scholarly journals Tetracycline Loaded Collagen/Hydroxyapatite Composite Materials for Biomedical Applications

2015 ◽  
Vol 2015 ◽  
pp. 1-5 ◽  
Author(s):  
Laura Cristina Rusu ◽  
Ioan Avram Nedelcu ◽  
Mădălina Georgiana Albu ◽  
Maria Sonmez ◽  
Georgeta Voicu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Composite Materials ◽  
Biomedical Applications ◽  
Second Step ◽  
Ternary Composite ◽  
Hydroxyapatite Composite ◽  
Vis Spectroscopy ◽  
Release Study ◽  
Scanning Electron

The paper describes the preparation, characterisation, and testing of tetracycline loaded collagen-carboxymethylcellulose/hydroxyapatite ternary composite materials. The synthesis of this drug delivery system consists in two steps: the first step is the mineralization of collagen-carboxymethylcellulose gel while the second step corresponds to the loading of the ternary composite material with tetracycline. The obtained DDS is characterised by physicochemical, morphological, and release behaviour by using FTIR spectroscopy and microscopy, scanning electron microscopy, and UV-VIS spectroscopy. Based on the release study, it can be assumed that tetracycline is released in a prolonged way, assuring at least 6 days of antiseptic properties.

scholarly journals Synthesis and Evaluation of AlgNa-g-poly(QCL-co-HEMA) Hydrogels as Platform for Chondrocyte Proliferation and Controlled Release of Betamethasone

2021 ◽  
Vol 22 (11) ◽  
pp. 5730
Author(s):  
Jomarien García-Couce ◽  
Marioly Vernhes ◽  
Nancy Bada ◽  
Lissette Agüero ◽  
Oscar Valdés ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Controlled Release ◽  
Biomedical Applications ◽  
Release Kinetics ◽  
Cell Types ◽  
Tissue Engineering Scaffolds ◽  
Almost All ◽  
Scanning Electron

Hydrogels obtained from combining different polymers are an interesting strategy for developing controlled release system platforms and tissue engineering scaffolds. In this study, the applicability of sodium alginate-g-(QCL-co-HEMA) hydrogels for these biomedical applications was evaluated. Hydrogels were synthesized by free-radical polymerization using a different concentration of the components. The hydrogels were characterized by Fourier transform-infrared spectroscopy, scanning electron microscopy, and a swelling degree. Betamethasone release as well as the in vitro cytocompatibility with chondrocytes and fibroblast cells were also evaluated. Scanning electron microscopy confirmed the porous surface morphology of the hydrogels in all cases. The swelling percent was determined at a different pH and was observed to be pH-sensitive. The controlled release behavior of betamethasone from the matrices was investigated in PBS media (pH = 7.4) and the drug was released in a controlled manner for up to 8 h. Human chondrocytes and fibroblasts were cultured on the hydrogels. The MTS assay showed that almost all hydrogels are cytocompatibles and an increase of proliferation in both cell types after one week of incubation was observed by the Live/Dead® assay. These results demonstrate that these hydrogels are attractive materials for pharmaceutical and biomedical applications due to their characteristics, their release kinetics, and biocompatibility.

scholarly journals GREEN TECHNOLOGY MEDIATED SYNTHESIS OF SILVER NANOPARTICLES FROM MOMORDICA CHARANTIA FRUIT EXTRACT AND ITS BACTERICIDAL ACTIVITY

2017 ◽  
Vol 10 (3) ◽  
pp. 196 ◽  
Author(s):  
S C Joshi ◽  
Utkarsh Kaushik ◽  
Aproova Upadhyaya ◽  
Priyanka Sharma
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Silver Nanoparticles ◽  
Atomic Force Microscope ◽  
Momordica Charantia ◽  
Diffusion Method ◽  
Fruit Extract ◽  
Atomic Force ◽  
Vis Spectroscopy ◽  
Scanning Electron

ABSTRACTObjective: The synthesis of nanoparticles from biological processes is evolving a new era of research interests in nanotechnology. Silver nanoparticlesare usually synthesized by chemicals and physical method, which are quite toxic and flammable in nature. This study deals with an environmentfriendly biosynthesis process of antibacterial silver nanoparticles using Momordica charantia fruit.Methods: AgNO3 (5 mM) was allowed to react with fruit extract of M. charantia. Biosynthesis of AgNPs was optimized by changing temperature,pH, and solvent. The silver nanoparticles so formed were characterized using ultraviolet-visible (UV-VIS) spectroscopy, Fourier transform infraredspectroscopy (FTIR), dynamic light scattering (DLS), atomic force microscope (AFM), and scanning electron microscopy (SEM).Results: UV-VIS spectra show absorption peak between 420 and 430 nm. The FTIR analysis showed the alcoholic, lactam, and nitro group presentin the plant extract, which were responsible for the reduction in AgNPs. The SEM images showed the size distribution of the nanoparticles and theaverage size was found to be 50-100 nm. By DLS analysis and AFM analysis, average sizes of the silver nanoparticles were of 150 nm. The results ofthese analyses confirmed the formation of silver nanoparticles. Silver nanoparticles were tested against Bacillus cereus and Staphylococcus epidermidisstrains using disc diffusion method and were found to be effective.Conclusion: Silver nanoparticles so synthesized in this study using fruit extract of M. charantia are simple, easy, and effective technique of nanoparticlesproduction.Keywords: Silver nanoparticles, Momordica charantia, Optimization, Antibacterial, Atomic force microscope, Scanning electron microscopy.

Influence of Sodium Hydroxide on the Properties of FGD Gypsum-Slag Composite Materials

2014 ◽  
Vol 675-677 ◽  
pp. 750-755
Author(s):  
Fang Huang ◽  
Bao Long Jiao ◽  
Dong Dong Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Composite Materials ◽  
Flexural Strength ◽  
Sodium Hydroxide ◽  
Setting Time ◽  
Maximal Strength ◽  
Action Mechanism ◽  
Fgd Gypsum ◽  
Scanning Electron

By examining the compressive and flexural strength of composite and using scanning electron microscopy (SEM), we analyzed the influence of sodium hydroxide on the properties of FGD gypsum and slag composite materials and discussed the influence of sodium hydroxide on the setting time and mechanical strength of the composite materials and presented the action mechanism of sodium hydroxide as a stimulator. The results show that when the content of sodium hydroxide was percent of 0.25, the maximal strength of FGD gypsum-slag composite materials was reached.

Biopolymer Encapsulation of PEI-Derivatives for Heavy Metal Sorption

2015 ◽  
Vol 1130 ◽  
pp. 529-532
Author(s):  
Caroline Bertagnolli ◽  
Thierry Vincent ◽  
Eric Guibal
Keyword(s):  
Electron Microscopy ◽  
Heavy Metal ◽  
Scanning Electron Microscopy ◽  
Composite Materials ◽  
Metal Sorption ◽  
Initial Concentration ◽  
Heavy Metal Sorption ◽  
Maximum Sorption ◽  
Complex Solutions ◽  
Scanning Electron

Composite materials have been synthesized by alginate or chitosan encapsulation of polyethylenimine (PEI) derivatives (obtained by glutaraldehyde grafting of histidine and carbon disulfide). Discrete or agglomerated PEI-derivative particles are immobilized in the macroporous network of biopolymer matrix (as shown by scanning electron microscopy and SEM-EDX analysis). The effect of pH and initial concentration on Zn (II) and Cu (II) sorption performance were analyzed. The incorporation of PEI-derivatives biopolymer matrix improves sorption performance in complex solutions (doped with CaCl2) compared to pristine biopolymer. Maximum sorption capacities range from 0.64 to 1 mmol L-1 for Zn (II) and from 1.13 to 1.67 mmol L-1 for Cu (II).

The adsorption of methylene blue on montmorillonite from acid solutions

Clay Minerals ◽  
2011 ◽  
Vol 46 (3) ◽  
pp. 461-471 ◽  
Author(s):  
Z. Klika ◽  
P. Pustková ◽  
M. Dudová ◽  
P. Čapková ◽  
Ch. Kliková ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Methylene Blue ◽  
Ion Exchange ◽  
Powder Diffraction ◽  
Acid Solutions ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Adsorption Wave ◽  
Scanning Electron

AbstractThe adsorption of methylene blue (MB) on montmorillonite from acid solutions has not yet been studied in detail. In this paper the adsorption of this dye on Ca/SAz montmorillonite from 0.32, 0.80 and 1.60 M HCl solutions at ambient temperature and after 2 hours leaching was carefully studied and evaluated. Under the above conditions the MB/SAz intercalates formed are practically insoluble. In contrast to the adsorption of methylene blue on montmorillonite from aqueous solutions, the adsorption from acid solutions consists of two adsorption waves. The intercalated samples from the first and second waves were studied using X-ray powder diffraction (XRD), FTIR, Vis spectroscopy, and scanning electron microscopy (SEM) equipped with a microprobe system. The adsorption of MB in the first wave is attributed to ion exchange of the dye cationic species (MB+, MB22+, H-aggregates, MBH2+ and H+) for the original interlayer cations of montmorillonite. The percentages of MBH2+ and H+ based on total adsorbed MB were estimated for varying HCl concentrations. The second adsorption wave is linked to the precipitation of MB species on the outer MB/SAz surface.

Cellulose Derivatives Based Membranes for Biomedical Applications

2015 ◽  
Vol 638 ◽  
pp. 27-30 ◽  
Author(s):  
Stefan Ioan Voicu ◽  
Alexandru Muhulet ◽  
Iulian Antoniac ◽  
Marijana Simina Corobea
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Comparative Study ◽  
Biomedical Applications ◽  
Cellulose Derivatives ◽  
Hydrodynamic Behavior ◽  
Flow Rates ◽  
Cellulose Acetate Membranes ◽  
Morphological Differences ◽  
Scanning Electron

This paper presents a comparative study of cellulose acetate membranes, respectively nitrocellulose membranes, synthesized under the same conditions for the retention of proteins from aqueous solutions. It has also been studied the hydrodynamic behavior of the membranes, measuring water, respectively ethanol flow rates, and the retention of proteins. The membranes have been characterized by scanning electron microscopy in order to study the morphological differences.

scholarly journals High-responsivity hybrid α-Ag2S/Si photodetector prepared by pulsed laser ablation in liquid

2020 ◽  
Vol 11 ◽  
pp. 1596-1607
Author(s):  
Raid A Ismail ◽  
Hanan A Rawdhan ◽  
Duha S Ahmed
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Laser Ablation ◽  
Energy Gap ◽  
Longitudinal Optical Phonon ◽  
Ambient Conditions ◽  
Optical Energy Gap ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Scanning Electron

We report the synthesis of α-Ag2S nanoparticles (NPs) by one-step laser ablation of a silver target in aqueous solution of thiourea (Tu, CH4N2S) mixed with cationic cetyltrimethylammonium bromide (CTAB) as surfactant. The effect of the CTAB surfactant on the structural, morphological, optical, and elemental composition of Ag2S NPs was evaluated using X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and UV–vis spectroscopy. The optical absorption decreased and the optical energy gap of α-Ag2S increased from 1.5 to 2 eV after the CTAB surfactant was added to the Tu solution. XRD studies revealed that the synthesized Ag2S NPs were polycrystalline with a monoclinic structure and that crystallinity of the nanoparticles was improved after adding CTAB. Raman studies revealed the presence of peaks related to Ag–S bonds (Ag modes) and the longitudinal optical phonon 2LO mode. Scanning electron microscopy investigations confirmed the production of monodisperse Ag2S NPs when using the CTAB surfactant. The optoelectronic properties of α-Ag2S/p-Si photodetector, such as current–voltage characteristics and responsivity in the dark and under illumination, were also improved after using the CTAB surfactant. The responsivity of the photodetector increases from 0.64 to 1.85 A/W at 510 nm after adding CTAB. The energy band diagram of the α-Ag2S/p-Si photodetector under illumination was constructed. The fabricated photodetectors exhibited reasonable stability after three weeks of storage under ambient conditions with a responsivity of 70% of the initial value.

Processability of Composite Materials Containing Chitosan

1990 ◽  
Vol 218 ◽  
Author(s):  
G. Graham Allan ◽  
Mutombo Muvundamina
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Composite Materials ◽  
Electron Spectroscopy ◽  
Surface Composition ◽  
Polypropylene Fibers ◽  
Acidic Solutions ◽  
Foreign Materials ◽  
Wetting Force ◽  
Scanning Electron

AbstractThe processability of polypropylene fibers into composite materials was characterized by dynamic wettability measurements. Single fibers were immersed in a series of aqueous acidic solutions of chitosan. Variations in the wetting force, observed for progressive and successive immersions of the fibers in the liquid, indicated adsorption of species out of the solution or the presence of foreign materials on the surface of the solid. The value of the advancing wetting force was used to assess the coating of the fibers by the liquid. Data on the surface composition of the fibers were obtained by electron spectroscopy for chemical analysis. The conditions of preparation of the composite materials containing chitosan were determined from the correlation of the observations on wettability, surface composition and scanning electron microscopy.

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