英文摘要 |
"In this study, a high-pressure homogenization method was used to develop a new type of Transfersome with three kind of silicon edge activators. The Transfersome made of P-12D has the smallest particle size, with an average particle size of 166.0 nm. Under the same silicon edge activator conditions, different lipid ratios have little effect on the particle size. In terms of the entrapment efficiency, the poor performance of the LP-18M Transfersome is presumed to be that the hydrophobic edge activator is not good for the relatively hydrophilic caffeine entrapment. P-15D-3 has the fastest relative deformability, 37.59% higher than Liposome (18.70 s). As a result, it was found that the smaller the proportion of edge activator added, the poorer the relative deformability. In the in vitro transdermal delivery test, P-15D-3 performed best, with a penetration flux of 0.43 mg/cm2‧hr, which was 22.22% higher than Tw80-1. The best formulation conditions is use PEG/PPG-15/15 Dimethicone as edge activator, add co-solvent 1, 3-BG, lipid ratio is 80:20, lipid concentration is 2%." |