Laser Science and Technology
Asraa B. Radhi; Khawla S. Khashan; Ghassan M. Sulaiman; Hamdoon A. Mohammed
Abstract
In this work, room temperature laser ablation with an iron target in water was used to create iron oxide nanoparticles (IONPs) with a different number of pulses (100, 200, 300, 400 and 500) at a constant energy of 200 mJ. The colloidal solutions of the IONPs were studied and the effects of the number ...
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In this work, room temperature laser ablation with an iron target in water was used to create iron oxide nanoparticles (IONPs) with a different number of pulses (100, 200, 300, 400 and 500) at a constant energy of 200 mJ. The colloidal solutions of the IONPs were studied and the effects of the number of pulses on the properties were investigated by Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), ultraviolet-visible spectroscopy (UV-VIS) and photoluminescence (PL). The FTIR spectra showed that the synthesised IONPs were formed, and the peaks appeared between (500-600) cm-1. FESEM images showed that the IONPs have hemispherical structures and become spherical with increasing laser pulses. They also exhibited a small aggregation due to electrostatic forces. The UV-VIS results showed that the IONPs had an absorption shoulder at 300-400 nm, which increased with the laser pulses. The PL spectra of the IONPs showed strong, sharp peaks in the UV region at 370 nm, the intensity of which increased with increasing pulse duration, while the density of the nanoparticles in the solution increased. In addition, the antibacterial activities were evaluated using an agar well diffusion assay against Pseudomonas aeruginosa (P. aeruginosa), Staphylococcus aureus (S. aureus), Streptococcus mutans (S. mutans) and Acinetobacter baumannii (A. baumannii). The result showed that the IONPs have good antibacterial activity, which increased with the laser pulses due to the increased concentration of IONPs. A hemolysis and in vitro toxicity test also evaluated the compatibility with human blood on red blood cells.
Laser Science and Technology
Mayyadah H. Mohsin; Khawla S. Khashan; Ghassan M. Sulaiman; Khalil A. A. Khalil
Abstract
A technique for exfoliating Boron nitride (BN) nanosheets was devised, which was then followed by a laser ablation-fragmentation process to produce lamellar hexagonal Boron nitride nanostructures (h-BNNs). The physicochemical properties of the nanoparticles were analysed to investigate the effect of ...
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A technique for exfoliating Boron nitride (BN) nanosheets was devised, which was then followed by a laser ablation-fragmentation process to produce lamellar hexagonal Boron nitride nanostructures (h-BNNs). The physicochemical properties of the nanoparticles were analysed to investigate the effect of laser energy and wavelength in the two-step pre-treatment procedure during BN synthesis. The X-ray diffraction (XRD) patterns showed no impurity phase structures, and only primary h-BN reflections were visible. It was discovered that the crystallite h-BNNs size ranged from 11 to 18 nm, and nanosecond laser energy was sufficient to transform BN into h-BNNs and a few nanotubes. Combining laser intensity and wavelength transformed the BN nanoparticle shape from haphazardly arranged platelets to melting-like formations. Fourier Transform infrared (FTIR) spectroscopy confirmed distinct observed changes in the size and melting behaviour in the h-BNNs and the sharp absorption peaks, which could indicate changes in their optical properties. Morphological characteristics and formation of the hexagonal phase of BN caused variations in optical properties and high-resolution transmission electron microscopy (HRTEM) results. Photoluminescence of h-BNNs was observed in the 250–600 nm range with peak emission at 485 nm. Due to its significant structural disorder, the h-BNNs exhibited a wide emission with a strong luminescence that remained largely continuous after 48 hours, resulting in a distinctive blue hue (470 and 485nm).
Biotechnology
Zainab S. Abbas; Ghassan M. Sulaiman; Majid S. Jabir; Hamdoon A. Mohammed; Salman A. A. Mohammed
Abstract
Galangin, a non-toxic phytochemical, is known to have a variety of therapeutic uses. This study looked into the role of inclusion complexes of galangin/β-cyclodextrin in increasing antioxidant activity over pure galangin. The role of this inclusion complex in increasing antioxidant activity in comparison ...
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Galangin, a non-toxic phytochemical, is known to have a variety of therapeutic uses. This study looked into the role of inclusion complexes of galangin/β-cyclodextrin in increasing antioxidant activity over pure galangin. The role of this inclusion complex in increasing antioxidant activity in comparison to pure galangin. In this study, hydrogen peroxide assays were used in vitro. Galangin demonstrated concentration-dependent scavenging action in the 2-50 µg mL-1 range, with the highest level of activity possible 92.00% at 50 µg mL-1. In pure galangin, a decrease of 85.00% was observed. The ferric thiocyanate lipoperoxidation method was clarified by using galangin and galangin/β-cyclodextrin and demonstrated concentration-dependent suppress lipid peroxidation in the 2-50 µg mL-1 range, at 50 µg mL-1, the highest level of activity was 70.00%. A 60.00% decrease in pure galangin was observed. Xanthine oxidase activity using uric acid was given. The co-incubation of galangin and galangin/β-cyclodextrin inhibited xanthine oxidase activity in a concentration-dependent manner in 2-50 µg mL-1 range, at 50 µg mL-1, the highest level of activity was 90.00%. Pure galangin showed an 82.00% decrease. There were no significant differences in absolute weight of mice organs and hematological parameters between pure galangin and galangin/ β-cyclodextrin when used concentration 80 mg kg-1, compared to control group. According to the findings, galangin combined with β-cyclodextrin has excellent properties as a therapeutic agent and food supplement.
Biotechnology
Zahraa A. Kadhim; Ghassan M. Sulaiman; Ahmed M. Al-Shammari; Hamdoon A. Mohammed; Salman A. A. Mohammed
Abstract
Glioblastoma multiforme (GBM) is one of the most life-threatening types of cancer that is difficult to treat. The search for effective yet safe therapy is progressing and non-conventional therapies such as using viruses as a smart and selective agent against cancer are promising. The aim of the study ...
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Glioblastoma multiforme (GBM) is one of the most life-threatening types of cancer that is difficult to treat. The search for effective yet safe therapy is progressing and non-conventional therapies such as using viruses as a smart and selective agent against cancer are promising. The aim of the study was the presence of a reliable method to use Newcastle disease virus (NDV) as an oncolytic agent against GBM, which attempted to propagate the NDV in laboratory experiments. Ahmed Majeed Hamza Al-Shammari-1 (AMHA1) attenuated strain of NDV was propagated in chicken embryos. The virus's tittered in Vero-slamed cells to determine the infective dose. MTT cell viability assay was used to investigate the killing effects of NDV on Ahmed-Majeed-Glioblastoma-Multiforme-2005 (AMGM5) human glioblastoma cancer cells derived from Iraqi patients. The infected cells' morphology was studied to measure the cytolytic effect of the NDV in cancer cells. Results showed that After 24 to 72 hours of inoculation, all of the chicken embryos died when the AMHA1 Iraqi NDV strain was injected. Cell viability assay showed that the NDV-AMHA1 strain has cytotoxicity at MOI of 0.1, 0.5, and 1 for 72 hours of exposure to cancer cells. The morphological analysis showed that NDV induces cell death in the infected cells with both necrotic and apoptotic features. In conclusion, the study focuses on the propagation of the oncolytic NDV as a biological agent capable of overcoming treatment resistance through infecting and replicating inside cancer.
Biotechnology
Ali A. Al-Jubori; Ghassan M. Sulaiman; Amer T. Tawfeeq
Abstract
Resveratrol (RES) is a bioactive molecule with potent antioxidant properties, and it constitutes an essential component of herbal medicine. This study was designed to use a nano-syntheses approach to encapsulate RES in Poloxamer 407 nanoparticles. This type of nano-construction has been employed in a ...
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Resveratrol (RES) is a bioactive molecule with potent antioxidant properties, and it constitutes an essential component of herbal medicine. This study was designed to use a nano-syntheses approach to encapsulate RES in Poloxamer 407 nanoparticles. This type of nano-construction has been employed in a variety of biological applications, both in vitro and in vivo. The contribution of this nano-construct is to increase antioxidant activity over the pure RES was investigate. 1,1-diphenyl-2-picryl hydrazyl (DPPH), and hydrogen peroxide radical scavenging assays were utilized in vitro. RES-loaded poloxamer 407 showed concentration-dependent scavenging action in the range of 20-80 µg.ml-1, with a maximum activity of 80.1% at 80 µg.ml-1. Whereas pure RES had a decrement of 61.7%. While the activity of positive control (Vit. C) was 93.2%. The magnitude of blood hemolysis examination was 3.9% at 80 µg.ml-1. That may indicate RES-loaded poloxamer 407 provide significant red blood cell protection. The pure RES did not prevent the appearance of abnormal cells (echinocytes), and that was cured by RES-loaded poloxamer 407. Finally, the safety of RES-loaded poloxamer 407 was assessed in vivo. Male mice were invested to detect the functions of their liver and kidney. A histopathological study was included as well. The findings showed that RES-loaded poloxamer 407 might have superior characters as a drug delivery system, nutritional supplements, and may be used in pharmaceutical products.
