Ibuprofen (an anti-inflammatory drug that is a crystalline solid at ambient temperature) has been
encapsulated in MCM-41 silica matrices with different pore diameters (35 and 116 Å). Its behavior has
been investigated by magic angle spinning (MAS) 1H, 13C, and 29Si solid-state NMR spectroscopy at
ambient and low temperature. This study reveals an original physical state of the drug in such materials.
At ambient temperature, ibuprofen is not in a solid state (crystalline or amorphous) and is extremely
mobile inside the pores, with higher mobility in the largest pores (116 Å). The interaction between
ibuprofen and the silica surface is weak, which favors fast drug release from this material in a simulated
intestinal or gastric fluid. The quasi-liquid behavior of ibuprofen allows the use of NMR pulse sequences
issued from solution-state NMR, such as the INEPT sequence, to characterize these solid-state samples.
The solid-state MAS NMR study shows that the proton of the carboxylic acid group of ibuprofen is in
a chemical exchange at ambient temperature. Furthermore, at low temperature (down to 223 K), NMR
spectroscopy results show that ibuprofen is able to crystallize inside the largest pores (116 Å), whereas
a glassy state is obtained for the smallest ones (35 Å).
Magnetic nanoparticles have attracted attention in modern medicine and pharmacology owing to their potential usefulness as contrast agents for MRI, as colloidal mediators for cancer magnetic hyperthermia or as active constituents of drug-delivery platforms. This review examines these in vivo applications through an understanding of the involved problems and the current and future possibilities for resolving them. A special emphasis is placed upon magnetic nanoparticle requirements from a physical viewpoint (e.g., relaxivity for MRI, specific absorption rate for hyperthermia and magnetic guidance), the factors affecting their biodistribution after intravenous injection (e.g., size and surface hydrophobic/hydrophilic balance) and the solutions envisaged for enhancing their half-life in the blood compartment and in targeting tumor cells.
A thermoresponsive hydrogel, poly(N‐isopropylacrylamide) (poly(NIPAM)), is synthesized in situ within an oxidized porous Si template, and the nanocomposite material is characterized. Infiltration of the hydrogel into the interconnecting nanoscale pores of the porous SiO2 host is confirmed by scanning electron microscopy. The optical reflectivity spectrum of the nanocomposite hybrid displays Fabry–Pérot fringes characteristic of thin film interference, enabling direct, real‐time observation of the volume phase transition of the confined poly(NIPAM) hydrogel. Reversible optical reflectivity changes are observed to correlate with the temperature‐dependent volume phase transition of the hydrogel, providing a new means of studying nanoscale confinement of responsive hydrogels. The confined hydrogel displays a swelling and shrinking response to changes in temperature that is significantly faster than that of the bulk hydrogel. The porosity and pore size of the SiO2 template, which are precisely controlled by the electrochemical synthesis parameters, strongly influence the extent and rate of changes in the reflectivity spectrum of the nanocomposite. The observed optical response is ascribed to changes in both the mechanical and the dielectric properties of the nanocomposite.
Ionogels containing imidazolium ibuprofenate have been shown to be an efficient drug releasing system with kinetics controlled by the nature of the silica wall.
Chitosan/silica hybrids were synthesized and shaped as microspheres, which may or may not present a core/shell structure, depending on the experimental conditions. The core is constituted by a homogeneous hybrid, while the shell is pure silica. The amino groups of the biopolymer are still accessible as active sites for heterogeneous catalysis.
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