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. 2015 Aug 4;9:4269–4277. doi: 10.2147/DDDT.S90706

Table 1.

The formulation, particle size, and specific surface area of the megestrol acetate solid dispersion nanoparticles prepared using the SAS process

Formulation Drug content (%) Mean particle size (nm) Specific surface area (m2/g)
Megestrol acetate:HPMC =1:2 95.1±2.6 135.8±18.2 96.16±1.69
Megestrol acetate:PVP K30 =1:2 95.9±3.7 310.9±30.3 40.21±1.33
Megestrol acetate:HPMC:Gelucire 44/14 =1:2:0.5 96.1±2.1 245.9±35.9 49.22±1.09
Megestrol acetate:HPMC:poloxamer 407 =1:2:0.5 95.8±2.3 229.7±21.6 51.13±1.03
Megestrol acetate:HPMC:Ryoto sugar ester L1695 =1:2:0.5 97.1±2.0 155.3±20.1 69.31±1.25
Megestrol acetate:HPMC:TPGS =1:2:0.5 97.7±1.9 495.2±65.3 33.11±1.19
Megestrol acetate:HPMC:Ryoto sugar ester L1695 =1:2:1 98.9±1.8 180.3±29.1 57.22±1.35

Notes:

The drug content (%) = weight of the loaded drug/weight of the feeding drug ×100. Data are expressed as mean ± standard deviation (n=3).

Abbreviations: SAS, supercritical antisolvent; HPMC, hydroxypropylmethyl cellulose; PVP, polyvinylpyrrolidone; TPGS, D-α-tocopheryl polyethylene glycol 1000 succinate.