최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
DataON 바로가기다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
Edison 바로가기다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
Kafe 바로가기국가/구분 | United States(US) Patent 등록 |
---|---|
국제특허분류(IPC7판) |
|
출원번호 | US-0692676 (2015-04-21) |
등록번호 | US-9272000 (2016-03-01) |
발명자 / 주소 |
|
출원인 / 주소 |
|
대리인 / 주소 |
|
인용정보 | 피인용 횟수 : 0 인용 특허 : 334 |
Provided are electrokinetically-altered fluids (gas-enriched electrokinetic fluids) comprising an ionic aqueous solution of charge-stabilized oxygen-containing nanostructures in an amount sufficient to provide modulation of at least one of cellular membrane potential and cellular membrane conductivi
Provided are electrokinetically-altered fluids (gas-enriched electrokinetic fluids) comprising an ionic aqueous solution of charge-stabilized oxygen-containing nanostructures in an amount sufficient to provide modulation of at least one of cellular membrane potential and cellular membrane conductivity, and therapeutic compositions and methods for use in treating diabetes and diabetes-associated conditions or disorders (e.g., insulin resistance), or symptoms thereof. Provided are electrokinetically-altered ioinic aqueous fluids optionally in combination with other therapeutic agents. Particular aspects provide for regulating or modulating intracellular signal transduction associated with said inflammatory responses by modulation of at least one of cellular membranes, membrane potential, membrane proteins such as membrane receptors, including but not limited to G-Protein Coupled Receptors (GPCR), and intercellular junctions (e.g., tight junctions, gap junctions, zona adherins and desmasomes). Other embodiments include particular routes of administration or formulations for the electrokinetically-altered fluids (e.g., electrokinetically-altered gas-enriched fluids and solutions) and therapeutic compositions.
1. A method for treating diabetes or a diabetes-associated condition or disorder, or symptoms thereof, comprising administering to a subject in need thereof a therapeutically effective amount of an oxygenated ionic aqueous solution of stabilized oxygen-containing nanobubbles having an average diamet
1. A method for treating diabetes or a diabetes-associated condition or disorder, or symptoms thereof, comprising administering to a subject in need thereof a therapeutically effective amount of an oxygenated ionic aqueous solution of stabilized oxygen-containing nanobubbles having an average diameter of less than 100 nanometers persisting in the ionic aqueous solution in an amount sufficient for treating diabetes or a diabetes-associated condition or disorder, or at least one symptom thereof. 2. The method of claim 1, wherein the stabilized oxygen-containing nanobubbles are the major gas-containing nanostructure species in the ionic aqueous solution. 3. The method of claim 1, wherein the percentage of dissolved oxygen molecules present in the ionic aqueous solution as the stabilized oxygen-containing nanobubbles is a percentage greater than 0.01%. 4. The method of claim 1, wherein the percentage of dissolved oxygen molecules present in the fluid as the stabilized oxygen gas-containing nanobubbles is a percentage greater than 50%. 5. The method of claim 1, wherein the stabilized oxygen-containing nanobubbles have an average diameter of less than 90 nm. 6. The method of claim 1, wherein the ionic aqueous solution comprises a saline solution. 7. The method of claim 1, wherein the ionic aqueous solution is superoxygenated. 8. The method of claim 1, wherein the ionic aqueous solution comprises a form of solvated electrons. 9. The method of claim 1, wherein the diabetes-associated condition or disorder comprises at least one selected from the group consisting of: diabetes; insulin-dependent diabetes mellitus or IDDM (Type 1); non-insulin dependent diabetes mellitus or NIDDM (Type 2); insulin resistance; and diabetic retinopathy. 10. The method of claim 9, wherein the diabetes-associated condition or disorder comprises at least one of diabetes and insulin resistance. 11. The method of claim 10, wherein the diabetes-associated condition or disorder comprises diabetes. 12. The method of claim 1, wherein the at least one symptom of the diabetes-associated condition or disorder is related to at least one condition selected from the group consisting of: chronic inflammation, acute inflammation, insulin resistance. 13. The method of claim 1, wherein the ionic aqueous solution modulates localized or cellular levels of nitric oxide. 14. The method of claim 1, wherein the ionic aqueous solution promotes a localized decrease at the site of administration of at least one cytokine selected from the group consisting of: IL-1beta, IL-8, TNF-alpha, and TNF-beta. 15. The method of claim 1, further comprising a synergistic or non-synergistic inhibition or reduction in inflammation by simultaneously or adjunctively treating the subject with another anti-inflammatory agent. 16. The method of claim 15, wherein said other anti-inflammatory agent comprises a steroid or glucocorticoid steroid. 17. The method of claim 16, wherein the glucocorticoid steroid comprises Budesonide or an active derivative thereof. 18. The method of claim 1, further comprising combination therapy, wherein at least one additional therapeutic agent is administered to the patient. 19. The method of claim 18, wherein the at least one additional therapeutic agent is selected from the group consisting of: Biguanides including metformin, buformin, and phenformin, insulin, alpha-glucosidase inhibitors, biguanides, DPP-4 inhibitors, meglitinides, sulfonylureas, thiazolidinediones, alpha-glucosidase inhibitors including, acarbose and miglitol, DPP-4 inhibitors including vildagliptin, sitagliptin, saxagliptin, linagliptin, and alogliptin, sulfonylureas including acetohexamide, chlorpropamide, tolbutamide, tolazamide, glipizide, gliclazide, glibenclamide (glyburide), gliquidone, glyclopyramide, and glimepiride, meglitinides including nateglinide, mitiglinide, and repaglinide. thiazolidinediones including troglitazone, pioglitazone, and rosiglitazone, inhibitors of MMPs including inhibitor of MMP-9 and MMP-2, short-acting β2-agonists, long-acting β2-agonists, anticholinergics, corticosteroids, systemic corticosteroids, mast cell stabilizers, leukotriene modifiers, methylxanthines, β2-agonists, albuterol, levalbuterol, pirbuterol, artformoterol, formoterol, salmeterol, anticholinergics including ipratropium and tiotropium; corticosteroids including beclomethasone, budesonide, flunisolide, fluticasone, mometasone, triamcinolone, methyprednisolone, prednisolone, prednisone; leukotriene modifiers including montelukast, zafirlukast, and zileuton; mast cell stabilizers including cromolyn and nedocromil; methylxanthines including theophylline; combination drugs including ipratropium and albuterol, fluticasone and salmeterol, budesonide and formoterol; antihistamines including hydroxyzine, diphenhydramine, loratadine, cetirizine, and hydrocortisone; immune system modulating drugs including tacrolimus and pimecrolimus; cyclosporine; azathioprine; mycophenolatemofetil; and combinations thereof. 20. The method of claim 18, wherein the at least one additional therapeutic agent is a thymic stromal lymphopoietin (TSLP) and/or thymic stromal lymphopoietin receptor (TSLPR) antagonist. 21. The method of claim 20, wherein the TSLP and/or TSLPR antagonist is selected from the group consisting of neutralizing antibodies specific for TSLP and the TSLP receptor, soluble TSLP receptor molecules, and TSLP receptor fusion proteins, including TSLPR-immunoglobulin Fc molecules or polypeptides that encode components of more than one receptor chain. 22. The method of claim 1, comprising administration to a cell network or layer, and further comprising modulation of an intercellular junction therein. 23. The method of claim 22, wherein the intracellular junction comprises at least one selected from the group consisting of tight junctions, gap junctions, zona adherins and desmasomes. 24. The method of claim 22, wherein the cell network or layers comprises at least one selected from the group consisting of endothelial cells, endothelial-astrocyte tight junctions in CNS vessels, blood-cerebrospinal fluid tight junctions or barrier, pulmonary epithelium-type junctions, bronchial epithelium-type junctions, and intestinal epithelium-type junctions. 25. The method of claim 1, wherein the oxygen in the ionic aqueous solution is present in an amount of at least 15 ppm at atmospheric pressure. 26. The method of claim 1, wherein the ionic aqueous solution comprises at least one of a form of solvated electrons, and electrokinetically modified or charged oxygen species. 27. The method of claim 26, wherein the solvated electrons or electrokinetically modified or charged oxygen species are present in an amount of at least 0.01 ppm. 28. The method of claim 27, wherein the ionic aqueous solution comprises solvated electrons stabilized, at least in part, by molecular oxygen. 29. The method of claim 1, wherein the amount of oxygen present in stabilized oxygen-containing nanobubbles of the ionic aqueous solution is at least 15 ppm oxygen at atmospheric pressure. 30. The method of claim 1, wherein treating comprises administration by at least one of topical, inhalation, intranasal, oral and intravenous routes. 31. The method of claim 1, wherein treating comprises modulation of intracellular NF-κB expression and/or activity. 32. The method of claim 5, wherein the stabilized oxygen-containing nanobubbles comprise stabilized oxygen-containing nanobubbles having an average diameter of less than 80 nanometers.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.