In Vitro Bioactivity Study on ZnI2-HAp Nanoparticles

2020 ◽  
Vol 15 (4) ◽  
pp. 523-531
Author(s):  
Mohammad Y. Alshahrani ◽  
H. Algarni ◽  
Ibrahim AlShahrani ◽  
I. S. Yahia ◽  
H. Y. Zahran ◽  
...  
Keyword(s):  
Fourier Transform ◽  
Sol Gel ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
Mouse Splenocytes ◽  
Fourier Transform Raman Spectroscopy ◽  
Sol Gel Process ◽  
Splenic Cells ◽  
Ft Ir

The manufactured powder of immaculate HAp which is doped with 1.0, 5.0, 10, 20, 30, and 40 in wt.% ZnI2 has been prepared via the sol–gel process. The characterization of samples was achieved by X-ray diffraction (XRD), Fourier Transform Infrared spectroscopy (FT-IR) and Fourier Transform Raman spectroscopy (FT- Raman). The morphology of the obtained HAp powder was studied through SEM analysis. The investigation proves that all prepared samples have the dimension of a nanoscale. The prepared powders were examined for its anti-growth, stimulatory/cytotoxic potentials on normal/activated mouse splenocytes in vitro as well as the lytic effects on red blood cells (RBCs). Results showed that different preparations of ZnI2 had anti-growth effects on normal mouse splenocytes. The pure HAp, 1% and 10% ZnI2 showed no effects on stimulated mouse splenic cells while the other preparations 5%, 20%, 30% and 40% ZnI2 showed inhibitory/cytotoxic effects. All ZnI2 preparations showed safe effects on RBCs.

Hydroxyapatite Nanostructure Doped by Lithium Iodide with Their Biological Activity

2020 ◽  
Vol 15 (5) ◽  
pp. 613-619
Author(s):  
Mohammad Y. Alshahrani ◽  
H. Algarni ◽  
Ibrahim AlShahrani ◽  
I. S. Yahia ◽  
H. Y. Zahran ◽  
...  
Keyword(s):  
Radiation Treatment ◽  
Sol Gel ◽  
Dimensional Structure ◽  
X Ray Diffraction ◽  
Inhibitory Effects ◽  
Lithium Iodide ◽  
Sol Gel Process ◽  
Splenic Cells ◽  
Low Dimensional

The nanostructure of biomaterial samples of Hydroxyapatite (HAp) was treated by microwave radiation treatment with different additives (1, 10, 20, 30 and 40 wt. in percent) of Lithium Iodide (LiI) using the known sol–gel process. The sample crystal structure was achieved through the analysis of X-ray diffraction and some associated parameters like that strain, grain size, and dislocation. The FTIR and Raman spectroscopy investigations identified effective functional groups and their modes. SEM conforms to the sample morphology's fine low-dimensional structure (10–28 nm). The various preparations were studied for their anti-proliferative/anticytotoxicity/stimulatory ability against normal and activated splenic cells of the mouse in vitro and for the lytic effects on red blood cells (RBCs). Results showed that various LiI additives have inhibitory effects on normal splenic cells of the mouse. The pure LiI and Li 10 had relaxing effects on splenic cells activated by the mouse while the other formulations (LiI 20, LiI 30 and LiI 40) displayed inhibitory/cytotoxic results besides that all preparation samples were safe effects to RBCs.

Luminescent Properties of Zn2SiO4:Eu3+,Dy3+ Phosphors via Sol-Gel Process

2012 ◽  
Vol 217-219 ◽  
pp. 733-736
Author(s):  
Xiu Mei Han ◽  
Shu Ai Hao ◽  
Ying Ling Wang ◽  
Gui Fang Sun ◽  
Xi Wei Qi
Keyword(s):  
Thermal Analysis ◽  
Ir Spectra ◽  
Sol Gel ◽  
Luminescent Properties ◽  
Photoluminescence Spectra ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sol Gel Process ◽  
Ft Ir

Zn2SiO4:Eu3+, Dy3+ phosphors have been prepared through the sol-gel process. X-ray diffraction (XRD), thermogravimetric and ddifferential thermal analysis (TG-DTA), FT-IR spectra and photoluminescence spectra were used to characterize the resulting phosphors. The results of XRD indicated that the phosphors crystallized completely at 1000oC. In Zn2SiO4:Eu3+,Dy3+ phosphors, the Eu3+ and Dy3+ show their characteristic red(613nm, 5D0-7F2), blue (481nm, 4F9/2–6H15/2) and yellow (577nm, 4F9/2–6H13/2) emissions.

scholarly journals Bismuth(III) bromide-thioamide complexes: synthesis, characterization and cytotoxic properties

2018 ◽  
Vol 41 (5-6) ◽  
pp. 143-154 ◽  
Author(s):  
M. Cakmak ◽  
I.I. Ozturk ◽  
C.N. Banti ◽  
M. Manoli ◽  
E. Moushi ◽  
...  
Keyword(s):  
Fourier Transform ◽  
Fetal Lung ◽  
Molecular Structures ◽  
X Ray Diffraction ◽  
Vis Spectroscopy ◽  
Normal Human ◽  
Ft Ir ◽  
Human Fetal Lung ◽  
Heterocyclic Thioamides

Abstract New bismuth(III) bromine compounds of the heterocyclic thioamides were prepared and structurally characterized. The reaction of heterocyclic thioamides with bismuth(III) bromide resulted in the formation of the {[BiBr2(μ2-Br)(MMI)2]2·CH3COCH3·H2O} (1), {[BiBr2(MBZIM)4]·Br·2H2O} (2), {[BiBr2(μ2-Br)(tHPMT)2]2·CH3CN} (3), {[BiBr2(μ2-Br)(PYT)2]2·CH3CN} (4) and {[BiBr2(μ2-Br)(MBZT)2]2 2CH3OH} (5) complexes (MMI: 2-mercapto-1-methylimidazole, MBZIM: 2-mercaptobenzimidazole, tHPMT: 2-mercapto-3,4,5,6-tetrahydro-pyrimidine, PYT: 2-mercaptopyridine and MBZT: 2-mercaptobenzothiazole). The complexes 1–5 were characterized by melting point (m.p.), elemental analysis (e.a.), molar conductivity, Fourier-transform infrared (FT-IR), Fourier-transform Raman (FT-Raman), nuclear magnetic resonance (1H and 13CNMR) spectroscopy, UV-Vis spectroscopy and thermogravimetric-differential thermal analysis (TG-DTA). The molecular structures of 1–5 were determined by single-crystal X-ray diffraction. Complex 2 is a first ionic monomuclear octahedral bismuth(III) bromide, while the complexes 1, 3–5 are the first examples of dinuclear bismuth(III) bromide derivatives. Complexes 1–5 were evaluated in terms of their in vitro cytotoxic activity against human adenocarcinoma breast (MCF-7) and cervix (HeLa) cells. The toxicity on normal human fetal lung fibroblast cells (MRC-5) was also evaluated. Moreover, the complexes 1–5 and free heterocyclic thioamide ligands were studied upon the catalytic peroxidation of the linoleic acid by the enzyme lipoxygenase (LOX).

Influence of Li2+ Doping on the Structural and Optical Properties of CaO Synthesized by Sol–Gel Process

2019 ◽  
Vol 07 (01n02) ◽  
pp. 1950002
Author(s):  
Nadir Lalou ◽  
Ahmed Kadari
Keyword(s):  
Optical Properties ◽  
Band Gap ◽  
Sol Gel ◽  
Calcium Nitrate ◽  
Lithium Nitrate ◽  
X Ray Diffraction ◽  
Structural And Optical Properties ◽  
Sol Gel Process ◽  
Ft Ir ◽  
First Time

This work proposes the synthesis of nanocrystalline calcium oxide (CaO) pure and doped with different concentrations of lithium (Li[Formula: see text]) ions by sol–gel process. Calcium nitrate (Ca(NO[Formula: see text]4H2O; 99.99%) and lithium nitrate (LiNO3; 99.99%) were used as precursors. The synthesized powders were characterized by several techniques such as: UV-Vis transmission spectroscopy, Fourier Transform Infra-red spectroscopy (FT-IR) and X-ray diffraction (XRD). The main objective of this paper is to study the influence of lithium (Li[Formula: see text] ratio) on the structural and optical properties of synthesized powders. The band gap values decreased with the increasing of Li[Formula: see text] ions in CaO lattice; the slight change in the band gap was directly related to the energy transfer between the CaO excited states and the 2s levels of Li[Formula: see text] ions. The influence of Li[Formula: see text] doping on the physical properties of CaO nanocrystalline will be studied for the first time in this work; no literature has previously published this kind of impurities.

Synthesis of V2O5 Powders by EDTA Assistance Ultrasound Sol-Gel Process

2012 ◽  
Vol 512-515 ◽  
pp. 207-210
Author(s):  
Quan Wen ◽  
Jian Feng Huang ◽  
Li Yun Cao ◽  
Jian Peng Wu
Keyword(s):  
Activation Energy ◽  
Raw Materials ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Calcination Temperatures ◽  
Sol Gel Process ◽  
Ft Ir ◽  
Precursor Powders ◽  
Influence Of Ph

V2O5 powders were successfully synthesized by the EDTA assistanced ultrasound sol-gel process using NH4VO3 and EDTA, NH3•H2O as raw materials. The synthesized activation energy and the influence of pH values and the calcination temperatures on the phases and microstructures of powders were particularly investigated. The precursor powders and the V2O5 powders were characterized by X-ray diffraction (XRD), fourier transform inelectron microscopy (FT-IR), scanning electron microscopy (SEM) and differential scanning calorimetry-thermal gravimetric (DSC-TG). Results show that the obtained products exhibit good crystallization under the conditions of pH=4, calcination temperature 400~500 °C and calcination time 0.5 h during the synthesizing process. The as-prepared V2O5 powders show preferred growth orientation along (001) plane at the pH=4. By DSC analysis, the ultrasonic cavitation result in the decrease in synthesized activation energy obviously than that was prepared without ultrasonic irradiation.

Apatite Formation on PDMS-Modified SiO2-CaO-P2O5 Hybrids Prepared with Different P2O5 Content by Sol-Gel Method

2004 ◽  
Vol 449-452 ◽  
pp. 1121-1124 ◽  
Author(s):  
Do Won Seo ◽  
J.G. Kim ◽  
Yun Hae Kim ◽  
Chin Myung Whang
Keyword(s):  
Sol Gel ◽  
Calcium Nitrate ◽  
Apatite Formation ◽  
Calcium Nitrate Tetrahydrate ◽  
X Ray Diffraction ◽  
Phosphate Ions ◽  
P2o5 Content ◽  
Sol Gel Process ◽  
Nitrate Tetrahydrate

Bioactive ORMOSILS (organically modified silicate), PDMS-CaO-SiO2-P2O5 with five different P2O5 content (0, 0.01, 0.03, 0.06, 0.09 mol%) have successfully been synthesized by sol-gel process. The hybrids have been prepared with polydimethylsiloxane (PDMS), tetraethoxysilane (TEOS), calcium nitrate tetrahydrate [Ca(NO3)2 4H2O] and triethyl phosphate (TEP) as starting materials and subsequently soaked into the simulated body fluid (SBF) for different period of time and the bioactivity of hybrids was determined by examining the apatite formation on the surface of the specimen by FT-IR, Thin-Film X-ray Diffraction, and Scanning Electron Microscopy (SEM). All of the prepared samples with different P2O5 content showed in vitro bioactivity. It was observed that the increase in P2O5 content up to 0.03 mole % increases the apatite formation compared to P2O5- free hybrids. However, further increase in P2O5 concentration slows down the formation of the apatite layer most probably due to the decrease of pH of SBF by dissolution of a large amount of phosphate ions.

Synthesis and Characterization of Siloxane-Polyurethane Hybrid Materials

2008 ◽  
Vol 396-398 ◽  
pp. 481-484
Author(s):  
Rodrigo Jiménez-Gallegos ◽  
L. Téllez-Jurado ◽  
Luis M. Rodríguez-Lorenzo ◽  
Julio San Román
Keyword(s):  
Hybrid Materials ◽  
Sol Gel ◽  
Proton Nuclear Magnetic Resonance ◽  
X Ray Diffraction ◽  
Organic Part ◽  
Sol Gel Process ◽  
Nmr Techniques ◽  
Ft Ir ◽  
Characterization Of Materials

This paper focuses on the preparation of siloxane-polyurethane hybrid materials using a sol-gel method. The global aim of the project is to tailor mechanical properties, degradability rate, bioactivity and biocompatibility to design scaffolds for musculoskeletal applications. A series of seven hybrid materials were synthesized with varying the proportion of polydimethylsiloxane (PDMS), and Polyurethane (PU). The organic part ratios (by weight) employed were (% PDMS:% PU) 30:0, 35:5, 20:10, 15:15, 10:20, 5:25, and 0:30. The organic part was reacted with constant 70 % TEOS to obtain the hybrid materials. A sol-gel process was selected for the synthesis of the hybrids. The characterization of materials was carried out by the fourier-infrared spectroscopy (FT-IR), x-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electronic microscopy (SEM) and proton nuclear magnetic resonance (1H-NMR) techniques in order to analyze the structure, microstructure and chemical composition of the hybrid materials. Gelification time depends on the proportion of PU used. When no PU is employed, the gel time is 8 hours but it rises up to 18 days for 30 % of polyurethane. Materials range from opaque to translucent but with a greater fragility for greater amounts of polyurethane. No differences in the bonding of materials could be appreciated.

scholarly journals In VitroBioactivity and Antimicrobial Tuning of Bioactive Glass Nanoparticles Added with Neem (Azadirachta indica) Leaf Powder

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
M. Prabhu ◽  
S. Ruby Priscilla ◽  
K. Kavitha ◽  
P. Manivasakan ◽  
V. Rajendran ◽  
...  
Keyword(s):  
Bioactive Glass ◽  
Azadirachta Indica ◽  
Sol Gel ◽  
Sem Analysis ◽  
Microbial Infection ◽  
X Ray Diffraction ◽  
Doped Glasses ◽  
Leaf Powder ◽  
Doped Glass

Silica and phosphate based bioactive glass nanoparticles (58SiO2-33CaO-9P2O5) with doping of neem (Azadirachta indica) leaf powder and silver nanoparticles were prepared and characterised. Bioactive glass nanoparticles were produced using sol-gel technique.In vitrobioactivity of the prepared samples was investigated using simulated body fluid. X-ray diffraction (XRD) pattern of prepared glass particles reveals amorphous phase and spherical morphology with a particle size of less than 50 nm. When compared to neem doped glass, better bioactivity was attained in silver doped glass through formation of hydroxyapatite layer on the surface, which was confirmed through XRD, Fourier transform infrared (FTIR), and scanning electron microscopy (SEM) analysis. However, neem leaf powder doped bioactive glass nanoparticles show good antimicrobial activity againstStaphylococcus aureusandEscherichia coliand less bioactivity compared with silver doped glass particles. In addition, the biocompatibility of the prepared nanocomposites reveals better results for neem doped and silver doped glasses at lower concentration. Therefore, neem doped bioactive glass may act as a potent antimicrobial agent for preventing microbial infection in tissue engineering applications.

Preparation and Characterization of Pr2Ti2O7 by Sol-Gel Process

2017 ◽  
Vol 748 ◽  
pp. 413-417
Author(s):  
Chun Yu Long ◽  
Fang Fang Peng ◽  
Min Min Jin ◽  
Pei Song Tang ◽  
Hai Feng Chen
Keyword(s):  
Methyl Orange ◽  
Single Phase ◽  
Raw Materials ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Illumination Time ◽  
X Ray ◽  
Sol Gel Process ◽  
Ft Ir

Using Pr (NO3)3, butyl titanate, ethylene glycol and citric acid as main raw materials, praseodymium titanate (Pr2Ti2O7) was prepared by the sol-gel process. The samples were characterized by means of X-ray diffraction (XRD), scanning electron microscope (SEM), thermal gravity-differential thermal analysis (TG-DTA), diffuse-reflection spectra (DRS) and Fourier transform infrared (FT-IR). The effect of different calcination temperature and illumination time on the photocatalytic properties of Pr2Ti2O7 was investigated. It was found that the single phase Pr2Ti2O7 could be obtained through sol-gel process and calcination at 1000 °C. The Pr2Ti2O7 samples calcination at 1000 °C were uniform , and the resulting product had a particle size of 200 nm and an optical band gap of 3.26 eV. Under ultraviolet light, the degradation of methyl orange arrived to 80.11% after 180 min of photocatalytic reaction. The Pr2Ti2O7 samples showed good photocatalytic activity for decomposition of methyl orange.

Sign in / Sign up

Export Citation Format

Share Document