The ultra-small hollow silica nanoparticles were synthesized using the prepared amorphous calcium carbonate (ACC) particles as a template. The ACC particles were firstly prepared by carbonation method, which procedure was conducted in the methanol solvent to form the Ca(OCH3)2 layers on the ACC particles. An effect of methanol concentration on the morphology of ACC particles was also investigated. The prepared ACC particles were directly coated by silica through adding tetraethoxysilane (TEOS) into the methanol solvent. Hence, the ACC-silica core-shell particles were obtained since the ACC particles have a positive charge and interact with hydrolyzed TEOS. The ACC particles could be stabilized through the reaction between methanol and calcium ions when the methanol concentration was increased over than 40?vol%. 相似文献
The drug release characteristics of calcium alginate hydrogels, (Ca-Alg), under an electric field assisted transdermal drug
delivery system were systematically investigated. The Ca-Alg hydrogels were prepared by the solution-casting using CaCl2 as a crosslinking agent. The diffusion coefficients and the release mechanism of the anionic model drugs, benzoic acid and
tannic acid, and a cationic model drug, folic acid on the Ca-Alg hydrogels were determined and investigated using a modified
Franz-Diffusion cell in an MES buffer solution of pH 5.5, at a temperature of 37°C, for 48 h. The influences of the crosslinking
ratio, —the mole of the crosslinking agent to the mole of the alginate monomer—mesh size, model drug size, drug charge, electric
field strength, and electrode polarity were systematically studied. The drug diffusion coefficient decreased with an increasing
crosslinking ratio and drug size for all of the model drugs. The drug diffusion coefficient is precisely controlled by an
applied electric field and the electrode polarity depending on the drug charge, suitable for a tailor-made transdermal drug
delivery system. 相似文献
Summary: In order to produce nanometer‐sized fibers at an industrial scale, not only the morphology but also the production rate of fibers is important. The effect of solvent properties and functionality on the production rate of electrospun PS nanofibers was investigated using eighteen different solvents. The solution concentration was varied between 10 and 30% w/v. Electrospinning of PS solutions was carried out at various applied voltages and tip‐to‐collector distances The production rate of the obtained PS nanofibers was quantified in terms of electrospinnability. We found that the chance for the resulting PS solution to be spinnable is greater for solvents with high dipole moment and low viscosity. The solvent that provided the highest electrospinnability for polystyrene was DMF and the functionalities that promoted high dipole moment and thus high spinnability were the carbonyl group and the nitrogen group with free electrons. General guidelines for choosing suitable solvents for successful production of electrospun nanofibers have also been proposed.
SEM image of PS 685D at 200× magnification and the %‐coverage of the fibers obtained by using DMF, chloroform, and 1,4‐dioxane. 相似文献