scholarly journals A facile approach towards copper oxide nanoparticles synthesis using Spirulina platensis and assessment of its biological activities

2018 ◽  
Vol 5 (10) ◽  
pp. 433-442 ◽  
Author(s):  
Priyanga Jayakrishnan ◽  
Sirajunnisa Abdul Razack ◽  
Keerthana Sivanesan ◽  
Pavithra Sellaperumal ◽  
Geethalakshmi Ramakrishnan ◽  
...  
Keyword(s):  
Copper Oxide ◽  
Spirulina Platensis ◽  
Biological Activities ◽  
Nanoparticle Synthesis ◽  
Cuo Nanoparticles ◽  
Metal Nanoparticle ◽  
Anticancer Activities ◽  
Cytotoxicity Activity ◽  
Ft Ir ◽  
Cuo Nanoparticle

There is a budding need to develop a method for environmentally benign metal nanoparticle synthesis, that do not use toxic chemicals in the synthesis protocols to avoid adverse effects in medical applications. The present investigation dealt with the synthesis of copper oxide (CuO) nanoparticles from blue green alga, Spirulina platensis. The algal extract consisting of phytochemicals was used as the reducing agent and copper sulphate as the substrate. Synthesised nanoparticles were characterized by UV-Vis spectrophotometry, FT-IR spectroscopy, XRD and SEM. Antibacterial and anticancer activities were assessed for the CuO nanoparticles. The results indicated that the formed CuO nanoparticles were observed to be nanosheets. FT-IR spectral analysis elucidated the occurrence of biomolecules required for the reduction of copper oxide ions. The synthesized nanoparticles were found to be effective at the concentration of 1 mg/mL against Escherichia coli, Bacillus subtilis, Pseudomonas aeruginosa and Serratia marcescens. The cytotoxicity activity of CuO nanoparticle was evaluated by MTT Assay against colon cancer cell lines and confirmed that CuO nanoparticle at a concentration of 125 µg/mL had cytotoxic activity. In conclusion, the CuO nanoparticles were synthesized at a low energy supply, in an ecologically safe mode which could be utilized for pharmacological applications and various biotechnological studies.

Characterization and Anticancer Activities of Green Synthesized CuO Nanoparticles, A Review

2020 ◽  
Vol 20 ◽  
Author(s):  
Seyedeh R. Alizadeh ◽  
Mohammad A. Ebrahimzadeh
Keyword(s):  
Drug Delivery ◽  
Cancer Therapy ◽  
Copper Oxide ◽  
Medical Science ◽  
Copper Oxide Nanoparticles ◽  
Cuo Nanoparticles ◽  
Oxide Nanoparticles ◽  
Anticancer Activities

Background: Cancer is defined as an abnormal/uncontrolled cell growth that shows rapid cell division. This disease is annually recognized in more than ten million people. Nanomaterials can be used as new strategies for cancer therapy. Nanostructured devices have developed for drug delivery and controlled release and created novel anticancer chemotherapies. Nanomaterials were taken into consideration because of their new properties, containing a large specific surface area and high reactivity. Copper oxide nanoparticles (CuONPs) have potential applications in many fields like heterogeneous catalysis, antibacterial, anticancer, antioxidant, antifungal, antiviral, imaging agents, and drug delivery agents in biomedicine. CuONPs display different physical properties, such as hightemperature superconductivity, electron correlation effects, and spin dynamics. NPs can be synthesized using different methods like physical, chemical, and biological methods. Methods: Copper oxide nanoparticles (CuONPs) have been suggested for its broad usage in biomedical applications. In this review, we tried to exhibit the results of significant anticancer activity of green synthesized CuONPs and their characterization by different analytical techniques such as UV-Vis, FT-IR, XRD, EDAX, DLS, SEM, and TEM. Results: The green method for the synthesis of CuO nanoparticles as eco-friendly, cost-effective, and facile method is the more effective method. Synthesized CuONPs from this method have an appropriate size and shape. The Green synthesized CuONPs exhibited high potential against several breast cancer (AMJ-13, MCF-7, and HBL-100 cell lines), cervical cancer (HeLa), colon cancer (HCT-116), gastric cancer (human adenocarcinoma AGS cell line), lung cancer (A549), leukemia cancer, and other cancers with the main toxicity approach of increasing ROS production. Conclusion: The present review confirms the importance of green synthesized CuO nanoparticles in medical science especially cancer therapy that exhibited high activity against different cancer in both in vitro and in vivo. The main toxicity approach of CuONPs is increasing the production of reactive oxygen species (ROS). It needs to perform more studies about in vivo cancer therapy and following clinical trial testing in the future. We believe that green synthesized CuO nanoparticles can be used for the improvement of different diseases.

Electrospun Nanofibers Embedded with Copper Oxide Nanoparticles to Improve Antiviral Function

2021 ◽  
Vol 21 (8) ◽  
pp. 4174-4178
Author(s):  
Wen Ying Cui ◽  
Hyun Jin Yoo ◽  
Yun Guang Li ◽  
Changyoon Baek ◽  
Junhong Min
Keyword(s):  
Electron Microscopy ◽  
Copper Oxide ◽  
Oxygen Plasma ◽  
H1n1 Virus ◽  
Polymer Surface ◽  
Electrospun Nanofibers ◽  
Cuo Nanoparticles ◽  
Epidemic Spread ◽  
Antiviral Efficacy ◽  
Cuo Nanoparticle

Many studies on anti-bacterial/antiviral surfaces have been conducted to prevent epidemic spread worldwide. Several nanoparticles such as those composed of silver and copper are known to have antiviral properties. In this study, we developed copper oxide (CuO) nanoparticle-incorporated nanofibers to inactivate or remove viruses. The CuO nanoparticle-incorporated nanofiber was fabricated with a hydrophobic polymer—polyvinylpyrrolidone (PVP)—using electrospinning, and CuO nanoparticles were exposed from the PVP polymer surface by etching the nanofiber with oxygen plasma. The fabrication conditions of electrospinning and oxygen plasma etching were investigated by scanning electron microscopy (SEM), and field emission transmission electron microscopy (FETEM)/ energy dispersive spectrometry (EDS). H1N1 virus was utilized as the target sample and quantified by RT-qPCR. The antiviral efficacy of CuO nanoparticle-incorporated nanofibers was compared against bare CuO nanoparticles. Overall, 70% of the viruses were inactivated after CuO nanoparticle-incorporated nanofibers were incubated with 102 pfu/mL of H1N1 virus solution for 4 h. This indicates that the developed CuO nanoparticle-incorporated nanofibers have noticeable antiviral efficacy. As the developed CuO nanoparticle-incorporated nanofibers exerted promising antiviral effects against H1N1 virus, it is expected to benefit global health by preventing epidemic spread.

scholarly journals CuO NANOPARTICLES: SYNTHESIS, CHARACTERIZATION AND THEIR BACTERICIDAL EFFICACY

2017 ◽  
Vol 9 (6) ◽  
pp. 71 ◽  
Author(s):  
Manyasree D ◽  
Kiran Mayi Peddi ◽  
Ravikumar R
Keyword(s):  
Staphylococcus Aureus ◽  
Antibacterial Activity ◽  
Copper Oxide ◽  
Cuo Nanoparticles ◽  
Proteus Vulgaris ◽  
X Ray Diffraction ◽  
Gram Positive ◽  
Gram Negative ◽  
X Ray ◽  
Ft Ir

Objective: In the present study copper oxide (CuO) nanoparticles were synthesized and characterized. The antibacterial activity of CuO nanoparticles was carried out against Escherichia coli, Proteus vulgaris, Staphylococcus aureus and Streptococcus mutans.Methods: The synthesis was carried out by coprecipitation method using copper sulfate and sodium hydroxide as precursors. The synthesized copper oxide nanoparticles were characterized by using X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FT-IR), UV-vis spectroscopy and scanning electron microscope (SEM) with Energy Dispersive X-ray Analysis (EDX) techniques. Besides, this study determines the antibacterial activity and minimum inhibitory concentration (MIC) of CuO nanoparticles against gram-positive (Staphylococcus aureus and Streptococcus mutans) and gram-negative (E. coli and Proteus vulgaris) bacteria.Results: The average crystallite size of CuO nanoparticles was found to be 19 nm by X-ray diffraction. FT-IR spectrum exhibited vibrational modes at 432 cm-1, 511 cm-1 and 611 cm-1were assigned for Cu-O stretching vibration. According to UV-Vis spectrum, two bands were observed at 402 nm and 422 nm. ED’s spectrum shows only elemental copper (Cu) and oxide (O) and no other elemental impurity was observed. The antimicrobial assay revealed that Proteus vulgaris showed a maximum zone of inhibition (37 mm) at 50 mg/ml concentration of CuO nanoparticles.Conclusion: In conclusion, copper oxide is a good antibacterial agent against both gram positive and gram-negative organisms.

scholarly journals Anti-inflammatory and Antimicrobial Potential of Cissus quadrangularis-Assisted Copper Oxide Nanoparticles

2021 ◽  
Vol 2021 ◽  
pp. 1-11
Author(s):  
S. Rajeshkumar ◽  
Soumya Menon ◽  
Venkat Kumar S ◽  
M. Ponnanikajamideen ◽  
Daoud Ali ◽  
...  
Keyword(s):  
Copper Oxide ◽  
Biomedical Applications ◽  
Nanoparticle Synthesis ◽  
Copper Oxide Nanoparticles ◽  
Oxide Nanoparticles ◽  
X Ray Diffraction ◽  
Atomic Force ◽  
Cissus Quadrangularis ◽  
Ft Ir ◽  
Anti Inflammatory

Recently, nontoxic origin-mediated synthesis of copper oxide nanoparticles acquires further recognition because of the key role of bioapplications. The plant Cissus quadrangularis is one most prominent herbs used in the treatment of diabetes, asthma, tissue regeneration, etc. In this study, we tested the process of copper oxide nanoparticle synthesis and their role in many functions from Cissus quadrangularis. The synthesis of copper oxide nanoparticles uses plant extract and characterization by X-ray diffraction, thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FT-IR), atomic force microscope (AFM), and scanning electron microscope (SEM). The synthesized nanoparticles were analyzed for their biomedical applications such as antibacterial, antifungal, antioxidant, antidiabetic, and anti-inflammatory activity and antiproteinase action. The results show that the C. quadrangularis plant-mediated nanoparticles may be used in many biomedical applications related to arthritis, diabetes, and the production of various antimicrobial products in the future.

scholarly journals Green Synthesis of Copper Oxide Nanoparticles from Magnolia Champaca Floral Extract and its Antioxidant & Toxicity Assay using Danio Rerio

2020 ◽  
Vol 8 (5) ◽  
pp. 5444-5449 ◽  
Keyword(s):  
Copper Oxide ◽  
Visible Spectrum ◽  
Spherical Shape ◽  
Copper Oxide Nanoparticles ◽  
Cuo Nanoparticles ◽  
Physiochemical Properties ◽  
Analytical Strategies ◽  
Ft Ir ◽  
Ir Analysis ◽  
Uv Visible

The biosynthesis of copper oxide (GS-CuO) nanoparticles utilizing Magnolia champaca floral extract was studied, where the Magnolia champaca was used for the reduction of precurosor to elemental CuO nanopartciles which also provides stabilization. Physiochemical properties of GS-CuO nanoparticles were described utilizing analytical strategies like UV-Vis, XRD, FT-IR, SEM, TEM, Zeta potential and DLS analysis. The UV-Visible spectrum gave maximum absorbance in the scale of 250-350 nm. The biosynthesized GS-CuO was crystallite in nature and it was investigated by XRD and was verified with JCPDS NO: 89-589. FT-IR analysis spectrum at 3302 cm-1 is assigned for alcoholic hydroxide group, 1022 cm-1 correspondings to CH3 shaking vibration respectively. The morphology of biosynthesized nanoparticles was between 20 to 40 nm and spherical shape was investigated utilizing TEM. The antoxidant potentiality of GS-CuO was evaluated by DPPH, ABST test, that demonstrated inhibition values at 76.30% and 66.46% respectively. Toxicity quality examination was performed utilizing morphological investigation, incubating, and viability rate examination on zebrafish embryonic model. The toxicity quality assessment with zebrafish uncovered organ advancement with various viability and hatching speed at 48 and 72 hpf with LC50 of 500 ± 15 mg/L.

scholarly journals Comparing study of CuO synthesized by biological and electrochemical methods for biological activity

2019 ◽  
Vol 30 (1) ◽  
pp. 94 ◽  
Author(s):  
Shaimaa Hamed Jaber
Keyword(s):  
Electron Microscopy ◽  
Copper Oxide ◽  
Electrochemical Method ◽  
Cuo Nanoparticles ◽  
Biological Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Average Size ◽  
Cuo Nanoparticle

In the present work, copper oxide (CuO) nanoparticles have been synthesized by two methods (electro chemical and biological method).The synthesized nanoparticles characterized by x-ray diffraction (XRD), Scanning Electron Microscopy(SEM) and transmission Electron Microscopy(TEM). results show that to copper oxide (CuO) nanoparticle have average size of (11-15)nm of electrochemical method and (6-12 ) nm of biological method by different technique CuO nanoparticles were applied to study the inhibition of bacterial using (staphylococcus and pseudomonas). The antibacterial activity of CuO nanoparticles show a higher inhibition of pseudomonas bacteria when a compared with staphylococcus bacteria.

Structure and Activity of Pentacyclic Triterpenes Codrugs. A Review

2021 ◽  
Vol 21 ◽  
Author(s):  
Justyna Żwawiak ◽  
Anna Pawełczyk ◽  
Dorota Olender ◽  
Lucjusz Zaprutko
Keyword(s):  
Biological Activities ◽  
Anticancer Activities ◽  
Drug Molecule ◽  
Pentacyclic Triterpene ◽  
Formation Pathway ◽  
Chemical Systems ◽  
Drug Molecules ◽  
Wide Range ◽  
Anti Hiv ◽  
Structure And Activity

: Triterpenes are a wide and important group of compounds that have several promising pharmacological properties, such as hepatoprotective, anti-inflammatory, anti-HIV, antioxidant, or anticancer activities. Such potent substances can be successfully incorporated in more complex chemical systems e.g. codrugs or pro-drugs that have better pharmacological profile. The codrug is connected with a drug formation pathway to chemically cohere at least two drug molecules to improve positive therapeutic efficiency or decrease side effects. The codrug can be cleaved in the organism to generate effective compounds previously used as substrates. This article presents an overview of codrugs that consist of pentacyclic triterpene moiety that is chosen as a basic codrug moiety due to their wide range of vital activities and another drug molecule fragment. It was found that triterpenoid codrugs are characterized by a wide range of biological activities. However, most of them have anticancer potency.

Synthesis of New α-Amino Phosphonates Containing 3-Amino-4(3H) Quinazolinone Moiety as Anticancer and Antimicrobial Agents: DFT, NBO, and Vibrational Studies

2018 ◽  
Vol 15 (2) ◽  
pp. 286-296 ◽  
Author(s):  
Mohamed K. Awad ◽  
Mahmoud F. Abdel-Aal ◽  
Faten M. Atlam ◽  
Hend A. Hekal
Keyword(s):  
Biological Activity ◽  
Cell Line ◽  
Quantum Chemical ◽  
Density Functional ◽  
Carcinoma Cell ◽  
Liver Carcinoma ◽  
Anticancer Activities ◽  
Functional Theory ◽  
Ft Ir ◽  
Good Agreement

Aim and Objective: Synthesis of new .-aminophosphonates containing quinazoline moiety through Kabachnik-Fields reaction in the presence of copper triflate catalyst [32], followed by studying their antimicrobial activities and in vitro anticancer activities against liver carcinoma cell line (HepG2) with the hope that new anticancer agents could be developed. Also, the quantum chemical calculations are performed using density functional theory (DFT) to study the effect of the changes of molecular and electronic structures on the biological activity of the investigated compounds. Materials and Method: The structures of the synthesized compounds are confirmed by FT-IR, 1H NMR, 13C NMR, 31P NMR and MS spectral data. The synthesized compounds show significant antimicrobial and also remarkable cytotoxicity anticancer activities against liver carcinoma cell line (HepG2). Density functional theory (DFT) was performed to study the effect of the molecular and electronic structure changes on the biological activity. Results: It was found that the electronic structure of the substituents affects on the reaction yield. The electron withdrawing substituent, NO2 group 3b, on the aromatic aldehydes gave a good yield more than the electron donating substituent, OH group 3c. The electron deficient on the carbon atom of the aldehydic group may increase the interaction of the Lewis acid (Cu(OTf)2) and the Lewis base (imine nitrogen), and accordingly, facilitate the formation of imine easily, which is attacked by the nucleophilic phosphite species to give the α- aminophosphonates. Conclusion: The newly synthesized compounds exhibit a remarkable inhibition of the growth of Grampositive, Gram-negative bacteria and fungi at low concentrations. The cytotoxicity of the synthesized compounds showed a significant cytotoxicity against the liver cancer cell line (HepG 2). Also, it was shown from the quantum chemical calculations that the electron-withdrawing substituent increases the biological activity of the α-aminophosphonates more than the electron donating group which was in a good agreement with the experimental results. Also, a good agreement between the experimental FT-IR and the calculated one was found.

scholarly journals Plant-Derived Nano and Microvesicles for Human Health and Therapeutic Potential in Nanomedicine

Pharmaceutics ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 498
Author(s):  
Mariaevelina Alfieri ◽  
Antonietta Leone ◽  
Alfredo Ambrosone
Keyword(s):  
Therapeutic Potential ◽  
Biological Activities ◽  
Plant Biotechnology ◽  
Bioactive Metabolites ◽  
Anticancer Activities ◽  
Long Distance ◽  
In Vivo Models ◽  
Therapeutic Tools

Plants produce different types of nano and micro-sized vesicles. Observed for the first time in the 60s, plant nano and microvesicles (PDVs) and their biological role have been inexplicably under investigated for a long time. Proteomic and metabolomic approaches revealed that PDVs carry numerous proteins with antifungal and antimicrobial activity, as well as bioactive metabolites with high pharmaceutical interest. PDVs have also been shown to be also involved in the intercellular transfer of small non-coding RNAs such as microRNAs, suggesting fascinating mechanisms of long-distance gene regulation and horizontal transfer of regulatory RNAs and inter-kingdom communications. High loading capacity, intrinsic biological activities, biocompatibility, and easy permeabilization in cell compartments make plant-derived vesicles excellent natural or bioengineered nanotools for biomedical applications. Growing evidence indicates that PDVs may exert anti-inflammatory, anti-oxidant, and anticancer activities in different in vitro and in vivo models. In addition, clinical trials are currently in progress to test the effectiveness of plant EVs in reducing insulin resistance and in preventing side effects of chemotherapy treatments. In this review, we concisely introduce PDVs, discuss shortly their most important biological and physiological roles in plants and provide clues on the use and the bioengineering of plant nano and microvesicles to develop innovative therapeutic tools in nanomedicine, able to encompass the current drawbacks in the delivery systems in nutraceutical and pharmaceutical technology. Finally, we predict that the advent of intense research efforts on PDVs may disclose new frontiers in plant biotechnology applied to nanomedicine.

Synthesis and characterization of a new series of thiadiazole derivatives as potential anticancer agents

2020 ◽  
Vol 26 (1) ◽  
pp. 6-13 ◽  
Author(s):  
Ulviye Acar Çevik ◽  
Derya Osmaniye ◽  
Serkan Levent ◽  
Begüm Nurpelin Sağlik ◽  
Betül Kaya Çavuşoğlu ◽  
...  
Keyword(s):  
Anticancer Agents ◽  
Biological Activities ◽  
Cancer Cell Line ◽  
Chemotherapeutic Agents ◽  
Anticancer Activities ◽  
Normal Tissues ◽  
H Nmr ◽  
Wide Range ◽  
Thiadiazole Derivatives ◽  
Low Efficiency

AbstractCancer is one of the most common causes of death in the world. Despite the importance of combating cancer in healthcare systems and research centers, toxicity in normal tissues and the low efficiency of anticancer drugs are major problems in chemotherapy. Nowadays the aim of many medical research projects is to discover new safer and more effective anticancer agents. 1,3,4-Thiadiazole compounds are important fragments in medicinal chemistry because of their wide range of biological activities, including anticancer activities. The aim of this study was to determine the capacity of newly synthesized 1,3,4-thiadiazole compounds as chemotherapeutic agents. The structures of the obtained compounds were elucidated using 1H-NMR, 13C-NMR and mass spectrometry. Although the thiadiazole derivatives did not prove to be significantly cytotoxic to the tumour tissue cultures, compound 4i showed activity against the C6 rat brain cancer cell line (IC50 0.097 mM) at the tested concentrations.

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