Next Article in Journal
Development of a Model for Genomic Prediction of Multiple Traits in Common Bean Germplasm, Based on Population Structure
Next Article in Special Issue
Co-Application of TiO2 Nanoparticles and Arbuscular Mycorrhizal Fungi Improves Essential Oil Quantity and Quality of Sage (Salvia officinalis L.) in Drought Stress Conditions
Previous Article in Journal
Green Revolution to Gene Revolution: Technological Advances in Agriculture to Feed the World
Previous Article in Special Issue
Maize Silk Biogenic Nanoceria (CeO2NPs) Enhanced Sequential Injection-Chemiluminescence Detection of Ferulic, Sinapic and p-Coumaric in Yellow Maize Kernels
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Plants
Volume 11
Issue 10
10.3390/plants11101293
plants-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Cytotoxic and Genotoxic Evaluation of Biosynthesized Silver Nanoparticles Using Moringa oleifera on MCF-7 and HUVEC Cell Lines

by
Hatice Alkan
1,
İbrahim Hakkı Ciğerci
1,*,
Muhammad Muddassir Ali
2,
Omer Hazman
3,
Recep Liman
4,
Florica Colă
5,* and
Elena Bonciu
5
1
Faculty of Science and Literature, Molecular Biology and Genetics Department, Afyon Kocatepe University, Afyonkarahisar 03200, Turkey
2
Institute of Biochemistry and Biotechnology, University of Veterinary and Animal Sciences Lahore, Punjab 54000, Pakistan
3
Faculty of Science and Literature, Department of Chemistry, Afyon Kocatepe University, Afyonkarahisar 03200, Turkey
4
Faculty of Arts and Sciences, Molecular Biology and Genetics Department, Uşak University, 1 Eylül Campus, Uşak 64300, Turkey
5
Faculty of Agronomy, Department of Agricultural and Forestry Technology, University of Craiova, 13 A.I. Cuza Street, 200585 Craiova, Romania
*
Authors to whom correspondence should be addressed.
Plants 2022, 11(10), 1293; https://doi.org/10.3390/plants11101293
Submission received: 11 April 2022 / Revised: 6 May 2022 / Accepted: 9 May 2022 / Published: 12 May 2022
(This article belongs to the Special Issue Impact of Metal and Metal Oxide Nanomaterials on Plant Research: Recent Advances and Challenges)
Browse Figures
Review Reports Versions Notes

Abstract

:
Nowadays, green synthesized nanoparticles (NPs) are extensively investigated to explore their biological potential. They are being explored to treat different infectious and cancerous diseases. Therefore, the current study was designed to evaluate the cytotoxic and genotoxic effects of biosynthesized silver nanoparticles (AgNPs) from the medicinal plant Moringa oleifera on breast cancer (MCF-7) and HUVEC (human umbilical vein endothelial cells) cell lines. M. oleifera-mediated AgNPs were synthesized from the M. oleifera extract (MOE) and then characterized through the use of a scanning electron microscope (SEM), X-ray diffraction (XRD) and UV–vis spectrophotometer. Biosynthesized AgNPs and MOE were employed on MCF-7 and HUVEC cell lines to evaluate their cytotoxic and genotoxic effects. More cytotoxic effects were observed by AgNPs and MOE on MCF-7 cell lines. The IC50 for biosynthesized AgNPs was found to be 5 μg/mL. DNA damage was also observed by the MOE and AgNPs on MCF-7 cell lines. However, non-significant DNA damage was observed by MOE and AgNPs on HUVEC cell lines. The findings of the current study revealed the cytotoxic and genotoxic effects of biosynthesized AgNPs on MCF-7 cell lines. However, these AgNPs were considered safe for normal HUVEC cell lines.

Graphical Abstract

1. Introduction

Green synthesis is the production of nanoparticles using environmentally suitable materials, such as bacteria, fungi and plants [1]. These green strategies are not just attractive, but also harmless, in comparison to the usual strategies used for synthesis, because they are very friendly to the ecosystem [2]. Several advantages can be obtained by the synthesis of biologically derived extracts, such as a higher production rate and, more importantly, the cheap downstream processing required for the production of the particles [3,4,5]. The synthesis of nanoparticles from plant extracts provides an excellent pathway for the production of nanoparticles that are not only attractive to the industries, but can also be produced on a massive scale. Different studies show that various plant extracts can be used for the formation of silver nanoparticles (AgNPs), having beneficial antimicrobial activities, including extracts of Acalypha indica leaves [3], Solidago altissima [6], Xanthium strumerium L. [3], Murraya koenigii (curry leaf) [7], Ocimum sanctum (Tulsi leaf) [8,9], extracts from seeds of Acacia farnesiana [10], Macrotyloma uniflorum [11], extracts obtained from the roots of Trianthema decandra [12], stem extracts of Ocimum sanctum [8], and even fruit extracts of Musa paradisiaca (banana) peels [13] and Carica papaya [14]. All these types of studies show that plant extracts possessing phytocompounds can serve as capping or reducing agents in the reaction of silver nitrate (AgNO3), which is commonly used to initiate the process of silver nanoparticle synthesis.
M. oleifera is an important multitasking crop [15]. The plant is considered to be a rare species because its leaves, seeds, pods and flowers are edible and contain many macro/micronutrients and bioactive substances [16]. Furthermore, the different uses of this plant for livestock (as an important element of feed, fodder and antibiotics), humans (as a food fortificant, cosmetic and cooking oil), and agricultural purposes (purification of water, biofuel and fertilizer) have been published [15,17]. Various parts of M. oleifera are commonly used as the major beneficial ingredients in dietary supplement production, because of their broad health-promoting properties [18,19]. The leaves, seeds, flowers and fruits of M. oleifera have great nutraceutical and antioxidant potential [15]. The leaves of Moringa contain calcium, potassium, iron, protein, vitamins, ascorbic acid, polyphenols, rutin, flavonoids, glycosides and carotenoids, which makes it a superfood for nourishment, and it also has ameliorative effects that combat different carcinogens and mutagens. M. oleifera contains biomolecules (such as carbohydrates, proteins and coenzymes) with exemplary potential to reduce metal salt in nanoparticles [20,21]. M. oleifera is also used to treat various kinds of illnesses [15], such as for the treatment of menstrual disorders, as a fertility enhancer and cardioprotective, and to reduce abortion [22].
Silver, however, serves some necessary functions as an antiseptic, because of its significant efficiency against about 650 types of disease-causing microorganisms, and it is actually an inorganic and nontoxic agent in its nature [23]. The usage of plant extracts for AgNPs production is not only economic, but also known for its cost effectiveness at the same time [24]. Recent documentations regarding silver plant nano-extracts have shown that it has a vast range of possible applications. Moreover, it has been stated and observed that the leaves of M. oleifera are major and primary sources of vitamin C, having a higher quantity of it than that of oranges and lemons, which are considered the main source of this compound [25].
By keeping in mind the great biological potential of M. oleifera and vast range of biological activities of silver, the purpose of this study was to control the biosynthesis of M. oleifera-mediated AgNPs to synergize their efficacy. Moreover, the chemopreventive properties of M. oleifera, through its biosynthesized AgNPs, were also investigated on breast cancer cell lines (Michigan Cancer Foundation-7; MCF-7) and HUVEC (human umbilical vein endothelial cells) cell lines. Both cell lines are important as laboratory model systems. Breast cancer is widespread throughout the world, so it is important to study which agents could be safely utilized for the treatment of breast cancer [25]. Moreover, as HUVECs are cells obtained from the endothelium of veins from the umbilical cord, these cells are normally considered to be excellent cell culture models to study the angiogenesis of endothelial cells after exposure to different mutagens or chemicals [26].

2. Results

2.1. Biosynthesis and Characterization of AgNPs

The color change from green to brown following the reaction indicated the formation of AgNPs (Figure 1A). The absorption of AgNPs in the range of 350–590 nm, using a UV–visible spectrophotometer, showed a strong and broad surface plasmon peak at 420 nm for biosynthesized AgNPs (Figure 1B). During the formation of AgNPs, changes in the pH value of the mixture were observed. After mixing the two solutions, the pH value measured at the first moment was 6.48, while the pH value at the end of 24 h decreased to 6.09. The surface structure of AgNPs was revealed to have a spherical shape by SEM (Figure 2). Properties such as the crystal structure and grain size of AgNPs were determined by the XRD method (Figure 3).
The obtained Bragg peaks were found to be consistent with crystallographic reflections from 111 (35.68°), 200 (51.62°), 220 (65.86°), and 311 (77.95°), which corresponds to the JCPDS pattern 04-0783. The average size was calculated as 12.09 nm.

2.2. Cytotoxic Effects of Biosynthesized AgNPs and Plant Extract on MCF-7 and HUVEC Cells

More cytotoxic effects were observed by both MOE and AgNPs on MCF-7 (Figure 4). The IC50 value was found to be 5 μg/mL for AgNPs. It was also determined that the AgNPs concentrations leading to cell death were cytotoxic at much lower concentrations compared to the plant extract (Figure 4).
Moreover, less cell viability % was observed after 72 h in MCF-7 cells, whereas the cell viability % was not significantly reduced in the HUVEC cell line (Figure 5) by both AgNPs and MOE. Microscopic images of reduced cell viability for both cell lines are shown in Figure 6 and Figure 7.

2.3. Genotoxic Effect of Biosynthesized AgNPs and Plant Extract on MCF-7 and HUVEC Cells

DNA damage was observed by both AgNPs and MOE in the MCF-7 cell line (Table 1) compared to the negative control groups.
The highest DNA damage (103.67 ± 6.03) was observed at 10 μg/mL in 72 h by the biosynthesized AgNPs. The least DNA damage (48.33 ± 2.52 a) was observed at 1.25 μg/mL in 24 h by the AgNPs in the MCF-7 cell line. This increase in DNA damage was found to be statistically significant. Moreover, similarly, more genotoxic effects were observed by the AgNPs and MOE compared with the positive control. However, MOE and AgNPs demonstrated an almost equal level of DNA damage as the positive control in the HUVEC cell line (Table 2). This indicates non-significant DNA damage in this cell line.

3. Discussion

In the current study, biosynthesized AgNPs demonstrated a brown color after their formation. AgNPs exhibit a brown color because of the surface plasmon phenomenon in aqueous solution, which has been previously reported [2,27]. Moreover, the effectiveness of the protocol utilized in the current study is apparent by the fact that the plant secretes carbohydrates, as is observed in Chorella vulgaris and in the reaction of AgNO3, in which complete reduction takes place at the temperature of 50 °C after 24 h [28]. This, in turn, indicates that there is time variation, which is linked with the type of reducing agent used for the production of nanoparticles.
The initial results of the microscopic analysis (SEM) showed that AgNPs were spherical. Furthermore, the particles’ appearance was in the form of heavy clusters, which is the result of the physical dehydration that occurred during the procedure of SEM sample preparation [29]. The extraction of M. oleifera leaves for AgNPs production in the current study was similar to that of the previous studies [30,31].
Previous studies show the similar consequences of green-synthesized silver nanoparticles in MCF-7 cells [10,32,33]. When there is some alteration in the cells, it has been shown that cell death occurs in the cells, due to the antitumor functions of silver nanoparticles. Similarly, [34] reported the anticancerous assessment of silver nanoparticles against MCF-7 cells. In addition to this, AgNPs can be used in some biochemical functions that enhance the anticancer activities in MCF-7 cells. The authors of [35,36] reported that AgNPs in combination with hyaluronic acid can induce cell death through self-eating, improper functioning of mitochondria, stoppage of cell division, and by inducing peroxidation of lipids.
The comet assay has already been used to assess the DNA damage of various nanoparticles, mutagens, and carcinogens via different model systems [37,38,39,40]. In the current study, genotoxic effects were observed by the biosynthesized AgNPs and MOE in the MCF-7 cell line. Silver nanoparticles have the ability to activate caspase enzymes, along with reactive oxygen species (ROS) that can cause damage to DNA, stress, improper protein folding, and cell death. It has been observed that when activation starts, the cleavage of caspase-3 occurs, and it is translocated through caspase-activated DNA (CAD), due to which DNA fragments are formed. This fragmentation of the nucleic acid by the enzymes is regarded as the main point of natural cell death that might happen at initial steps [41]. A similar observation was reported by [42], who reported the consequences of silver nanoparticles on cellular functions. On the other hand, a predicted mechanism showed that damage to DNA can be due to ROS. ROS are free radicals that are produced in living organisms to perform the normal cellular functions. When there is no appropriate level or amount of ROS present, this decreased level of reactive oxygen species leads to improper functioning of cellular mechanisms, which will induce damage to DNA, peroxidation of fatty acids and cell death [43].
However, M. oleifera has different biological functions. A variety of these anti-oxidant functions are dependent on the pods, flowers and leaves of seedlings [44]. The initial extracts consist of a variety of mixtures, which have biologically active ingredients. These mixtures can induce cytotoxicity and genotoxicity [45]. Therefore, this property is utilized in the current study to find the anti-cancerous effects through its cytotoxic and genotoxic evaluation via the biosynthesis of M. oleifera AgNPs. This study revealed the cytotoxic effects of AgNPs and MOE on both HUVEC and MCF-7 cells. Previously, the cytotoxic effects of M. oleifera extracts on human cancer cells, such as pancreatic cancer cells (Panc-1) [46], colon cancer cells (SW480 and HCT18) [47], and KB tumor cells [48], have been reported. AgNPs synthesis using plant extracts is a good alternative to physical and chemical methods, and can be a potential alternative agent in breast cancer treatment [49].
A rise in the activeness of phytoconstituents (total phenolic compounds and total flavonoids) by the use of AgNPs during the process of plant extraction has already been observed [50]. Moreover, the effectiveness of the total antioxidant is increased by the use of AgNPs, and scavenging activity occurs against the free radicals ABTS and DPPH, which increases cytotoxicity, and this is effective against colon cancer cell growth [50,51].
In recent studies, the ability of silver nanoparticles to reduce cell viability and increase apoptosis in different cancer cells has come to the forefront. For this reason, research has led to the selection of natural compounds with anticancer effects for the synthesis of silver nanoparticles, which have valuable properties against cancer cells, but a low effect on normal cells [34,42].

4. Materials and Methods

4.1. Preparation of Bio-Synthesized Silver Nanoparticles

M. oleifera leaves were pulverized and 0.5 gm powder was weighed and mixed with 50 mL of distilled H2O. The mixture was heated in a microwave oven (600 W, 50 Hz) for 2 min and the extract was further filtered through Whatman no.1 filter paper. An aqueous solution of AgNO3 (1 mM) was prepared and used for the synthesis of AgNPs at room temperature. For the biosynthesis of AgNPs, 980 mL of 1 mM AgNO3 solution and 20 mL M. oleifera extract (MOE) were mixed. This mixture was heated in a microwave oven (600 W, 50 Hz) for 2 min. The color changed from green to brown, indicating the formation of AgNPs [50].

4.2. Characterization of Bio-Synthesized Nanoparticles

After 24 h, the sample taken from the AgNPs solution was examined using a UV–vis spectrophotometer at wavelengths in the range of 320–500 nm. The pH value of the synthesized AgNPs was also measured using a pH meter at the time of creating the first mixture and at the end of 24 h [52,53]. The formation, particle shape and size of the synthesized AgNPs were examined by SEM analysis and the characteristic diffraction of each crystal was analyzed by XRD analysis [54]. Properties such as crystal structure and grain size of AgNPs were determined by the XRD method [50,55]. Characteristic Ag peaks were obtained by takeover XRD spectra of AgNPs synthesized with MOE and 1 mM AgNO3 solution at 300 rpm with a magnetic stirrer at 80 °C for 60 min.

4.3. Cell Culture

The human breast cancer cell line MCF-7 and HUVEC cell lines were cultured in RPMI-1640 medium containing 10% fetal bovine serum, 100 μg/mL streptomycin, 100 U/mL penicillin and 2 mM l-glutamic acid. Culture was obtained under sterile conditions at 37 °C in an incubator with 5% CO2 [56].

4.4. MTT Test

Cell viability was evaluated by the 3-(4,5-dimethylthiazol-2-YL)-2,5-diphenyltetrazolium bromide (MTT) test. Briefly, cells were counted and then seeded into 24-well plates. MCF-7 and HUVEC cells were incubated with biosynthesized AgNPs and MOE at different concentrations (1.25–10 µg/mL; 1–100 µg/mL) for 24, 48 and 72 h, respectively. MTT (5 mg/mL) was added (80 μL) to each well and incubated for 4 h. At the end of 4 h, purple-colored formazone crystals formed and those were further dissolved in 800 μL dimethyl sulfoxide (DMSO). Optical density (OD) was measured using a multi-well spectrophotometer (ELISA) plate reader at a wavelength of 540 nm. Concentration (IC50 value) of biosynthesized NPs showing 50% reduction in cell viability was determined. Cells untreated with AgNPs were used as the control.

4.5. Comet Test

DNA damage was determined by the comet method, as described by [57,58]. Briefly, cells mixed with low-melting agarose were embedded on pre-coated slides of normal-melting agarose. Then, slides were kept in lysis solution and electrophoresis was carried out. This comet-shaped DNA was then stained using ethidium bromide and made visible through a fluorescent microscope. Cells were counted using a fluorescence microscope, as described by [59,60,61].

4.6. Statistical Analysis

Results were expressed as the mean ± standard deviation of three independent experiments. The results of the comet analysis were calculated with the Duncan multi-distribution test (p < 0.05).

5. Conclusions

Biosynthesized NPs are considered to be safer and to have excellent biological potential against cancerous cell lines. Previously, no documented study has been found on the genotoxic and anticancerous assessment of M. oleifera-mediated AgNPs on MCF-7 and HUVEC cells, or the comparison between them. It was concluded that biosynthesized AgNPs from MOE exhibited anti-cancerous effects on MCF-7 cells. The MOE extracts also showed cytotoxic and genotoxic effects on MCF-7 cells. Biosynthesized AgNPs and MOE demonstrated that these are considered safe for normal HUVEC cells, as non-significant cytotoxic and DNA damage was observed in this cell line. However, the molecular anti-cancerous mechanism should be further evaluated to better understand its anti-cancerous effects.

Author Contributions

Conceptualization, H.A. and İ.H.C.; methodology, M.M.A.; validation, O.H., R.L. and H.A; formal analysis, O.H.; investigation, M.M.A. and F.C.; data curation, R.L. and E.B.; writing—original draft preparation, İ.H.C.; writing—review and editing, F.C.; visualization, R.L. and E.B.; supervision, İ.H.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Patra, J.K.; Baek, K.H. Green nanobiotechnology: Factors affecting synthesis and characterization techniques. J. Nanomater. 2014, 2014, 417305. [Google Scholar] [CrossRef] [Green Version]
  2. Veerasamy, R.; Xin, T.Z.; Gunasagaran, S.; Xiang, T.F.W.; Yang, E.F.C.; Jeyakumar, N.; Dhanaraj, S.A. Biosynthesis of silver nanoparticles using mangosteen leaf extract and evaluation of their antimicrobial activities. J. Saudi Chem. Soc. 2011, 15, 113–120. [Google Scholar] [CrossRef] [Green Version]
  3. Liu, B.; Xie, J.; Lee, J.; Ting, Y.; Chen, J.P. Optimization of high-yield biological synthesis of single-crystalline gold nanoplates. J. Phys. Chem. B 2005, 109, 15256–15263. [Google Scholar] [CrossRef] [PubMed]
  4. Moodley, J.S.; Krishna, S.B.N.; Pillay, K.; Govender, P. Green synthesis of silver nanoparticles from Moringa oleifera leaf extracts and its antimicrobial potential. Adv. Nat. Sci. Nanosci. Nanotechnol. 2018, 9, 015011. [Google Scholar] [CrossRef] [Green Version]
  5. Das, V.L.; Thomas, R.; Varghese, R.T.; Soniya, E.; Mathew, J.; Radhakrishnan, E. Extracellular synthesis of silver nanoparticles by the Bacillus strain CS 11 isolated from industrialized area. 3 Biotech 2014, 4, 121–126. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Kumar, V.A.; Uchida, T.; Mizuki, T.; Nakajima, Y.; Katsube, Y.; Hanajiri, T.; Maekawa, T. Synthesis of nanoparticles composed of silver and silver chloride for a plasmonic photocatalyst using an extract from a weed Solidago altissima (goldenrod). Adv. Nat. Sci. Nanosci. Nanotechnol. 2016, 7, 015002. [Google Scholar] [CrossRef]
  7. Christensen, L.; Vivekanandhan, S.; Misra, M.; Mohanty, A.K. Biosynthesis of silver nanoparticles using Murraya koenigii (curry leaf): An investigation on the effect of broth concentration in reduction mechanism and particle size. Adv. Mater. Lett. 2011, 2, 429–434. [Google Scholar] [CrossRef]
  8. Ahmad, N.; Sharma, S.; Alam, M.K.; Singh, V.; Shamsi, S.; Mehta, B.; Fatma, A. Rapid synthesis of silver nanoparticles using dried medicinal plant of basil. Colloids Surf. B Biointerfaces 2010, 81, 81–86. [Google Scholar] [CrossRef]
  9. Malapermal, V.; Botha, I.; Krishna, S.B.N.; Mbatha, J.N. Enhancing antidiabetic and antimicrobial performance of Ocimum basilicum, and Ocimum sanctum (L.) using silver nanoparticles. Saudi J. Biol. Sci. 2017, 24, 1294–1305. [Google Scholar] [CrossRef]
  10. Yallappa, S.; Manjanna, J.; Peethambar, S.; Rajeshwara, A.; Satyanarayan, N. Green synthesis of silver nanoparticles using Acacia farnesiana (Sweet Acacia) seed extract under microwave irradiation and their biological assessment. J. Clust. Sci. 2013, 24, 1081–1092. [Google Scholar] [CrossRef]
  11. Vidhu, V.; Aromal, S.A.; Philip, D. Green synthesis of silver nanoparticles using Macrotyloma uniflorum. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 2011, 83, 392–397. [Google Scholar] [CrossRef] [PubMed]
  12. Geethalakshmi, R.; Sarada, D. Gold and silver nanoparticles from Trianthema decandra: Synthesis, characterization, and antimicrobial properties. Int. J. Nanomed. 2012, 7, 5375–5384. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Bankar, A.; Joshi, B.; Kumar, A.R.; Zinjarde, S. Banana peel extract mediated novel route for the synthesis of silver nanoparticles. Colloids Surf. Physicochem. Eng. Asp. 2010, 368, 58–63. [Google Scholar] [CrossRef]
  14. Jain, D.; Daima, H.K.; Kachhwaha, S.; Kothari, S. Synthesis of plant-mediated silver nanoparticles using papaya fruit extract and evaluation of their anti microbial activities. Dig. J. Nanomater. Biostruct. 2009, 4, 557–563. [Google Scholar]
  15. Falowo, A.B.; Mukumbo, F.E.; Idamokoro, E.M.; Lorenzo, J.M.; Afolayan, A.J.; Muchenje, V. Multi-functional application of Moringa oleifera Lam. in nutrition and animal food products: A review. Food Res. Int. 2018, 106, 317–334. [Google Scholar] [CrossRef] [PubMed]
  16. Rocchetti, G.; Pagnossa, J.P.; Blasi, F.; Cossignani, L.; Piccoli, R.H.; Zengin, G.; Montesano, D.; Cocconcelli, P.S.; Lucini, L. Phenolic profiling and in vitro bioactivity of Moringa oleifera leaves as affected by different extraction solvents. Food Res. Int. 2020, 127, 108712. [Google Scholar] [CrossRef]
  17. Valenga, M.G.P.; Boschen, N.L.; Rodrigues, P.R.P.; Maia, G.A.R. Agro-industrial waste and Moringa oleifera leaves as antioxidants for biodiesel. Ind. Crops Prod. 2019, 128, 331–337. [Google Scholar] [CrossRef]
  18. Sengev, A.I.; Abu, J.O.; Gernah, D.I. Effect of Moringa oleifera leaf powder supplementation on some quality characteristics of wheat bread. Food Nutr. Sci. 2013, 4, 270–275. [Google Scholar]
  19. Hassan, F.A.; Bayoumi, H.M.; El-Gawad, M.; Enab, A.; Youssef, Y. Utilization of Moringa oleifera leaves powder in production of yoghurt. Int. J. Dairy Sci. 2016, 11, 69–74. [Google Scholar] [CrossRef] [Green Version]
  20. Siddhuraju, P.; Becker, K. Antioxidant properties of various solvent extracts of total phenolic constituents from three different agroclimatic origins of drumstick tree (Moringa oleifera Lam.) leaves. J. Agric. Food Chem. 2003, 51, 2144–2155. [Google Scholar] [CrossRef]
  21. Ndong, M.; Uehara, M.; Katsumata, S.; Sato, S.; Suzuki, K. Preventive effects of Moringa oleifera (Lam) on hyperlipidemia and hepatocyte ultrastructural changes in iron deficient rats. Biosci. Biotech. Biochem. 2007, 71, 1826–1833. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Nwamarah, J.U.; Otitoju, O.; Otitoju, G.T. Effects of Moringa oleifera Lam. aqueous leaf extracts on follicle stimulating hormone and serum cholesterol in Wistar rats. Afr. J. Biotech. 2015, 14, 181–186. [Google Scholar] [CrossRef]
  23. Popescu, M.; Velea, A.; Lőrinczi, A. Biogenic production of nanoparticles. Dig. J. Nanomater. Biostruct. 2010, 5, 1035–1040. [Google Scholar]
  24. Allafchian, A.; Mirahmadi-Zare, S.; Jalali, S.; Hashemi, S.; Vahabi, M. Green synthesis of silver nanoparticles using phlomis leaf extract and investigation of their antibacterial activity. J. Nanostruct. Chem. 2016, 6, 129–135. [Google Scholar] [CrossRef] [Green Version]
  25. Comşa, S.; Cîmpean, A.M.; Raica, M. The Story of MCF-7 Breast Cancer Cell Line: 40 years of Experience in Research. Anticancer Res. 2015, 35, 3147–3154. [Google Scholar] [PubMed]
  26. Grossini, E.; Garhwal, D. The Potential Role of Peripheral Oxidative Stress on the Neurovascular Unit in Amyotrophic Lateral Sclerosis Pathogenesis: A Preliminary Report from Human and In Vitro Evaluations. Biomedicines 2022, 10, 691. [Google Scholar] [CrossRef]
  27. Mbailao, M.; Mianpereum, T.; Albert, N. Proximal and elemental composition of Moringa oleifera (Lam) leaves from three regions of Chad. J. Food Res. Sci. 2014, 3, 12–20. [Google Scholar] [CrossRef]
  28. Govindappa, M.; Farheen, H.; Chandrappa, C.; Rai, R.V.; Raghavendra, V.B. Mycosynthesis of silver nanoparticles using extract of endophytic fungi, Penicillium species of Glycosmis mauritiana, and its antioxidant, antimicrobial, anti-inflammatory and tyrokinase inhibitory activity. Adv. Nat. Sci. Nanosci. Nanotechnol. 2016, 7, 035014. [Google Scholar] [CrossRef]
  29. Ebrahiminezhad, A.; Bagheri, M.; Taghizadeh, S.M.; Berenjian, A.; Ghasemi, Y. Biomimetic synthesis of silver nanoparticles using microalgal secretory carbohydrates as a novel anticancer and antimicrobial. Adv. Nat. Sci. Nanosci. Nanotechnol. 2016, 7, 015018. [Google Scholar] [CrossRef]
  30. Sadeghi, B.; Gholamhoseinpoor, F. A study on the stability and green synthesis of silver nanoparticles using Ziziphora tenuior (Zt) extract at room temperature. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 2015, 134, 310–315. [Google Scholar] [CrossRef]
  31. Sathyavathi, R.; Krishna, M.; Rao, D.N. Biosynthesis of silver nanoparticles using Moringa oleifera leaf extract and its application to optical limiting. J. Nanosci. Nanotechnol. 2011, 11, 2031–2035. [Google Scholar] [CrossRef] [PubMed]
  32. Shousha, W.G.; Aboulthana, W.M.; Salama, A.H.; Saleh, M.H.; Essawy, E.A. Evaluation of the biological activity of Moringa oleifera leaves extract after incorporating silver nanoparticles, in vitro study. Bull. Nat. Res. Cent. 2019, 43, 212. [Google Scholar] [CrossRef] [Green Version]
  33. Vivek, R.; Thangam, R.; Muthuchelian, K.; Gunasekaran, P.; Kaveri, K.; Kannan, S. Green biosynthesis of silver nanoparticles from Annona squamosa leaf extract and its in vitro cytotoxic effect on MCF-7 cells. Process Biochem. 2012, 47, 2405–2410. [Google Scholar] [CrossRef]
  34. Sadat Shandiz, S.A.; Shafiee Ardestani, M.; Shahbazzadeh, D.; Assadi, A.; Ahangari Cohan, R.; Asgary, V.; Salehi, S. Novel imatinib-loaded silver nanoparticles for enhanced apoptosis of human breast cancer MCF-7 cells. Artif. Cells Nanomed. Biotechnol. 2017, 45, 1082–1091. [Google Scholar] [CrossRef] [PubMed]
  35. Sriram, M.I.; Kanth, S.B.M.; Kalishwaralal, K.; Gurunathan, S. Antitumor activity of silver nanoparticles in Dalton’s lymphoma ascites tumor model. Int. J. Nanomed. 2010, 5, 753–762. [Google Scholar]
  36. Liang, J.; Zeng, F.; Zhang, M.; Pan, Z.; Chen, Y.; Zeng, Y.; Xu, Y.; Xu, Q.; Huang, Y. Green synthesis of hyaluronic acid-based silver nanoparticles and their enhanced delivery to CD44+ cancer cells. RSC Adv. 2015, 5, 43733–43740. [Google Scholar] [CrossRef]
  37. Kaygisiz, S.Y.; Ciğerci, I.H. Genotoxic evaluation of different sizes of iron oxide nanoparticles and ionic form by SMART, Allium and comet assay. Toxicol. Ind. Health 2017, 33, 802–809. [Google Scholar] [CrossRef]
  38. Ciğerci, I.H.; Liman, R.; Özgül, E.; Konuk, M. Genotoxicity of indium tin oxide by Allium and Comet tests. Cytotechnology 2015, 67, 157–163. [Google Scholar] [CrossRef] [Green Version]
  39. Liman, R.; Ali, M.M.; Istifi, E.S.; Ciğerci, I.H.; Bonciu, E. Genotoxic and cytotoxic efects of pethoxamid herbicide on Allium cepa cells and its molecular docking studies to unravel genotoxicity mechanism. Environ. Sci. Pollut. Res. 2022. [Google Scholar] [CrossRef]
  40. Ali, M.M.; Cigerci, I.H. Anti-cancerous efficacy of alcoholic and aqueous extracts from an endemic plant Thermopsis turcica on Liver Carcinoma. Br. J. Pharm. Res. 2017, 16, 1–5. [Google Scholar] [CrossRef]
  41. Anandalakshmi, K.; Venugobal, J.; Ramasamy, V. Characterization of silver nanoparticles by green synthesis method using Pedalium murex leaf extract and their antibacterial activity. Appl. Nanosci. 2016, 6, 399–408. [Google Scholar] [CrossRef] [Green Version]
  42. Bin-Jumah, M.; Monera, A.A.; Albasher, G.; Alarifi, S. Effects of green silver nanoparticles on apoptosis and oxidative stress in normal and cancerous human hepatic cells in vitro. Int. J. Nanomed. 2020, 15, 1537–1548. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Arora, S.; Jain, J.; Rajwade, J.; Paknikar, K. Cellular responses induced by silver nanoparticles: In vitro studies. Toxicol. Lett. 2008, 179, 93–100. [Google Scholar] [CrossRef] [PubMed]
  44. Forman, H.J.; Torres, M. Reactive oxygen species and cell signaling: Respiratory burst in macrophage signaling. Am. J. Respir. Crit. Care Med. 2002, 166 (Suppl. 1), S4–S8. [Google Scholar] [CrossRef]
  45. Ali, K.; Iqbal, A.; Bukhari, S.; Safdar, S.; Raiz, A.; Ali, W.; Hussain, A.; Javid, A.; Hussain, M.; Ali, M. Amelioration potential of Moringa oleifera extracts against sodium arsenate induced embryotoxicity and genotoxicity in mouse (Mus musculus). Braz. J. Biol. 2021, 83, e248022. [Google Scholar] [CrossRef]
  46. Yumnamcha, T.; Nongthomba, U.; Devi, M.D. Phytochemical screening and evaluation of genotoxicity and acute toxicity of aqueous extract of Croton tiglium L. Int. J. Sci. Res. Publ. 2014, 4, 2250–3153. [Google Scholar]
  47. Berkovich, L.; Earon, G.; Ron, I.; Rimmon, A.; Vexler, A.; Lev-Ari, S. Moringa Oleifera aqueous leaf extract down-regulates nuclear factor-kappaB and increases cytotoxic effect of chemotherapy in pancreatic cancer cells. BMC Complement. Altern. Med. 2013, 13, 212. [Google Scholar] [CrossRef] [Green Version]
  48. Pamok, S.; Vinitketkumnuen, S.S.U.; Saenphet, K. Antiproliferative effect of Moringa oleifera Lam. and Pseuderanthemum palatiferum (Nees) Radlk extracts on the colon cancer cells. J. Med. Plants Res. 2012, 6, 139–145. [Google Scholar]
  49. Sreelatha, S.; Jeyachitra, A.; Padma, P. Antiproliferation and induction of apoptosis by Moringa oleifera leaf extract on human cancer cells. Food Chem. Toxicol. 2011, 49, 1270–1275. [Google Scholar] [CrossRef]
  50. Aydın, Ç.; Pehlivanoğlu, S. Synthesis of Silver Nanoparticles using Rosmarinus officinalis and Cytotoxic Effect on MCF-7 Human Breast Cancer Cells. SDU J. Health Sci. Inst. 2019, 10, 172–176. [Google Scholar]
  51. Abdel-Aziz, M.S.; Shaheen, M.S.; El-Nekeety, A.A.; Abdel-Wahhab, M.A. Antioxidant and antibacterial activity of silver nanoparticles biosynthesized using Chenopodium murale leaf extract. J. Saudi Chem. Soc. 2014, 18, 356–363. [Google Scholar] [CrossRef] [Green Version]
  52. Aboulthana, W.; Sayed, H. How to use green technology to enhance antioxidant efficiency of plant extracts: A novel strategy. J. Appl. Pharm. 2018, 10, 264–267. [Google Scholar]
  53. Nartop, P. Use of biosynthetic silver nanoparticles in the surface sterilization of Pyracantha coccinea stem explants. Pamukkale Univ. J. Eng. Sci. 2016, 23, 759–761. [Google Scholar] [CrossRef] [Green Version]
  54. Nartop, P. Use of herbal drug extracts as reducing agents for green synthesis of silver nanoparticles. Eskiseh. Technol. Univ. J. Sci. Technol. C-Life Sci. Biotechnol. 2019, 8, 50–60. [Google Scholar]
  55. Günay, K.; Leblebici, Z.; Koca, F.D. Çinko nanopartiküllerinin (ZnO NP) biyosentezi, karakterizasyonu ve anti-bakteriyel etkisinin incelenmesi. Nevşehir Bilim ve Teknol. Derg. 2021, 10, 56–66. [Google Scholar]
  56. Acar, Ç.A.; Pehlivanoglu, S. Biosynthesis of silver nanoparticles using Rosa canina extract and its anti-cancer and anti-metastatic activity on human colon adenocarcinoma cell line HT29. Mehmet Akif Ersoy University. J. Health Sci. Inst. 2019, 7, 124–131. [Google Scholar]
  57. Dağlıoğlu, C. Using inorganic nanoparticle-based drug delivery systems against human colon cancer cells: Effect of particle size on anticancer activity. J. Polytec-Politek Derg. 2020, 23, 171–179. [Google Scholar]
  58. Ali, M.M.; Ciğerci, İ.H. Genotoxic Evaluation of an Endemic Plant Thermopsis turcica Extracts on Liver Cancer Cell Line. Pak. J. Zool. 2019, 51, 355–357. [Google Scholar] [CrossRef]
  59. Liman, R.; Acikbas, Y.; Ciğerci, İ.H.; Ali, M.M.; Kars, M.D. Cytotoxic and genotoxic assessment of silicon dioxide nanoparticles by allium and comet tests. Bull Environ. Contam. Toxicol. 2020, 104, 215–221. [Google Scholar] [CrossRef]
  60. Liman, R.; Ali, M.M.; Ciğerci, İ.H.; İstifli, E.S.; Sarıkurkcu, C. Cytotoxic and genotoxic evaluation of copper oxychloride through Allium test and molecular docking studies. Environ. Sci. Pollut. Res. 2021, 28, 44998–45008. [Google Scholar] [CrossRef]
  61. Liman, R.; Başbuğ, B.; Ali, M.M.; Acikbas, Y.; Ciğerci, İ.H. Cytotoxic and genotoxic assessment of tungsten oxide nanoparticles in Allium cepa cells by Allium ana-telophase and comet assays. J. Appl. Genet. 2021, 62, 85–92. [Google Scholar] [CrossRef] [PubMed]
Plants 11 01293 g001 550
Figure 1. (A) Biosynthesis of silver nanoparticles, (B) along with UV–visible spectrophotometer image.
Figure 1. (A) Biosynthesis of silver nanoparticles, (B) along with UV–visible spectrophotometer image.
Plants 11 01293 g001
Plants 11 01293 g002 550
Figure 2. Image of scanning electron microscope (SEM) for the biosynthesized nanoparticles.
Figure 2. Image of scanning electron microscope (SEM) for the biosynthesized nanoparticles.
Plants 11 01293 g002
Plants 11 01293 g003 550
Figure 3. Image of X-ray diffraction for the biosynthesized nanoparticles.
Figure 3. Image of X-ray diffraction for the biosynthesized nanoparticles.
Plants 11 01293 g003
Plants 11 01293 g004 550
Figure 4. Cytotoxic effect of biosynthesized silver AgNPs and M. oleifera extract (MOE) on cell viability of MCF-7. Cells were treated at various concentrations of AgNPs and MOE for 24, 48 and 72 h, and cytotoxicity was determined by MTT. Results are expressed as the mean ± standard deviation of three independent experiments.
Figure 4. Cytotoxic effect of biosynthesized silver AgNPs and M. oleifera extract (MOE) on cell viability of MCF-7. Cells were treated at various concentrations of AgNPs and MOE for 24, 48 and 72 h, and cytotoxicity was determined by MTT. Results are expressed as the mean ± standard deviation of three independent experiments.
Plants 11 01293 g004
Plants 11 01293 g005 550
Figure 5. Cytotoxic effect of biosynthesized silver nanoparticles (AgNPs) and M. oleifera extract (MOE) on cell viability of HUVEC cell line.
Figure 5. Cytotoxic effect of biosynthesized silver nanoparticles (AgNPs) and M. oleifera extract (MOE) on cell viability of HUVEC cell line.
Plants 11 01293 g005
Plants 11 01293 g006 550
Figure 6. (a) Microscopic image of MCF-7 cells after 72 h. MCF-7 cells are well developed and confluent. (b) Microscopic image of MCF-7 cells after exposure to NP dosing. Reduced cell viability and less confluence are apparent after dosing.
Figure 6. (a) Microscopic image of MCF-7 cells after 72 h. MCF-7 cells are well developed and confluent. (b) Microscopic image of MCF-7 cells after exposure to NP dosing. Reduced cell viability and less confluence are apparent after dosing.
Plants 11 01293 g006
Plants 11 01293 g007 550
Figure 7. (a) Microscopic image of HUVEC cells after 72 h before exposure to NP doses. Cells are well developed and confluent. (b) Microscopic image of HUVEC cells after exposure to NP dosing. Reduced cell viability and less confluence are apparent after dosing.
Figure 7. (a) Microscopic image of HUVEC cells after 72 h before exposure to NP doses. Cells are well developed and confluent. (b) Microscopic image of HUVEC cells after exposure to NP dosing. Reduced cell viability and less confluence are apparent after dosing.
Plants 11 01293 g007
Table
Table 1. DNA damage at different concentrations of M. oleifera extracts (MOE) and biosynthesized AgNPs in MCF-7 cell lines.
Table 1. DNA damage at different concentrations of M. oleifera extracts (MOE) and biosynthesized AgNPs in MCF-7 cell lines.
GroupsConcentrations (µg/mL)DNA Damage (Arbitrary Unit)
Mean ± Standard Deviation (SD)
24 h48 h72 h
Control-48.67 ± 5.03 a50.33 ± 5.51 a53.33 ± 5.86 a
Cisplatin119 53.67 ± 5.51 ab63.33 ± 11.55 ab67.67 ± 12.42 ab
MOE10066 ± 4.58 b107.33 ± 8.08 c122.67 ± 6.43 f
1059.33 ± 8.08 ab85 ± 11.36 d99.67 ± 19.4 e
159.67 ± 3.51 ab85 ± 7.94 d97 ± 12.12 de
AgNPs1061.33 ± 10.07 ab77.67 ± 4.51 bd103.67 ± 6.03 ef
552 ± 11.14 a74.33 ± 7.64 bd90.33 ± 14.05 cde
2.555.67 ± 9.07 ab73 ± 5.2 bd79 ± 9.54 bcd
1.2548.33 ± 2.52 a67.33 ± 2.08 b71.33 ± 11.02 abc
In each column, means (±SD) with similar letters indicate no significance at p ≤ 0.05, depending on the Duncan multi-distribution test.
Table
Table 2. DNA damage at different concentrations of M. oleifera extracts (MOE) and biosynthesized AgNPs in HUVEC cell lines.
Table 2. DNA damage at different concentrations of M. oleifera extracts (MOE) and biosynthesized AgNPs in HUVEC cell lines.
GroupsConcentrations (µg/mL)DNA Damage (Arbitrary Unit)
Mean ± Standard Deviation (SD)
24 h48 h72 h
Control-9.67 ± 2.08 a9 ± 1 a9 ± 1.73 a
Cisplatin3423.17 ± 2.51 ab33.13 ± 21.12 ab37.67 ± 11.12 ab
MOE1009.33 ± 0.58 a7 ± 1.73 b8 ± 1 ab
109.67 ± 1.15 a7 ± 1 b7.33 ± 1.53 ab
17.67 ± 2.08 a6.33 ± 0.58 b7 ± 1 ab
AgNPs108.67 ± 2.08 a6.67 ± 0.58 b7.33 ± 0.58 ab
59.67 ± 2.08 a7 ± 1 b6.67 ± 0.58 ab
2.59.33 ± 0.58 a6.33 ± 1.53 b6 ± 1 b
1.258.33 ± 0.58 a6 b6.33 ± 0.58 b
In each column, means (±SD) with similar letters indicate no significance at p ≤ 0.05, depending on the Duncan multi-distribution test.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Alkan, H.; Ciğerci, İ.H.; Ali, M.M.; Hazman, O.; Liman, R.; Colă, F.; Bonciu, E. Cytotoxic and Genotoxic Evaluation of Biosynthesized Silver Nanoparticles Using Moringa oleifera on MCF-7 and HUVEC Cell Lines. Plants 2022, 11, 1293. https://doi.org/10.3390/plants11101293

AMA Style

Alkan H, Ciğerci İH, Ali MM, Hazman O, Liman R, Colă F, Bonciu E. Cytotoxic and Genotoxic Evaluation of Biosynthesized Silver Nanoparticles Using Moringa oleifera on MCF-7 and HUVEC Cell Lines. Plants. 2022; 11(10):1293. https://doi.org/10.3390/plants11101293

Chicago/Turabian Style

Alkan, Hatice, İbrahim Hakkı Ciğerci, Muhammad Muddassir Ali, Omer Hazman, Recep Liman, Florica Colă, and Elena Bonciu. 2022. "Cytotoxic and Genotoxic Evaluation of Biosynthesized Silver Nanoparticles Using Moringa oleifera on MCF-7 and HUVEC Cell Lines" Plants 11, no. 10: 1293. https://doi.org/10.3390/plants11101293

APA Style

Alkan, H., Ciğerci, İ. H., Ali, M. M., Hazman, O., Liman, R., Colă, F., & Bonciu, E. (2022). Cytotoxic and Genotoxic Evaluation of Biosynthesized Silver Nanoparticles Using Moringa oleifera on MCF-7 and HUVEC Cell Lines. Plants, 11(10), 1293. https://doi.org/10.3390/plants11101293

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop