摘要
To further explore the wonder of nano technology in drug delivery system, the combination of micelles and mesoporous silica was conducted for delivering poorly water soluble nifedipine (NFP). Double-nano silica xerogel (DN-SX) with both micelles and nanopores was prepared and silica xerogel with only nanopores (SN-SX) was made for comparison. Characteristics of DN-SX and SN-SX, including morphology, porous structure and crystalline state were investigated and pharmaceutical performances of drug loaded carriers were studied. The micelles in DN-SX contributed to achieve larger mesopores and enhanced NFP dissolution better than SN-SX. How responses of drug release amount and reduced drug release amount reacted as changing each influencing factor was elucidated by Box–Behnken experimental design. With the DN-SX obtained by optimization, in vivo pharmacokinetic study result demonstrated that the relative bioavailability of NFP loaded DN-SX and NFP loaded SN-SX were 216.84% and 161.14%, respectively. Therefore, the optimized DN-SX with double-nano structure was of great value for designing poorly water soluble drug delivery system.
危险品化学品经营许可证(带存储)