Non-Aqueous Water-Miscible Materials as Vehicles for Drug Delivery
A pharmaceutical composition includes at least one pharmaceutical component having a low aqueous solubility and at least one non-aqueous water-miscible material. Such a pharmaceutical composition is useful in providing a therapeutically meaningful amount of such pharmaceutical component at a target tissue. The pharmaceutical composition is particularly suitable for administration to or into an ocular environment to treat or control an ocular disease, disorder, or condition.
1 . A method of preparing a pharmaceutical composition comprising the steps of:
a) providing a non-aqueous water-miscible material;
b) solubilizing in the non-aqueous water-miscible material a pharmaceutical component having a low aqueous solubility,
wherein the pharmaceutical component is solubilizable in the non-aqueous water-miscible material in an amount sufficient to obtain a therapeutically effective concentration of the pharmaceutical composition; and
wherein the non-aqueous water-miscible material is present in the composition in an amount sufficient to deliver a therapeutically effective amount of the pharmaceutical component when the composition is administered into a target tissue.
2 . The method of claim 1 , wherein the non-aqueous water-miscible material is selected from the group consisting of alkanols having 1-6 carbon atoms, arylalkanols having 5 to 10 carbon atoms, polyols having 2 to 6 carbon atoms, n-methylpyrrolidone, polyalkylene glycols, polyglycerin, triacetin, dimethyl acetimide, dimethyl sulfoxide, ascorbic acid, phosphate buffer vehicle systems, isotonic vehicles, modified vegetable oils or petroleum jelly, as well as aqueous solutions containing alkyl cellulose materials, carbopol, polyvinyl alcohol, polyvinyl pyrrolidone, isopropyl myristate, other ophthalmic field employed, non-toxic, pharmaceutically acceptable organic and inorganic carriers, derivatives thereof, and mixtures thereof.
3 . The method of claim 1 , wherein the non-aqueous water-miscible material is mixed with water to provide a mixture of aqueous and non-aqueous materials.
4 . The method of claim 1 , wherein the sufficient amount of the pharmaceutical component solubilizable in the non-aqueous water-miscible material is an amount of at least about 0.1 mg/g.
5 . The method of claim 1 , wherein the pharmaceutical component is a member selected from the group consisting of: anti-inflammatory agents, anti-infective agents, anti-allergic agents, antiproliferative agents, anti-angiogenic agents, anti-oxidants, antihypertensive agents, neuroprotective agents, cell receptor agonists, cell receptor antagonists, immunomodulating agents, immunosuppressive agents, IOP lowering agents, beta adrenoceptor antagonists, alpha-2 adrenoceptor agonists, carbonic anhydrase inhibitors, cholinergic agonists, prostaglandins and prostaglandin receptor agonists, angiotensin converting enzyme (“ACE”) inhibitors, AMPA receptor antagonists, NMDA antagonists, angiotensin receptor antagonists, somatostatin agonists, mast cell degranulation inhibitors, alpha-adrenergic receptor blockers, alpha-2 adrenoceptor antagonists, thromboxane A2 mimetics, protein kinase inhibitors, prostaglandin F derivatives, prostaglandin-2 alpha antagonists, cyclooxygenase-2 inhibitors, muscarinic agents, and combinations thereof.
6 . The method of claim 1 , further comprising the step of sterilizing the composition.
7 . A pharmaceutical composition comprising:
a pharmaceutical component having a low aqueous solubility; the pharmaceutical component being present in the composition in an amount that is therapeutically effective when the composition is administered to or into a target tissue; and
a non-aqueous water-miscible material in an amount sufficient to solubilize said therapeutically effective amount of the pharmaceutical component.
8 . The pharmaceutical composition of claim 7 , wherein the pharmaceutical component is solubilized in the non-aqueous water-miscible material in an amount of at least about 0.1 mg/g.
9 . The pharmaceutical composition of claim 7 , wherein the pharmaceutical component is selected from the group consisting of anti-inflammatory agents, anti-infective agents, anti-allergic agents, antiproliferative agents, anti-angiogenic agents, anti-oxidants, antihypertensive agents, neuroprotective agents, cell receptor agonists, cell receptor antagonists, immunomodulating agents, immunosuppressive agents, IOP lowering agents, beta adrenoceptor antagonists, alpha-2 adrenoceptor agonists, carbonic anhydrase inhibitors, cholinergic agonists, prostaglandins and prostaglandin receptor agonists, angiotensin converting enzyme (“ACE”) inhibitors, AMPA receptor antagonists, NMDA antagonists, angiotensin receptor antagonists, somatostatin agonists, mast cell degranulation inhibitors, alpha-adrenergic receptor blockers, alpha-2 adrenoceptor antagonists, thromboxane A2 mimetics, protein kinase inhibitors, prostaglandin F derivatives, prostaglandin-2 alpha antagonists, cyclooxygenase-2 inhibitors, muscarinic agents, and combinations thereof.
10 . The pharmaceutical composition of claim 9 , wherein the composition further includes water mixed with the non-aqueous water-miscible material.
11 . The pharmaceutical composition of claim 10 , wherein the non-aqueous water-miscible material is selected from the group consisting of alkanols having 1 to 10 carbon atoms, arylalkanols having 5 to 14 carbon atoms, polyols having 2 to 12 carbon atoms, n-methylpyrrolidone, polyalkylene glycols, polyglycerin, triacetin, dimethyl acetimide, dimethyl sulfoxide, ascorbic acid, phosphate buffer vehicle systems, isotonic vehicles, modified vegetable oils or petroleum jelly, as well as aqueous solutions containing alkyl cellulose materials, carbopol, polyvinyl alcohol, polyvinyl pyrrolidone, isopropyl myristate, other ophthalmic field employed, non-toxic, pharmaceutically acceptable organic and inorganic carriers, derivatives thereof, and mixtures thereof.
12 . The pharmaceutical composition of claim 9 , wherein the non-aqueous water-miscible material is compatible with ocular tissue.
13 . The pharmaceutical composition of claim 11 , further comprising an additive selected from the group consisting of preservatives, anti-oxidants, surfactants, buffering agents, tonicity-adjusting agents, emulsifying agents, derivatives thereof, and combinations thereof.
14 . The pharmaceutical composition of claim 10 , wherein the composition has a viscosity of between about 10 cp to about 10,000 cp.
15 . The pharmaceutical composition of claims 7 , wherein said pharmaceutical component comprises a compound having Formula V.
16 . The pharmaceutical composition of claims 7 , wherein said pharmaceutical component comprises a compound having Formula II.
17 . A method of treating or controlling an ocular disease, disorder, or condition, the method comprising:
administering to or into an ocular environment a therapeutically effective amount of a mixture comprising a pharmaceutical component having low aqueous solubility solubilized in a non-aqueous water-miscible material, to treat or control said disease, disorder, or condition.
18 . The method of claim 17 , wherein the ocular disease, disorder, or condition is selected from the group consisting of diabetic retinopathy, diabetic macular edema, cystoid macular edema, age macular degeneration (including the wet and dry form), optic neuritis, retinitis, chorioretinitis, intermediate and posterior uveitis, choroidal neovascuralization, anterior uveitis (including iritis and iridocyclitis), keratitis, conjunctivitis, keratoconjunctivitis (including vernal keratoconjunctivitis (or “VKC”) and atopic keratoconjunctivitis), corneal ulcer, corneal edema, sterile corneal infiltrates, anterior scleritis, episcleritis, blepharitis, and post-operative (or post-surgical) ocular inflammation resulting from procedures such as photorefractive keratectomy, cataract removal surgery, intraocular lens (“IOL”) implantation, laser-assisted in situ keratomileusis (“LASIK”), conductive keratoplasty, radial keratotomy, and combinations thereof.
19 . The method of claim 17 , wherein said administering is carried out by topical administration to treat or control an anterior-segment ocular disease, disorder, or condition.
20 . The method of claim 17 , wherein said administering is carried out by intravitreal administration to treat or control a posterior-segment ocular disease, disorder, or condition.