Methods and compositions for reducing neurodegeneration in amyotrophic lateral sclerosis

• US 20060142241A1
• Filed: 10/31/2005
• Published: 06/29/2006
• Est. Priority Date: 11/01/2004
• Status: Abandoned Application

• Current Assignee: Seo Hong Yoo
• Original Assignee: Seo Hong Yoo
• Inventors: Yoo, Seo Hong
• Application Number:
  US11/263,087
• Publication Number:
  US 20060142241A1
• Time in Patent Office: Days
• US Class Current: 514/59
• CPC Class Codes: A61K 31/56 Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
• CPC Class Codes: A61K 31/575 substituted in position 17 beta by a chain of three or more carbon atoms, e.g. cholane, cholestane, ergosterol, sitosterol
• CPC Class Codes: A61K 31/715 Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
• CPC Class Codes: A61K 31/718 Starch or degraded starch, e.g. amylose, amylopectin
• CPC Class Codes: A61K 47/36 Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
• CPC Class Codes: A61K 9/0095 Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches A61K9/0007 takes precedence; eatable gels or foams A61K9/0056; oral mucosa adhesive forms A61K9/006
• CPC Class Codes: A61K 9/08 Solutions composition of solutions A61K47/00
• CPC Class Codes: A61P 25/00 Drugs for disorders of the nervous system
• CPC Class Codes: A61P 25/14 for treating abnormal movements, e.g. chorea, dyskinesia
• CPC Class Codes: A61P 25/16 Anti-Parkinson drugs
• CPC Class Codes: A61P 25/28 for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: Y02A 50/30 Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

The present disclosure is related to clear aqueous solutions of one or more bile acids and either an aqueous soluble starch conversion product or a non-starch polysaccharide. Solutions of the disclosure may be administered to a subject in conjunction with a pharmaceutical compound having a therapeutic effect in subjects with a neurodegenerative disease and/or a motor neuron disease. In some embodiments, the disease is amyotrophic lateral sclerosis.

Claims

1. A method of ameliorating or treating at least one symptom of a neurodegenerative diseases in a subject comprising:

administering to a subject a clear aqueous solution comprising;

(a) a first material selected from the group consisting of a bile acid, an aqueous soluble derivative of a bile acid, a bile acid salt, and a bile acid conjugated with an amine by an amide linkage;

(b) a carbohydrate selected from the group consisting of an aqueous soluble starch conversion product or an aqueous soluble non-starch polysaccharide;

(c) water, wherein the first material and the carbohydrate both remain in solution for all pH values of the solution within a selected range of pH values.

2. A method according to claim 1, wherein the neurodegenerative disease is selected from the group consisting of Parkinson'"'"'s disease, Huntington'"'"'s disease, Alzheimer'"'"'s disease, amyotrophic lateral sclerosis, stroke, and spinal cord injury.

3. A method according to claim 2, wherein the neurodegenerative disease is amyotrophic lateral sclerosis.

4. A method according to claim 3, wherein the amyotrophic lateral sclerosis is advanced amyotrophic lateral sclerosis.

5. A method according to claim 1, wherein the symptom is selected from the group consisting of shortened lifespan and paralysis.

6. A method according to claim 1, wherein subject is a mammal.

7. A method according to claim 1, wherein subject is a human.

8. A method according to claim 1, wherein the first material is present in therapeutically active amount.

9. A method according to claim 1, wherein the first material is selected from the group consisting of chenodeoxycholic acid, cholic acid, hyodeoxycholic acid, deoxycholic acid, 7-oxolithocholic acid, lithocholic acid, iododeoxycholic acid, iocholic acid, tauroursodeoxycholic acid, taurochenodeoxycholic acid, taurodeoxycholic acid, glycoursodeoxycholic acid, taurocholic acid, glycocholic acid, their derivatives at a hydroxyl or carboxylic acid group on the steroid nucleus, their salts, or their conjugates with amines.

10. A method according to claim 1, wherein the aqueous soluble starch conversion product is selected from the group consisting of maltodextrin, dextrin, liquid glucose, corn syrup solid, and soluble starch.

11. A method according to claim 1, wherein the selected pH range is between approximately 1 and approximately 10 inclusive.

12. A method according to claim 1, wherein the first material is ursodeoxycholic acid or sodium salt of ursodeoxycholic acid.

13. A method according to claim 1, wherein the aqueous soluble starch conversion product is maltodextrin.

14. A method according to claim 1, wherein the aqueous soluble non-starch polysaccharide are selected from the group consisting of dextran, guar gum, pectin, indigestible soluble fiber.

15. A method of ameliorating or treating at least one symptom of a motor neuron disease in a subject comprising:

administering to a subject a clear aqueous solution comprising;

(a) a first material selected from the group consisting of a bile acid, an aqueous soluble derivative of a bile acid, a bile acid salt, and a bile acid conjugated with an amine by an amide linkage;

(b) a carbohydrate selected from the group consisting of an aqueous soluble starch conversion product or an aqueous soluble non-starch polysaccharide;

(c) water, wherein the first material and the carbohydrate both remain in solution for all pH values of the solution within a selected range of pH values.

16. A method according to claim 15, wherein the motor neuron disease is selected from the group consisting of amyotrophic lateral sclerosis, progressive bulbar palsy, pseudobulbar palsy, primary lateral sclerosis, progressive muscular atrophy, and post-polio syndrome.

17. A method according to claim 16, wherein the motor neuron disease is amyotrophic lateral sclerosis.

18. A method according to claim 17, wherein the amyotrophic lateral sclerosis is advanced amyotrophic lateral sclerosis.

19. A method according to claim 15, wherein the symptom is selected from the group consisting of shortened lifespan and paralysis.

20. A method according to claim 15, wherein subject is a mammal.

21. A method according to claim 15, wherein subject is a human.

22. A method according to claim 15, wherein the first material is present in therapeutically active amount.

23. A method according to claim 15, wherein the first material is selected from the group consisting of chenodeoxycholic acid, cholic acid, hyodeoxycholic acid, deoxycholic acid, 7-oxolithocholic acid, lithocholic acid, iododeoxycholic acid, iocholic acid, tauroursodeoxycholic acid, taurochenodeoxycholic acid, taurodeoxycholic acid, glycoursodeoxycholic acid, taurocholic acid, glycocholic acid, their derivatives at a hydroxyl or carboxylic acid group on the steroid nucleus, their salts, or their conjugates with amines.

24. A method according to claim 15, wherein the aqueous soluble starch conversion product is selected from the group consisting of maltodextrin, dextrin, liquid glucose, corn syrup solid, and soluble starch.

25. A method according to claim 15, wherein the selected pH range is between approximately 1 and approximately 10 inclusive.

26. A method according to claim 15, wherein the first material is ursodeoxycholic acid or sodium salt of ursodeoxycholic acid.

27. A method according to claim 15, wherein the aqueous soluble starch conversion product is maltodextrin.

28. A method according to claim 15, wherein the aqueous soluble non-starch polysaccharide are selected from the group consisting of dextran, guar gum, pectin, indigestible soluble fiber.

29. A method for ameliorating or treating at least one symptom of a neurodegenerative disease or at least one symptom of a motor neuron disease in a subject comprising:

administering a pharmaceutical compound to the subject; and

administering to the subject a clear aqueous solution comprising;

(a) a first material selected from the group consisting of a bile acid, an aqueous soluble derivative of a bile acid, a bile acid salt, and a bile acid conjugated with an amine by an amide linkage;

(b) a carbohydrate selected from the group consisting of an aqueous soluble starch conversion product or an aqueous soluble non-starch polysaccharide;

(c) water, wherein the first material and the carbohydrate both remain in solution for all pH values of the solution within a selected range of pH values;

30. A method according to claim 29, wherein the subjects is a mammal.

31. A method according to claim 29, wherein the subjects is a human.

32. A method according to claim 29, wherein the administering a pharmaceutical compound and the administering a clear aqueous solution occur at the same time.

33. A method according to claim 29, wherein the administering a pharmaceutical compound and the administering a clear aqueous solution occur at different moments within a defined period of time.

34. A method according to claim 33, wherein the administering a pharmaceutical compound occurs before the administering a clear aqueous solution.

35. A method according to claim 33, wherein the administering a pharmaceutical compound occurs after the administering a clear aqueous solution.

36. A method according to claim 29, wherein the administering a pharmaceutical compound further comprises administering a plurality of doses of the pharmaceutical compound.

37. A method according to claim 29, wherein the administering a clear aqueous solution further comprises administering a plurality of doses of the clear aqueous solution.

38. A method according to claim 37, wherein the administering a pharmaceutical compound further comprises administering a plurality of doses of the pharmaceutical compound.

39. A method according to claim 38, wherein the administering a pharmaceutical compound further comprises administering at least one dose of the pharmaceutical compound after the administering a clear aqueous solution.

40. A method according to claim 38, wherein the administering a pharmaceutical compound further comprises administering at least one dose of the pharmaceutical compound before the administering a clear aqueous solution.

41. A method according to claim 38, wherein the administering a clear aqueous solution further comprises administering at least one dose of the clear aqueous solution after the administering a pharmaceutical compound.

42. A method according to claim 38, wherein the administering a clear aqueous solution further comprises administering at least one dose of the clear aqueous solution before the administering a pharmaceutical compound.

43. A method according to claim 38, wherein the administering a clear aqueous solution and the administering a pharmaceutical compound occur concurrently for each dose.

44. A method according to claim 43, wherein the clear aqueous solution further comprises the pharmaceutical compound.

45. A method according to claim 29, wherein the first material is present in therapeutically active amount.

46. A method according to claim 29, wherein the first material is selected from the group consisting of chenodeoxycholic acid, cholic acid, hyodeoxycholic acid, deoxycholic acid, 7-oxolithocholic acid, lithocholic acid, iododeoxycholic acid, iocholic acid, tauroursodeoxycholic acid, taurochenodeoxycholic acid, taurodeoxycholic acid, glycoursodeoxycholic acid, taurocholic acid, glycocholic acid, their derivatives at a hydroxyl or carboxylic acid group on the steroid nucleus, their salts, or their conjugates with amines.

47. A method according to claim 29, wherein the aqueous soluble starch conversion product is selected from the group consisting of maltodextrin, dextrin, liquid glucose, corn syrup solid, and soluble starch.

48. A method according to claim 29, wherein the selected pH range is between approximately 1 and approximately 10 inclusive.

49. A method according to claim 29, wherein the first material is ursodeoxycholic acid or sodium salt of ursodeoxycholic acid.

50. A method according to claim 29, wherein the aqueous soluble starch conversion product is maltodextrin.

51. A method according to claim 29, wherein the aqueous soluble non-starch polysaccharide are selected from the group consisting of dextran, guar gum, pectin, indigestible soluble fiber.

52. A method according to claim 29, wherein the neurodegenerative disease or motor neuron disease is selected from the group consisting of Parkinson'"'"'s disease, Huntington'"'"'s disease, Alzheimer'"'"'s disease, amyotrophic lateral sclerosis, stroke, spinal cord injury, progressive bulbar palsy, pseudobulbar palsy, primary lateral sclerosis, progressive muscular atrophy, and post-polio syndrome.

53. A method according to claim 52, wherein the neurodegenerative disease or motor neuron disease is amyotrophic lateral sclerosis.

54. A method according to claim 29, wherein the pharmaceutical compound decreases motor neuron death.

55. A method according to claim 54, wherein the pharmaceutical compound that decreases motor neuron death is selected from the group consisting of Pasiniazide, Benzthiazide, Prednisolone, Menthol, Mebhydrolin Naphthalenesulfonate, Trichlormethiazide, Oxytetracycline, Arcaine sulphate, Erythromycin, Glutathione, Trioxsalen, NylidrinHCL, Desmethyldiazepam, Thonzylamine HCL, Valproate Na, Aminophenazone, Sulfamethizole, Droperidol, 2-Thiouracil, Kynurenic acid, Fusidic acid, Leucovorin Ca, Sparteine sulfate, Amygdalin, Pramoxine HCL, Furosemide, Dinitolmide, Budesonide, Flopropione, Fluorometholone, anti-inflammatory), N-Formylmethionylphenylalanine, Thiopental Na, Lansoprazole, Bretylium Tosylate, Cefamandole Na, Oxybendazole, Cycloleucylglycine, Dantrolene Na, Tetroquinone, piperazine, Aesculin, Ethisterone, Dimethadione, Griseofulvin, Acetaminosalol, Isoguvacine HCL, Putrescine DIHCL, Emetine HCL, Sulfanilamide, Mimosine, Acetylcholine, Pralidoxime Mesylate, LysylTryptophanyl-Lysine, Hecogenin, Prednisolone acetate, Albendazole, Hydrochlorothiazide, Demeclocycline HCL, Nitrofurazone, Dicloxacillin Na, alpha-Tocopherol, Tetracycline HCL, Fenofibrate, Probenecid, Tretinoin, Acetaminophen, Hydrastinine HCL, d[-Arg-2]Kyotorphin acetate, NMDA, Cefinetazole Na, Ribavirin, O-Benzyl-L-Serine, Picrotoxin, Oxethazine, Sulfathiazole, Trichlormethine, Nabumetone, Chloramphenicol, riluzole, ginseng and its extract, glycyrrhizin and glycyrrhizic acid, derivatives of carboquinone, coenzyme Q10, creatine, insulin-like growth factor-1, minocycline, mecamserin, xaliproden, gabapentin, dextromethorphan, talampanel, IL-1, TR-500, procysteine, brain derived neurotrophic factor, baclofen, tizanidin, benzodiazepines, glycopyrrolate, atropine, quinine, phenyloin and morphine.

56. A method according to claim 29, wherein the pharmaceutical compound is selected from the group consisting of hormones, hormone antagonists, analgesic, antipyretics, anti-inflammatory drugs, immunoactive drugs, antineoplastic drugs, antibiotics, anti-inflammatory agents, sympathomimetic drugs, anti-infective drugs, anti-tumor agents, and anesthetics.

57. A method according to claim 29, wherein the pharmaceutical compound is selected from the group consisting of insulin, heparin, calcitonin, ampicillin, octreotide, sildenafil citrate, calcitriol, dihydrotachysterol, ampomorphine, yohimbin, trazodone, acyclovir, amantadine •

HCl, rimantadine•

HCl, cidofovir, delavirdine•

mesylate, didanosine, famciclovir, forscarnet sodium, fluorouracil, ganciclovir sodium, idoxuridine, interferon-_, lamivudine, nevirapine, penciclovir, ribavirin, stavudine, trifluridine, valacyclovir•

HCl, zalcitabine, zidovudine, indinavir•

H2SO4, ritonavir, nelfinavir•

CH3SO3H, saquinavir•

CH3SO3H, d-penicillamine, chloroquine, hydroxychloroquine, aurothioglucose, gold sodium-thiomalate, auranofin levamisole, DTC, isoprinosine, methyl inosine monophosphate, muramyl dipeptide, diazoxide, hydralazine•

HCl, minoxidil, dipyridamole, isoxsuprine•

HCl, niacin, nylidrin•

HCl, phentolamine, doxazosin•

CH3SO3H, prazosin•

HCl, terazocin•

HCl, clonidine•

HCl, nifedipine, molsidomine, amiodarone, acetylsalicylic acid, verapamil, diltiazem, nisoldipine, isradipine, bepridil, isosorbide•

dinitrate, pentaerythrytol•

tetranitrate, nitroglycerin, cimetidine, famotidine, nizatidine, ranitidine, lansoprazole, omeprazole, misoprostol, sucralfate, metoclopramide•

HCl, erythromycin, bismuth compound, alprostadil, albuterol, pirbuterol, terbutaline•

H2SO4, salmetrol, aminophylline, dyphylline, ephedrine, ethylnorepinephrine, isoetharine, isoproterenol, metaproterenol, n-docromil, oxy triphylline, theophylline, bitolterol, fenoterol, budesonide, flunisolide, beclomethasone•

dipropionate, fluticasone•

propionate, codeine, codeine sulfate, codeine phosphate, dextromethorphan•

HBr, triamcinolone•

acetonide, montelukast sodium, zafirlukast, zileuton, cromolyn sodium, ipratropium bromide, nedocromil sodium benzonate, diphenhydramine•

HCl, hydrocodone•

bitartarate, methadone•

HCl, morphine sulfate, acetylcysteine, guaifenesin, ammonium carbonate, ammonium chloride, antimony potassium tartarate, glycerin, terpin•

hydrate, colfosceril palmitate, atorvastatin•

calcium, cervastatin•

sodium, fluvastatin•

sodium, lovastatin, pravastatin•

sodium, simvastatin, picrorrhazia kurrva, andrographis paniculata, moringa oleifera, albizzia lebeck, adhata vasica, curcuma longa, momordica charantia, gymnema sylvestre, terminalia arjuna, azadirachta indica, tinosporia cordifolia, metronidazole, amphotericin B, clotrimazole, fluconazole, haloprogin, ketoconazole, griseofulvin, itraconazole, terbinafin•

HCl, econazole•

HNO3, miconazole, nystatin, oxiconazole•

HNO3, sulconazole•

HNO3, cetirizine•

2HCl, dexamethasone, hydrocortisone, prednisolone, cortisone, catechin and its derivatives, glycyrrhizin, glycyrrhizic acid, betamethasone, ludrocortisone•

acetate, flunisolide, fluticasone•

propionate, methyl prednisolone, somatostatin, lispro, glucagon, proinsulin, insoluble insulins, acarbose, chlorpropamide, glipizide, glyburide, metformin•

HCl, repaglinide, tolbutamide, amino acid, colchicine, sulfinpyrazone, allopurinol, piroxicam, tolmetin sodium, indomethacin, ibuprofen, diflunisal, mefenamic acid, naproxen, and trientine.

58. A clear aqueous solution comprising:

(a) a first material selected from the group consisting of a bile acid, an aqueous soluble derivative of a bile acid, a bile acid salt, and a bile acid conjugated with an amine by an amide linkage;

(b) a carbohydrate selected from the group consisting of an aqueous soluble starch conversion product or an aqueous soluble non-starch polysaccharide;

(c) a pharmaceutically effective amount of a pharmaceutical compound that decreases motor neuron death; and

(d) water,

wherein the first material, the carbohydrate, and the riluzole all remain in solution for all pH values of the solution within a selected range of pH values.

59. A clear aqueous solution according to claim 58, wherein the first material is present in a neuroprotective amount.

60. A clear aqueous solution according to claim 58, wherein the pharmaceutical compound remains in solution for all pH values within the selected range.

61. A clear aqueous solution according to claim 58, wherein the first material is ursodeoxycholic acid.

62. A clear aqueous solution according to claim 58, wherein the first material is the sodium salt of ursodeoxycholic acid.

63. A clear aqueous solution according to claim 58, wherein the first material is selected from the group consisting of chenodeoxycholic acid, cholic acid, hyodeoxycholic acid, deoxycholic acid, 7-oxolithocholic acid, lithocholic acid, iododeoxycholic acid, iocholic acid, tauroursodeoxycholic acid, taurochenodeoxycholic acid, taurodeoxycholic acid, glycoursodeoxycholic acid, taurocholic acid, glycocholic acid, their derivatives at a hydroxyl or carboxylic acid group on the steroid nucleus, their salts, or their conjugates with amines.

64. A clear aqueous solution according to claim 58, wherein the selected pH range is between approximately 1 and approximately 10 inclusive.

65. A clear aqueous solution according to claim 58, wherein the aqueous soluble starch conversion product is selected from the group consisting of maltodextrin, dextrin, liquid glucose, corn syrup solid, and soluble starch.

66. A clear aqueous solution according to claim 58, wherein the aqueous soluble starch conversion product is maltodextrin.

67. A clear aqueous solution according to claim 58, wherein the aqueous soluble non-starch polysaccharide is selected from the group consisting of dextran, guar gum, pectin, indigestible soluble fiber.

68. A clear aqueous solution according to claim 58, wherein the pharmaceutical compound is selected from the group consisting of Pasiniazide, Benzthiazide, Prednisolone, Menthol, Mebhydrolin, Naphthalenesulfonate, Trichlormethiazide, Oxytetracycline, Arcaine sulphate, Erythromycin, Glutathione, Trioxsalen, NylidrinHCL, Desmethyldiazepam, Thonzylamine HCL, Valproate Na, Aminophenazone, Sulfamethizole, Droperidol, 2-Thiouracil, Kynurenic acid, Fusidic acid, Leucovorin Ca, Sparteine sulfate, Amygdalin, Pramoxine HCL, Furosemide, Dinitolmide, Budesonide, Flopropione, Fluorometholone, anti-inflammatory), N-Formylmethionylphenylalanine, Thiopental Na, Lansoprazole, Bretylium Tosylate, Cefamandole Na, Oxybendazole, Cycloleucylglycine, Dantrolene Na, Tetroquinone, piperazine, Aesculin, Ethisterone, Dimethadione, Griseofulvin, Acetaminosalol, Isoguvacine HCL, Putrescine DIHCL, Emetine HCL, Sulfanilamide, Mimosine, Acetylcholine, Pralidoxime Mesylate, LysylTryptophanyl-Lysine, Hecogenin, Prednisolone acetate, Albendazole, Hydrochlorothiazide, Demeclocycline HCL, Nitrofurazone, Dicloxacillin Na, alpha-Tocopherol, Tetracycline HCL, Fenofibrate, Probenecid, Tretinoin, Acetaminophen, Hydrastinine HCL, d[-Arg-2]Kyotorphin acetate, NMDA, Cefinetazole Na, Ribavirin, O-Benzyl-L-Serine, Picrotoxin, Oxethazine, Sulfathiazole, Trichlormethine, Nabumetone, Chloramphenicol, riluzole, ginseng and its extract, glycyrrhizin and glycyrrhizic acid, derivatives of carboquinone, coenzyme Q10, creatine, insulin-like growth factor-1, minocycline, mecamserin, xaliproden, gabapentin, dextromethorphan, talampanel, IL-1, TR-500, procysteine, brain derived neurotrophic factor, baclofen, tizanidin, benzodiazepines, glycopyrrolate, atropine, quinine, phenyloin and morphine.