Aerosil

Co-crystallization of drugs with benign co-formers is promising for enhancing dissolution rate of poorly soluble drugs. The… Expand

The main objective of this study was to prepare a solid form of lipid-based self-emulsifying drug delivery system (SEDDS) by… Expand

The thermal stability and kinetics of non-isothermal degradation of polypropene and polypropene composites filled with 20 mass… Expand

TiO2 nanotubes (TNTs) with large aspect ratio and large specific surface area were prepared from P25 (Nippon Aerosil) and applied… Expand

The solid dispersion particles of indomethacin (IMC) were prepared with different types of silica, non-porous (Aerosil 200) or… Expand

PurposeTo obtain free flowing, stable, amorphous solid dispersions (SDs) of simvastatin (SIM), a drug with relatively lower glass… Expand

Theophylline-loaded microparticles of a lipid carrier, Precirol ATO 5, were prepared by the ultrasonic spray-congealing method… Expand

Sustained-release nitrendipine microspheres were prepared in liquid system by quasi-emulsion solvent diffusion method, in which… Expand

A molecular precursor approach involving simple grafting procedures was used to produce site-isolated titanium-supported… Expand

High-resolution calorimetric studies have been made of the liquid crystal phase transitions for several dispersions of 70… Expand