Self-nanoemulsion of poorly soluble drugs
The present disclosure pertains to pharmaceutical formulation comprising low aqueous solubility drug, a solubilizer, and optionally at least one pharmaceutically acceptable excipient that form dispersions when exposed to an aqueous environment.
1. A pharmaceutical formulation comprising:
a) abiraterone;
b) propylene glycol monocaprylate; and
c) an emulsifier.
2. The pharmaceutical formulation of claim 1 , wherein the pharmaceutical formulation forms an emulsion when exposed to an aqueous environment; and further wherein a mean particle size (D50) of a droplet of the emulsion in said aqueous environment ranges from about 50 nm to about 800 nm.
3. The pharmaceutical formulation of claim 2 , wherein the mean particle size (D50) ranges from about 50 nm to about 200 nm.
4. The pharmaceutical formulation of claim 1 , wherein a difference in a solubility parameter of the active pharmaceutical ingredient and a solubility parameter of the non-aqueous solubilizer ranges from about 2 (MPa) 1/2 to about 7 (MPa) 1/2 .
5. The pharmaceutical formulation of claim 1 , wherein the emulsifier is selected from the group consisting of polyethoxylated oils, polysorbates, sorbitan esters of fatty acids, and combinations thereof.
6. The pharmaceutical formulation of claim 1 , further comprising a crystallization inhibitor.
7. The pharmaceutical formulation of claim 6 , wherein the crystallization inhibitor is selected from the group consisting of polyvinylpyrrolidones, cellulose ethers, and combinations thereof.
8. The pharmaceutical formulation of claim 1 , further comprising a co-solvent.
9. The pharmaceutical formulation of claim 8 , wherein the co-solvent is selected from the group consisting of propylene glycol, low molecular weight polyethylene glycols, triacetin, triethyl citrate, ethanol, glycofurol, and combinations thereof.
10. The pharmaceutical formulation of claim 1 , wherein the formulation is in a dosage form comprising a capsule.
11. A method of forming a nanoemulsion in an aqueous fluid comprising, mixing the pharmaceutical formulation of claim 1 in an aqueous fluid.