Multiparticulates comprising low-solubility drugs and carriers that result in rapid drug release
Multiparticulates of low-solubility drugs and carriers that result in rapid release of the drug are disclosed.
1 . A pharmaceutical composition comprising multiparticulates, said multiparticulates comprising a drug having an aqueous solubility of less than about 1 mg/mL at pH 6-7 and a sugar alcohol selected from the group consisting of mannitol, erythritol, and mixtures thereof, wherein said multiparticulates have a volume-weighted mean diameter of from about 10 μm to about 1000 μm, and wherein said sugar alcohol makes up at least 30 wt % of said multiparticulates and has a ratio of melting temperature to glass transition temperature in degrees Kelvin of at least about 1.5.
2 . The composition of claim 1 wherein said drug and said sugar alcohol together constitute at least 60 wt % of the total mass of said multiparticulate.
3 . The composition of claim 1 wherein said multiparticulates consist essentially of said drug and said sugar alcohol.
4 . The composition of claim 3 wherein said sugar alcohol makes up at least about 60 wt % of said multiparticulates.
5 . The composition of claim 1 wherein said multiparticulates have volume-weighted mean diameter of from about 30 μm to about 300 μm,
6 . (canceled)
7 . The composition of claim 1 wherein said sugar alcohol is mannitol.
8 . (canceled)
9 . The composition of claim 1 wherein said drug is selected from the group consisting of acyclovir, amlodipine, apomorphine, atorvastatin, celecoxib, chlorthalidone, clarithromycin, digitoxin, digoxin, erythromycin, famotidine, fluconazole, glipizide, griseofulvin, lidocaine, nadolol, nelfinavir, nifedipine, paroxetine, phenobarbital, prednisolone, sertraline, sildenafil, spironolactone, testosterone, thiabendazole, torcetrapib, valdecoxib, voriconazole, ziprasidone, and pharmaceutically acceptable forms thereof.
10 . The composition of claims 1 - 5 wherein said composition, following administration to a phosphate-buffered solution consisting essentially of an aqueous solution of 50 mM KH 2 PO 4 and 0.5 wt % polyoxyethylene 20 oleate at pH 7.3, releases at least 80 wt % of said drug from said composition within about 3 minutes following administration.
11 - 16 . (canceled)
17 . A pharmaceutical composition comprising multiparticulates, said multiparticulates comprising a low-solubility drug and a pore-forming carrier, wherein said pore-forming carrier is selected from the group consisting of (i) a mixture of glyceryl dibehenate and polyethylene glycol behenate, (ii) an anionic emulsifying wax and (iii) mixtures thereof.
18 . The composition of claim 17 wherein pore-forming carrier (i) comprises approximately equal amounts of glyceryl dibehenate and polyethylene glycol behenate.
19 . The composition of claim 17 wherein pore-forming carrier (ii) comprises a mixture of cetyl alcohol, stearyl alcohol, water and sodium lauryl sulfate.
20 . The composition of claim 17 wherein said pore-forming carrier and said low-solubility drug constitute at least about 50 wt % of the total mass of said multiparticulate.
21 . The composition of claim 17 wherein said drug has an aqueous solubility of less than about 10 mg/mL at pH 6-7.
22 . The composition of claim 21 wherein said drug is selected from the group consisting of acyclovir, amlodipine, apomorphine, atorvastatin, celecoxib, chlorthalidone, clarithromycin, digitoxin, digoxin, erythromycin, famotidine, fluconazole, glipizide, griseofulvin, lidocaine, nadolol, nelfinavir, nifedipine, paroxetine, phenobarbital, prednisolone, sertraline, sildenafil, spironolactone, testosterone, thiabendazole, torcetrapib, valdecoxib, voriconazole, ziprasidone, and pharmaceutically acceptable forms thereof.
23 . The composition of claims 17 - 22 further comprising a dissolution enhancer selected from the group consisting of surfactants, alcohols, sugars, salts, amino acids, and mixtures thereof.
24 - 27 . (canceled)