共 110 条
[1]
Bermejo M(2020)Mechanistic physiologically-based biopharmaceutics modeling (PBBM) approach to assess the in vivo performance of an orally administered drug product: From IVIVC to IVIVP Pharmaceutics 12 74-4304
[2]
Hens B(2017)In vivo dissolution and systemic absorption of immediate release ibuprofen in human gastrointestinal tract under fed and fasted conditions Mol Pharm 14 4295-163
[3]
Dickens J(2014)The Biopharmaceutics Classification System: subclasses for in vivo predictive dissolution (IPD) methodology and IVIVC Eur J Pharm Sci 57 152-338
[4]
Mudie D(2017)Investigation of the effect of solubility increase at the main absorption site on bioavailability of BCS class II drug (risperidone) using liquisolid technique Drug Deliv 24 328-392
[5]
Paixão P(2018)Amorphous solid dispersions and nanocrystal technologies for poorly water-soluble drug delivery – an update Int J Pharmaceutics 535 379-175
[6]
Tsume Y(2020)The potential of nanofibers to increase solubility and dissolution rate of the poorly soluble and chemically unstable drug lovastatin Int J Pharmaceutics 573 167-17
[7]
Sun D(2020)Impact of nanoparticle size and solid state on dissolution rate by investigating modified drug powders Powder Technol 376 12-1617
[8]
Baker JR(2012)Improvement in solubility of poor water-soluble drugs by solid dispersion Int J Pharm Investig 2 1607-1344
[9]
Wen B(2011)Physical stability of salts of weak bases in the solid-state J Pharm Sci 100 1334-556
[10]
Frances A(2014)Combined use of crystalline sodium salt and polymeric precipitation inhibitors to improve pharmacokinetic profile of ibuprofen through supersaturation AAPS PharmSciTech 15 536-356