scholarly journals Cupric Oxide Nanoparticles Induce Cellular Toxicity in Liver and Intestine Cell Lines

2020 ◽  
Vol 10 (2) ◽  
pp. 213-220 ◽  
Author(s):  
Mahmoud Abudayyak ◽  
Elif Guzel ◽  
Gül Özhan

Purpose: The wide application of cupric oxide nanoparticles (copper (II) oxide, CuO-NPs) in various fields has increased exposure to the kind of active nanomaterials, which can cause negative effects on human and environment health. Although CuO-NPs were reported to be harmful to human, there is still a lack information related to their toxic potentials. In the present study, the toxic potentials of CuO-NPs were evaluated in the liver (HepG2 hepatocarcinoma) and intestine (Caco-2 colorectal adenocarcinoma) cells. Methods: After the characterization of particles, cellular uptake and morphological changes were determined. The potential of cytotoxic, genotoxic, oxidative and apoptotic damage was investigated with several in vitro assays. Results: The average size of the nanoparticles was 34.9 nm, about 2%-5% of the exposure dose was detected in the cells and mainly accumulated in different organelles, causing oxidative stress, cell damages, and death. The IC50 values were 10.90 and 10.04 µg/mL by MTT assay, and 12.19 and 12.06 µg/mL by neutral red uptake (NRU) assay, in HepG2 and Caco-2 cells respectively. Apoptosis assumes to the main cell death pathway; the apoptosis percentages were 52.9% in HepG2 and 45.5% in Caco-2 cells. Comet assay result shows that the highest exposure concentration (20 µg/mL) causes tail intensities about 9.6 and 41.8%, in HepG2 and Caco-2 cells, respectively. Conclusion: CuO-NPs were found to cause significant cytotoxicity, genotoxicity, and oxidative and apoptotic effects in both cell lines. Indeed, CuO-NPs could be dangerous to human health even if their toxic mechanisms should be elucidated with further studies.

2020 ◽  
Vol 9 (1) ◽  
Author(s):  
Khwaja Salahuddin Siddiqi ◽  
M. Rashid ◽  
A. Rahman ◽  
Tajuddin ◽  
Azamal Husen ◽  
...  

Abstract Background Biogenic fabrication of nanoparticles from naturally occurring biomaterials involves plants, herbs, bacteria and fungi using water as neutral solvent, while chemical synthesis involves hazardous chemicals and leaves unwanted byproduct which unnecessarily pollute the environment. In order to prevent atmospheric pollution a safe, clean and green strategy for the synthesis of cupric oxide nanoparticles from aqueous leaf extract of Diospyros montana has been employed. D. montana of Ebenaceae family is a poisonous tropical plant which grows wild in Asia. Its extract is commonly known as fish poison. The rate of formation of NPs from plant extract is thought to be facile and rapid relative to those formed by fungi and bacteria, but it depends on the concentration of reducing chemicals available in the extract. We report, in this communication, a benign method of biogenic synthesis of cupric oxide nanoparticles (CuO-NPs) from leaf extract of D. montana and their characterization by UV–visible, FTIR, SEM, TEM, DLS, SAED and EDX analyses. Their antimicrobial activity against seven Gram-positive and four Gram-negative bacteria has been screened. Photocatalytic degradation of methylene blue by ascorbic acid as reducing agent and cupric oxide nanoparticles as catalyst has been done under sunlight. Results Cupric oxide nanoparticles of varying size starting from 5.9 to 21.8 nm have been fabricated from aqueous leaf extract of D. montana at room temperature. The pure extract absorbs at 273 nm while CuO-NPs exhibit a broad peak at 320 nm. FTIR spectrum of the leaf extract shows the presence of a double quinonoid molecule. There are three types of CuO-NPs with different hydrodynamic radii. Their average hydrodynamic radii fall between 495 ± 346 nm. SEM and TEM images show spherical shaped CuO-NPs of different size. SAED suggests crystalline nature of CuO-NPs. They are highly polydispersed in solution. EDX analysis reveals the presence of Ca, C, O, Na and Si besides copper. Oxygen content is over 50% by mass. Reduction of methylene blue dye (MB) by ascorbic acid as reducing agent, in presence of CuO-NPs as catalyst, has been achieved in 90 s at room temperature while their reduction by ascorbic acid alone takes more than 10 min. Antibacterial activity of CuO-NPs against seven Gram-positive (Staphylococcus aureus, Streptococcus mutans, Streptococcus pyogenes, Streptococcus viridans, Staphylococcus epidermidis, Corynebacterium xerosis and Bacillus cereus) and four Gram-negative bacterial strains (Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and Proteus vulgaris) has been investigated. The results indicated that NPs are highly effective against growth inhibition of Gram-positive bacteria than Gram-negative bacteria. Copper oxide nanoparticles are even more toxic than the standard antibiotic, norfloxacin. Conclusion In this project cupric oxide NPs of 5.9–21.8 nm have been fabricated from aqueous leaf extract of D. montana. It is most inexpensive and easy process to fabricate NPs from plant material because no toxic chemicals are used. Since CuO-NPs are toxic to several Gram-positive and Gram-negative bacterial strains, attempt may be made to use them as antibacterial agent to protect food, vegetable and crops. Also, the reduction of methylene blue dye by ascorbic acid as reducing agent in presence of CuO NPs as catalyst has been done very efficiently at a rapid rate which prompts us to use them as catalyst in the reduction of dyes, other toxic materials and industrial effluents. Further investigation of other beneficial properties of CuO-NPs can also be explored.


2019 ◽  
Vol 6 (2) ◽  
pp. 432-443
Author(s):  
J. Vassallo ◽  
K. Tatsi ◽  
R. Boden ◽  
R. D. Handy

This study looks at the potential for ingested nanomaterials dosed in soil, to become bioaccessible for human intestinal absorption.


2021 ◽  
Author(s):  
Chetan Kumar ◽  
Rajnesh Kumar Sharma

Abstract Present study was aimed to investigate the effect of temperature on the shape and size of nanoparticles and related cytotoxicity of these particles on ovarian granulosa cells. Cupric oxide nanoparticles (CuONPs) were synthesized using a simple, efficient, and reproducible precipitation method involving reduction of Cu metal salt with sodium hydroxide and then incubation of the precipitates at 70oC for 5 hrs. Subsequently, this prepared sample was divided into 3 subsamples and incubated at 3 different temperatures i.e. 70oC, 150oC, and 350oC for a time duration of 5 hrs. to study the effect of temperature on the particles. The products were characterized by XRD, FTIR, HRTEM, and FESEM. Characterization of the particles revealed that all particles were monoclinic crystalline in nature and had a size range from 9 nm - 60 nm. Particles were of different shapes; spherical, needle, and capsule. Toxicity of each particle was determined on granulosa cells by exposing them for 24 hrs. at 2 different doses. Toxicological results showed the size and shape-related toxicity of nanoparticles; particles which were spherical shape were significantly more toxic than capsule-shaped particles.


1997 ◽  
Vol 272 (13) ◽  
pp. 8836
Author(s):  
Etienne Decroly ◽  
Sandrine Wouters ◽  
Carlo Di Bello ◽  
Claude Lazure ◽  
Jean-Marie Ruysschaert ◽  
...  
Keyword(s):  

2021 ◽  
Vol 23 (Supplement_6) ◽  
pp. vi222-vi222
Author(s):  
Breanna Mann ◽  
Noah Bell ◽  
Denise Dunn ◽  
Scott Floyd ◽  
Shawn Hingtgen ◽  
...  

Abstract Brain cancers remain one of the greatest medical challenges. The lack of experimentally tractable models that recapitulate brain structure/function represents a major impediment. Platforms that enable functional testing in high-fidelity models are urgently needed to accelerate the identification and translation of therapies to improve outcomes for patients suffering from brain cancer. In vitro assays are often too simple and artificial while in vivo studies can be time-intensive and complicated. Our live, organotypic brain slice platform can be used to seed and grow brain cancer cell lines, allowing us to bridge the existing gap in models. These tumors can rapidly establish within the brain slice microenvironment, and morphologic features of the tumor can be seen within a short period of time. The growth, migration, and treatment dynamics of tumors seen on the slices recapitulate what is observed in vivo yet is missed by in vitro models. Additionally, the brain slice platform allows for the dual seeding of different cell lines to simulate characteristics of heterogeneous tumors. Furthermore, live brain slices with embedded tumor can be generated from tumor-bearing mice. This method allows us to quantify tumor burden more effectively and allows for treatment and retreatment of the slices to understand treatment response and resistance that may occur in vivo. This brain slice platform lays the groundwork for a new clinically relevant preclinical model which provides physiologically relevant answers in a short amount of time leading to an acceleration of therapeutic translation.


2021 ◽  
Author(s):  
◽  
Peter Barwell

<p>The cell kinetics and morphological changes during late ventral body wall development of the embryonic chick were studied, particularly midline degeneration and the medial migration of lateral tissues. An histological examination of these events was undertaken, along with autoradiography to determine the duration of the cell cycle, followed by teratological studies involving the prevention of differentiative events in the cell death pathway, using BrDU and Janus B Green as agents. The effects of cell cycle blockade on rates of cell death were also examined, as was the tissues ability to express differentiative features in vitro. Ventral body wall (VBW) cell death was classified as apoptosis, and was involved in two distinct events. Medial migration of lateral tissues began at day 5 of development, with widespread VBW apoptosis being seen by day 6, limited to the original mesoderm of the region. A later precise line of apoptosis (the VBL), involving both ectodermal cells of the midline ectodermal ruffle and the underlying mesodermal cells, was observed at day 7, spreading in a rostral to caudal fashion down the embryo, appearing as the migratory lateral tissues fused in the midline body wall. Increases in the amount of cell death are matched by decreases in the MI, such that at its peak (day 7.5 of development) the cell death rate is sufficiently greater than both the cell proliferation and immigration rates that a state of negative tissue growth ensues. The histological half-life of the apoptotic bodies approximates 3.8 hours. The ability to undergo apoptosis at day 7 is dependent upon a differentiative event around day 4 of incubation, and involves signal mechanisms intrinsic to the VBW tissues. BrDU application was found to inhibit apoptotic differentiation, in contrast to Janus B Green, which had a more generalised teratogenic effect on the region as a whole. Tissue culturing experiments revealed that an ectodermal-mesodermal interaction is important in regulating the extent of mesodermal apoptosis, the ectoderm playing a maintenance role for the mesoderm. Dead cells derive from the cycling cell population, as shown by the occurrence of labelled dead cells after autoradiography, and by the prevention of apoptosis by a cell cycle blockade, and by the production of a semi-synchronised wave of apoptoses after release of this blockade. These cell blockading results further suggest that entry into the apoptotic death program requires cells to be in a particular cell cycle stage, and it seems most likely that the decision to die was made in early G1. Tissue and cell growth rates, cell loss and death rates, cell birth rates and cell immigration rates were all determined for the VBW region throughout the time period studied.</p>


Sign in / Sign up

Export Citation Format

Share Document