Table 6.
Categories | Year | |||
---|---|---|---|---|
~1980 | 1980~1996 | 1997~2003 | 2004~2010 | |
Model drug | Diflunisal, diazepam | sulfathiazole, paracetamol, zolpidem, glucosamine | sibutramine, tranilast, megestrol acetate | felodipine, kinetisola, itraconazole, ketoprofen, glibenclamide |
Carrier | polyethlene glycol 6000, amphiphilicity | sodium lauryl sulfate, hydroxypropyl methylcellulose, eudragit, cellulose derivative matrice, lactose, polyethlene glycol, povidone-sodium, cholate-phospholipid mixed micelle | N/A | Polyvinylpyrrolidone |
Preparation method | N/A | spray | supercritical fluid | fusion production, hot-melt extruded, supercritical antisolvent process |
Characterizations | N/A | N/A | N/A | thermoanalytical measurement, NMR atomic force microscopy |
Mechanism | N/A | amorphous drug stabilization, sustained-release, thermal behavior, dissolution behaviour | crystalline property, solid nano dispersion system | binary dispersion, quantifying drug crystallinity, in vivo drug absorption, drug-release properties, ab initio polymer selection, physical stability studies, acidic decomposition characteristic, free amorphous solid dispersion, glassy form, drug-carrier interaction, heterogeneity, excipient distribution, phase diagram, enthalpy relaxation studies, crystal engineering principle, moisture, miscibility |