxypropyl-
trimethoxysilane to improve flexural strength and hardness. Nanotechnology also brings
hope and new vistas in improving the adhesion and durability of implants. Carbon nan-
otubes, polyvinyl alcohol, and silica-based NPs were used in addition to calcium phosphate
to synthesize nanocomposites and sometimes scaffolds for improving mechanical strength
and tissue regeneration [104]. In addition, the improvement of calcium carbonate-silicone
dioxide NPs improves tear strength and hardness of maxillofacial silicone elastomers [105].
In another study, Persson et al. synthesized glass-ceramic in Zirconia-silica NPs using the
sol-gel method to improve the corrosion resistance and hardness [106].
Few commercial products are also available in the market to understand the potential
of nanotechnology in prosthodontics. Clearfil Majesty Posterior is a product (a superfilled
nanohybrid composite) of Kuraray America and is an ideal amalgam alternative (92% filled
with nano-sized alumina and glass materials) and shows high physical properties with
superior surface wear resistance [107]. PremiseTM , a product of Kerr corporation (84%
filled), a nanocomposite that shows significant improvement in durability, wettability, and
sculptability [108].
2.5. Orthodontics
Orthodontic brackets and archwires are important components for desired tooth move-
ment. However, it may take time to acquire better holding and stability due to frictional
forces between orthodontic wires and brackets [109]. To trace these issues, coating these
components using nanotechnology is used. Nowadays, Fullerene like Molybdenum and
tungsten disulfide NPs are used as dry (solid) lubricants for stainless steel archwires to
reduce the friction [110]. Moreover, it was found that maintaining oral hygiene is more dif-
ficult during orthodontic therapy due to microbial colonization (e.g., Streptococcus mutans,
Staphylococcus aureus, etc.), a biofilm of bacterial plaque and enamel decalcification. Sev-
eral studies have been reported using nanotechnology-based approaches like elastomeric
ligatured supported NPs (Benzocaine and Ag) to show anticariogenic, antimicrobial activ-
ity [111] and nanocomposites (Ag NPs with ZnO, chlorhexidine) of adhesive types/bands
to elicit improved tensile strength, anti-inflammatory properties [112]. Akarajarasrod et al.
reported improved antibacterial activities of orthodontic adhesives when incorporated
with gold NPs [113]. In a study, a comparative evaluation between orthodontic adhesive
containing silver NPs and conventional orthodontic adhesives was reported by Ahn et al.
This study illustrates that newer orthodontic adhesives prevent enamel demineralization
better than conventional adhesives [114]. Another study showed that the inclusion of
TiO2 NPs in orthodontic composites improved the antibacterial activity without losing the
integrity of shear bond strength [115]. Moreover, it was found that copper material was
more stable (physically or chemically) and economical than silver material. Eshed et al.
also showed a significant inhibitor effect when copper oxide NPs were incorporated with
adhesive [116,117].
Further, nanotechnology brings new hope to orthodontic therapy by utilizing nanocoat-
ing over temporary anchorage devices, especially mini-screws, for improving wettability
and anti-inflammatory activities [118]. Overall, the use of nanotechnology in orthodontics
and prosthetics opens the door to reducing/avoidance of demineralization and shows
more anchorage leads to improved patient compliance [119].
2.6. Periodontology and Bone Regeneration

Due to several factors like genetics, smoking, poor oral hygiene, and obesity, periodon-
titis occurs, leading to the destruction of the tooth and its surrounding structure (including
the cementum, alveolar bone, and ligament). Therefore, the overall aim of periodontal
therapeutics is to repair or for bone regeneration [120]. Several aspects have been studied
but found shortcomings. Nanotechnology has also gained popularity in this field, reducing
dentin hypersensitivity, drug delivery, and bone regeneration.
Dentinal hypersensitivity is one of the major concerns patients face in periodontal dis-
eases. HA NPs (HA NPs) were studied and clinically used in toothpaste and mouth wash
(nano-XIM of FLUIDINOVA, S.A. Portugal) as these particles are highly effective in sealing
dentin tubules and preventing nerve revelation. These NPs also showed higher binding to
teeth surface, thus promoting enamel remineralization [121,122]. Moreover, drug-loaded
NPs and scaffolds are also interestingly popular for tissue regeneration and healing peri-
odontal diseases [123]. Various biodegradable polymers like Poly(Lactic acid-Glycolic acid)
(PLGA) based NPs were successfully formulated to deliver therapeutic actives like minocy-
cline to show sustained release patterns in periodontal infections [124]. HA-NPs loaded
tetracycline were also synthesized and promoted the proliferation of periodontal ligament
cells [125]. Further, tetracycline NPs have also been investigated for periodontal treatment
as well. There are various commercially available tetracycline-loaded microsphere patches,
such as Arestin® (Valeant, Bridgewater, MA, USA) and Nanogen® (Orthogen, Springfield,
IL, USA), already in the market. These are intended for insertion within the periodontal
pocket, which releases the drug into the affected area in a sustained manner. Various growth
factors (e.g., Bone Morphogenetic Protein-2 and Fibroblast) loaded NPs were synthesized to
initiate the alveolar bone cell differentiation process [126]. Furthermore, various scaffolds
based on nano-engineering exhibited potential in bone repair due to mimic of native tissue
construct. Various electrospun nanofibres (prepared by PLGA or gelatin) were utilized to
grow the human periodontal ligament (PDL) cells by exhibiting the optimum cell adhesion
and differentiation process [127]. Also, the scaffolds containing nano-HA and nano-alginate
were prepared to culture human PDL cells [128]. Besides polymeric nanofibers, various
biomimetic self-assembling peptides (e.g., P11 -4) were also studied and evaluated to treat
early caries lesions [129]. Moreover, green chemistry-based biomaterials were also invented
and utilized for oral bone regeneration. Gandolfi et al. formulated a hydrogel consisting of
polysaccharides (copolymers of L-guluronate and D-mannuronate) and peptide (gelatin)

matrix activated with biominerals (calcium silicate, dicalcium phosphate dehydrate) type
of fillers and evaluated this green hydrogel for bone regeneration [130]. Also, they had
developed Poly-lactic acid (PLA) based scaffolds loaded in exosomes with suitable minerals
(calcium silicate and dicalcium phosphate dehydrate; DCPD) to improve the osteogenic
strength of human adipose-derived mesenchymal stem cells [131]. In another study, Tat-
ullo et al. developed an innovative scaffold for regeneration of periapical and alveolar
bones using polymeric (PLA) base doped with minerals (hydraulic calcium silicate and
DCPD) seeded with human mesenchymal stem cells of the inflammatory periapical cyst.
These scaffolds were produced by thermally induced phase separation technique, whereas
other techniques are also utilized to produce polymeric scaffolds: electrospinning, salt
leaching, and 3D printing [132]. Further, many porous nano-scaffold have been in use for
tooth extraction site preservation. Nano-HA mineralized silk fibroin porous scaffold is
biocompatible in nature and helps in bone regeneration. The porous nature simulated the
biological bone structure and induced osteogenesis in in vitro cell line culture [133].
2.7. Dental Implants

For many decades, dental implants have been used and applied to restore or replace
teeth. However, attaining osseointegration and managing infection associated with im-
plants (metallic type) are still an issue to explore [134]. Various studies have been reported
for using different surface modifications to improve these issues, as surface modification
also affects the biological regenerative process (adsorption of proteins, adhesion, differentia-
tion, and proliferation of cells, which further initiates tissue regeneration). Nanotechnology-
based coating over the surface of titanium and tetragonal Zirconia implants was studied
to improve the biological and mechanical properties [135]. Further, Silica nanocomposites
were utilized and coated over the surface of implants to improve mechanical strength
and bone growth [136]. Moreover, the implant surface can be treated/modified by HA
nanocrystals [137] and Calcium-phosphorus NPs for ameliorating bone regeneration [138].
In addition to the advantages of metal and ceramic-based dental implants, several limi-
tations like toxicities and corrosive behavior are also associated with them. To overcome
these challenges, less toxic plant-derived biomaterials are used in the production of dental
implants [139]. A recent study reported that gold NPs were photo-fabricated from aqueous
bark extract of Salacia chinensis and applied in dental implants, where it was shown its
biocompatibility with blood and high osseoinductive potential when evaluating the cell
viability with MG-63 bone osteosarcoma cell lines [140]. Another approach to improving
osseointegrity of dental implants is the use of calcium phosphate nanoparticles coated
over the surface of TiO2 implants [141]. In another study of rats with ovariectomized
induced osteoporosis, where chitosan gold NPs carrying the c-myb gene improved the
osseointegration of dental implants [142].
2.8. Regulatory Framework

Although nanomaterials have solved various challenges associated with dentistry.
However, various concerns such as toxicity and regulations are not solved fully and
need to be understood to explore nanotechnology potential fully. In comparison to the
conventional materials/formulations in dentistry, nanomaterials show different responses
due to their unique physiochemical properties such as size, interaction with different
cell membranes and other biological macromolecules, and different pharmacokinetics
parameters. Therefore, more understanding of these interactions, toxicity assessment
(especially immunotoxicology and impurity profiling), in vitro–in vivo modeling, and
regulations are necessary to increase the commercialization success rate of nanomaterials,
especially in dentistry [143].
NPs induced toxicity symptoms can be easily understood by different nanomaterials
utilized in dentistry. Carbon nanotubes used in dental coating showed some inflammatory
reactions when in contact with some biological membrane [144]. Moreover, during the
preparation of nanomaterials, exposure to them by inhalation may cause toxic symptoms in

the lungs. Exposure to titanium dioxide (TiO2 ) NPs may impose a risk of lung cancer [145]
and impair spatial cognitive performance [146]. HA NPs employed in a dental filling bind
with blood proteins, form a complex that is killed by macrophages, and then transferred
to major vascular organs, such as the lung and spleen, which shows toxic responses [147].
In addition, genotoxic and immunotoxic effects were exhibited by silica and zirconium
nanomaterials primarily due to reactive oxygen species (ROS) [148,149].
Unique physio-chemical properties, surface charge, and the high surface-to-volume
ratio of NPs act as a basis for transporting them into the cells to illustrate toxic effects.
Different scientific reports revealed the internalization process of NPs in the mammalian
cells and expressed the endocytosis as a transport mechanism through clathrin mediation
and scavenging receptors. However, the interactions of nanomaterials with alveolar bone
and gingival mucosa are still unknown and need to be explored clinically [150]. Moreover,
the presumed mechanism for toxicity is the induction of cellular oxidative leading to more
production of ROS, which further leads to altering cell signaling cascades, generating
protein radicals and lipid peroxidation, DNA damage, initiation of inflammatory responses,
and eventually cell death [151]. Recently, metals in dentistry have raised another challenge
and concern for environmentalists. Grinding of resin-based dental materials results in
wastewater pollution, especially in the case of using micro-nano particles making their way
from dental sinks to the wider environment leading to potential toxicity concerns [152].
Especially after the ‘Minamata convention,’ the use of mercury amalgam is being replaced
with resin formulation in dentistry [153]. However, scientists present the solution for
remediation of heavy metal poisoning in waste dental water using NPs only. These specified
nano pollution absorbers and efficiently eradicate heavy metals from water due to their
higher surface area and porous nature [154].y
In a nutshell, to fasten the regulatory submissions and commercialization of nanoma-
terials in dentistry, more understanding of material selection (whether it is biocompatible
and biodegradable or not), particle size, surface charge, and interaction with biological
membranes are required.
3. Future of Nanodentisty
Undoubtedly nanodentistry confers numerous advantages over conventional systems,
such as higher bio-regeneration, a notable antimicrobial effect due to anti-biofilm properties,
increased hardness of composites, and better sealing of fillers, but at the same time, its
overpricing, precise placement, associated toxicity, costly development, and international
regulations limit the clinical exploration. Though despite all the stated hurdles, scientists are
now working hard to find the least expensive methods to synthesize NP scaffolds that fits
in the regulatory framework as well as assist in placing the NPs into the right place. There
are multiple unconventional NPs, including nanodiamonds, quantum dots, nanoshells, and
carbon nanotubes, which have been explored widely in research and have better outcomes
to be used in future commercial markets. Its superior surface and chemical nature make it
a very suitable candidate for use as a filler in dental nanocomposite fabrication.
3.1. 3D Printing
3D printing is one technique that is being employed for the synthesis of the most
complex gematrical scaffold that might be difficult to make when using different processes.
Chau et al. fabricated vancomycin releasing polycaprolactone/nHA nanocomposite using
3D modeling. The scaffolds showed higher strength and sustained drug release for up to
14 days which may assist tissue regeneration with antimicrobial activity [155]. However,
despite the success in bone regeneration scaffold synthesis, little research has been done in
the nanodentistry domain, making it a potential area for future research.
3.2. Nanobots
To overcome the already stated shortcomings, i.e., precise placement, nanorobots have
been invented. These are specialized tools to carry out programmed penetrations, clean
the decayed tissue, and place composites to the required site using 3D filling technology.
Dasgupta et al. published the use of magnetic nanobots incorporated in root canal opera-
tions. These nanobots could go deeper into the dentin, which is difficult using conventional
methods. The special retrieval process of nanobots also made a better choice [156]. These
nanobots work using a special algorithm or software. In 2015, Razavi et al. demonstrated
simulation for dental restoration. The inclusion of robotics increases the speed by eight
times [157].
3.3. Nanozymes
Inorganic NPs showing enzyme-like properties are termed nanozymes. They are
less costly, easy to synthesize, more stable, and highly efficient compared to their natural
counterparts. They are vastly used for their theranostic applications. Zhang et al. developed
DNA nanozymes for biosensing the presence of dental bacteria [158]. Similarly, Huang et al.
presented bifunctional nanozymes that specifically inhibit the pathogenic Streptococcus
mutans (pathogen) but not the commensal, Streptococcus oralis using iron oxide nanozymes
having oxidase kind activity [159].
4. Conclusions
Conventional dentistry is enriched by revolutionized nanotechnology despite the
many irrefutable lacunas that limit its clinical exploration. Research in the field of nanoden-
tistry is still lagging as compared to other biological research areas. More patient-centered
research will help to boost the development of nanotheranostics that should not only be
efficacious but, at the same time should be affordable. Moreover, the true potential has
still not been unleashed in the case of nanodentistry until now; metallic/polymeric NPs
have only been explored vastly, but drug-eluting NPs research still has gigantic leaps
to follow. Although challenges are huge, a collaborative scientific effort will make the
impossible possible.
Funding: This work was supported by the Deanship of Scientific Research, King Faisal University,
Saudi Arabia (Grant number NA000111).
Data Availability Statement: Not applicable.
Acknowledgments: All the authors thank the Deanship of Scientific Research, King Faisal University,
Saudi Arabia, for supporting this project.
Conflicts of Interest: The authors declare no conflict of interest.
References
1. Drexler, K.E. Nanotechnology: From Feynman to Funding. Bull. Sci. Technol. Soc. 2004, 24, 21–27. [CrossRef]
2. Freitas, R.A., Jr. Nanodentistry. J. Am. Dent. Assoc. 2000, 131, 1559–1565. [CrossRef] [PubMed]
3. McKenna, G. Nutrition and Oral Health; Springer: Berlin/Heidelberg, Germany, 2021.
4. Nelson, S.J. Wheeler’s Dental Anatomy, Physiology and Occlusion-E-Book; Elsevier Health Sciences: Amsterdam, The Netherlands, 2014.
5. Palumbo, A. The anatomy and physiology of the healthy periodontium. In Gingival Diseases-Their Aetiology, Prevention and
Treatment; Intech: Manila, Thailand, 2011; pp. 1–21.
6. Sasalawad, S.S.; Sathyajith, N.N.; Shashibhushan, K.; Poornima, P.; Hugar, S.M.; Roshan, N.M.; Reviews, M. “Nanodentistry”-The
Next Big Thing Is Small. Int. J. Contemp. Dent. Med. Rev. 2014, 2014.
7. Bapat, R.A.; Joshi, C.P.; Bapat, P.; Chaubal, T.V.; Pandurangappa, R.; Jnanendrappa, N.; Gorain, B.; Khurana, S.; Kesharwani, P.
The use of nanoparticles as biomaterials in dentistry. Drug Discov. Today 2018, 24, 85–98. [CrossRef]
8. Yudaev, P.; Chuev, V.; Klyukin, B.; Kuskov, A.; Mezhuev, Y.; Chistyakov, E.J.P. Polymeric Dental Nanomaterials: Antimicrobial
Action. Polymers 2022, 14, 864. [CrossRef]
9. Limeback, H. Comprehensive Preventive Dentistry; John Wiley & Sons: Hoboken, NJ, USA, 2012.
10. Sawarkar, H.A.; Kashyap, P.P.; Kaur, C.D.; Pandey, A.K.; Biswas, D.K.; Singh, M.K.; Dhongade, H.K. Antimicrobial and TNF-α
Inhibitory Activity of Barleria prionitis and Barleria grandiflora: A comparative Study. Indian J. Pharm. Sci. 2016, 50, 409–417.
[CrossRef]
11. Pitts, N.B.; Zero, D.T.; Marsh, P.D.; Ekstrand, K.; Weintraub, J.A.; Ramos-Gomez, F.; Tagami, J.; Twetman, S.; Tsakos, G.; Ismail, A.
Dental caries. Nat. Rev. Dis. Primers 2017, 3, 17030. [CrossRef]
12. Larsen, T.; Fiehn, N.E. Dental biofilm infections–An update. Apmis 2017, 125, 376–384. [CrossRef]
13. Soumo, G.; Sangamitra, A. Review of Nanotechnology in dentistry. J. Adv. Med. Dent. Sci. Res. 2021, 7, 65–67.
14. Weir, M.D.; Kaner, P.; Marin, A.; Andrianov, A.K. Ionic Fluoropolyphosphazenes as Potential Adhesive Agents for Dental
Restoration Applications. Regen. Eng. Transl. Med. 2021, 7, 10–20. [CrossRef]
15. Baier, R.E. Surface behaviour of biomaterials: The theta surface for biocompatibility. J. Mater. Sci. Mater. Med. 2006, 17, 1057–1062.
[CrossRef] [PubMed]
16. Khan, S.T.; Al-Khedhairy, A.A.; Musarrat, J. ZnO and TiO2 nanoparticles as novel antimicrobial agents for oral hygiene: A review.
J. Nanopart. Res. 2015, 17, 276. [CrossRef]
17. Ingram, G.; Horay, C.; Stead, W. Interaction of Zinc with Dental Mineral. Caries Res. 1992, 26, 248–253. [CrossRef] [PubMed]
18. Pal, S.; Tak, Y.K.; Song, J.M. Does the Antibacterial Activity of Silver Nanoparticles Depend on the Shape of the Nanoparticle? A
Study of the Gram-Negative Bacterium Escherichia coli. Appl. Environ. Microbiol. 2007, 73, 1712–1720. [CrossRef]
19. Wang, L.; Hu, C.; Shao, L. The antimicrobial activity of nanoparticles: Present situation and prospects for the future. Int. J.
Nanomed. 2017, 12, 1227–1249. [CrossRef]
20. Eslami, N.; Rajabi, O.; Ghazvini, K.; Barati, S.; Ahrari, F. The antimicrobial sensitivity of Streptococcus mutans and Streptococcus
sangius to colloidal solutions of different nanoparticles applied as mouthwashes. Dent. Res. J. 2015, 12, 44. [CrossRef]
21. Ahmed, O.; Sibuyi, N.R.S.; Fadaka, A.O.; Madiehe, M.A.; Maboza, E.; Meyer, M.; Geerts, G.J.P. Plant Extract-Synthesized Silver
Nanoparticles for Application in Dental Therapy. Pharmaceutics 2022, 14, 380. [CrossRef]
22. Ahghari, M.R.; Soltaninejad, V.; Maleki, A.J. Synthesis of nickel nanoparticles by a green and convenient method as a magnetic
mirror with antibacterial activities. Sci. Rep. 2020, 10, 12627. [CrossRef]
23. Yazdanian, M.; Rostamzadeh, P.; Rahbar, M.; Alam, M.; Abbasi, K.; Tahmasebi, E.; Tebyaniyan, H.; Ranjbar, R.; Seifalian, A.;
Yazdanian, A. The Potential Application of Green-Synthesized Metal Nanoparticles in Dentistry: A Comprehensive Review.
Bioinorg. Chem. Appl. 2022, 2022, 2311910. [CrossRef]
24. Zhang, K.; Melo, M.A.S.; Cheng, L.; Weir, M.D.; Bai, Y.; Xu, H.H. Effect of quaternary ammonium and silver nanoparticle-
containing adhesives on dentin bond strength and dental plaque microcosm biofilms. Dent. Mater. 2012, 28, 842–852. [CrossRef]
25. Cheng, L.; Zhang, K.; Weir, M.D.; Melo, M.A.S.; Zhou, X.; Xu, H.H. Nanotechnology strategies for antibacterial and remineralizing
composites and adhesives to tackle dental caries. Nanomedicine 2015, 10, 627–641. [CrossRef] [PubMed]
26. Magalhaes, A.P.R.; Santos, L.B.; Lopes, L.G.; Estrela, C.R.d.A.; Estrela, C.; Torres, É.M.; Bakuzis, A.F.; Cardoso, P.C.; Carrião, M.S.
Nanosilver application in dental cements. Int. Sch. Res. Not. 2012, 2012, 265438. [CrossRef]
27. Daliri, K.; Seifi-Shalamzari, N.; Saeida-Ardekani, M.; Ekraminasab, S.; Neamatzadeh, H.J. Neonatology. Application of Golden
Nanoparticles against Streptococcus Mutans for Prevention of Caries Lesions. World J. Peri Neonatol. 2020, 3, 56–61.
28. Zhang, M.; Liu, X.; Xie, Y.; Zhang, Q.; Zhang, W.; Jiang, X.; Lin, J.J. Biological safe gold nanoparticle-modified dental aligner
prevents the Porphyromonas gingivalis biofilm formation. ACS Omega 2020, 5, 18685–18692. [CrossRef]
29. Kamath, K.A.; Nasim, I.; Rajeshkumar, S. Evaluation of the re-mineralization capacity of a gold nanoparticle-based dental varnish:
An in vitro study. J. Conserv. Dent. 2020, 23, 390.
30. Kovtun, A.; Kozlova, D.; Ganesan, K.; Biewald, C.; Seipold, N.; Gaengler, P.; Arnold, W.H.; Epple, M. Chlorhexidine-loaded
calcium phosphate nanoparticles for dental maintenance treatment: Combination of mineralising and antibacterial effects. RSC
Adv. 2012, 2, 870–875. [CrossRef]
31. Liu, Y.; Huang, Y.; Kim, D.; Ren, Z.; Oh, M.J.; Cormode, D.P.; Hara, A.T.; Zero, D.T.; Koo, H. Ferumoxytol nanoparticles target
biofilms causing tooth decay in the human mouth. Nano Lett. 2021, 21, 9442–9449. [CrossRef]
32. Drukteinis, S. Hydraulic calcium silicate-based materials for root canal obturation. Clin. Dent. Rev. 2022, 6, 1. [CrossRef]
33. Lv, K.L.; Zhang, J.X.; Meng, X.C.; Li, X.Y. Remineralization Effect of the Nano-HA Toothpaste on Artificial Caries. Key Eng. Mater.
2007, 330–332, 267–270. [CrossRef]
34. Huang, S.; Gao, S.; Yu, H.J.B.m. Effect of nano-hydroxyapatite concentration on remineralization of initial enamel lesion in vitro.
Biomed. Mater. 2009, 4, 034104. [CrossRef]
35. Liang, K.; Weir, M.D.; Reynolds, M.A.; Zhou, X.; Li, J.; Xu, H.H. Poly (amido amine) and nano-calcium phosphate bonding agent
to remineralize tooth dentin in cyclic artificial saliva/lactic acid. Mater. Sci. Eng. C 2017, 72, 7–17. [CrossRef] [PubMed]
36. Nguyen, S.; Hiorth, M.; Rykke, M.; Smistad, G. Polymer coated liposomes for dental drug delivery–Interactions with parotid
saliva and dental enamel. Eur. J. Pharm. Sci. 2013, 50, 78–85. [CrossRef] [PubMed]
37. Pistone, S.; Rykke, M.; Smistad, G.; Hiorth, M. Polysaccharide-coated liposomal formulations for dental targeting. Int. J. Pharm.
2017, 516, 106–115. [CrossRef] [PubMed]
38. Backlund, C.J.; Worley, B.V.; Schoenfisch, M.H. Anti-biofilm action of nitric oxide-releasing alkyl-modified poly (amidoamine)
dendrimers against Streptococcus mutans. Acta Biomater. 2016, 29, 198–205. [CrossRef]
39. Liang, K.; Wang, S.; Tao, S.; Xiao, S.; Zhou, H.; Wang, P.; Cheng, L.; Zhou, X.; Weir, M.D.; Oates, T.W.; et al. Dental remineralization
via poly (amido amine) and restorative materials containing calcium phosphate nanoparticles. Int. J. Oral Sci. 2019, 11, 1–12.
[CrossRef]
40. Chen, L.; Chen, W.; Yu, Y.; Yang, J.; Jiang, Q.; Wu, W.; Yang, D. Effect of chlorhexidine-loaded poly(amido amine) dendrimer on
matrix metalloproteinase activities and remineralization in etched human dentin in vitro. J. Mech. Behav. Biomed. Mater. 2021,
121, 104625. [CrossRef]
41. Yang, L.; Schoenfisch, M. Nitric Oxide-Releasing Hyperbranched Polymers as Antibacterial Agents Against Dental Pathogens.
ACS Appl. Bio. Mater. 2019, 4, 8.
42. Wu, D.; Yang, J.; Li, J.; Chen, L.; Tang, B.; Chen, X.; Wu, W.; Li, J. Hydroxyapatite-anchored dendrimer for in situ remineralization
of human tooth enamel. Biomaterials 2013, 34, 5036–5047. [CrossRef]
43. A Mostafa, D.; Bayoumi, F.S.; Taher, H.M.; Abdelmonem, B.H.; Eissa, T.F. Antimicrobial potential of mentha spp. essential oils as
raw and loaded solid lipid nanoparticles against dental caries. Res. J. Pharm. Technol. 2020, 13, 4415. [CrossRef]
44. Wassel, M.O.; Khattab, M.A. Antibacterial activity against Streptococcus mutans and inhibition of bacterial induced enamel
demineralization of propolis, miswak, and chitosan nanoparticles based dental varnishes. J. Adv. Res. 2017, 8, 387–392. [CrossRef]
45. Patil, A.G.; Jobanputra, A. Rutin-Chitosan Nanoparticles: Fabrication, Characterization and Application in Dental Disorders.
Polym. Technol. Eng. 2015, 54, 202–208. [CrossRef]
46. Covarrubias, C.; Trepiana, D.; Corral, C. Synthesis of hybrid copper-chitosan nanoparticles with antibacterial activity against
cariogenic Streptococcus mutans. Dent. Mater. J. 2018, 37, 379–384. [CrossRef] [PubMed]
47. Javed, R.; Rais, F.; Kaleem, M.; Jamil, B.; Ahmad, M.A.; Yu, T.; Qureshi, S.W.; Ao, Q. Chitosan capping of CuO nanoparticles: Facile
chemical preparation, biological analysis, and applications in dentistry. Int. J. Biol. Macromol. 2020, 167, 1452–1467. [CrossRef]
[PubMed]
48. Cheng, L.; Weir, M.D.; Xu, H.H.K.; Antonucci, J.M.; Lin, N.J.; Lin-Gibson, S.; Xu, S.M.; Zhou, X. Effect of amorphous calcium
phosphate and silver nanocomposites on dental plaque microcosm biofilms. J. Biomed. Mater. Res. Part B Appl. Biomater. 2012, 100,
1378–1386. [CrossRef] [PubMed]
49. González-Luna, P.-I.; Martínez-Castañón, G.-A.; Zavala-Alonso, N.-V.; Patiño-Marin, N.; Niño-Martínez, N.; Morán-Martínez, J.;
Ramírez-González, J.-H. Bactericide Effect of Silver Nanoparticles as a Final Irrigation Agent in Endodontics on Enterococcus
faecalis: An Ex Vivo Study. J. Nanomater. 2016, 2016, 7597295. [CrossRef]
50. Tagad, C.; Dugasani, S.R.; Aiyer, R.; Park, S.; Kulkarni, A.; Sabharwal, S. Green synthesis of silver nanoparticles and their
application for the development of optical fiber based hydrogen peroxide sensor. Sensors Actuators B: Chem. 2013, 183, 144–149.
[CrossRef]
51. Fayaz, A.M.; Balaji, K.; Kalaichelvan, P.; Venkatesan, R. Fungal based synthesis of silver nanoparticles—An effect of temperature
on the size of particles. Colloids Surf. B Biointerfaces 2009, 74, 123–126. [CrossRef]
52. Inbakandan, D.; Kumar, C.; Bavanilatha, M.; Ravindra, D.N.; Kirubagaran, R.; Khan, S.A. Ultrasonic-assisted green synthesis of
flower like silver nanocolloids using marine sponge extract and its effect on oral biofilm bacteria and oral cancer cell lines. Microb.
Pathog. 2016, 99, 135–141. [CrossRef]
53. Favaro, J.C.; Detomini, T.R.; Maia, L.P.; Poli, R.C.; Guiraldo, R.D.; Lopes, M.B.; Berger, S.B. Anticaries Agent Based on Silver
Nanoparticles and Fluoride: Characterization and Biological and Remineralizing Effects—An In Vitro Study. Int. J. Dent. 2022,
2022, 1–11. [CrossRef]
54. Alcudia, A.; Begines, B.; Rodriguez-Lejarraga, P.; Greyer, V.; Godinho, V.C.F.; Pajuelo, E.; Torres, Y. Development of porous
silver nanoparticle/polycaprolactone/polyvinyl alcohol coatings for prophylaxis in titanium interconnected samples for dental
implants. Colloids Interface Sci. Commun. 2022, 48, 100621. [CrossRef]
55. Toledano, M.; Vallecillo-Rivas, M.; Aguilera, F.S.; Osorio, M.T.; Osorio, E.; Osorio, R. Polymeric zinc-doped nanoparticles for high
performance in restorative dentistry. J. Dent. 2021, 107, 103616. [CrossRef] [PubMed]
56. Tiwari, A.K.; Jha, S.; Agrawal, R.; Mishra, S.K.; Pathak, A.K.; Singh, A.K.; Dikshit, A.; Awasthi, R.R. Anti-bacterial efficacy of
phyto-synthesized zinc oxide nanoparticles using murraya paniculata l. leaf extract. Sciences 2022, 4, 7.
57. Heydari, S.; Asefnejad, A.; Nemati, N.H.; Goodarzi, V.; Vaziri, A. Fabrication of multicomponent cellulose/polypyrrole composed
with zinc oxide nanoparticles for improving mechanical and biological properties. React. Funct. Polym. 2021, 170, 105126.
[CrossRef]
58. Bai, X.; Lin, C.; Wang, Y.; Ma, J.; Wang, X.; Yao, X.; Tang, B. Preparation of Zn doped mesoporous silica nanoparticles (Zn-MSNs)
for the improvement of mechanical and antibacterial properties of dental resin composites. Dent. Mater. 2020, 36, 794–807.
[CrossRef] [PubMed]
59. Memarzadeh, K.; Sharili, A.S.; Huang, J.; Rawlinson, S.C.; Allaker, R.P. Nanoparticulate zinc oxide as a coating material for
orthopedic and dental implants. J. Biomed. Mater. Res. Part A 2015, 103, 981–989. [CrossRef] [PubMed]
60. Ergun, G.; ATAOL, A.S.; Şahin, Z.; Saraç, N.; Baygar, T.; Uğur, A. Antibiofilm Evaluation of Two Different Denture Liners
Incorporated with Zirconium Oxide Nanoparticles. Cumhur. Dent. J. 2021, 25, 9–19. [CrossRef]
61. Chau, T.P.; Veeraragavan, G.R.; Narayanan, M.; Chinnathambi, A.; Alharbi, S.A.; Subramani, B.; Brindhadevi, K.; Pimpimon,
T.; Pikulkaew, S. Green synthesis of Zirconium nanoparticles using Punica granatum (pomegranate) peel extract and their
antimicrobial and antioxidant potency. Environ. Res. 2022, 209, 112771. [CrossRef]
62. Almutairi, B.; Binhasan, M.; Shabib, S.; Al-Qahtani, A.S.; Tulbah, H.I.; Al-Aali, K.A.; Vohra, F.; Abduljabbar, T. Adhesive bond
integrity of silanized zirconia nanoparticles in polymeric resin dentin bonding agent. An FTIR, SEM, TEM and Micro-tensile
experiment. Int. J. Adhes. Adhes. 2021, 114, 103069. [CrossRef]
63. Argueta-Figueroa, L.; Morales-Luckie, R.A.; Scougall-Vilchis, R.J.; Olea-Mejía, O.F. Synthesis, characterization and antibacterial
activity of copper, nickel and bimetallic Cu–Ni nanoparticles for potential use in dental materials. Prog. Nat. Sci. Mater. Int. 2014,
24, 321–328. [CrossRef]
64. Choe, Y.-E.; Kim, Y.-J.; Jeon, S.-J.; Ahn, J.-Y.; Park, J.-H.; Dashnyam, K.; Mandakhbayar, N.; Knowles, J.C.; Kim, H.-W.; Jun, S.-K.;
et al. Investigating the mechanophysical and biological characteristics of therapeutic dental cement incorporating copper doped
bioglass nanoparticles. Dent. Mater. 2021, 38, 363–375. [CrossRef]
65. Chung, J.H.; Kim, Y.K.; Kim, K.H.; Kwon, T.Y.; Vaezmomeni, S.Z.; Samiei, M.; Aghazadeh, M.; Davaran, S.; Mahkam, M.; Asadi, G.;
et al. Synthesis, characterization, biocompatibility of hydroxyapatite–natural polymers nanocomposites for dentistry applications.
Artif. Cells Nanomed. Biotechnol. 2016, 44, 277–284. [CrossRef] [PubMed]
66. Sharifi, S.; Khosroshahi, A.Z.; Dizaj, S.M.; Rezaei, Y. Preparation, Physicochemical Assessment and the Antimicrobial Action of
Hydroxyapatite–Gelatin/Curcumin Nanofibrous Composites as a Dental Biomaterial. Biomimetics 2021, 7, 4. [CrossRef] [PubMed]
67. Abdelshafi, M.A.; Fathy, S.M.; Elkhooly, T.A.; Reicha, F.M.; Osman, M.F. Bond strength of demineralized dentin after synthesized
collagen/hydroxyapatite nanocomposite application. J. Mech. Behav. Biomed. Mater. 2021, 121, 104590. [CrossRef]
68. Imani, M.M.; Kiani, M.; Rezaei, F.; Souri, R.; Safaei, M. Optimized synthesis of novel hydroxyapatite/CuO/TiO2 nanocomposite
with high antibacterial activity against oral pathogen Streptococcus mutans. Ceram. Int. 2021, 47, 33398–33404. [CrossRef]
69. Balu, S.K.; Sampath, V.; Andra, S.; Alagar, S.; Vidyavathy, S.M. Fabrication of carbon and silver nanomaterials incorporated
hydroxyapatite nanocomposites: Enhanced biological and mechanical performances for biomedical applications. Mater. Sci. Eng.
C 2021, 128, 112296. [CrossRef] [PubMed]
70. Rashahmadi, S.; Hasanzadeh, R.; Mosalman, S. Improving the Mechanical Properties of Poly Methyl Methacrylate Nanocompos-
ites for Dentistry Applications Reinforced with Different Nanoparticles. Polym. Technol. Eng. 2017, 56, 1730–1740. [CrossRef]
71. Mateescu, M.; Vlase, G.; Jumanca, D.; Galuscan, A.; Avram, C.; Vlase, T. Comparative Study Regarding Thermal Behaviour of
Mixtures Based on Hydroxyapatite and Methacrylate for Dental Use. Mater. Plast. 2021, 58, 1–10. [CrossRef]
72. Mallakpour, S.; Khani, M.; Mallakpour, F.; Fathi, M. Preparation and Characterization of Polyvinylpyrrolidone/L-leucine Amino
Acid–Modified Montmorillonite/Chiral Diacid–Functionalized Mg-Substituted Fluorapatite Nanocomposites by Ultrasonic-
Assisted Rapid Process. Polym. Technol. Eng. 2017, 57, 28–37. [CrossRef]
73. Deng, F.; Fu, L.-H.; Ma, M.-G. Microwave-assisted rapid synthesis and characterization of CaF 2 particles-filled cellulose
nanocomposites in ionic liquid. Carbohydr. Polym. 2015, 121, 163–168. [CrossRef]
74. Sözügeçer, S.; Bayramgil, N.P. Preparation and characterization of polyacrylic acid-hydroxyapatite nanocomposite by microwave-
assisted synthesis method. Heliyon 2021, 7, e07226. [CrossRef]
75. Karthik, K.; Dhanuskodi, S.; Gobinath, C.; Prabukumar, S.; Sivaramakrishnan, S. Multifunctional properties of microwave assisted
CdO–NiO–ZnO mixed metal oxide nanocomposite: Enhanced photocatalytic and antibacterial activities. J. Mater. Sci. Mater.
Electron. 2018, 29, 5459–5471. [CrossRef]
76. Raho, R.; Paladini, F.; Lombardi, F.A.; Boccarella, S.; Zunino, B.; Pollini, M. In-situ photo-assisted deposition of silver particles on
hydrogel fibers for antibacterial applications. Mater. Sci. Eng. C 2015, 55, 42–49. [CrossRef] [PubMed]
77. Aseena, S.; Abraham, N.; Babu, V.S. Synthesis of ZnO/CNT Nanocomposite by Microwave and Ultrasound Assisted Two
Step Process. In Proceedings of the 2019 International Conference on Vision Towards Emerging Trends in Communication and
Networking (ViTECoN), Vellore, India, 30–31 March 2019; pp. 1–4.
78. Suzuki, T.; Lee, C.H.; Chen, M.; Zhao, W.; Fu, S.; Qi, J.J.; Chotkowski, G.; Eisig, S.; Wong, A.; Mao, J. Induced Migration of Dental
Pulp Stem Cells for in vivo Pulp Regeneration. J. Dent. Res. 2011, 90, 1013–1018. [CrossRef] [PubMed]
79. Rodríguez-Lozano, F.J.; Guerrero-Gironés, J.; Pecci-Lloret, M.R.; Pecci-Lloret, M.P. Stem cells for endodontic regeneration. In
Biomaterials in Endodontics; Elsevier: Amsterdam, The Netherlands, 2022; pp. 273–283.
80. Hanafy, A.K.; Shinaishin, S.F.; Eldeen, G.N.; Aly, R.M. Nano Hydroxyapatite & Mineral Trioxide Aggregate Efficiently Promote
Odontogenic Differentiation of Dental Pulp Stem Cells. Open Access Maced. J. Med Sci. 2018, 6, 1727–1731. [PubMed]
81. Li, Z.; Xie, K.; Yang, S.; Yu, T.; Xiao, Y.; Zhou, Y. Multifunctional Ca–Zn–Si-based micro-nano spheres with anti-infective, anti-
inflammatory, and dentin regenerative properties for pulp capping application. J. Mater. Chem. B 2021, 9, 8289–8299. [CrossRef]
[PubMed]
82. SSinjari, B.; Pizzicannella, J.; D’Aurora, M.; Zappacosta, R.; Gatta, V.; Fontana, A.; Trubiani, O.; Diomede, F. Curcumin/Liposome
Nanotechnology as Delivery Platform for Anti-inflammatory Activities via NFkB/ERK/pERK Pathway in Human Dental Pulp
Treated With 2-HydroxyEthyl MethAcrylate (HEMA). Front. Physiol. 2019, 10, 633. [CrossRef]
83. Kim, J.; Shukla, R.; Casagrande, L.; Sedgley, C.; Nör, J.; Baker, J., Jr.; Hill, E.E. Differentiating dental pulp cells via RGD-dendrimer
conjugates. J. Dent. Res. 2010, 89, 1433–1438. [CrossRef]
84. A Elgendy, A.; Fayyad, D.M. Cell viability and apoptotic changes of dental pulp stem cells treated with propolis, chitosan, and
their nano counterparts. Tanta Dent. J. 2017, 14, 198. [CrossRef]
85. Tondnevis, F.; Ketabi, M.; Fekrazad, R.; Sadeghi, A.; Abolhasani, M.M. Using Chitosan Besides Nano Hydroxyapatite and
Fluorohydroxyapatite Boost Dental Pulp Stem Cell Proliferation. J. Biomim. Biomater. Biomed. Eng. 2019, 42, 39–50. [CrossRef]
86. Baskar, K.; Karthikeyan, B.S.; Gurucharan, I.; Mahalaxmi, S.; Rajkumar, G.; Dhivya, V.; Kishen, A. Eggshell derived nano-
hydroxyapatite incorporated carboxymethyl chitosan scaffold for dentine regeneration: A laboratory investigation. Int. Endod. J.
2021, 55, 89–102. [CrossRef]
87. Lee, D.-K.; Kim, S.V.; Limansubroto, A.N.; Yen, A.; Soundia, A.; Wang, C.-Y.; Shi, W.; Hong, C.; Tetradis, S.; Kim, Y.; et al.
Nanodiamond–Gutta Percha Composite Biomaterials for Root Canal Therapy. ACS Nano 2015, 9, 11490–11501. [CrossRef]
[PubMed]
88. Vagropoulou, G.; Trentsiou, M.; Georgopoulou, A.; Papachristou, E.; Prymak, O.; Kritis, A.; Epple, M.; Chatzinikolaidou, M.;
Bakopoulou, A.; Koidis, P. Hybrid chitosan/gelatin/nanohydroxyapatite scaffolds promote odontogenic differentiation of dental
pulp stem cells and in vitro biomineralization. Dent. Mater. 2020, 37, e23–e36. [CrossRef] [PubMed]
89. Alipour, M.; Pouya, B.; Aghazadeh, Z.; SamadiKafil, H.; Ghorbani, M.; Alizadeh, S.; Aghazadeh, M.; Abdolahinia, E.D. The
Antimicrobial, Antioxidative, and Anti-Inflammatory Effects of Polycaprolactone/Gelatin Scaffolds Containing Chrysin for
Regenerative Endodontic Purposes. Stem Cells Int. 2021, 2021, 3828777. [CrossRef] [PubMed]
90. Alipour, M.; Firouzi, N.; Aghazadeh, Z.; Samiei, M.; Montazersaheb, S.; Khoshfetrat, A.B.; Aghazadeh, M. The osteogenic
differentiation of human dental pulp stem cells in alginate-gelatin/Nano-hydroxyapatite microcapsules. BMC Biotechnol. 2021,
21, 6. [CrossRef]
91. Ilyas, K.; Qureshi, S.W.; Afzal, S.; Gul, R.; Yar, M.; Kaleem, M.; Khan, A.S. Microwave-assisted synthesis and evaluation of type 1
collagen–apatite composites for dental tissue regeneration. J. Biomater. Appl. 2018, 33, 103–115. [CrossRef]
92. Liao, S.; Watari, F.; Zhu, Y.; Uo, M.; Akasaka, T.; Wang, W.; Xu, G.; Cui, F. The degradation of the three layered nano-carbonated
hydroxyapatite/collagen/PLGA composite membrane in vitro. Dent. Mater. 2007, 23, 1120–1128. [CrossRef]
93. Wang, W.; Liao, S.; Zhu, Y.; Liu, M.; Zhao, Q.; Fu, Y. Recent applications of nanomaterials in prosthodontics. J. Nanomater. 2015,
2015, 3. [CrossRef]
94. Van Noort, R.; Barbour, M. Introduction to Dental Materials-E-Book; Elsevier Health Sciences: Amsterdam, The Netherlands, 2014.
95. Praveena, C.; Manne, P.; Kalluri, L.; Anne, R. Nanobiomaterials and their application in prosthodontics. In Dental Applications of
Nanotechnology; Chaughule, R.S., Ed.; Springer: Cham, Switzerland, 2018; pp. 177–201.
96. Ali, N.A.; Hussein, S.I.; Asafa, T.B.; Abd-Elnaiem, A.M. Mechanical properties and electrical conductivity of poly (methyl
methacrylate)/multi-walled carbon nanotubes composites. Iran. J. Sci. Technol. Trans. A Sci. 2020, 44, 1567–1576. [CrossRef]
97. Zafar, M.S. Prosthodontic applications of polymethyl methacrylate (PMMA): An update. Polymers 2020, 12, 2299. [CrossRef]
98. Chowdhary, R. Effect of adding silver nanoparticle on physical and mechanical properties of maxillofacial silicone elastomer
material-an in-vitro study. J. Prosthodont. Res. 2020, 64, 431–435.
99. Kodal, M.; Şirin, H.; Karaağaç, B.; Özkoç, G. Improved interfacial adhesion with the help of functional polyhedral oligomeric
silsesquioxanes in silicone rubber/rayon fiber composites: Physical, mechanical, thermal, and morphological properties. Polym.
Eng. Sci. 2020, 60, 1958–1972. [CrossRef]
100. Gendreau, L.; Loewy, Z.G. Epidemiology and etiology of denture stomatitis. J. Prosthodont. Implant. Esthet. Reconstr. Dent. 2011,
20, 251–260. [CrossRef] [PubMed]
101. Guo, Z.; Pereira, T.; Choi, O.; Wang, Y.; Hahn, H.T. Surface functionalized alumina nanoparticle filled polymeric nanocomposites
with enhanced mechanical properties. J. Mater. Chem. 2006, 16, 2800–2808. [CrossRef]
102. Carrillo-Cotto, R.; Etges, A.; Jardim, P.S.; Torre, E.; Kaizer, M.R.; Ferrúa, C.P.; Nedel, F.; Cuevas-Suárez, C.E.; Moraes, R.R.
Cytotoxicity of contemporary resin-based dental materials in contact with dentin. Eur. J. Oral Sci. 2020, 128, 436–443. [CrossRef]
103. de Oliveira, A.D.; Beatrice, C.A.G. Polymer nanocomposites with different types of nanofiller. In Nanocomposites: Recent Evolutions;
Sivasankaran, S., Ed.; IntechOpen: London, UK, 2018; pp. 103–104.
104. Praveena, C.; Chaughule, R.S.; Satyanarayana, K. Nanotechnology in Implant Dentistry. In Advances in Dental Implantology Using
Nanomaterials and Allied Technology Applications; Springer: Berlin/Heidelberg, Germany, 2021; pp. 1–23.
105. Al-Samaray, M.; Al-Somaiday, H.; Rafeeq, A.K. Effect of Adding Different Concentrations of CaCO3-SiO2 Nanoparticles on Tear
Strength and Hardness of Maxillofacial Silicone Elastomers. Nano Biomed. Eng. 2021, 13, 257–263. [CrossRef]
106. Persson, C.; Unosson, E.; Ajaxon, I.; Engstrand, J.; Engqvist, H.; Xia, W. Nano grain sized zirconia–silica glass ceramics for dental
applications. J. Eur. Ceram. Soc. 2012, 32, 4105–4110. [CrossRef]
107. Yılmaz, M.N.; Gul, P. Monomer release from dental restorative materials containing dimethacrylate resin after bleaching. Clin.
Oral Investig. 2022, 1–16. [CrossRef]
108. Saber, M.H.; Loomans, A.; Zohairy, A.E.; Dörfer, C.E.; El-Badrawy, W. Evaluation of proximal contact tightness of Class II resin
composite restorations. Oper. Dent. 2010, 35, 37–43. [CrossRef]
109. De Stefani, A.; Bruno, G.; Preo, G.; Gracco, A. Application of Nanotechnology in Orthodontic Materials: A State-of-the-Art
Review. Dent. J. 2020, 8, 126. [CrossRef]
110. Gracco, A.; Dandrea, M.; Deflorian, F.; Zanella, C.; De Stefani, A.; Bruno, G.; Stellini, E. Application of a molybdenum and
tungsten disulfide coating to improve tribological properties of orthodontic archwires. Nanomaterials 2019, 9, 753. [CrossRef]
111. Yin, I.X.; Zhang, J.; Zhao, I.S.; Mei, M.L.; Li, Q.; Chu, C.H. The antibacterial mechanism of silver nanoparticles and its application
in dentistry. Int. J. Nanomed. 2020, 15, 2555. [CrossRef] [PubMed]
112. Bapat, R.A.; Chaubal, T.V.; Joshi, C.P.; Bapat, P.R.; Choudhury, H.; Pandey, M.; Gorain, B.; Kesharwani, P. An overview of
application of silver nanoparticles for biomaterials in dentistry. Mater. Sci. Eng. C 2018, 91, 881–898. [CrossRef] [PubMed]
113. Akarajarasrod, P.; Dechkunakorn, S.; Tantivitayakul, P.; Punnakitikashem, P.; Wichai, W.; Whitis, P.P.; Anuwongnukroh, N.
Antibacterial Effect of Experimental Orthodontic Adhesives Containing Gold Nanoparticles against Streptococcus mutans and
Streptococcus sobrinus. Key Eng. Mater. 2021, 904, 301–308. [CrossRef]
114. Alam, M.K.; Alsuwailem, R.; Alfawzan, A.A. Antibacterial activity and bond strength of silver nanoparticles modified orthodontic
bracket adhesive: A systematic review and meta-analysis of in-vitro and in-vivo studies. Int. J. Adhes. Adhes. 2022, 113, 103040.
[CrossRef]
115. Poosti, M.; Ramazanzadeh, B.; Zebarjad, M.; Javadzadeh, P.; Naderinasab, M.; Shakeri, M.T. Shear bond strength and antibacterial
effects of orthodontic composite containing TiO2 nanoparticles. Eur. J. Orthod. 2013, 35, 676–679. [CrossRef]
116. Eshed, M.; Lellouche, J.; Matalon, S.; Gedanken, A.; Banin, E. Sonochemical coatings of ZnO and CuO nanoparticles inhibit
Streptococcus mutans biofilm formation on teeth model. Langmuir ACS J. Surf. Colloids 2012, 28, 12288–12295. [CrossRef]
117. Toodehzaeim, M.H.; Zandi, H.; Meshkani, H.; Hosseinzadeh Firouzabadi, A. The Effect of CuO Nanoparticles on Antimicrobial
Effects and Shear Bond Strength of Orthodontic Adhesives. J. Dent. (Shiraz Iran.) 2018, 19, 1–5.
118. Batra, P. Applications of Nanoparticles in Orthodontics. In Dental Applications of Nanotechnology; Springer: Berlin/Heidelberg,
Germany, 2018; pp. 81–105.
119. Zakrzewski, W.; Dobrzynski, M.; Dobrzynski, W.; Zawadzka-Knefel, A.; Janecki, M.; Kurek, K.; Lubojanski, A.; Szymonowicz, M.;
Rybak, Z.; Wiglusz, R.J. Nanomaterials Application in Orthodontics. Nanomaterials 2021, 11, 337. [CrossRef]
120. Flemmig, T.F. Periodontitis. Ann. Periodontol. 1999, 4, 32–37. [CrossRef]
121. Barone, M.; Malpassi, M. Clinical trial of a 15% supermicronized hydroxyapatite gel for dentin hypersensitivity. G. Ital. Di Endod.
1991, 5, 43–47.
122. Gopinath, N.M.; John, J.; Nagappan, N.; Prabhu, S.; Kumar, E.S. Evaluation of dentifrice containing nano-hydroxyapatite for
dentinal hypersensitivity: A randomized controlled trial. J. Int. Oral Health JIOH 2015, 7, 118. [PubMed]
123. Ding, Q.; Cui, J.; Shen, H.; He, C.; Wang, X.; Shen, S.G.; Lin, K. Advances of nanomaterial applications in oral and maxillofacial
tissue regeneration and disease treatment. Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 2021, 13, e1669. [CrossRef] [PubMed]
124. Kashi, T.S.J.; Eskandarion, S.; Esfandyari-Manesh, M.; Marashi, S.M.A.; Samadi, N.; Fatemi, S.M.; Atyabi, F.; Eshraghi, S.;
Dinarvand, R. Improved drug loading and antibacterial activity of minocycline-loaded PLGA nanoparticles prepared by
solid/oil/water ion pairing method. Int. J. Nanomed. 2012, 7, 221.
125. Madhumathi, K.; Kumar, T.S. Regenerative potential and anti-bacterial activity of tetracycline loaded apatitic nanocarriers for the
treatment of periodontitis. Biomed. Mater. 2014, 9, 035002. [CrossRef]
126. Funda, G.; Taschieri, S.; Bruno, G.A.; Grecchi, E.; Paolo, S.; Girolamo, D.; Del Fabbro, M. Nanotechnology scaffolds for alveolar
bone regeneration. Materials 2020, 13, 201. [CrossRef]
127. Inanç, B.; Arslan, Y.E.; Seker, S.; Elçin, A.E.; Elçin, Y.M. Periodontal ligament cellular structures engineered with electrospun poly
(DL-lactide-co-glycolide) nanofibrous membrane scaffolds. J. Biomed. Mater. Res. Part A Off. J. Soc. Biomater. Jpn. Soc. Biomater.
Aust. Soc. Biomater. Korean Soc. Biomater. 2009, 90, 186–195. [CrossRef]
128. Jang, H.J.; Lee, E.C.; Kwon, G.J.; Seo, Y.K. The effect of coated nano-hydroxyapatite concentration on scaffolds for osteogenesis. J.
Biomater. Appl. 2020, 34, 827–839. [CrossRef]
129. Brunton, P.A.; Davies, R.P.W.; Burke, J.L.; Smith, A.; Aggeli, A.; Brookes, S.J.; Kirkham, J. Treatment of early caries lesions using
biomimetic self-assembling peptides—A clinical safety trial. Br. Dent. J. 2013, 215, E6. [CrossRef]
130. Gandolfi, M.G.; Zamparini, F.; Valente, S.; Parchi, G.; Pasquinelli, G.; Taddei, P.; Prati, C. Green Hydrogels Composed of Sodium
Mannuronate/Guluronate, Gelatin and Biointeractive Calcium Silicates/Dicalcium Phosphate Dihydrate Designed for Oral Bone
Defects Regeneration. Nanomaterials 2021, 11, 3439. [CrossRef]
131. Gandolfi, M.G.; Gardin, C.; Zamparini, F.; Ferroni, L.; Esposti, M.D.; Parchi, G.; Ercan, B.; Manzoli, L.; Fava, F.; Fabbri, P. Mineral-
doped poly (L-lactide) acid scaffolds enriched with exosomes improve osteogenic commitment of human adipose-derived
mesenchymal stem cells. Nanomaterials 2020, 10, 432. [CrossRef]
132. Tatullo, M.; Spagnuolo, G.; Codispoti, B.; Zamparini, F.; Zhang, A.; Esposti, M.D.; Aparicio, C.; Rengo, C.; Nuzzolese, M.; Manzoli,
L. PLA-based mineral-doped scaffolds seeded with human periapical cyst-derived MSCs: A promising tool for regenerative
healing in dentistry. Materials 2019, 12, 597. [CrossRef] [PubMed]
133. Nie, L.; Zhang, H.; Ren, A.; Li, Y.; Fu, G.; Cannon, R.D.; Ji, P.; Wu, X.; Yang, S. Nano-hydroxyapatite mineralized silk fibroin
porous scaffold for tooth extraction site preservation. Dent. Mater. 2019, 35, 1397–1407. [CrossRef] [PubMed]
134. Pye, A.; Lockhart, D.; Dawson, M.; Murray, C.; Smith, A. A review of dental implants and infection. J. Hosp. Infect. 2009, 72,
104–110. [CrossRef] [PubMed]
135. He, X.; Reichl, F.-X.; Milz, S.; Michalke, B.; Wu, X.; Sprecher, C.M.; Yang, Y.; Gahlert, M.; Röhling, S.; Kniha, H. Titanium and
zirconium release from titanium-and zirconia implants in mini pig maxillae and their toxicity in vitro. Dent. Mater. 2020, 36,
402–412. [CrossRef]
136. Rashti, A.; Yahyaei, H.; Firoozi, S.; Ramezani, S.; Rahiminejad, A.; Karimi, R.; Farzaneh, K.; Mohseni, M.; Ghanbari, H.
Development of novel biocompatible hybrid nanocomposites based on polyurethane-silica prepared by sol gel process. Mater. Sci.
Eng. C 2016, 69, 1248–1255. [CrossRef]
137. Yamada, M.; Ueno, T.; Tsukimura, N.; Ikeda, T.; Nakagawa, K.; Hori, N.; Suzuki, T.; Ogawa, T. Bone integration capability of
nanopolymorphic crystalline hydroxyapatite coated on titanium implants. Int. J. Nanomed. 2012, 7, 859.
138. Krupa, D.; Baszkiewicz, J.; Kozubowski, J.; Lewandowska-Szumieł, M.; Barcz, A.; Sobczak, J.; Biliński, A.; Rajchel, A. Effect of
calcium and phosphorus ion implantation on the corrosion resistance and biocompatibility of titanium. Bio-Med. Mater. Eng.
2004, 14, 525–536.
139. Jeevanandam, J.; Danquah, M.K.; Pan, S. Plant-derived nanobiomaterials as a potential next generation dental implant surface
modifier. Front. Mater. 2021, 8, 130. [CrossRef]
140. Jadhav, K.; Rajeshwari, H.; Deshpande, S.; Jagwani, S.; Dhamecha, D.; Jalalpure, S.; Subburayan, K.; Baheti, D. Phytosynthesis of
gold nanoparticles: Characterization, biocompatibility, and evaluation of its osteoinductive potential for application in implant
dentistry. Mater. Sci. Eng. C 2018, 93, 664–670. [CrossRef]
141. Subramani, K.; Lavenus, S.; Rozé, J.; Louarn, G.; Layrolle, P. Impact of nanotechnology on dental implants. In Emerging
Nanotechnologies in Dentistry; Subramani, K., Ahmed, W., Eds.; Elsevier: Amsterdam, The Netherlands, 2018; pp. 83–97.
142. Takanche, J.S.; Kim, J.-E.; Kim, J.-S.; Lee, M.-H.; Jeon, J.-G.; Park, I.-S.; Yi, H.-K. Chitosan-gold nanoparticles mediated gene
delivery of c-myb facilitates osseointegration of dental implants in ovariectomized rat. Artif. Cells Nanomed. Biotechnol. 2018, 46,
S807–S817. [CrossRef]
143. Bansal, V.; Katiyar, S.S.; Dora, C.P. Toxicity aspects: Crucial obstacles to clinical translation of nanomedicines. In Direct Nose-to-
Brain Drug Delivery; Elsevier: Amsterdam, The Netherlands, 2021; pp. 485–494.
144. Kou, W.; Akasaka, T.; Watari, F.; Sjögren, G. An in vitro evaluation of the biological effects of carbon nanotube-coated dental
zirconia. Int. Sch. Res. Not. 2013, 2013. [CrossRef] [PubMed]
145. Canu, I.G.; Gaillen-Guedy, A.; Wild, P.; Straif, K.; Luce, D. Lung cancer mortality in the French cohort of titanium dioxide workers:
Some aetiological insights. Occup. Environ. Med. 2020, 77, 795–797. [CrossRef] [PubMed]
146. Naima, R.; Imen, M.; Mustapha, J.; Hafedh, A.; Kamel, K.; Mohsen, S.; Salem, A. Acute titanium dioxide nanoparticles exposure
impaired spatial cognitive performance through neurotoxic and oxidative mechanisms in Wistar rats. Biomarkers 2021, 26, 760–769.
[CrossRef] [PubMed]
147. Wang, J.; Wang, L.; Fan, Y. Adverse biological effect of TiO2 and hydroxyapatite nanoparticles used in bone repair and replacement.
Int. J. Mol. Sci. 2016, 17, 798. [CrossRef] [PubMed]
148. Atalay, H.; Çelik, A.; Ayaz, F. Investigation of genotoxic and apoptotic effects of zirconium oxide nanoparticles (20 nm) on L929
mouse fibroblast cell line. Chem.-Biol. Interact. 2018, 296, 98–104. [CrossRef] [PubMed]
149. Li, L.; Deng, Y.; Meng, X.; Chang, H.; Ling, C.; Li, D.; Wang, Q.; Lu, T.; Yang, Y.; Song, G. Genotoxicity evaluation of silica
nanoparticles in murine: A systematic review and meta-analysis. Toxicol. Mech. Methods 2022, 32, 1–17. [CrossRef] [PubMed]
150. Pokrowiecki, R.; Pałka, K.; Mielczarek, A. Nanomaterials in dentistry: A cornerstone or a black box? Nanomedicine 2018, 13,
639–667. [CrossRef]
151. Fu, P.P.; Xia, Q.; Hwang, H.-M.; Ray, P.C.; Yu, H. Mechanisms of nanotoxicity: Generation of reactive oxygen species. J. Food Drug
Anal. 2014, 22, 64–75. [CrossRef]
152. Reidelbach, C.; Garcia-Käufer, M.; Wingert, N.; Arif, A.; Vach, K.; Hellwig, E.; Gminski, R.; Polydorou, O. Cytotoxicity and
estrogenicity in simulated dental wastewater after grinding of resin-based materials. Dent. Mater. 2021, 37, 1486–1497. [CrossRef]
153. Binner, H.; Kamali, N.; Harding, M.; Sullivan, T. Characteristics of wastewater originating from dental practices using predomi-
nantly mercury-free dental materials. Sci. Total Environ. 2022, 814, 152632. [CrossRef]
154. Thangavelu, L.; Veeraragavan, G.R.; Mallineni, S.K.; Devaraj, E.; Parameswari, R.P.; Syed, N.H.; Dua, K.; Chellappan, D.K.;
Balusamy, S.R.; Bhawal, U.K. Role of Nanoparticles in Environmental Remediation: An Insight into Heavy Metal Pollution from
Dentistry. Bioinorg. Chem. Appl. 2022, 2022. [CrossRef] [PubMed]
155. Chou, P.-Y.; Chou, Y.-C.; Lai, Y.-H.; Lin, Y.-T.; Lu, C.-J.; Liu, S.J. Fabrication of drug-eluting nano-hydroxylapatite filled polycapro-
lactone nanocomposites using solution-extrusion 3D printing technique. Polymers 2021, 13, 318. [CrossRef] [PubMed]
156. Dasgupta, D.; Peddi, S.S.; Saini, D.K.; Ghosh, A. Implantation and Retrieval of Magnetic Nanobots for Treatment of Endodontic
Re-Infection in Human Dentine; Cambridge University Press: Cambridge, UK, 2021.
157. Razavi, M.; Talebi, H.; Zareinejad, M.; Dehghan, M.R. A GPU-implemented physics-based haptic simulator of tooth drilling. Int.
J. Med. Robot. Comput. Assist. Surg. 2015, 11, 476–485. [CrossRef] [PubMed]
158. Zhang, L.; Qi, Z.; Zou, Y.; Zhang, J.; Xia, W.; Zhang, R.; He, Z.; Cai, X.; Lin, Y.; Duan, S.Z.; et al. Engineering DNA–nanozyme
interfaces for rapid detection of dental Bacteria. ACS Appl. Mater. Interfaces 2019, 11, 30640–30647. [CrossRef] [PubMed]
159. Huang, Y.; Liu, Y.; Shah, S.; Kim, D.; Simon-Soro, A.; Ito, T.; Hajfathalian, M.; Li, Y.; Hsu, J.C.; Nieves, L.M.; et al. Precision
targeting of bacterial pathogen via bi-functional nanozyme activated by biofilm microenvironment. Biomaterials 2021, 268, 120581.
[CrossRef]

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Nanomaterials 2022, 12, 1676. https://doi.org/10.3390/nano12101676 https://www.mdpi.com/journal/nanomaterials

orthodontics. Primarily, dental practitioners focus on the prophylactic treatment of dental

Table 1. Research topic click number in PubMed.

Nanotechnology Nanoparticle Nano Nano

Nanomaterials 2022, 12, x FOR PEER REVIEW 3 of 21

Figure 2. Various synthesis approaches implemented in nanodentistry.

It is already mentioned that understanding the biomatters helps to make biomimick-

Material used in Nano-dentistry

Lithium Disilicate Inorganic

Silica Calcium Phosphate

Figure 3. Diagrammatic illustration to provide basic material classes used in dentistry.

Application of Nanomaterials in dentistry

Periodontology and bone

Figure 4. Pictorial representation

Drug Delivery System Characteristic Action Reference

Drug Delivery System Characteristic Action Reference

2.2. Tooth Restoration

Nanocomposites) employing ultrasonic waves as an energy source [72]. While various

2.4.1. Removable Type

2.4.2. Fixed Type

2.6. Periodontology and Bone Regeneration

polysaccharides (copolymers of L-guluronate and D-mannuronate) and peptide (gelatin)

2.7. Dental Implants

2.8. Regulatory Framework

preparation of nanomaterials, exposure to them by inhalation may cause toxic symptoms in

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