Microbicidal activity of TiO2 nanoparticles synthesised by sol–gel method

In this study, the authors investigated antimicrobial activity of TiO₂ nanoparticles (NPs) synthesised by sol–gel method. As synthesised TiO₂ NPs were characterised by X‐ray diffraction, scanning electron microscopy and ultraviolet‐visible absorption spectroscopy. The antimicrobial activity of calcined TiO₂ nanoparticle samples was examined in day light on Gram positive bacteria (Staphylococcus aureus, Streptococcus pneumonia and Bacillus subtilis), Gram negative bacteria (Proteus vulgaris, Pseudomonas aeruginosa and Escherichia coli) and fungal test pathogen Candida albicans. The synthesised TiO₂ NPs were found to be effective in visible light against Streptococcus pneumonia, Staphylococcus aureus, Proteus vulgaris, Pseudomonas aeruginosa and Candida albicans.Inspec keywords: titanium compounds, microorganisms, nanomedicine, biomedical materials, nanofabrication, sol‐gel processing, ultraviolet spectra, visible spectra, X‐ray diffraction, scanning electron microscopy, nanoparticles, antibacterial activityOther keywords: microbicidal activity, titanium dioxide nanoparticle, sol‐gel method, antimicrobial activity, X‐ray diffraction, scanning electron microscopy, ultraviolet‐visible absorption spectroscopy, Gram positive bacteria, Staphylococcus aureus, Streptococcus pneumonia, Bacillus subtilis, TiO₂ , Candida albicans, fungal test pathogen, Escherichia coli, Pseudomonas aeruginosa, Proteus vulgaris, Gram negative bacteria     

Functionalisation of Fe3 O4 nanoparticles by 2‐((pyrazol‐4‐yl) methylene) hydrazinecarbothioamide enhances the apoptosis of human breast cancer MCF‐7 cells

Cancer is a major cause of death. Thus, the incidence and mortality rate of cancer is globally important. Regarding vast problems caused by chemotherapy drugs, efforts have progressed to find new anti‐cancer drugs. Pyrazole derivatives are known as components with anti‐cancer properties. In here, Fe₃ O₄ nanoparticles were first functionalized with (3‐chloropropyl) trimethoxysilane, then 2‐((pyrazol‐4‐yl) methylene) hydrazinecarbothioamide (P) was anchored on the surface of magnetic nanoparticles (PL). The synthesized nano‐compounds were characterized using Fourier transform infrared spectroscopy, X‐ray diffraction, scanning electron microscopy, Zeta potential, dynamic light scattering, and energy‐dispersive x‐ray spectrometry analyses. The cytotoxicity effect was evaluated using MTT assay, apoptosis test by Flow cytometry, cell cycle analysis, Caspase‐3 activity assay and Hoechst staining on MCF‐7 cell line. The high toxicity for tumor cells and low toxicity on normal cells (MCF10A) was considered as an important feature (selectivity index, 10.9). Based on results, the IC50 for P and PL compounds were 157.80 and 131.84 μM/ml respectively. Moreover, apoptosis inducing, nuclear fragmentation, Caspase 3 activity and induction of cell rest in sub‐G1 and S phases, were also observed. The inhibitory effect of PL was significantly higher than P, which could be due to the high penetrability of Fe₃ O₄ nanoparticles.Inspec keywords: magnetic particles, drugs, nanomedicine, biochemistry, cancer, light scattering, scanning electron microscopy, molecular biophysics, iron compounds, electrokinetic effects, nanofabrication, tumours, X‐ray diffraction, cellular biophysics, nanoparticles, biomedical materials, toxicology, nanomagnetics, Fourier transform infrared spectra, enzymes, X‐ray chemical analysisOther keywords: anticancer properties, Fe₃ O₄ magnetic nanoparticles, (3‐chloropropyl) trimethoxysilane, energy‐dispersive X‐ray spectrometry, cell cycle analysis, MCF‐7 cell line, tumour cells, human breast cancer MCF‐7 cells, mortality rate, pyrazole derivatives, 2‐((pyrazol‐4‐yl) methylene) hydrazinecarbothioamide, chemotherapy drugs, heterocyclic components, nanocompounds, X‐ray diffraction, scanning electron microscopy, Zeta potential, dynamic light scattering, cytotoxicity effect, MTT assay, apoptosis test, caspase‐3 activity assay, Hoechst staining, MCF10A nontumourigenic cells, cell rest induction, nuclear fragmentation, Fe₃ O₄      

Biosynthesis of zinc oxide nanoparticles using anjbar (root of Persicaria bistorta) extract and their cytotoxic effects on human breast cancer cell line (MCF‐7)

Biosynthesis of nanoparticles (NPs) using biomass is now one of the best methods for synthesising NPs due to their nontoxic and biocompatibility. Plants are the best choice among all biomass to synthesise large‐scale NPs. The objectives of this study were to synthesise zinc oxide nanoparticles (ZnO‐NPs) using Anjbar (root of Persicaria bistorta) [An/ZnO‐NPs] and investigate the cytotoxic and anti‐oxidant effects. For this purpose, the An/ZnO‐NPs were synthesised by using Bistort extract and characterised using UV–Visible spectroscopy, transmission electron microscope, field emission scanning electron microscope, x‐ray diffraction and Fourier‐transform infrared spectroscopy. The cytotoxic effects of the An/ZnO‐NPs on MCF‐7 cells were followed by 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide assays at 24, 48, and 72 h. Nuclear morphology changed and apoptosis in cells was investigated using acridine orange/propodium iodide (AO/PI) staining and flow cytometry analysis. The pure biosynthesised ZnO‐NPs were spherical in shape and particles sizes ranged from 1 to 50 nm. Treated MCF‐7 cells with different concentrations of ZnO‐NPs inhibited cell viability in a time‐ and dose‐dependent manner with IC50 about 32 μg/ml after 48 h of incubation. In flow cytometry analysis the sub‐G1 population, which indicated apoptotic cells, increased from 12.6% at 0 μg/ml (control) to 92.8% at 60 μg/ml, 48 h after exposure. AO/PI staining showed that the treated cells displayed morphologic evidence of apoptosis, compared to untreated groups. Inspec keywords: cancer, cellular biophysics, toxicology, particle size, nanofabrication, X‐ray diffraction, nanomedicine, nanoparticles, ultraviolet spectra, scanning electron microscopy, visible spectra, transmission electron microscopy, patient treatment, field emission electron microscopy, Fourier transform infrared spectra, drug delivery systemsOther keywords: anjbar, cytotoxic effects, human breast cancer cell line, biomass, transmission electron microscope, field emission scanning electron microscope, Fourier‐transform infrared spectroscopy, flow cytometry analysis, ZnO‐NPs inhibited cell viability, antioxidant effects, MCF‐7 cells, biosynthesised ZnO‐NP, biosynthesised ZnO‐NP, acridine orange‐propodium iodide staining, An‐ZnO‐NP, Persicaria bistorta, zinc oxide nanoparticle biosynthesis, 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide     

CdO nanoparticles,c‐MWCNT nanoparticles and CdO nanoparticles/c‐MWCNT nanocomposite fibres: in vitro assessment of anti‐proliferative and apoptotic studies in HeLa cancer cell line

A simple ultrasonic assisted chemical technique was used to synthesise cadmium oxide (CdO) nanoparticles (NPs) and CdO NPs/c‐Multiwalled carbon nanotube (c‐MWCNT) nanocomposite fibres.To confirm the physio‐chemico properties and to analyse surface morphology of the obtained nanomaterials X‐Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and field emission scanning electron microscopy (FESEM) were performed. To evaluate the anti‐cancer property of CdO NPs, c‐MWCNT NPs and CdO NPs/c‐MWCNT nanocomposite fibres, an anti‐proliferative assay test (Methylthiazolyl diphenyl‐ tetrazolium bromide ‐ MTT assay) were performed on HeLa cells which further estimated IC50 value (Least concentration of sample in which nearly 50% of cells remain alive) under in‐vitro conditions. On comparison, CdONPs/c‐MWCNT based system was found to be superior by achieving 52.3% cell viability with its minimal IC50 value of 31.2 μg/ml. Lastly, the CdO NPs based system was taken up for an apoptotic study using DNA fragmentation assay for estimating its ability to cleave the DNA of the HeLa cells into internucleosomal fragments using the agarose gel electrophoresis method. In conclusion, based on our observations, CdO NPs/c‐MWCNT hybrid based system can be further used for the development of efficient drug delivery and therapeutic systems.Inspec keywords: drug delivery systems, electrophoresis, oxidation, toxicology, DNA, nanoparticles, drugs, field emission electron microscopy, scanning electron microscopy, nanofabrication, surface morphology, cancer, X‐ray diffraction, nanomedicine, cellular biophysics, filled polymers, biomedical materials, molecular biophysics, biochemistry, Fourier transform infrared spectra, multi‐wall carbon nanotubesOther keywords: c‐MWCNT nanoparticles, apoptotic study, HeLa cancer cell line, cadmium oxide nanoparticles, c‐MWCNT NPs, anti‐proliferative assay test [methyl thiazolyl diphenyl‐tetrazolium bromide assay], human epithelioid cervix carcinoma cells, live cells, CdO NP‐based system, IC50 concentration, HeLa cell line, cell deaths, CdO‐C     

Silver nanoparticles biosynthesised using Centella asiatica leaf extract: apoptosis induction in MCF‐7 breast cancer cell line

The aim of this study was to green synthesised silver nanoparticles (AgNPs) using Centella asiatica leaf extract and investigate the cytotoxic and apoptosis‐inducing effects of these nanoparticles in MCF‐7 breast cancer cell line. The characteristics and morphology of the green synthesised AgNPs were evaluated using transmission electron microscopy, scanning electron microscopy, UV–visible spectroscopy, X‐ray diffraction, and Fourier‐transform infrared spectroscopy. The MTT assay was used to investigate the anti‐proliferative activity of biosynthesised nanoparticles in MCF‐7 cells. Apoptosis test was performed using flow cytometry and expression of caspase 3 and 9 genes. The spherical AgNPs with an average size of 19.17 nm were synthesised. The results showed that biosynthesised AgNPs exhibited cytotoxicity, anti‐cancer, apoptosis induction, and increased expression of genes encoding for caspases 3 and 9 in MCF‐7 cancer cells in a concentration‐ and time‐dependent manner. It seems that green synthesised AgNPs have potential uses for pharmaceutical industries.Inspec keywords: ultraviolet spectra, transmission electron microscopy, cellular biophysics, infrared spectra, visible spectra, nanofabrication, cancer, toxicology, nanomedicine, nanoparticles, biomedical materials, scanning electron microscopy, silver, Fourier transform spectra, X‐ray diffraction, genetics, enzymes, botany, biochemistryOther keywords: spherical AgNPs, biosynthesised AgNPs, anti‐cancer, apoptosis induction, green synthesised AgNPs, MCF‐7 breast cancer cell line, green synthesised silver nanoparticles, Ag, caspase gene expression, flow cytometry, anti‐proliferative activity, MTT assay, pharmaceutical industries, cytotoxicity, UV–visible spectroscopy, nanoparticle morphology, scanning electron microscopy, Centella asiatica leaf extract, biosynthesised nanoparticles, Fourier‐transform infrared spectroscopy, transmission electron microscopy     

Synthesis,characterisation and potential biomedical applications of magnetic core–shell structures: carbon‐, dextran‐, SiO2 ‐ and ZnO‐coated Fe3 O4 nanoparticles

Due to the strong effect of nanoparticles'' size and surface properties on cellular uptake and bio‐distribution, the selection of coating material for magnetic core–shell nanoparticles (CSNPs) is very important. In this study, the effects of four different biocompatible coating materials on the physical properties of Fe₃ O₄ (magnetite) nanoparticles (NPs) for different biomedical applications are investigated and compared. In this regard, magnetite NPs are prepared by a simple co‐precipitation method. Then, CSNPs including Fe₃ O₄ as a core and carbon, dextran, ZnO (zincite) and SiO₂ (silica) as different shells are synthesised using simple one‐ or two‐step methods. A comprehensive study is carried out on the prepared samples using X‐ray diffraction, vibrating sample magnetometry, transmission electron microscopy and Fourier transform infrared spectroscopy analyses. According to the authors'' findings, it is suggested that carbon‐ and dextran‐coated magnetite NPs with high M _s have great potential in the application of magnetic resonance imaging contrast agents. Moreover, silica‐coated magnetite NPs with high coercivity are potentially suitable candidates for hyperthermia and ZnO‐coated Fe₃ O₄ is potentially suitable for photothermal therapy.Inspec keywords: iron compounds, carbon, silicon compounds, zinc compounds, nanomedicine, biomedical materials, nanofabrication, nanoparticles, magnetic particles, coatings, X‐ray diffraction, magnetometry, transmission electron microscopy, Fourier transform spectra, infrared spectra, biomedical MRI, hyperthermia, radiation therapyOther keywords: biomedical applications, magnetic core‐shell nanoparticles, CSNP, cellular uptake, biodistribution, coating material, biocompatible coating materials, co‐precipitation, dextran, zincite, silica, X‐ray diffraction, vibrating sample magnetometry, transmission electron microscopy, Fourier transform infrared spectroscopy, magnetic resonance imaging contrast agents, hyperthermia, photothermal therapy, SiO₂ ‐Fe₃ O₄ , ZnO‐Fe₃ O₄