Showing 4 results for Chitosan
M. Raz, F. Moztarzadeh, M.a. Shokrgozar, M. Ashuri, M. Tahriri,
Volume 32, Issue 2 (12-2013)
Abstract
In this project, we prepared biomimetic nanocomposite scaffolds from gelatin and chitosan and hydroxyapatite and subsequently the scaffolds were evaluated by common used bulk technique. For this purpose, the nanocomposite hydrogel/apatite bone tissue engineering scaffolds were fabricated using applied biomimetic method accompanied with freeze drying technique. The apatite was precipitated using double diffusion mechanism within gelatin hydrogel in similar pH and temperature to the human body. Chitosan initial percentage (20, 30 and 40%) was set as variables. Nanocomposites were soaked in glutaraldehyde solution in order to enhance mechanical properties and make them insoluble in water. Diffusion of calcium and phosphate from lateral hydrogel into the middle hydrogel caused formation of parallel white layer-formed precipitate. Analysis of precipitates formed within middle hydrogel for the samples, showed that detected materials are composed of carbonated hydroxyapatite and dicalcium phosphate dihydrate (DCPD, brushite). Also, mechanical behavior obtained for the scaffolds were comparable with spongy bone. With increasing chitosan in the composite scaffold, the water up-take was increased from 379 to 661%. Phase composition, microstructure and structural groups in the composite samples were also characterized by X-Ray Diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infra-red (FTIR) analyses. Eventually, the obtained results showed that the composite contains 20% chitosan had appropriate properties for fabricating bone scaffold.
F. Soleimani, R. Emadi,
Volume 38, Issue 3 (12-2019)
Abstract
In this study, polycaprolactone/chitosan/1% baghdadite composite coating was applied on anodized AZ91 alloy to improve the corrosion rate of AZ91 alloy in simulated body fluid (SBF) solution for long immersion times, control its degradability and enhance its bioactivity. By applying the composite coating and after seven days of immersion in a phosphate buffer solution, the corrosion rate decreased from 0.21 mg/h.cm2 (for AZ91 sample) to 0.1 mg/h.cm2 (for anodized AZ91 sample). Formation of apatite layer on the surface of specimens is considered a criterion for bioactivity. In order to evaluate the ability of specimens to get covered by an apatite, the SBF test was used. Application of the composite coating yielded the highest ability for apatite formation, controlled release of ions, and the lowest corrosion rate in the SBF so that it could be considered a good choice for bone implants.
N. Poursharifi, D. Semnani, P. Soltani, S. Amanpour,
Volume 38, Issue 4 (1-2020)
Abstract
In this study, seven-layer nanofiber structures consisting of polycaprolactone/ chitosan polymers loaded with methotrexate and 5-fluorouracil anti-cancer drugs, for controlled drug delivery, were produced and evaluated. For this purpose, the second, fourth and sixth layers were loaded with drug and placed between the drug-free layers. The surface morphology of drug-free and drug-loaded nanofibers was investigated by scanning electron microscopy (SEM) and Fourier transform infrared spectrometry (FTIR) was used to study their chemical structure. The drug release rate in phosphate buffered saline (pH=7.4) and the released drug concentration were measured by spectrophotometry. Mechanical properties of single- and multi-layered samples were also investigated. SEM images showed formation of uniform and beadless fibers. FTIR spectrum confirmed presence of the drugs in the polymer mixture with no interaction. It was found that by increasing the chitosan content, a brittle structure with decreased elongation is formed. The release behavior of methotrexate and 5-Fluoracil drugs in neutral pH environment for 26 days was evaluated and the results exhibited a slow and sustained release.
Sh. Talebniya, M. R. Saeri, I. Sharifi, A. Doostmohammadi,
Volume 41, Issue 1 (8-2022)
Abstract
Magnetic nanoparticles are of interest in various research fields such as magnetic fluids, catalysts, biotechnology, medicine, information storage, and environmental issues. However, spinel ferrite magnetic nanoparticles with proper magnetic properties could not be used alone in these applications because of their lack of biocompatibility and instability in aqueous solutions. Surface coating is an effective strategy to eliminate or minimize this issue. In this study, FeFe2O4 and ZnFe2O4 spinel ferrites were synthesized using the reverse co-precipitation method under a nitrogen gas atmosphere. The magnetic behavior of the particles, determined by a vibrating magnetometer (VSM) showed the saturation magnet (Ms) values of the FeFe2O4 and ZnFe2O4 spinel. Fourier-transform infrared (FTIR) spectra showed two high-frequency bands v1 and v2 at about 554-578 and 368-397 cm-1, respectively, which were related to the spinel structure. Finally, the synthesized FeFe2O4 nanoparticles were coated with chitosan and polyethylene glycol (PEG) biopolymers. The TEM and FTIR analysis indicated that the magnetic nanoparticles were uniformly coated by the biopolymers.
