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Biofabrication of silver nanoparticles from various plant extracts: blessing to nanotechnology

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Nanotechnology is influencing life in many ways. Researchers are developing their interest in biofabrication of silver nanoparticles because of its excellent properties and boundless utilisation in almost every branch of science. Plant extract is used to synthesise silver nanoparticles and reduce silver ion, and act as capping and reducing agent. The phyto-chemicals and metabolites present in the extract help in biogenic reduction of silver ion, forming non-toxic nanoparticles. This review focuses on the green synthesis of nanoparticles from various plants and their parts as an easy and eco-friendly approach.
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International Journal of Environmental Analytical
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Biofabrication of silver nanoparticles from various
plant extracts: blessing to nanotechnology
Aiman Zafar, Rose Rizvi & Irshad Mahmood
To cite this article: Aiman Zafar, Rose Rizvi & Irshad Mahmood (2019): Biofabrication of silver
nanoparticles from various plant extracts: blessing to nanotechnology, International Journal of
Environmental Analytical Chemistry, DOI: 10.1080/03067319.2019.1622698
To link to this article: https://doi.org/10.1080/03067319.2019.1622698
Published online: 04 Jun 2019.
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REVIEW ARTICLE
Biofabrication of silver nanoparticles from various plant
extracts: blessing to nanotechnology
Aiman Zafar, Rose Rizvi and Irshad Mahmood
Department of Botany, Aligarh Muslim University, Aligarh, India
ABSTRACT
Nanotechnology is inuencing life in many ways. Researchers are
developing their interest in biofabrication of silver nanoparticles
because of its excellent properties and boundless utilisation in
almost every branch of science. Plant extract is used to
synthesise silver nanoparticles and reduce silver ion, and act as
capping and reducing agent. The phyto-chemicals and metabo-
lites present in the extract help in biogenic reduction of silver ion,
forming non-toxic nanoparticles. This review focuses on the green
synthesis of nanoparticles from various plants and their parts as an
easy and eco-friendly approach.
ARTICLE HISTORY
Received 12 April 2019
Accepted 15 May 2019
KEYWORDS
Biofabrication;
nanotechnology; plant
extract; silver nanoparticles
1. Introduction
Nanotechnology is being considered as the most advance form of technology in the
recent years, due to its impact on various scientic research areas such as food industry,
agriculture, crop improvement, electronics, photonics, medicine, textile, catalyst and
space industries [15]. Nanoparticles can be classied on the basis of dimensions (1D,
2D, 3D), shape (spherical, tubular, irregular shape), morphology, size and composition
[6,7]. They can also be categorised as natural and engineered nanoparticles on the basis
of their source of inference and extraction [8]. According to Uddin [9] nanoparticles can
be obtained from nature and can be extracted by natural processes such as biodegrada-
tion and biomineralisation. Nanoparticles are further chiey categorised as organic
nanoparticles (comprising carbon nanoparticles) and inorganic nanoparticles comprising
of metal nanoparticles (platinum, palladium, silver, gold, etc.), magnetic nanoparticles
and semi-conductor nanoparticles (titanium oxide and zinc oxide). Now a days there is
increase in the production of metal nanoparticles because of their superior quality and
functional exibility. The process of fabrication of nanoparticles can be achieved by
either top-downor bottom-upapproaches [10,11] which include several methods such
as physical methods (arc discharge, pyrolysis, etching, inert gas condensation, etc.),
chemical methods (sol gel process, tollens method, vapour deposition, photo induced
reduction, etc.) and biological methods (by Fungi, bacteria, enzymes, plant parts). In
top-downmethod, fabrication of nanoparticles is done by reduction in size (by physical
and chemical method) from starting material and in bottom-upapproach, nanoparti-
cles are fabricated from tiny units by joining molecules, atoms and smaller particles
CONTACT Aiman Zafar aimanzafar94@gmail.com
INTERNATIONAL JOURNAL OF ENVIRONMENTAL ANALYTICAL CHEMISTRY
https://doi.org/10.1080/03067319.2019.1622698
© 2019 Informa UK Limited, trading as Taylor & Francis Group
[11,12]. These methods are quite expensive, requires high maintenance, and chemicals
used in fabrication are very perilous to both humans and environment [13,14]. Hence,
this review emphasises the role of dierent plant extracts for the biofabrication of
nanoparticles as a green, safe and a non-toxic approach.
1.1. Need and importance of biosynthesis of nanoparticles
The synthesis of nanoparticles from top-downand bottom-upapproach is exorbitant
as well as dangerous but biosynthesis of nanoparticles from plants is an expedient and
a green approach. Prerequisite of chemical synthesis are several purications, utilisation
of explosive solvents, escalated consumption of methods like sonication, sophisticated
instruments and perilous release of byproducts. These are demerits of chemical synth-
esis. The scaling up of physical method is a tough job and the nanoparticles formed
have a very short shelf life and low thermal stability. Microbe mediated synthesis also
requires high lab maintenance cost of microorganisms. Due to these snags, scientists
and researchers felt to develop a method that is easy, eco-friendly, cost eective and
free of toxic materials. According to Husen and Siddiqui [15] nanoparticles (NPs) can be
chemically synthesised by various conventional methods but biosynthesis curbs the
atmosphere from pollution. So, biosynthesis or biofabrication (from fungi, bacteria and
plant extract) is manifested as a blessing in the eld of Nanotechnology.
2. Biosynthesis of silver nanoparticles
There are several reports of nanoparticles synthesised from fungi and bacteria by various
researchers as a part of green and biological synthesis.
2.1. Mechanism, synthesis and characterisation of nanoparticles from fungi
Fungi are used for synthesis of silver nanoparticles because of their high tolerance power
and ability to bioaccumulate metals [16,17]. Biofabrication of silver nanoparticles from fungi
is a strenuous process requiring biomolecules as both stabilising and reducing agents
[18,19]. Predominantly, in fungi the NADH/NADPH dependent enzyme is involved in the
stabilisation and reduction of silver ions. Biomolecules such as enzymes [20], biosurfactants
and proteins present in microorganisms (fungi, bacteria) act as powerful reducing, capping
and stabilising agents in synthesis [21] and [22] have suggested that silver ions are extra-
cellularly reduced in water to form stable silver nanoparticles from fungi. The rst step in the
synthesis is the reduction of silver ion, Ag(I) to Ag(0). Then the particles are stabilised to
avoid clumping and maintaining their distance, which would otherwise result in fusion and,
ultimately, the formation of bigger particles. [18][23] reported 515 nm silver nanoparticles
from Fusarium oxysporum by enzymatic method reducing metal ions and thus developing
a fungal-based method for synthesis of nanomaterials. [23] observed the role of NADPH-
dependent reductase in the reduction of silver ion. [24]usedAspergillus avus for the
biosynthesis of silver nanoparticles. The nanoparticles formed were conrmed by ultraso-
nication and ultraviolet-visible spectroscopy (UV-Vis) spectroscopy showing absorbance
peak at 425 nm. The particles formed were monodispersed and having a size range of
8.92 ± 1.61 nm. The reduction of ions is because of proteins in the fungal ltrate [12]
2A. ZAFAR ET AL.
exposed Verticillium fungal biomass to aqueous Ag+ ions which resulted in intracellular
synthesis of silver nanoparticles of 25 ± 12 nm in size. Electron microscopyof thin sections of
fungal cells further showed that silver nanoparticles were formed beneath the cell wall, by
ions reduction in cell membrane due to enzymes. The metal ions were non-toxic to the cell
wall. Extracellular synthesis of nanoparticles fromFusarium semitectum was reported by [25].
The nanoparticles were formed by reduction of ions in the ltrate solution. The silver ions
are reduced due to the release of proteins (having tryptophan and tyrosine residues) into
the solution by fungus and coupling of NADH reductase with electron shuttle. TEM studies
depicted that the size range from 10 to 60 nm and were spherical [26]observedthe
extracellular synthesis of Ag-NPs using fungus Cladosporium cladosporioides and the size
of nanoparticles was measured by TEM analysis and were 10100 nm in size [27] reported
the synthesis of silver nanoparticles from Aspergillus terreus by reduction of aqueous Ag+ ion
with the fungus ltrate. The reaction occurred at room temperature and bioreduction of
AgNPs was analysed by UV-Vis spectroscopy, and characterisationwas done by transmission
electron microscopy and X-ray diraction. Reduced nicotinamide adenine nucleotide acted
as reducing agent for the formation of nanoparticles as reported by [27]. The synthesised
AgNPs were 120 nm in size and spherical. Silver nanoparticles were also biofabricated
using fungal culture of Trametes trogii, a white rot fungus by [14]. The activity of enzyme
caused the reduction of nanoparticles and capping by the interaction of Cys-Cys and the
sulfhydryl moiety.
2.2. Mechanism, synthesis and characterisation of nanoparticles from bacteria
[28] reported the biosynthesis of silver nanoparticles from Bacillus brevis(NCIM 2533). The
synthesised nanoparticles were analysed by surface plasmon resonance and UV-Vis spectro-
scopy showed the absorbance at 420 nm. SEM characterisation determined the size of
nanoparticles ranging between 42 and 68 nm. The presence of bioactive compounds was
further assured by FTIR analysis. Proteins in the bacterial extract have high binding capacity
with silver ions and can act as capping and stabilising agent [29] elucidated the extracellular
synthesis of silver nanoparticles from ltrate of an endophytic bacterium, Pantoea ananatis.
The synthesised AgNPs were characterised by UV-Vis spectroscopy, transmission electron
microscopy (TEM), scanning electron microscopy (SEM) and energydispersive X-ray spectro-
scopy (EDX), FTIR, and Zeta potential. FTIR studies revealed that binding of amino groups
with the surface of silver nanoparticles has acted as capping agent. Further the peak
depicted that the presence of proteins, phenols and carboxylic acid in the solution behaved
as reducing agent in the fabrication of nanoparticles. The analysis depicted that nanopar-
ticles formed were 35.02 ± 13.41 nm and spherical.
The nanoparticles synthesised from fungi and bacteria is a slow process and requires
high lab maintenance cost with production of less biomass when compared to nano-
particles synthesised from plant extracts. Thus, the use of plant parts and their extracts
becomes a feasible method to synthesise nanoparticles.
2.3. Green synthesis of silver nanoparticles from plant extract
In biosynthesis of silver nanoparticles by plant extracts, the extract is added to silver
nitrate solution at room temperature and is kept in dark for the synthesis. Colour change
INTERNATIONAL JOURNAL OF ENVIRONMENTAL ANALYTICAL CHEMISTRY 3
of the solution marks the synthesis and characterisation is done by UV-Vis Spectroscopy,
SEM, TEM, FTIR, EDX, XRD to measure the size and shape of the particles. Researchers
have used spices, vegetables, medicinal plants and weeds to bio-fabricate silver nano-
particles from dierent parts (leaf, stem, bark, fruit, etc.) of the plant. The reduction of
silver ions is because of the various metabolites and phytochemicals present in plants
which includes ketones, carboxylic acids, avonoids, phenolic compounds, carbohy-
drates, aldehydes, terpenoids and amides. These phytochemicals are water-soluble and
are subjected to act as reducing agent for the metal ions in synthesis [30,31]. The rate
and amount of production of nanoparticles is inuenced by the nature of plant extract,
its concentration, pH, temperature and concentration of metal ion [11,32].
[33] Biosynthesised spherical nanoparticles of 5.2 ± 4.2 nm in size from Aloe vera leaf extract
[34] reported the biosynthesis of silver nanoparticles from leaf extract of Amaranthus gang-
eticus. The nanoparticles obtained were 1116 nm in size and exhibited antimicrobial activity
towards bacteria (Gram positive, Gram negative) and fungus [35] synthesised silver nanopar-
ticles from twig extract of Amaranthus viridis. The twig extract reduced silver ions in 10 mins,
depicting it as a fast and eco-friendly method of synthesis. The particles were spherical and
520 nm in size as inferred by the SEM and TEM analysis and showed antibacterial activity.
Silver ions could be reduced to nanoparticles by plant extract of Mentha piperita [36]. The
characterisation by SEM, EDX revealed that the particles were spherical and 90 nm in size. The
results depicted that the reduction was imputed to menthol present in the leaf extract and
nanoparticles were inhibitory against Staphylococcus aureus and Escherichia coli [37]usedleaf
extract of Acalypha indica to fabricate silver nanoparticles of size 2030 nm within 30 min.
These nanoparticles also showed antibacterial activity against waterborne pathogens, Vibrio
cholerae and Escherichia coli [38] observed the synthesis of silver nanoparticles from Ocimum
sanctum dried stem and root. The broth of the plant is used as a reducing agent for the
synthesis of Ag nanoparticles at room temperature. Silver nanoparticles were synthesised from
thefruitextractofTanacetum vulgare by [39]. Synthesis of the nanoparticles was further
inferred by UV-Vis spectroscopy and TEM [40] reported the extracellular synthesis of silver
nanoparticles from Emblica ocinalis fruit extract. The fruit extract acted as reducing agent and
the nanoparticles measuring 1020 nm were formed [41]reported the formation of silver
nanoparticles from Terminalia chebula fruit extract and nanoparticles were found to be highly
stable at neutral pH. The phytochemicals present in the fruit extract and high zeta potential are
responsible for the stability of nanoparticles. XRD and EDX characterisation showed that silver
nanoparticles were crystalline and having face centred cubic geometry orientation. TEM
revealed that nanoparticles were 25 nm in size. The biosynthesised nanoparticles showed
catalytic activity on the reduction of methylene blue [42] illustrated biofabrication of Silver
nanoparticles from seed extract of Artocarpus heterophyllus. The seed is made up of a lectin,
Jacalin having various biological activities. The seed extract reduced silver ions when seed
extract solution and silver nitrate solution was autoclaved at 121°C, 15 psi, for 5 mins. The
average size of nanoparticles was 10.78 nm and were irregular when characterised. Silver
nanoparticles formed exhibited strong antibacterial property against Bacillus cereus, Bacillus
subtilis, Staphyloccocus aureus and Pseudomonas aeruginosa [43]usedfruitextractofCrataegus
douglasii as reducing agent and fabricated silver nanoparticles measuring 29.28 nm and were
spherical, showed antimicrobial property against Staphylococcus aureus and Escherichia coli.
The method of fabrication is illustrated in Figure 1 and the other plants and parts utilised in the
fabrication are listed in Table 1.
4A. ZAFAR ET AL.
3. Applications of silver nanoparticles
Biosynthesised silver nanoparticles are being used in several in vitro studies to check their
anti-microbial activities like antibacterial, antifungal, antiviral, anticancer, etc. [9597]. Silver
nanoparticles are also utilised in medicine as antimicrobial agent [11,98,99], wound dres-
sings, and agriculture engineering [18,100]. Silver nanoparticles are now utilised in ban-
dages and dentistry. The bond strength of orthodontic adhesives was enhanced by the
addition of nanoparticles [18,101]. Endodontic llings coated with nanoparticles were
ecient against bacterial pathogens such as Enterococcus faecalis, Streptococcus milleri
Figure 1. Illustration of green synthesis of silver nanoparticles from plant extract and their applica-
tion in various scienticelds.
INTERNATIONAL JOURNAL OF ENVIRONMENTAL ANALYTICAL CHEMISTRY 5
Table 1. Biofabricated silver nanoparticles from dierent plants and their parts.
Plant Part used
Size of
AgNPs Phytochemicals involved in reduction References
Alfalfa Sprouts 24nm [44]
Argemone
mexicana
Leaf 30 nm Leaf proteins and metabolites [45]
Chenopodium
album
Leaf 1030 nm Oxalic acid, (COOH)
2
,oxalate, Aldehydes [32]
Chenopodium
aristatum
Stem 336 nm Functional Groups: OH, NH, CH, C=O [46]
Chenopodium
murale
Leaf 3050 nm Phenolic Compounds and Flavonoides [47]
Desmodium
trifolium
Whole
plant
520 nm Polyphenols, avonoids, sterols, ascorbic acid [48]
Euphorbia hirta Leaf 4050 nm [49]
Lepidium draba Root 2080 nm Aldehydes, carboxylic acids, glycosidic and phenolics
compound
[50]
Ipomoea carnea Leaf, Stem
and
Root
Amide groups of proteins and the phenolic groups [51]
Lantana camara Leaf 35 nm Alcohols, alkenes [52]
Parthenium Leaf 50 nm [53]
Solidago
altissima
Leaf P, sulphur, and Cl [54]
Calotropis
gigantean
Leaf 83.7 nm Secondary amines [55]
Calotropis
procera
Flower 35 nm Phytochemicals [56]
Amaranthus
gangeticus
Leaf 1115 nm Hydrogen bonded OH and NH2 groups in the amino
acids
[34]
Amaranthus
viridis
Twig 520 nm Alcohols, phenols, proteins [35]
Abutilon indicum Leaf 525 nm Flavonoids, polyphenols, saponins and alkaloids [57]
Eclipta prostrata Leaf 3560 nm [58]
Abutilon indicum Leaf Nitrate reductase enzyme (protein) [59]
Pomegranate Peel 313 nm Polyphenolic compound (Punicalagin), avonoids and
tannins
[60]
Tansy Fruit 1040 nm [39]
Water hyacinth Cellulose 5.69 ± 5.89 Either acetyl and uronic ester linkage of carboxylic group of
the ferulic and p-coumeric acids of lignin and/or
hemicelluloses
[61]
Saraca asoca Leaf 24.85 nm Secondary metabolites [62]
Coccinia grandis Fruit 2530 nm Alcohols, phenols [63]
Silybum
marianum
Fruit 25.26 nm Flavonoids group (avolignans) [64]
Berberis vulgare Leaf, Root 3070 nm Phytochemical compounds [97]
Enicostemma
axillare
Leaf 1520 nm Alcohol, carboxylic acid, ether and esters [65]
Parkia speciosa
Hassk
Pods 2050 nm Phenolic compounds [66]
Orange Peel 91 nm Flavonoids [67]
Alstonia
scholaris
Bark 50 nm Functional organic groups (carboxyl and amine), proteins [68]
Lens culinaris Seed 13 nm [69]
Dalbergia sissoo Leaf 555 nm Flavones, Iso-avones, avonols, neoavonols and
coumarins
[70]
Pongam pinnata
L. Pierre
Leaf 38 nm Flavones [71]
Catharanthus
roseus
Root 3555 nm Aliphatic amines and alkanes [72]
Tea Leaf 20 nm Polyphenols, protein, and amino acid [30]
Syzygium cumini Bark 2060 nm Phenols, Alkaloids, tannins [73]
(Continued)
6A. ZAFAR ET AL.
and Streptococcus aurens [18,102]. Silver ions are toxic to bacterial cells and hamper the cell
permeability, inactivate proteins and hinder in DNA replication. Application of nanoparti-
cles is also emerging in the eld of agriculture as nanoparticles are found to increase the
plant growth and decrease the disease incidence of the plant pathogens [103] studied the
eect of foliar application at dierent concentration of silver nanoparticles in
Trigonellafoenum-graecum and concluded that the plant growth, physiological aspects,
yield, and antioxidant activity were high in plants treated with nanoparticles. Silver act as
potent growth simulator [104] and growth was also enhanced in wheat [105], mung bean
[106]Bacopa monnieri [107], Brassica juncea [108], common bean and corn [109][110]
reported that silver nanoparticles synthesised from Euporbia tirucalli (Et-AgNPs) were fatal
to second stage juveniles of root-knot nematode, Meloidogyne incognita and also inhibited
egg hatching (in-vitro). In pot trial of tomato also Meloidogyne incognita infestation was
reduced when the roots were treated with Et-AgNPs. From this study, it was inferred that
Table 1. (Continued).
Plant Part used
Size of
AgNPs Phytochemicals involved in reduction References
Terminalia
arjuna
Bark 2100 nm Phenols [74]
Polyalthia
longifolia
Leaf 58 nm [75]
Cinnamomum
camphora
Leaf 5580 nm Polyol componentsand the water-soluble heterocyclic
components
[76]
Ficus
benghalensis
Extract 16 nm [77]
Pelargonium
graveolens
Leaf 1640 nm Terpenoids (citronellol and geraniol) [78]
Vitis vinifera Fruit 3040 nm Carboxylic acids, esters, alcohols, amides, amines [79]
Musa
paradisiacal
Peel 20 nm Functional groups (carboxyl, amine and hydroxyl) [80]
Rheum
palmatum
Root 121 2 nm Phenolic compound, ester, and anthraquinone [81]
Excoecaria
agallocha
Leaf 20 nm Phenolic compounds, avonoids, methylene groups,
amides and carboxylate groups
[82]
Ampelocissus
latifolia
Root 3545 nm Flavonoids, tannins, alkaloids or terpenoids [83]
Erythrina indica
lam
Root 20118 nm Functional groups such as OH, CO groups, Alkaloids
and phenols
[84]
Delphinium
denudatum
Root 85 nm Terpenoids [85]
Glycyrrhiza
glabra
Root 20 nm Flavonoids, terpenoids and thiamine [86]
Zingiber
ocinale
Root 1020 nm Alkaloids and avonoids, [87]
Panax ginseng Root 100 nm Phenolic acids, avonoids, ginsenosides and
polysaccharides
[95]
Ocimum
sanctum
Leaf 430 nm Alcohols, phenols, carbonyl group of amino acid [88]
Malus domestica Fruit 20 nm Protein and ascorbic acid [89]
Olive Leaf 2025 nm Oleuropein and its derivatives [90]
Chrysanthemum
indicum
Leaf 1729 nm Flavonoids, terpenoids and glycosides, [91]
Achiella
bieberstennii
Flower 12 ± 2 nm Phytochemicals [92]
Nelumbo
nucifera
Leaf 45 nm C=O group, methoxy compounds [93]
Aloe vera Leaf 70 nm Carbonyl group of amino acid, nitriles [94]
INTERNATIONAL JOURNAL OF ENVIRONMENTAL ANALYTICAL CHEMISTRY 7
Et-AgNPs are helpful in the management of M. incognita. Silver nanoparticles are used in
food packaging to increase the shelf life of products [111] and also in minimising the
microbial population in waste water management [21,112].
4. Future prospects
Silver nanoparticles are widely applicable in medicine, environment, agriculture, human
pathology, management of various plant diseases, cosmetics, drug delivery, food, dentistry,
etc. Biofabrication of AgNPs from plant is not only used as it is safe and benign technique
but due to large production of nanoparticles in bulk quantity. The advantage of using plant
extract in synthesis is that the phyto-chemicals present in the extract act as both reducing
and capping agent. Thus, making it a simple, easy, fast, cost eective and an eco-friendly
approach. The utilisation of plant extract will reduce the use of chemicals in fabrication and
will produce chemical free nanoparticles. The plant mediated synthesises will overcome the
use of organisms and their maintenance for production of nanoparticles. Nanotechnology
is emerging as potent eld in every possible aspect of the living world and is a boon to the
scientic and research area.
Disclosure statement
No potential conict of interest was reported by the authors.
References
[1] Y. Shen and P.N. Prasad, Appl. Phys. B 74, 641 (2002). doi:10.1007/s003400200851.
[2] A.V. Zayats and I.I. Smolyaninov, J. Opt. A: 5, S16 (2003). doi:10.1088/1464-4258/5/4/353.
[3] F. Jotterand and A.A. Alexander, in Biomedical Nanotechnology, edited by S.J. Hurst (Humana
Press, New York, 2011).
[4] S.B. Kalidindi and B.R. Jagirdar, Chem. Sus. Chem. 5,65(2012). doi:10.1002/cssc.201100377.
[5] M.L. Etheridge, S.A. Campbell, A.G. Erdman, C.L. Haynes, S.M. Wolf and J. McCullough,
Nanomed. Nanotech. Boil. Med. 9,1(2013). doi:10.1016/j.nano.2012.05.013.
[6] C. Buzea, I.I. Pacheco and K. Robbie, Biointerphases 2,17(2007). doi:10.1116/1.2815690.
[7] B. Novack and T.D. Bucheli, Environ. Pollut. 150,5(2007). doi:10.1016/j.envpol.2007.06.006.
[8] G. Lidén, Ann. Occup. Hyg. 55,1(2011).
[9] I. Uddin, P. Poddar, U. Kumar, N. Phogat and J. Green, Sci. Tech. 1,48(2013).
[10] S. Sepeur, Nanotechnology: Technical Basics and Applications, Vincentz Network (GmbH &
Co KG, Hannover, 2008).
[11] A.K. Mittal, Y. Chisti and U.C. Banerjee, Biotechnol. Adv. 31, 346 (2013). doi:10.1016/j.
biotechadv.2013.01.003.
[12] P. Mukherjee, A. Ahmad, D. Mandal, S. Senapati, S.R. Sainkar, M.I. Khan, R. Parischcha, P.
V. Ajaykumar, M. Alam, R. Kumar and M. Sastry, Nano. Lett. 1, 515 (2001). doi:10.1021/
nl0155274.
[13] K. Punjabi, P. Choudhary, L. Samant, S. Mukherjee, S. Vaidya and A. Chowdhary, Int. J. Pharm.
Sci. Rev. Res. 30, 219 (2015).
[14] J.M. Kobashigawa, C.A. Robles, M.L.M. Ricci and C.C. Carmarán, Saudi J. Biol. Sci. 2018.
doi:10.1016/j.sjbs.2018.09.006
[15] A. Husen and K.S. Siddiqi, Nanoscale Res. Lett. 9, 229 (2014). doi:10.1186/1556-276X-9-229.
[16] M. Sastry, A. Ahmad, M.I. Khan and R. Kumar, Current Sci. 85,162 (2003).
8A. ZAFAR ET AL.
[17] M. Raque, I. Sadaf, M.S. Raque and M.B. Tahir, Artif. Cells Nanomed. Biotechn. 45, 1272
(2017). doi:10.1080/21691401.2016.1241792.
[18] D.M. Ledwith, A.M. Whelan and J.M. Kelly, J. Mater. Chem. 17, 2459 (2007). doi:10.1039/
b702141k.
[19] E. Wanarska and I. Maliszewska, Bioorganic. Chem. 2019. doi:10.1016/j.bioorg.2019.02.028
[20] D. Mandal, M.E. Bolander, D. Mukhopadhyay, G. Sarkar and P. Mukherjee, Appl. Microbiol.
Biotechnol. 69, 485 (2006). doi:10.1007/s00253-005-0179-3.
[21] N. Duran, P.D. Marcato, G.I.H. De Souza, O.L. Alves and E. Esposito, J. Biomed. Nanotechnol.
3, 203 (2007). doi:10.1166/jbn.2007.022.
[22] V. Ingle, M. Rai, A. Gade and M. Bawaskar, J. Nanopart. Res. 11, 2079 (2009). doi:10.1007/
s11051-008-9573-y.
[23] A. Ahmad, P. Mukherjee, S. Senapati, D. Mandal, M.I. Khan, R. Kumar and M. Sastry, Colloid
Surf. B 28, 313 (2003). doi:10.1016/S0927-7765(02)00174-1.
[24] N. Vigneshwaran, N.M. Ashtaputre, P.V. Varadarajan, R.P. Nachane, K.M. Paralikar and R.
H. Balasubramanya, Mater. Lett. 61, 1413 (2007). doi:10.1016/j.matlet.2006.07.042.
[25] S. Basavaraja, S.D. Balaji, L. Arunkumar, A.H. Rajasab and A. Venkataraman, Mater. Res. Bull.
43, 1164 (2008). doi:10.1016/j.materresbull.2007.06.020.
[26] D.S. Balaji, S. Basavaraja, R. Deshpande, D.B. Mahesh, B.K. Prabhakar and A. Venkataraman,
Colloids Surf. B 68,88(2008). doi:10.1016/j.colsurfb.2008.09.022.
[27] G. Li, D. He, Y. Qian, B. Guan, S. Gao, Y. Cui, K. Yokoyama and L. Wang, Int. J. Mol. Sci. 13, 466
(2012). doi:10.3390/ijms13010466.
[28] M. Saravanan, S.K. Barik, D. MubarakAli, P. Prakash and A. Pugazhendhi, Microb. Pathog. 116,
221 (2018). doi:10.1016/j.micpath.2018.01.038.
[29] T. Monowar, M.S. Rahman, S.J. Bhore and G. Raju, Molecules 6,23(2018).
[30] Q. Suna, X. Cai, J. Li, M. Zheng, Z. Chen and C.P. Yu, Colloids Surf. A 444, 226 (2014).
doi:10.1016/j.colsurfa.2013.12.065.
[31] S. Ahmed, M. Ahmad, B.L. Swami and S. Ikram, J. Raditn. Res. Appl. Sci. 9,1(2016).
[32] A.D. Dwivedi and K. Gopal, Colloids Surf. A 369,27(2010). doi:10.1016/j.
colsurfa.2010.07.020.
[33] S.P. Chandran, M. Chaudhary, R. Pasricha, A. Ahmad and M. Sastry, Biotechnol. Prog. 22, 577
(2006). doi:10.1021/bp0501423.
[34] H. Kolya, P. Maiti, A. Pandey and T. Tripathy, J. Analyt. Sci. Tech. 6,33(2015). doi:10.1186/
s40543-015-0074-1.
[35] R. Koyyati, V.B. Nagati, R. Nalvothula, R. Merugu, K.R. Kudle, P. Marx and P.R.M. Padigya, Int.
J. Res. Pharm. Sci. 5,32(2014).
[36] D. MubarakAli, N. Thajuddin, K. Jeganathan and M. Gunasekaran, Colloids Surf. B 85, 360
(2011). doi:10.1016/j.colsurfb.2011.03.009.
[37] C. Krishnaraj, E.G. Jagan, S. Rajasekar, P. Selvakumar, P.T. Kalaichelvan and N.J.C.S.B.
B. Mohan, Colloids Surf. B 76,50(2010). doi:10.1016/j.colsurfb.2009.10.008.
[38] N. Ahmad, S. Sharma, M.K. Alam, V.N. Singh, S.F. Shamsi, B.R. Mehta and A. Fatma, Colloid
Surf. B 81,81(2010). doi:10.1016/j.colsurfb.2010.06.029.
[39] S.P. Dubey, M. Lahtinen and M. Sillanpää, Process Biochem. 45, 1065 (2010). doi:10.1016/j.
procbio.2010.03.024.
[40] B. Ankamwar, C. Damle, A. Ahmad and M. Sastry, J. Nanosci. Nanotech. 5, 1665 (2005).
doi:10.1166/jnn.2005.184.
[41] T.J.I. Edison and M.G. Sethuraman, Process Biochem. 47, 1351 (2012). doi:10.1016/j.
procbio.2012.04.025.
[42] U.B. Jagtap and V.A. Bapat, Indust. Crops Prodt. 46, 132 (2013). doi:10.1016/j.
indcrop.2013.01.019.
[43] M.G. Moghaddam and R.H. Dabanlou, J. Indust. Eng. Chem. 20, 739 (2014). doi:10.1016/j.
jiec.2013.09.005.
[44] J.L. Gardea-Torresdey, E. Gomez, J.R. Peralta-Videa, J.G. Parsons, H. Troiani and M. Jose-
Yacaman, Langmuir 19, 1357 (2003). doi:10.1021/la020835i.
INTERNATIONAL JOURNAL OF ENVIRONMENTAL ANALYTICAL CHEMISTRY 9
[45] A. Singh, D. Jain, M.K. Upadhyay, N. Khandelwal and H.N. Verma, Dig. J. Nanomater. Bios. 5,
483 (2010).
[46] C.G. Yuan, C. Huo, B. Gui, P. Liu and C. Zhang, J. Cluster Sci. 28, 1319 (2017). doi:10.1007/
s10876-016-1147-z.
[47] M.S. Abdel-Aziz, M.S. Shaheen, A.A. El-Nekeety and M.A. Abdel-Wahhab, J. Saudi Chem. Soct.
18, 356 (2014). doi:10.1016/j.jscs.2013.09.011.
[48] N. Ahmad, S. Sharma, V.N. Singh, S.F. Shamsi, A. Fatma and B.R. Mehta, Biotech. Res. Int.
2011. doi:10.4061/2011/454090
[49] E.K. Elumalai, T.N.V.K.V. Prasad, J. Hemachandran, S.V. Therasa, T. Thirumalai and E. David,
J. Pharm. Sci. Res. 2, 549 (2010).
[50] F. Benakashani, A. Allafchia and H.A.S. Jalali, Green Chem. Lett. Rev. 10, 324 (2017).
doi:10.1080/17518253.2017.1363297.
[51] S.U. Ganaie, T. Abbasi, J. Anuradha and S.A. Abbasi, J. King Saud Univer. Sci. 26, 222 (2014).
doi:10.1016/j.jksus.2014.02.004.
[52] B. Ajitha, Y.A.K. Reddy, S. Shameer, K.M. Rajesh, Y. Suneetha and P.S. Reddy, J. Photochem.
Photobio. B: Bio. 149,84(2015). doi:10.1016/j.jphotobiol.2015.05.020.
[53] V. Parashar, R. Parashar, B. Sharma and A.C. Pandey, Dig. J. Nanomat. Biostruc. 4,45(2009).
[54] V.A. Kumar, T. Uchida, T. Mizuki, Y. Nakajima, Y. Katsube, T. Hanajiri and T. Maekawa, Adv.
Nat. Sci. 7, 015002 (2016).
[55] J. Sivakumar, C. Premkumar, P. Santhanam and N. Saraswathi, African J. Basic Appl. Sci. 3,
265 (2011).
[56] S.A. Babu and H.G. Prabu, Mater. Lett. 65, 1675 (2011). doi:10.1016/j.matlet.2011.02.071.
[57] R. Mata, J.R. Nakkala and S.R. Sadras, Colloids Surf. B 128, 276 (2015). doi:10.1016/j.
colsurfb.2015.01.052.
[58] G. Rajakumar and A.A. Rahuman, Acta Trop. 118, 196 (2011). doi:10.1016/j.
actatropica.2011.03.003.
[59] M. Prathap, A. Alagesan and B.R. Kumar, J. Nanostruct. Chem. 4, 106 (2014). doi:10.1007/
s40097-014-0106-1.
[60] M. Nasiriboroumand, M. Montazer and H. Barani, J. Photochemi. Photobiol. B: Bio. 179,98
(2018). doi:10.1016/j.jphotobiol.2018.01.006.
[61] T. Mochochoko, O.S. Oluwafemi, D.N. Jumbam and S.P. Songca, Carbohydr. Polym. 98, 290
(2013). doi:10.1016/j.carbpol.2013.05.038.
[62] S. Fatema, M. Shirsat, M. Farooqui and M.A. Pathan, Int. J. Nano Dimension 10, 163 (2019).
[63] M. Ahmaruzzaman, Indian J. Chem. Tech. 25, 475 (2019).
[64] Z.M. Ayad, O.M.S. Ibrahim and L.W. Omar, Adv. Anim. Vet. Sci. 7, 122 (2019).
[65] S. Raj, S.C. Mali and R. Trivedi, Biochem. Biophys. Res. Commun. 503, 2814 (2018).
doi:10.1016/j.bbrc.2018.08.045.
[66] I. Fatimah, J. Adv. Res. 7, 961 (2018).
[67] M.A. Awad, A.A. Hendi, K.M. Ortashi, D.F. Elradi, N.E. Eisa, L.A. Al-Lahieb and A.A. Awad, Int.
J. Physical Sci. 9,34(2014). doi:10.5897/IJPS2013.4080.
[68] P. Shetty, N. Supraja, M. Garud and T.N.V.K.V. Prasad, J. Nanostructure Chem. 4, 161 (2014).
doi:10.1007/s40097-014-0132-z.
[69] S. Shams, S.H. Pourseyedi and H. Hashemipour, Int. J. Nanosci. Nanotechnol. 10, 127 (2014).
[70] C. Singh, R.K. Baboota, P.K. Naik and H. Singh, Adv. Mater Lett. 3, 279 (2012). doi:10.5185/
amlett.2011.10312.
[71] R.W. Raut, N.S. Kolekar, J.R. Lakkakula, V.D. Mendhulkar and S.B. Kashid, Nano-Micro Lett. 2,
106 (2010). doi:10.1007/BF03353627.
[72] T. Rajagopal, I.A.A. Jemimah, P. Ponmanickam and M. Ayyanar, J. Environ. Boil. 36, 1283
(2015).
[73] R. Prasad and V.S. Swamy, J. Nanoparticles 2013. doi:10.1155/2013/431218
[74] Q. Ahmed, N. Gupta, A. Kumar and S. Nimesh, Artif. Cells Nanomed. Biotechn. 45, 1192
(2017). doi:10.1080/21691401.2016.1215328.
[75] T.N.V.K.V. Prasad and E.K. Elumalai, Asian Pac. J. Trop. Biomed. 1,439 (2011). doi:10.1016/
S2221-1691(11)60096-8.
10 A. ZAFAR ET AL.
[76] J. Huang, Q. Li, D. Sun, Y. Lu, Y. Su, X. Yang and J. Hong, Nanotechnology 18, 105104 (2007).
doi:10.1088/0957-4484/18/49/495102.
[77] A. Saxena, R.M. Tripathi, F. Zafar and P. Singh, Mater. Lett. 67,91(2012). doi:10.1016/j.
matlet.2011.09.038.
[78] S.S. Shankar, A. Ahmad and M. Sastry, Biotechnol. Prog. 19, 1627 (2003). doi:10.1021/
bp034070w.
[79] G. Gnanajobitha, K. Paulkumar, M. Vanaja, S. Rajeshkumar, C. Malarkodi, G. Annadurai and
C. Kannan, J. Nanostruct. Chem. 67,1(2013).
[80] A. Bankar, B. Joshi, A.R. Kumar and S. Zinjarde, Colloids Surf. A: Physicochem. Eng. Asp. 368,
58 (2010). doi:10.1016/j.colsurfa.2010.07.024.
[81] S. Arokiyaraj, S. Vincent, M. Saravanan, Y. Lee, Y.K. Oh and K.H. Kim, Artif. Cells Nanomed.
Biotechn. 45, 372 (2017). doi:10.3109/21691401.2016.1160403.
[82] R. Bhuvaneswari, R.J. Xavier and M. Arumugam, J. Parasit. Dis. 41, 180 (2017). doi:10.1007/
s12639-016-0773-6.
[83] M. Kishore and Y.H. Rao, Mater. Today Proc. 5, 26271 (2018).
[84] P. Rathi Sre, M. Rek, R. Poovazhagi, M.A. Kumar and K. Murugesan, Spectrochim. Acta Part A
135, 1137 (2015). doi:10.1016/j.saa.2014.08.019.
[85] G. Suresh, P.H. Gunasekar, D. Kokila, D. Prabhu, D. Dinesh, N. Ravichandran and G.V. Siva,
Spectrochim. Acta Part A 127,61(2014). doi:10.1016/j.saa.2014.02.030.
[86] S. Dinesh, S. Karthikeyan and P. Arumugam, Arch. Appl. Sci. Res. 4, 178 (2012).
[87] P. Velmurugan, K. Anbalagan, M. Manosathyadevan, K.J. Lee, M. Cho, S.M. Lee, J.H. Park, S.
G. Oh, K.S. Bang and B.T. Oh, Bioprocess. Biosys. Eng. 37, 1935 (2014). doi:10.1007/s00449-
014-1169-6.
[88] G. Singhal, R. Bhavesh, K. Kasariya, A.R. Sharma and R.P. Singh, J. Nanopart. Res. 13, 2981
(2011). doi:10.1007/s11051-010-0193-y.
[89] K. Roy, C.K. Sarkar and C.K. Ghosh, Dig. J. Nanomater. Biostruct. 9, 1137 (2014).
[90] M.M. Khalil, E.H. Ismail, K.Z. El-Baghdady and D. Mohamed, Arabian J. Chem. 7,1131 (2014).
doi:10.1016/j.arabjc.2013.04.007.
[91] S. Arokiyaraj, M.V. Arasu, S. Vincent, N.U. Prakash, S.H. Choi, Y.K. Oh and K.H. Kim, Int.
J. Nanomedicine 9, 379 (2014). doi:10.2147/IJN.S53546.
[92] J. Baharara, F. Namvar, T. Ramezani, N. Hosseini and R. Mohamad, Molecules 19, 4624 (2014).
doi:10.3390/molecules190811211.
[93] T. Santhoshkumar, A.A. Rahuman, G. Rajakumar, S. Marimuthu, A. Bagavan, C. Jayaseelan
and C. Kamaraj, Parasitol. Res. 108, 693 (2011). doi:10.1007/s00436-010-2115-4.
[94] S. Medda, A. Hajra, U. Dey, P. Bose and N.K. Mondal, Appl. Nanosci. 5, 875 (2015).
doi:10.1007/s13204-014-0387-1.
[95] P. Singh, Y.J. Kim, C. Wang, R. Mathiyalagan and D.C. Yang, Artif. Cells Nanomed. Biotechn.
44, 1150 (2016).
[96] G. Lakshmanan, A. Sathiyaseelan, P.T. Kalaichelvan and K. Murugesan, Karbala Int. J. Mod.
Sci. 4,61(2018). doi:10.1016/j.kijoms.2017.10.007.
[97] M. Behravan, A.H. Panache, A. Naghizadeh, M. Ziaee, R. Madhavi and A. Mirzapour, Int.
J. Biolo. Macromol. 124, 148 (2019). doi:10.1016/j.ijbiomac.2018.11.101.
[98] M. Rai, A. Yadav and A. Gade, Biotechnol. Adv. 27,76(2009). doi:10.1016/j.
biotechadv.2008.09.002.
[99] S. Ravindra, Y.M. Mohan, N.N. Reddy and K.M. Raju, Colloids Surf. A 367,31(2010).
doi:10.1016/j.colsurfa.2010.06.013.
[100] W. He, X. Liu, A. Kienzle, W.E.G. Mculler and Q. Feng, J. Nanosci. Nanotechnol. 16, 219 (2016).
doi:10.1166/jnn.2016.10728.
[101] A. Akhavan, A. Sodagar, F. Mojtahedzadeh and K. Sodagar, Acta. Odontol. Scand. 71, 1038
(2013). doi:10.3109/00016357.2012.741699.
[102] J.H. Lee, Y.M. Huh, Y.W. Jun, J.W. Seo, J.T. Jang, H.T. Song, S. Kim, E.J. Cho, H.G. Yoon, J.S. Suh
and J. Cheon, Nat. Med. 13,95(2007). doi:10.1038/nm1467.
[103] M.S. Sadak, Bull. Natl. Res. Cent. 43,3
8(2019). doi:10.1186/s42269-019-0077-y.
[104] K. Sharon, A. Choudhry and R. Kumar, J. Phytol. 2,83(2010).
INTERNATIONAL JOURNAL OF ENVIRONMENTAL ANALYTICAL CHEMISTRY 11
[105] A. Razzaq, R. Ammara, H.M. Jhanzab, T. Mahmood, A. Hafeez and S. Hussain, J. Nanosci. Tech.
2,55(2016).
[106] S. Najaand R. Jamei, J. Stress Physiol. Biochem 10, 316 (2014).
[107] C. Krishnaraj, E.G. Jagan, R. Ramachandran, S.M. Abirami, N. Mohan and P.T. Kalaichelvan,
Process Biochem. 4,51(2012).
[108] P. Sharma, D. Bhatt, M.G. Zaidi, P.P. Saradhi, P.K. Khanna and S. Arora, Appl. Biochem.
Biotechnol. 167, 2225 (2012). doi:10.1007/s12010-012-9759-8.
[109] H.M.H. Salama, Int. Res. J. Biotechnol. 3, 190 (2012b).
[110] D. Kalaiselvi, Crop Prot. 117, 108 (2019). doi:10.1016/j.cropro.2018.11.020.
[111] H.J. Malmiri, Z. Sayyar, N. Anarjan and A. Berenjian, Nanobiotechnology in Food: Concepts,
Applications and Perspectives (Springer, Cham, 2019).
[112] N.T. Giao, T. Limpiyakorn, P.T. Ratpukdi and S.S. Ratpukdi, Water Sci. Tech. 79, 1007 (2019).
doi:10.2166/wst.2019.075.
12 A. ZAFAR ET AL.
... The structure of AgNPs is important for their physicochemical characteristics, which include optical, magnetic, and electronic properties. Different crystal forms, such as body-centered cubic (BCC), hexagonal close-packed (HCP), and FCC, may be found in AgNPs (Terenteva, Apyari, Kochuk, Dmitrienko, & Zolotov, 2017;Zafar, Rizvi, & Mahmood, 2019). The FCC structure, which has a high degree of symmetry, is the most often seen in AgNPs. ...
Chapter
Human health and environmental safety are threatened on a worldwide scale by effluent pollution generated from chemical industries that contaminate water sources with heavy metals, inorganic pollutants, and organic pollutants. Silver nanoparticles (AgNPs) outperform other metal nanoparticles (MNPs) in several ways, including their high surface-to-volume ratio, shape and size diversity, and inexpensive cost. As a result, they are valuable in a wide range of applications and research domains. MNPs can typically be prepared through chemical and physical processes. However, these approaches involve the generation of toxic by-products in the synthesis protocol. The green synthesis method that uses plant products is considered to be important and better than other methods because it is a one-pot synthesis, affordable, and avoids the need for chemical reducing and stabilizing agents. This chapter describes in detail the plant-mediated synthesis of AgNPs, their photocatalytic and antibacterial applications, and the in vitro characterization techniques used for evaluating the nanoparticles.
... In the case of silver nanoparticles, a negative zeta potential is preferred for stability and dispersion in the solution. This is because silver nanoparticles tend to adsorb negatively charged biomolecules, such as DNA and proteins, which can lead to aggregation if the surface charge is not sufficient to counteract the attractive van der Waals forces [44]. Hence, in this study, high zeta potential indicated the high stability of AgNPs@sa and prevented the aggregation. ...
... Natural products have emerged and become of great interest in nanoparticle synthesis, particularly with respect to green chemistry. 7,8 Recently, natural products such as vegetables, seaweed, algae, enzymes, arthropods, and plants have begun to be used in the synthesis of nanoparticles. Among them, plant extracts are widely used due to their abundance and bioactive compound content. ...
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Nanoparticles have attracted great interest recently due to their application in many fields. In this study, an eco-friendly, scalable, cost-effective method was used for the synthesis of silver nanoparticles (s-AgNPs) using the fruit extract of Sphaerophysa kotschyana as a reducing agent, and their structure was elucidated by extensive spectroscopic techniques. The color change from yellow to dark brown indicated the formation of s-AgNPs. In the UV-Vis spectrum, the maximum absorption was observed at 437 nm. Fourier transform infrared (FTIR) spectroscopy displayed the functional group of the natural compounds in the extract that capped and stabilized the s-AgNPs. The characteristic hydroxyl vibrational signal appeared at 3168 cm–1. The X-ray diffraction (XRD) pattern indicated that the s-AgNPs were face-centered cubic crystalline structures. Scanning electron microscopy (SEM) exhibited the spherical-shaped nanoparticles with an average size of 67.37 nm. The antioxidant activity of the extract and s-AgNPs was established using the DPPH, ABTS, and FRAP assays. In the DPPH test, the effect of s-AgNPs was observed to be significantly higher than that of the extract, and the activity of s-AgNPs in the FRAP test was also reported to be higher than the extract. In the ABTS assay, the s-AgNPs displayed outstanding activity, which was even better than the standards. Consequently, s-AgNPs synthesized from S. kotschyana are promising drug products for diseases caused by oxidative stress.
... In this method, physical vapor deposition, mechanical methods, thermal methods and sputtering methods are used. One the other hand, NPs are formed by decomposing solution of materials through bottomup; this is usually treated with the applying of chemical vapor deposition, sol-gel and biological synthesis methods [6][7][8][9]. ...
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Currently, eco-friendly, cost-effective, and simple synthesis techniques are drawing the attention of nanoparticle researchers. The conversion of silver ions to silver nanoparticles (AgNPs) is carried out using the Adenia trilobata leaf extract, which is capable of acting as an exclusive reducing agent. AgNPs show very crucial antibacterial properties and are nontoxic for humans. The color of the solution changes from light blue to brown, ensuring the formation on nanoparticles. The biosynthesized AgNPs are incorporated into cotton fiber, and their antibacterial activity on gram negative ( E. coli) bacteria has been studied. The UV/Vis and absorption spectroscopy analysis shows a surface plasmon resonance peak at 445 nm. The x-ray diffraction measurement reveals peaks at 38.02 and 44.23, and the average particle size is 18.30 nm. Field emission scanning electron microscopy has been performed to find the size, shape, and morphology of the treated nanoparticles and the AgNP-incorporated cotton fiber. The Fourier transform infrared spectroscopy result shows the presence of functional groups of AgNPs and capping agents. The antibacterial activity on gram negative ( E. coli) bacterial strains for the both cases showed a promising result.
... Nanotechnology is an important science that has been advancing rapidly in recent times, dealing with nano-scale materials in the range of 1 to 100 nm and their application areas [1]. The different metals have been used for nanoparticle synthesis. ...
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Nanotechnology is arising as a fast-developing research discipline with many usages areas. The silver nanoparticles synthesis (sm-AgNPs) is accomplished by reduction of silver ions in treatment with aqueous extract of Sideritis montana L. leaves. The colour change from yellow to dark brown confirmed the structures. The spectroscopic studies revealed the desired structure. In the UV-Vis spectrum, the maximum absorption was observed at 480 nm. The diffraction peaks (2θ) at the degrees of 38.14°, 44.29°, 64.48°, and 77.38° can correspond to 111, 200, 220, and 311 facets that indicates the nanostructure to be a face-centered cubic unit structure. The scanning electron microscope (SEM) and dynamic light scattering (DLS) analyses indicated that the synthesized nanoparticles were spherical with an average particle size of 36.42 nm. The zeta potential of sm-AgNPs was found as -35.2 mV which indicated the repulsion among nanoparticles and their stability. The peaks from Fourier transform infrared spectrometer (FTIR) were associated with the phenols, flavonoids, terpenoids, and alkaloids, indicating that the corresponding compounds might act as reducing agents. The photocatalytic effect of sm-AgNPs was examined by degradation of methylene blue and sm-AgNPs were able to degrade the dye by about 67% at 96 h.
... 17 The bottom-up method is a constructive approach where nanoparticles are prepared from the fusion of tiny particles and atoms to form particles of nanosize. 18 Top-down and bottom-up methods may be obtained for the preparation of nanoparticles by applying various physical, chemical and biological methods. The physical techniques involve arc discharge, ultrasonication, inert gas condensation, microwave (MW) irradiation, pyrolysis and etching, whereas the chemical process involves mixing of precursors with reducing and stabilizing agents. ...
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Full-text available
Salvia aethiopis L. was heated in distilled water for 2 hours. After filtration, water extract was treated with silver nitrate for 2 hours at 60°C to yield the silver nanoparticles (Sa-AgNPs). The structure of silver nanoparticles was elucidated by spectroscopic methods such as Ultraviolet-visible (UV-Vis), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and Scanning electron microscope (SEM). The maximum absorption in UV-Vis spectrum was observed at 508 nm. XRD pattern at ( 2 θ) 38.1°, 44.3°, 64.4°, and 77.4° degrees can be assigned to the (111), (200), (220) and (311) Bragg’s reflections of the face-centered cubic crystalline structure. The average size of Sa-AgNPs was found as 74.09 nm by SEM analysis. The characteristic hydroxyl vibration signal appeared at 3222 cm − 1 . Antioxidant activity of extract and Sa-AgNPs were carried out using DPPH • , ABTS •+ FRAP assay. The Sa-AgNPs revealed the considerable ABTS •+ scavenging effect with the value of 4.93 (IC 50 , µg/mL) compared to BHT (IC 50 , µg/mL, 8.34). However, Sa-AgNPs displayed the lower DPPH • activity (IC 50 , µg/mL, 24.37) than that of the standard BHT (IC 50 , µg/mL, 9.67). The reducing power activity of Sa-AgNPs was found as 4.52 (µmol TE/mg extract) while the standard BHT value was 488 (µmol TE/mg extract).
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Nanobiotechnology has been emerging as an interdisciplinary act which converges materials and living organisms at nanoscale and proved to be one of the potential tools in nanotechnology to address some of the critical problems. Production of biogenic metallic nanoparticles using microorganisms and other living organisms including plants is been an attracting research activity. Herein, we report the synthesis of silver nanoparticles (AgNPs) using the bark extract of Alstonia scholaris, one of the most important medicinal plants and their promising antimicrobial activity. Stable AgNPs were formed by treating 10 % of A. scholaris bark extract with the aqueous solution of AgNO3 (1 mM). The formation of AgNPs was confirmed by UV–visible spectroscopic analysis and recorded the localized surface plasmon resonance of AgNPs at 432 nm. Fourier transform infrared spectroscopic analysis revealed that primary and secondary amine groups in combination with the proteins present in the bark extract are responsible for the reduction and stabilization of the AgNPs. X-ray diffraction micrograph indicated the face-centered cubic structure of the formed AgNPs, and morphological studies including size (average size 50 nm) were carried out using transmission electron microscopy. The hydrodynamic diameter (111.7 nm) and zeta potential (−18.9 mV) were measured using the dynamic light scattering technique. The antimicrobial activity of A. scholaris bark-extract-mediated AgNPs was evaluated (in vitro) against fungi, Gram-negative and Gram-positive bacteria using disc diffusion method.
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Abstract Background The use of nanotechnology can ensure food security via improving crop production. Nanoparticles have the ability to enhance growth and yield of different plants such as fenugreek (Trigonella foenum-graecum) (Fabaceae). The present work aims to study the role of silver nanoparticles (AgNPs) on growth, some biochemical aspects, and the yield both quantitatively and qualitatively of fenugreek plant. AgNPs were synthesized by chemical reduction of silver nitrate with trisodium citrate. Results Foliar application of AgNPs with different concentrations (20, 40, and 60 mg/l) improved the growth parameters of fenugreek plant (e.g., shoot length, number of leaves/plant, and shoot dry weight) and increased some biochemical aspects such as photosynthetic pigment (chlorophyll a, chlorophyll b, and carotenoids) and indole acetic acid (IAA) contents thus enhanced the yield quantity (number of pods/plant, number of seeds/pod, weight of seeds/plant, and seed index) and quality (carbohydrate%, protein%, phenolics, flavonoids, and tannins contents) of the yielded seeds as well as increasing antioxidant activity of the yielded seeds. Conclusion The most effective treatment was 40 mg/l as it caused the highest increases in the studied parameters.
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This study was carried out to synthesis of silver nanoparticles (AgNPs) by using Silybummarianum fruit extract which is very simple and eco-friendly method. The separation of this nanoparticle was performed by centrifugation while the identification was by UV-Visible spectroscopy, X-ray diffraction, Fourier Transmission Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM) methods. Reduction of the Ag+ to Ag0 during exposure to the S. marianum fruit extract was followed by color change of the solution from colorless, yellow to dark brown within 24 hours. It is observed that surface Plasmon resonance peaks of the maximum absorbance of silver-nanoparticles occurs at 425 nm, indicating that AgNPs were produced. Involvement of the flavonoids group (flavolignans) in the synthesized AgNPs was manifested from the result of the FTIR. Particle size was recorded according to the data exhibited from the XRD results at 2θ around 25 nm which was calculated by using the Dubai-Scherrer equation. The silver nanoparticles synthesized by the help of silymarin fruit extract were scanned using SEM. From the SEM image reveals that the silver nanoparticle seems to be spherical in shape. From the results of the current study concluded that silymarin fruit extract could be considered as a good source for synthesis of stable AgNPs in short time, and the process of synthesis was simple, low cost and eco-friendly.
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Most recently, silver nanoparticles due to antibacterial properties have been considered in medical science. So the aim of the study was green synthesis of silver nanoparticles using Berberis vulgaris leaf and root aqueous extract and its antibacterial activity. After collection, identification and extraction of Berberis vulgaris was performed production of silver nanoparticles. In the study effect of parameters such as AgNO3 concentration (0.5, 1, 3, 10 mM), aqueous extract (3, 5, 10, 15, 30 mL) and contact time (1, 2, 6, 12, 24 h) were investigated in the synthesis of nanoparticles and also the antibacterial effect of these nanoparticles was studied on Escherichia coli and Staphylococcus aureus bacteria by Disk diffusion test and Minimum Inhibitory Concentration test (MIC). According to XRD results and analysis of TEM, nanoparticles have spherical shapes and size of 30 to 70 nm. On the other hand antibacterial tests showed these nanoparticles have more antibacterial activity more than other extracts. Result showed the biosynthesis of silver nanoparticles using aqueous extract of Berberis vulgaris is a clean, inexpensive and safe method that has not been used any toxic substance and consequently does not side effects and this nanoparticles has a high antibacterial activity.
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Silver nanoparticles (AgNPs) were biosynthesized using fungal extract of Trametes trogii, a white rot basidiomycete involved in wood decay worldwide, which produces several ligninolytic enzymes. According to previous studies using fungi, enzymes are involved in nanoparticles synthesis, through the so-called green synthesis process, acting as reducing and capping agents. Understanding which factors could modify nanoparticles’ shape, size and production efficiency is relevant. The results showed that under the protocol used in this work, this strain of Trametes trogii is able to synthesize silver nanoparticles with the addition of silver nitrate (AgNO3) to the fungal extract obtained with an optimal incubation time of 72 h and pH 13, using NaOH to adjust pH. The progress of the reaction was monitored using UV–visible spectroscopy and synthesized AgNPs was characterized by scanning electron microscope (SEM), through in-lens and QBDS detectors, and energy-dispersive X-ray spectroscopy (EDX). Additionally, SPR absorption was modeled using Mie theory and simple nanoparticles and core-shell configurations were studied, to understand the morphology and environment of the nanoparticles. This protocol represents a simple and cheap synthesis in the absence of toxic reagents and under an environmentally friendly condition.
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