Claims for Patent: 10,786,444

Summary for Patent: 10,786,444

Title:	PH dependent carriers for targeted release of pharmaceuticals along the gastrointestinal tract, compositions therefrom, and making and using same
Abstract:	Novel drug carriers capable of targeted and/or pH dependent release of biologically active agents into selected pH environments including the gastrointestinal (GI), ophthalmic, urinary, or reproductive tracts. Unexpectedly, carriers including free fatty acids (FFA) are able to deliver biologically active agents to various pH environments. Such targeted delivery is tailorable and useful for active agents that are: (a) injurious to the upper GI tract (esophagus, stomach, and duodenum), (b) acid labile, (c) impermeable/insoluble compounds in GI fluids, (d) susceptible to first pass metabolism, and/or (e) cause stomach irritation, upset, or dyspepsia.
Inventor(s):	Upendra Marathi, Susann Childress, Shaun Gammill, Robert W. Strozier
Assignee:	Plx Acquisition Company LLC
Application Number:	US16/833,371
Patent Claims:	1. A method of targeting release of a biologically active agent to the small intestine of a subject, comprising orally administering to the subject an ingestible pharmaceutical composition, wherein the composition comprises a suspension of solid particles of a biologically active agent in a non-aqueous liquid carrier, wherein the non-aqueous liquid carrier is an oil, and wherein the carrier comprises: (a) at least about 10 wt. % of free monocarboxylic acid having at least 8 carbons, wherein the monocarboxylic acid is liquid at room temperature; and (b) less than about 10 wt. % zwitterionic phospholipid; wherein the pharmaceutical composition releases a lesser amount of active agent at a pH of <3 than at pH>3, and wherein the pharmaceutical composition is formulated in the absence of a solvent. 2. The method of claim 1, wherein the composition consists essentially of a suspension of solid biologically active agent in the non-aqueous liquid carrier. 3. The method of claim 1, wherein the carrier further comprises a neutral lipid. 4. The method of claim 1, wherein the non-aqueous liquid carrier comprises at least about 14 wt. % of free monocarboxylic acid having at least 8 carbons. 5. The method of claim 4, wherein the carrier comprises less than about 7.5 wt. % of zwitterionic phospholipid. 6. The method of claim 1, wherein: (a) less than about 20% of the biologically active agent is released from the non-aqueous liquid carrier at pH<3; and (b) greater than about 50% of the biologically active agent is released from the non-aqueous liquid carrier at pH>3. 7. The method of claim 1, wherein the non-aqueous liquid carrier releases a lesser amount of biologically active agent at pH<5 than at pH>5. 8. The method of claim 1, wherein the weight ratio of the active agent to the non-aqueous liquid carrier is between about 50: about 1 and about 1: about 10. 9. The method of claim 1, wherein the carrier comprises one monocarboxylic acid or a plurality of monocarboxylic acids. 10. The method of claim 1, wherein the carrier comprises a mixture of different monocarboxylic acids having at least 8 carbons. 11. The method of claim 1, wherein the carrier comprises up to about 40 wt. % monocarboxylic acids. 12. The method of claim 1, wherein the biologically active agent comprises at least one agent selected from the group consisting of an acid-labile pharmaceutical agent, an anti-depressant, an anti-diabetic agent, an anti-epileptic agent, an anti-fungal agent, an anti-malarial agent, an anti-muscarinic agent, an anti-neoplastic agent, an immunosuppressant, an anti-protozoal agent, an anti-tussive, a neuroleptics, a beta-blocker, a cardiac inotropic agent, a corticosteroid, an anti-parkinsonian agent, a gastrointestinal agent, histamine, a histamine receptor antagonist, a keratolytic, a lipid regulating agent, a muscle relaxant, a nitrate, an anti-anginal agent, a nutritional agent, an opioid analgesic, a sex hormone, a stimulant, a nutraceutical, a peptide, a protein, a therapeutic protein, a nucleoside, a nucleotide, DNA, RNA, a glycosaminoglycan, an acid-labile drug, (+)-N{3-[3-(4-fluorophenoxy)phenyl]-2-cyclopenten-1-yl}-N-hydroxyurea, amylase, aureomycin, bacitracin, beta carotene, cephalosporins, chloromycetin, cimetidine, cisapride, cladribine, clorazepate, deramciclane, didanosine, digitalis glycosides, dihydrostreptomycin, erythromycin, etoposide, famotidine, a hormone, estrogen, insulin, adrenalin, heparin, lipase, milameline, novobiocin, pancreatin, penicillin salts, polymyxin, pravastatin, progabide, protease, quinapril, quinoxaline-2-carboxylic acid, [4-(R)carbamoyl-1-(S-3-fluorobenzyl-2-(S),7-dihydroxy-7-methyloctyl]amide, quinoxaline-2-carboxylic acid[1-benzyl-4-(4,4-difluoro-1-hydroxy-cyclohexyl)-2-hydroxy-4-hydroxycarbamoyl-butyl]-amide ranitidine, streptomycin, subtilin, sulphanilamide, a proton pump inhibitors, esomeprazole, lansoprazole, minoprazole, omeprazole, pantoprazole and rabeprazole. 13. The method of claim 1, wherein the biologically active agent is an acid-labile drug. 14. The method of claim 13, wherein the acid-labile drug is selected from the group consisting of heparin, insulin, erythropoietin, pancreatin, lansoprazole, omeprazole, pantoprazole, rabeprazole, penicillin salts, benzathine penicillin, polymyxin, sulphanilamide, and erythromycin. 15. The method of claim 1, wherein the non-aqueous liquid carrier further comprises at least one component selected from the group consisting of an adjuvant, a mixture of adjuvants, an antioxidant, a mixture of antioxidants, a viscomodulator, a mixture of viscomodulators, and a permeability-improving agent. 16. The method of claim 1, wherein the non-aqueous liquid carrier is substantially free of fatty acid salt. 17. A method of targeting release of a non-steroidal anti-inflammatory drug (NSAID) to the small intestine of a subject, comprising orally administering to the subject an ingestible pharmaceutical composition, wherein the composition comprises a suspension of solid particles of a weak-acid NSAID in a non-aqueous liquid carrier, wherein the non-aqueous liquid carrier is an oil, and wherein the carrier comprises: (a) at least about 10 wt. % of free monocarboxylic acid having at least 8 carbons, wherein the monocarboxylic acid is liquid at room temperature; and (b) less than about 10 wt. % zwitterionic phospholipid; wherein the pharmaceutical composition releases a lesser amount of active agent at a pH of <3 than at pH>3, and wherein the pharmaceutical composition is formulated in the absence of a solvent. 18. The pharmaceutical composition of claim 17, wherein the NSAID is selected from the group consisting of ibuprofen, piroxicam, salicylate, aspirin, naproxen, indomethacin, diclofenac, mefenamic acid, COX2 inhibitors, and any mixture thereof. 19. The method of claim 18, wherein the NSAID is selected from the group consisting of aspirin, naproxen, indomethacin and mefenamic acid. 20. The method of claim 17, wherein: (a) the NSAID is released at pH values of less than pH 2 at a rate of less than about 20% in thirty minutes, and (b) the NSAID is released at pH values above about pH 3, at a rate of greater than about 80% in thirty minutes. 21. The method of claim 1, wherein the amount of zwitterionic phospholipids is selected from the group consisting of about 0.5 wt. %, about 1 wt. %, about 2 wt. %, about 2.5 wt. %, about 5 wt. %, and about 7.5 wt. %.