WO1989000848A1 - Procede permettant de traiter des tissus osseux et de leur administrer des medicaments - Google Patents
Procede permettant de traiter des tissus osseux et de leur administrer des medicaments Download PDFInfo
- Publication number
- WO1989000848A1 WO1989000848A1 PCT/US1987/003505 US8703505W WO8900848A1 WO 1989000848 A1 WO1989000848 A1 WO 1989000848A1 US 8703505 W US8703505 W US 8703505W WO 8900848 A1 WO8900848 A1 WO 8900848A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- oxygenated
- perfluorocarbon
- drugs
- tissue
- fluid
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 27
- 239000003814 drug Substances 0.000 title claims abstract description 23
- 229940079593 drug Drugs 0.000 title claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 18
- 239000001301 oxygen Substances 0.000 claims abstract description 18
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000012530 fluid Substances 0.000 claims abstract description 12
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 8
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 8
- 229940124597 therapeutic agent Drugs 0.000 claims abstract description 7
- 210000001519 tissue Anatomy 0.000 claims description 18
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 7
- 239000000839 emulsion Substances 0.000 claims description 5
- 230000003110 anti-inflammatory effect Effects 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 210000004877 mucosa Anatomy 0.000 claims description 4
- 239000003242 anti bacterial agent Substances 0.000 claims description 3
- 229940088710 antibiotic agent Drugs 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 230000001706 oxygenating effect Effects 0.000 claims description 2
- -1 perfluorocarbon compound Chemical class 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 description 5
- 239000008280 blood Substances 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 230000001225 therapeutic effect Effects 0.000 description 4
- 206010002383 Angina Pectoris Diseases 0.000 description 3
- 208000027418 Wounds and injury Diseases 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 208000014674 injury Diseases 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 208000003322 Coinfection Diseases 0.000 description 2
- 208000004210 Pressure Ulcer Diseases 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
- 239000013589 supplement Substances 0.000 description 2
- 230000002459 sustained effect Effects 0.000 description 2
- 230000000699 topical effect Effects 0.000 description 2
- QZCJOXAIQXPLNS-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,4a,5,5,6,6,7,7,8,8,8a-octadecafluoronaphthalene 4-(2-aminoethyl)benzene-1,2-diol Chemical compound NCCc1ccc(O)c(O)c1.FC1(F)C(F)(F)C(F)(F)C2(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C2(F)C1(F)F QZCJOXAIQXPLNS-UHFFFAOYSA-N 0.000 description 1
- 208000002874 Acne Vulgaris Diseases 0.000 description 1
- 206010017711 Gangrene Diseases 0.000 description 1
- CEAZRRDELHUEMR-URQXQFDESA-N Gentamicin Chemical compound O1[C@H](C(C)NC)CC[C@@H](N)[C@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](NC)[C@@](C)(O)CO2)O)[C@H](N)C[C@@H]1N CEAZRRDELHUEMR-URQXQFDESA-N 0.000 description 1
- 229930182566 Gentamicin Natural products 0.000 description 1
- 229920001612 Hydroxyethyl starch Polymers 0.000 description 1
- 206010028851 Necrosis Diseases 0.000 description 1
- 239000004100 Oxytetracycline Substances 0.000 description 1
- 108010093965 Polymyxin B Proteins 0.000 description 1
- 201000004681 Psoriasis Diseases 0.000 description 1
- 208000000453 Skin Neoplasms Diseases 0.000 description 1
- 206010040943 Skin Ulcer Diseases 0.000 description 1
- 241000383675 Trama Species 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 206010000496 acne Diseases 0.000 description 1
- 230000003143 atherosclerotic effect Effects 0.000 description 1
- 230000036770 blood supply Effects 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 229960005091 chloramphenicol Drugs 0.000 description 1
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 125000004855 decalinyl group Chemical class C1(CCCC2CCCCC12)* 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 230000036074 healthy skin Effects 0.000 description 1
- 229960000890 hydrocortisone Drugs 0.000 description 1
- 229940050526 hydroxyethylstarch Drugs 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229960003255 natamycin Drugs 0.000 description 1
- NCXMLFZGDNKEPB-FFPOYIOWSA-N natamycin Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C[C@@H](C)OC(=O)/C=C/[C@H]2O[C@@H]2C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 NCXMLFZGDNKEPB-FFPOYIOWSA-N 0.000 description 1
- 235000010298 natamycin Nutrition 0.000 description 1
- 239000004311 natamycin Substances 0.000 description 1
- 230000017074 necrotic cell death Effects 0.000 description 1
- 150000002926 oxygen Chemical class 0.000 description 1
- 238000006213 oxygenation reaction Methods 0.000 description 1
- 229960000625 oxytetracycline Drugs 0.000 description 1
- IWVCMVBTMGNXQD-PXOLEDIWSA-N oxytetracycline Chemical compound C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-PXOLEDIWSA-N 0.000 description 1
- 235000019366 oxytetracycline Nutrition 0.000 description 1
- 229950008618 perfluamine Drugs 0.000 description 1
- 239000010702 perfluoropolyether Substances 0.000 description 1
- RVZRBWKZFJCCIB-UHFFFAOYSA-N perfluorotributylamine Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F RVZRBWKZFJCCIB-UHFFFAOYSA-N 0.000 description 1
- JAJLKEVKNDUJBG-UHFFFAOYSA-N perfluorotripropylamine Chemical compound FC(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)F JAJLKEVKNDUJBG-UHFFFAOYSA-N 0.000 description 1
- 229920000024 polymyxin B Polymers 0.000 description 1
- 229960005266 polymyxin b Drugs 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000037390 scarring Effects 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 231100000019 skin ulcer Toxicity 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
- A61K9/0026—Blood substitute; Oxygen transporting formulations; Plasma extender
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/02—Halogenated hydrocarbons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/02—Halogenated hydrocarbons
- A61K31/025—Halogenated hydrocarbons carbocyclic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/08—Plasma substitutes; Perfusion solutions; Dialytics or haemodialytics; Drugs for electrolytic or acid-base disorders, e.g. hypovolemic shock
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Definitions
- the invention relates to a method for a treatment of and the administration of drugs to body tissues and surfaces.
- this invention particularly relates to the treatment of structures such as the skin or mucosa which are in need of enhanced or supplemental oxygen supply.
- This invention also relates to the treatment of individuals or tissues within individuals which may additionally or alternatively require the administration of drugs.
- Yet another long sought goal of medical science is ' an effective, non-invasive technique for the percutaneous administration of drugs.
- Most known methods are not well suited to be used by patents (e.g., intraveneous injection) or result in poor absorption and utilization of the drug (e.g., enceric administration). It is therefore an object of this invention to provide a method of treatment which will supplement or restore the-;; oxygen supply to damaged tissues. It is also an object of this invention to provide a method of treatment which facilitates the effective percutaneous administration of drugs which can be useful in the treatment of disease and especially useful in the treatment of damaged or diseased mucosa or skin.
- damaged bodily tissue is treated by oxygenating a pharmaceutically acceptable liquid with a therapeutically effective amount of oxygen and then applying the oxygenated liquid to the affected tissue.
- another therapeutic agent is dissolved or suspended in the liquid in addition to • or in place of oxygen.
- This therapeutic agent may be selected from an exceptionally wide variety of drugs including antibiotics, anti-inflamatories or mixtures of such agents or drugs.
- Another highly useful group of therapeutic agents are those which are useful in treating skin diseases such as acne, psoriasis, angina pectoris or skin cancers.
- perfluorinated hydrocarbons are generally insoluble in water it is highly preferred that an aqueous emulsion of the perfluorinated hydrocarbons to be used.
- Fluosol-DA Green Cross
- Oxypherol-ET Alpha Therapeutic Corporation. The composition of Oxypherol-ET is set forth in Table II.
- the Oxypheral-ET formulation may be modified by increasing the hydroxyethyl starch level to from 5- to 20%.
- the oxygenation of the perfluorocarbon or perfluorocarbon emulsion used in the process of the present invention can be carried out by exposing the fluid to an atmosphere of at least 75% oxygen, although an atmosphere of at least 95% oxygen is preferred. This is most effectively accomplished by bubbling oxygen at slightly greater than atmqspheric pressure through the perfluorocarbon. Once oxygenated, the perfluorocarbon or perfluorocarbon emulsion may be applied directly to damaged tissue.
- Perfluorocarbon preparations are known to be able to dissolve at least 40% of oxygen and it is desirable to use fully saturated preparations when treating oxygen starved tissues. However, even oxygen starved tissues benefit substantially from the use of 25% solutions.
- the oxygenated fluid should be applied to the affected tissue at regular intervals to obtain maximum therapeutic effect. It is expected that it will be necessary to reapply the oxygenated fluid to the affected tissue 2 to 6 times each day.
- topical or percutaneous administration of drugs can be accomplished with special advantage by the process of the present invention and the absorption of drugs is accomplished with suprising effectiveness.
- the affected tissue has suffered injury as a result of a trama or where secondary infection is present or seriously possible, it will be advisable to include a therapeutic concentration of an appropriate antibotic in the oxygenated perfluorocarbon fluid.
- Therapeutic concentrations of some suitable topical antibotics are set forth in Table III.
- Polymyxin B 0.5-1.5% by wt.
- an anti-inflamatory agent may be included in the oxygen-containing liquid which is used in the present invention.
- an anti-inflamatory agent may be included in the oxygen-containing liquid which is used in the present invention.
- hydrocortisone 0.5 to 1.5% by weight
- Other therapeutic agents which may be used include nordihydroquaiaretic acid and its derivatives, the usefulness of which is described in co-pending United States Patent Application No. 699,923, filed February 2, 1985.
- a wide variety of drugs can be administered with exceptional effectiveness through healthy skin by the process of the present invention. This process, therefore, has broad application in the percutaneous administration of drugs without regard to its usefulness as an oxygen supply technique.
- a bedsore may be treated by applying to it sufficient volume of oxygenated Oxypherol-ET to completely over the sore.
- the sore can be seen to begin to heal within 2 weeks and heal completely in about 4 weeks as the above described procedure is repeated every 12 hours.
- nitroglycern can be dissolved in the above-mentioned perfluorocarbon composition and applied in a patch on the skin of a patient suffering from angina pectoris. This procedure can provide immediate and sustained relief to the patient.
- Oxypherol-ET oxygenated Oxypherol-ET to completely over the sore.
- the sore can be seen to begin to heal within 2 weeks and heal completely in about 4 weeks as the above described procedure is repeated every 12 hours.
- nitroglycern can be dissolved in the above-mentioned perfluorocarbon composition and applied in a patch on the skin of a patient suffering from angina pectoris. This procedure can provide immediate and sustained relief to the patient.
Landscapes
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
On applique un fluide oxygéné aux tissus corporels abîmés, permettant ainsi aux tissus d'être oxygénés. On peut oxygéner et utiliser dans ce procédé des hydrocarbures perfluorés. Divers agents thérapeutiques peuvent être mélangés au fluide oxygéné et administrés aux tissus abîmés.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US90983286A | 1986-09-19 | 1986-09-19 | |
US909,832 | 1986-09-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1989000848A1 true WO1989000848A1 (fr) | 1989-02-09 |
Family
ID=25427897
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1987/003505 WO1989000848A1 (fr) | 1986-09-19 | 1987-08-18 | Procede permettant de traiter des tissus osseux et de leur administrer des medicaments |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0324802A4 (fr) |
JP (1) | JPH01503146A (fr) |
AU (1) | AU2807689A (fr) |
WO (1) | WO1989000848A1 (fr) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0493677A2 (fr) * | 1991-01-03 | 1992-07-08 | Chiron Adatomed Pharmazeutische und Medizintechnische Gesellschaft mbH | Solution pour le recollage d'une rétine décollée à la choroide |
EP0494974A1 (fr) * | 1989-10-04 | 1992-07-22 | Alliance Pharmaceutical Corporation | Emulsions de fluorocarbone contenant des agents anti-inflammatoires a base d'acides amines ainsi que des systemes de tampons |
EP0576537A1 (fr) * | 1991-03-21 | 1994-01-05 | Escalon Ophthalmics, Inc. | Extraction de corps etrangers dans des cavites corporelles a l'aide de liquides d'extraction |
DE4221256A1 (de) * | 1992-06-26 | 1994-01-05 | Lancaster Group Ag | Galenische Zusammensetzung für die topische Anwendung |
WO1994024223A1 (fr) * | 1993-04-21 | 1994-10-27 | Gordon Stead | Epaississement des liquides fluorures |
EP0670159A1 (fr) * | 1994-02-22 | 1995-09-06 | Hoechst Aktiengesellschaft | Emulsions d'huile contenant de fluorocarbures |
US5637318A (en) * | 1992-06-26 | 1997-06-10 | Lancaster Group Ag | Dermatological agent for assisting the transport of oxygen in the skin |
US5641509A (en) * | 1992-06-26 | 1997-06-24 | Lancaster Group Ag | Preparation for topical use |
US5643601A (en) * | 1992-06-26 | 1997-07-01 | Lancaster Group Ag | Phospholipid-and fluorocarbon-containing cosmetic |
US5733939A (en) * | 1993-09-29 | 1998-03-31 | Alliance Pharmaceutical Corp. | Fluorocarbons as anti-inflammatory agents |
US5750141A (en) * | 1993-04-08 | 1998-05-12 | The University Of Queensland | Administration of vaso-active agent and therapeutic agent |
US5847009A (en) * | 1986-01-14 | 1998-12-08 | Alliance Pharmaceutical Corp. | Prophylaxis in the parenteral administration of particulate dispersions in fluorocarbon emulsions |
US5929039A (en) * | 1993-11-15 | 1999-07-27 | Baker Medical Research Institute | Method for treating cardiac dysfunction and pharmaceutical compositions useful therefor |
US20120225102A1 (en) * | 2008-11-25 | 2012-09-06 | Oxygen Biotherapeutics, Inc. | Perfluorocarbon gel formulations |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5061688A (en) * | 1988-08-19 | 1991-10-29 | Illinois Institute Of Technology | Hemoglobin multiple emulsion |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4186423A (en) * | 1976-10-01 | 1980-01-29 | Matsushita Electric Industrial Company, Limited | Solid electrolyte capacitor using oxide of Ru, Rh, Re, Os or Ir as electrolyte |
US4366169A (en) * | 1979-06-25 | 1982-12-28 | Sun Tech, Inc. | Use of perfluorocarbons as wound treatment |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE881267A (fr) * | 1980-01-18 | 1980-05-16 | Stein Karl N | Methode pour le traitement de brulures de la peau chez les mammiferes |
EP0112658B1 (fr) * | 1982-11-26 | 1991-08-07 | Children's Hospital Medical Center | Dispositif extraoculaire pour le traitement de l'oeil |
-
1987
- 1987-08-18 WO PCT/US1987/003505 patent/WO1989000848A1/fr not_active Application Discontinuation
- 1987-08-18 JP JP1500105A patent/JPH01503146A/ja active Pending
- 1987-08-18 EP EP19880903116 patent/EP0324802A4/en not_active Withdrawn
- 1987-08-18 AU AU28076/89A patent/AU2807689A/en not_active Abandoned
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4186423A (en) * | 1976-10-01 | 1980-01-29 | Matsushita Electric Industrial Company, Limited | Solid electrolyte capacitor using oxide of Ru, Rh, Re, Os or Ir as electrolyte |
US4366169A (en) * | 1979-06-25 | 1982-12-28 | Sun Tech, Inc. | Use of perfluorocarbons as wound treatment |
Non-Patent Citations (1)
Title |
---|
See also references of EP0324802A4 * |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5847009A (en) * | 1986-01-14 | 1998-12-08 | Alliance Pharmaceutical Corp. | Prophylaxis in the parenteral administration of particulate dispersions in fluorocarbon emulsions |
US6361792B1 (en) | 1987-08-05 | 2002-03-26 | Alliance Pharmaceutical Corp. | Lipid dispersions and methods of use |
EP0494974A1 (fr) * | 1989-10-04 | 1992-07-22 | Alliance Pharmaceutical Corporation | Emulsions de fluorocarbone contenant des agents anti-inflammatoires a base d'acides amines ainsi que des systemes de tampons |
EP0494974A4 (en) * | 1989-10-04 | 1992-09-02 | Alliance Pharmaceutical, Inc. | Fluorocarbon emulsions containing amino acid based anti-inflammatory agents and buffer systems |
EP0493677A3 (en) * | 1991-01-03 | 1992-12-23 | Adatomed Pharmazeutische Und Medizin-Technische Gesellschaft Mbh | Solution for the reattachment of a detached retina to the choroid |
EP0493677A2 (fr) * | 1991-01-03 | 1992-07-08 | Chiron Adatomed Pharmazeutische und Medizintechnische Gesellschaft mbH | Solution pour le recollage d'une rétine décollée à la choroide |
US5397805A (en) * | 1991-01-03 | 1995-03-14 | Adatomed Pharmazeutische Und Medizintechnische Gesellschaft Mbh | Treatment liquid for reapplying (unfolding) detached retina to the chorioid of the eye |
EP0576537A4 (fr) * | 1991-03-21 | 1995-05-03 | Escalon Ophthalmics Inc | Extraction de corps etrangers dans des cavites corporelles a l'aide de liquides d'extraction. |
EP0576537A1 (fr) * | 1991-03-21 | 1994-01-05 | Escalon Ophthalmics, Inc. | Extraction de corps etrangers dans des cavites corporelles a l'aide de liquides d'extraction |
WO1994000110A1 (fr) * | 1992-06-26 | 1994-01-06 | Lancaster Group Ag | Composition galenique pour application topique |
DE4221256A1 (de) * | 1992-06-26 | 1994-01-05 | Lancaster Group Ag | Galenische Zusammensetzung für die topische Anwendung |
US5637318A (en) * | 1992-06-26 | 1997-06-10 | Lancaster Group Ag | Dermatological agent for assisting the transport of oxygen in the skin |
US5641509A (en) * | 1992-06-26 | 1997-06-24 | Lancaster Group Ag | Preparation for topical use |
US5643601A (en) * | 1992-06-26 | 1997-07-01 | Lancaster Group Ag | Phospholipid-and fluorocarbon-containing cosmetic |
US5750141A (en) * | 1993-04-08 | 1998-05-12 | The University Of Queensland | Administration of vaso-active agent and therapeutic agent |
WO1994024223A1 (fr) * | 1993-04-21 | 1994-10-27 | Gordon Stead | Epaississement des liquides fluorures |
US5733939A (en) * | 1993-09-29 | 1998-03-31 | Alliance Pharmaceutical Corp. | Fluorocarbons as anti-inflammatory agents |
US5929039A (en) * | 1993-11-15 | 1999-07-27 | Baker Medical Research Institute | Method for treating cardiac dysfunction and pharmaceutical compositions useful therefor |
EP0670159A1 (fr) * | 1994-02-22 | 1995-09-06 | Hoechst Aktiengesellschaft | Emulsions d'huile contenant de fluorocarbures |
US20120225102A1 (en) * | 2008-11-25 | 2012-09-06 | Oxygen Biotherapeutics, Inc. | Perfluorocarbon gel formulations |
Also Published As
Publication number | Publication date |
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EP0324802A1 (fr) | 1989-07-26 |
JPH01503146A (ja) | 1989-10-26 |
EP0324802A4 (en) | 1991-07-24 |
AU2807689A (en) | 1989-03-01 |
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