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. Author manuscript; available in PMC: 2014 Aug 30.
Published in final edited form as: Int J Pharm. 2012 Aug 25;453(1):198–214. doi: 10.1016/j.ijpharm.2012.08.042

Table 2.

Representative nanocrystal or nanoemulsion based formulations of poorly soluble drugs that are currently available commercially

Formulation approach Commercial name Drug Free drug solubility (μg/ml) Major indication Dosage form
Nanocrystal Triglide® Fenofibrate 0.3 123 Hypercholesterolemia Tablet
Rapamune® Sirolimus 2.6 124 Immunosuppresion Tablet
Emend® Aprepitant 3 - 7125 Antiemetic Capsule
Tricor® Fenofibrate 0.3 Hypercholesterolemia Tablet
Megace ES® Megestrol Antianorexia Suspension (oral)
Invenga™ Paliperidonepalmitate 11 – 30 126 Schizophrenia Suspension (intramuscular)

Nanoemulsion Estrasorb® Estradiol 2 127 Menopausal vasomotor symptoms Emulsion (topical)
Restasis® Cyclosporine 20 128 Chronic dry eye Emulsion (ophthalmic)
SandimmunNeoral® Cyclosporine 20 128 Prophylaxis of organ rejection following organ transplant SMEDDS
Norvir® Ritonavir 1 129 HIV infection SMEDDS
Fortovase®* Saquinavir 29 130 HIV infection SMEDDS

SMEDDS: self-microemulsifying drug delivery system

*

Currently discontinued in the US