Home About us Contact
|
Home About us Contact | ||
|
|
||
Chitosan Matrix (chitosan + matrix)
Selected AbstractsChitosan/Gold Nanocomposites: Chitosan Films Doped with Gold Nanorods as Laser-Activatable Hybrid Bioadhesives (Adv. Mater.ADVANCED MATERIALS, Issue 38 201038/2010) The cover image represents an inside view of a laser-activated gold nanorod/chitosan film. Gold nanorods dispersed throughout the polymeric chitosan matrix absorb incident near-infrared laser light. The photothermal conversion from the gold nanorods activates the surrounding chitosan strands to mediate functional adhesion with biological tissue, as discussed in work reported on p. 4313 by Paolo Matteini and co-workers. [source] Structure determination of diclofenac in a diclofenac-containing chitosan matrix using conventional X-ray powder diffraction dataJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2 2004Nongnuj Muangsin The structure determination of diclofenac embedded in a diclofenac-containing chitosan matrix using conventional X-ray powder diffraction data is demonstrated. It reveals that sodium diclofenac, the starting material in the preparation of a controlled-release diclofenac-containing chitosan matrix, changes to diclofenac acid in space group C2/c in the matrix. Simple methods were employed for handling the sample to obtain X-ray powder diffraction data of sufficiently high quality for the determination of the crystal structure of diclofenac embedded in chitosan. These involved grinding and sieving several times through a micro-mesh sieve to obtain a suitable particle size and a uniformly spherical particle shape. A traditional technique for structure solution from X-ray powder diffraction data was applied. The X-ray diffraction intensities were extracted using Le Bail's method. The structure was solved by direct methods from the extracted powder data and refined using the Rietveld method. For comparison, the single-crystal structure of the same drug was also determined. The result shows that the crystal structure solved from conventional X-ray powder diffraction data is in good agreement with that of the single crystal. The deviations of the differences in bond lengths and angles are of the order of 0.030,Å and 0.639°, respectively. [source] Growth of osteoblast-like cells on biomimetic apatite-coated chitosan scaffoldsJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2008I. Manjubala Abstract Porous scaffold materials that can provide a framework for the cells to adhere, proliferate, and create extracellular matrix are considered to be suitable materials for bone regeneration. Interconnected porous chitosan scaffolds were prepared by freeze-drying method, and were mineralized by calcium and phosphate solution by double-diffusion method to form nanoapatite in chitosan matrix. The mineralized chitosan scaffold contains hydroxyapatite nanocrystals on the surface and also within the pore channels of the scaffold. To assess the effect of apatite and porosity of the scaffolds on cells, human osteoblast (SaOS-2) cells were cultured on unmineralized and mineralized chitosan scaffolds. The cell growth on the mineralized scaffolds and on the pure chitosan scaffold shows a similar growth trend. The total protein content and alkaline phosphatase enzyme activity of the cells grown on scaffolds were quantified, and were found to increase over time in mineralized scaffold after 1 and 3 weeks of culture. The electron microscopy of the cell-seeded scaffolds showed that most of the outer macropores became sealed off by a continuous layer of cells. The cells spanned around the pore wall and formed extra cellular matrix, consisting mainly of collagen in mineralized scaffolds. The hydroxyproline content also confirmed the formation of the collagen matrix by cells in mineralized scaffolds. This study demonstrated that the presence of apatite nanocrystals in chitosan scaffolds does not significantly influence the growth of cells, but does induce the formation of extracellular matrix and therefore has the potential to serve for bone tissue engineering. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008 [source] Formulation pH modulates the interaction of insulin with chitosan nanoparticlesJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 6 2002Zengshuan Ma Abstract Previous studies on chitosan-insulin nanoparticles have reported diverse encapsulation efficiency and insulin release profiles despite similar formulation and preparation procedures. This study examined the efficiency and mechanism of association of insulin with chitosan nanoparticles in the pH range of 2.3 to 6.3. Nanoparticles of 237 to 235 nm were prepared by ionotropic gelation of chitosan with tripolyphosphate counterions. Insulin was quantified by an RP-HPLC method. The insulin association efficiency (AE) spanned a broad range from 2 to 85%, and was highly sensitive to formulation pH. Highest AE was measured at insulin loading concentrations,,,4.28 U/mL and pH 6.1, close to the pI of native insulin and the pKa of chitosan. This association, attributed to physical adsorption of insulin through hydrophobic interactions with chitosan, was labile, and the associated insulin rapidly and completely released by dilution of the nanoparticles in aqueous media of pH 2 to 7.4. AE obtained at pH 5.3 was less than half that measured at pH 6.1 at corresponding insulin concentration, but the association at pH 5.3 appeared to be based on stronger interactions, because the release of insulin was pH-dependent and recovery was less than 25% even upon disintegration of the chitosan matrix. Interaction of insulin with the chitosan nanoparticles rendered the protein more susceptible to acid and enzymatic hydrolyses, the effects being more predominant in nanoparticles prepared at pH 5.3 than at pH 6.1. © 2002 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 91:1396,1404, 2002 [source] Preparation and characterization of chitosan/KSF biocomposite filmPOLYMER COMPOSITES, Issue 8 2009Aylin Alt Chitosan,clay biocomposites have been prepared in which KSF-montmorillonite (KSF) is used as filler and diluted acetic acid is used as solvent for dissolving and dispersing chitosan and montmorillonite, respectively. The effect of KSF loadings in biocomposites has been investigated. The characterization with different methods (FTIR, DSC, TGA, SEM, and XRD) on chitosan/KSF biocomposites systems was examined. Morphology and properties of chitosan biocomposites have been studied compared with those of pure chitosan. The FTIR and SEM results indicated the formation of an intercalated-and-exfoliated structure at low KSF content and an intercalated-and-flocculated structure at high KSF content. The thermal stability and the mechanical properties of the composites were also examined by DSC, TGA/DTG, and tensile strength measurements, respectively. The dispersed clay improves the thermal stability of the matrix systematically with the increase of clay loading. Tensile strength of a chitosan film was enhanced until the clay ratio up to 2 wt% and elongation-at break decreased with addition of clay into the chitosan matrix. The XRD results confirmed the intercalation of the biopolymer in the clay interlayer by the decrease of 2, values while the chitosan,clayratio increases. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers [source] Effect of spatial architecture on cellular colonizationBIOTECHNOLOGY & BIOENGINEERING, Issue 1 2006Yan Huang Abstract The spatial cell-material interaction remains vital issue in forming biodegradable scaffolds in Tissue Engineering. In this study, to understand the influence of spatial architecture on cellular behavior, 2D and 3D chitosan scaffolds of 50,190 kD and >310 kD MW were synthesized through air drying and controlled rate freezing/lypohilization technique, respectively. In addition, chitosan was emulsified with 19, 76, and 160 kD 50:50 poly lactide-co-glycolide (PLGA) using 1,2-Dimyristoyl-sn-Glycero-3-Phosphocholine (DMPC) as stabilizer. 2D and 3D scaffolds were formed by air drying and lyophilization as before. Tensile and compressive properties of films and scaffolds were analyzed in wet conditions at 37°C. Alterations in the cell spreading, proliferation, and cytoskeletal organization of human umbilical vein endothelial cells (HUVECs) and mouse embryonic fibroblasts (MEFs) were studied. These results showed that the formed 3D chitosan scaffolds had interconnected open pore architecture (50,200 µm size). HUVECs and MEFs had reduced spreading areas and circular morphology on 2D chitosan membranes compared with 3D chitosan scaffolds. The fluorescence photomicrographs for actin (using Alexa Fluor 488 phalloidin) and cytoplasm staining (using carboxyfluorescein diacetate-succinimidyl ester) demonstrated that the cells spread within 3D chitosan matrix. 2D and 3D emulsified chitosan and chitosan/PLGA scaffolds reduced the spreading of HUVECs and MEFs even further. Proliferation results, analyzed via MTT-Formazan assay and BrdU uptake assay, correlated with the spreading characteristics. The reductions in cell spreading area on emulsified surfaces were not detrimental to the viability and endocytic activity but to proliferation. The observed alterations in cellular colonization are in part due to the substrate stiffness and surface topography. In summary, these results suggest a significant influence of spatial architecture on cellular colonization. © 2005 Wiley Periodicals, Inc. [source] | |||||||||||||