In Situ Loading of Basic Fibroblast Growth Factor Within Porous Silica Nanoparticles for a Prolonged Release

Basic fibroblast growth factor (bFGF), a protein, plays a key role in wound healing and blood vessel regeneration. However, bFGF is easily degraded in biologic systems. Mesoporous silica nanoparticles (MSNs) with well-tailored porous structure have been used for hosting guest molecules for drug delivery. Here, we report an in situ route to load bFGF in MSNs for a prolonged release. The average diameter (d) of bFGF-loaded MSNs is 57 ± 8 nm produced by a water-in-oil microemulsion method. The in vitro releasing profile of bFGF from MSNs in phosphate buffer saline has been monitored for 20 days through a colorimetric enzyme linked immunosorbent assay. The loading efficiency of bFGF in MSNs is estimated at 72.5 ± 3%. In addition, the cytotoxicity test indicates that the MSNs are not toxic, even at a concentration of 50 μg/mL. It is expected that the in situ loading method makes the MSNs a new delivery system to deliver protein drugs, e.g. growth factors, to help blood vessel regeneration and potentiate greater angiogenesis

Mesoporous silica nanoparticles with tunable pore size for tailored gold nanoparticles

The aim of this paper was to verify a possible correlation between the pore-size of meso- porous silica nanoparticles (MSNs) and the sizes of gold nanoparticles (AuNPs) obtained by an impreg- nation of gold(III) chloride hydrate solution in the MSNs, followed by a specific thermal treatment. Mesoporous silica nanoparticles with tunable pore diameter were synthesized via a surfactant-assisted method. Tetraethoxysilane as silica precursor, cetyl- trimethylammonium bromide (CTAB) as surfactant and toluene as swelling agent were used. By varying the CTAB–toluene molar ratio, the average dimension of the pores could be tuned from 2.8 to 5.5 nm. Successively, thiol groups were grafted on the surface of the MSNs. Finally, the thermal evolution of the gold salt, followed by ‘‘in situ’’ X-ray powder diffraction (XRPD) and thermogravimetric analysis (TGA), revealed an evident correlation among the degradation of the thiol groups, the pore dimension of the MSNs and the size of the AuNPs. The samples were characterized by means of nitrogen adsorption– desorption, transmission electron microscopy, small- angle X-ray scattering, XRPD ‘‘in situ’’ by synchro- tron radiation, and ‘‘ex situ’’ by conventional tech- niques, diffuse reflectance infrared Fourier transform spectroscopy, and TGA

Improved Natural Mordenite as Low-Cost Catalyst for Glycerol Acetalization Into Solketal-An Effective Fuel Additive

The increase in biodiesel production results in an excessive amount of crude glycerol byproduct. Therefore, production of solketal –an effective additive of gasoline fuel-from glycerol and acetone via catalytic acetalization could improve the added value of glycerol. This study investigates enhancement of natural mordenite catalytic properties through the hydrothermal recrystallization method for glycerol acetalization. The hydrothermal temperature was varied at 150, 170 and 190o C to form ZT 150, ZT 170 and ZT 190, respectively. The samples were characterized by using the x-ray diffraction and the scanning electron microscope-Energy dispersive X-Ray. They were later used as catalysts for glycerol acetalization with acetone. The best obtained catalyst was further studied to explore the effect of acetone to glycerol ratio. The glycerol conversion was determined using the ASTM D7637-10 titration method. Solketal product was identified by using the Fourier transform infrared spectroscopy. The results showed that the recrystallization temperature affected the intensity of the mordenite phase and quartz impurity phase in the modified zeolites. A high recrystallization temperature led to a higher phase of mordenite, peaking at 170o C, beyond which the quartz impurity phase increased. Glycerol acetalization conversions over zeolite parent, ZT 150, ZT 170 and ZT190 with acetone to glycerol ratio of 3 were 16.1, 30.4, 33.9 and 32.5%, respectively. When the ratio of acetone to glycerol was increased to 12, the glycerol conversion over ZT 170 catalyst reached 59%, a good starting point for further modifications. Overall finding demonstrated a straight-forward fabrication of catalyst from natural resource to enhance glycerol as the biodiesel production by-product into a higher value end-product of solketal