SI9200312A - Transdermally administered system containing acetylsalicylic acid for thrombosis therapy - Google Patents
Transdermally administered system containing acetylsalicylic acid for thrombosis therapy Download PDFInfo
- Publication number
- SI9200312A SI9200312A SI19929200312A SI9200312A SI9200312A SI 9200312 A SI9200312 A SI 9200312A SI 19929200312 A SI19929200312 A SI 19929200312A SI 9200312 A SI9200312 A SI 9200312A SI 9200312 A SI9200312 A SI 9200312A
- Authority
- SI
- Slovenia
- Prior art keywords
- acetylsalicylic acid
- asa
- pharmaceutically acceptable
- transdermal
- acceptable salts
- Prior art date
Links
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 title claims abstract description 18
- 229960001138 acetylsalicylic acid Drugs 0.000 title claims abstract description 18
- 238000002560 therapeutic procedure Methods 0.000 title claims abstract description 13
- 208000007536 Thrombosis Diseases 0.000 title abstract description 4
- 239000013543 active substance Substances 0.000 claims abstract description 21
- 150000003839 salts Chemical class 0.000 claims abstract description 16
- 230000002785 anti-thrombosis Effects 0.000 claims description 10
- 239000010410 layer Substances 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 10
- 239000003146 anticoagulant agent Substances 0.000 claims description 9
- 239000011159 matrix material Substances 0.000 claims description 9
- 239000012528 membrane Substances 0.000 claims description 9
- 239000011241 protective layer Substances 0.000 claims description 9
- 230000037317 transdermal delivery Effects 0.000 claims description 6
- 239000002674 ointment Substances 0.000 claims description 3
- 239000006071 cream Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 230000007246 mechanism Effects 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims 1
- 230000005611 electricity Effects 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 239000004793 Polystyrene Substances 0.000 description 12
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 9
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 8
- 230000001070 adhesive effect Effects 0.000 description 8
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 8
- 229920006267 polyester film Polymers 0.000 description 7
- 230000000202 analgesic effect Effects 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000012790 adhesive layer Substances 0.000 description 5
- 229960004889 salicylic acid Drugs 0.000 description 5
- 230000000699 topical effect Effects 0.000 description 5
- BODMYPYTCKYRSP-UHFFFAOYSA-N 1,1-dioctylcyclohexane Chemical compound CCCCCCCCC1(CCCCCCCC)CCCCC1 BODMYPYTCKYRSP-UHFFFAOYSA-N 0.000 description 4
- 206010061218 Inflammation Diseases 0.000 description 4
- 208000002193 Pain Diseases 0.000 description 4
- 230000001754 anti-pyretic effect Effects 0.000 description 4
- 239000002221 antipyretic Substances 0.000 description 4
- -1 glycerol ester Chemical class 0.000 description 4
- 230000002757 inflammatory effect Effects 0.000 description 4
- 230000004054 inflammatory process Effects 0.000 description 4
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229920004939 Cariflex™ Polymers 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 210000004369 blood Anatomy 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 239000003094 microcapsule Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 229920001195 polyisoprene Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 230000001225 therapeutic effect Effects 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000003623 enhancer Substances 0.000 description 2
- 210000001035 gastrointestinal tract Anatomy 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 208000010125 myocardial infarction Diseases 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 206010048620 Intracardiac thrombus Diseases 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 102000004005 Prostaglandin-endoperoxide synthases Human genes 0.000 description 1
- 108090000459 Prostaglandin-endoperoxide synthases Proteins 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 208000007814 Unstable Angina Diseases 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 208000005298 acute pain Diseases 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 230000000747 cardiac effect Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229960000800 cetrimonium bromide Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 208000029078 coronary artery disease Diseases 0.000 description 1
- 239000003246 corticosteroid Substances 0.000 description 1
- 229960001334 corticosteroids Drugs 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005370 electroosmosis Methods 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 230000000306 recurrent effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000452 restraining effect Effects 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229920006268 silicone film Polymers 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000003637 steroidlike Effects 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 229940100640 transdermal system Drugs 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
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
- A61K9/703—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
- A61K9/7038—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer
- A61K9/7046—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds
- A61K9/7053—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds, e.g. polyvinyl, polyisobutylene, polystyrene
- A61K9/7061—Polyacrylates
-
- 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
- A61K31/60—Salicylic acid; Derivatives thereof
-
- 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
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
- A61K9/703—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
- A61K9/7084—Transdermal patches having a drug layer or reservoir, and one or more separate drug-free skin-adhesive layers, e.g. between drug reservoir and skin, or surrounding the drug reservoir; Liquid-filled reservoir patches
-
- 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
-
- 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
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4142483 | 1991-12-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
SI9200312A true SI9200312A (en) | 1993-06-30 |
Family
ID=6447817
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI19929200312A SI9200312A (en) | 1991-12-20 | 1992-11-10 | Transdermally administered system containing acetylsalicylic acid for thrombosis therapy |
Country Status (23)
Country | Link |
---|---|
US (2) | US6264978B1 (no) |
EP (1) | EP0617623B1 (no) |
JP (1) | JP3748270B2 (no) |
KR (2) | KR100267442B1 (no) |
AT (1) | ATE217528T1 (no) |
AU (1) | AU667067B2 (no) |
CA (1) | CA2125662C (no) |
CZ (1) | CZ285190B6 (no) |
DE (2) | DE4241128C2 (no) |
DK (1) | DK0617623T3 (no) |
ES (1) | ES2176197T3 (no) |
FI (1) | FI113838B (no) |
HR (1) | HRP921157A2 (no) |
HU (1) | HU221679B1 (no) |
IL (1) | IL103917A (no) |
NO (1) | NO306599B1 (no) |
NZ (1) | NZ246158A (no) |
PT (1) | PT617623E (no) |
SI (1) | SI9200312A (no) |
SK (1) | SK67094A3 (no) |
WO (1) | WO1993012799A1 (no) |
YU (1) | YU75093A (no) |
ZA (1) | ZA922814B (no) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5240917A (en) * | 1991-04-03 | 1993-08-31 | Keimowitz Rudolph M | Suppression of thromboxane levels by percutaneous administration of aspirin |
WO1994013302A1 (de) * | 1991-12-20 | 1994-06-23 | Lts Lohmann Therapie-Systeme Gmbh & Co. Kg | Ein acetylsalicylsäure enthaltendes transdermales verabreichungssystem für die antithrombotische therapie und die krebsprophylaxe |
US6071896A (en) * | 1992-06-16 | 2000-06-06 | Gundersen Clinic, Ltd. | Suppression of thromboxane levels by percutaneous administration of aspirin |
PL174770B1 (pl) * | 1992-12-07 | 1998-09-30 | Lohmann Therapie Syst Lts | Przezskórny układ terapeutyczny do terapii przeciwzakrzepowej i/lub zapobiegania chorobom nowotworowym oraz sposób wytwarzania przezskórnego układu terapeutycznego do terapii przeciwzakrzepowej i/lub zapobiegania chorobom nowotworowym |
DE4332093C2 (de) * | 1993-09-22 | 1995-07-13 | Lohmann Therapie Syst Lts | Transdermales therapeutisches System mit dem Wirkstoff Acetylsalicylsäure und Verfahren zu seiner Herstellung |
DE4429663C2 (de) * | 1994-08-20 | 1997-09-11 | Lohmann Therapie Syst Lts | Transdermales therapeutisches System mit Hydrolyseschutz |
WO1997004758A1 (en) * | 1995-07-27 | 1997-02-13 | Cal International Limited | Pharmaceutical preparation for percutaneous absorbtion |
AU6708996A (en) * | 1995-07-27 | 1997-02-26 | Cal International Limited | Transdermal nitrate formulation |
GB2319473A (en) * | 1995-07-27 | 1998-05-27 | Cal Int Ltd | Transdemal patch containing aspirin |
EP0784975B1 (en) * | 1995-12-26 | 2005-10-19 | Teikoku Seiyaku Kabushiki Kaisha | Use of acetylsalicylic acid in the manufacture of a drug for the treatment of skin injuries |
DE19601487C2 (de) * | 1996-01-17 | 2001-09-13 | Micronas Gmbh | Vorrichtung zum Behandeln von malignen Gewebsveränderungen |
JPH1112177A (ja) | 1997-06-25 | 1999-01-19 | Teikoku Seiyaku Co Ltd | 安定なアスピリン含有外用製剤 |
DE19949252B4 (de) * | 1999-10-13 | 2004-02-12 | Lts Lohmann Therapie-Systeme Ag | Verwendung eines superfiziellen therapeutischen Systems zur topischen Applikation von Acetylsalicylsäure zur Behandlung von Akne-Erkrankungen und Verfahren zu seiner Herstellung |
JP2001187739A (ja) * | 1999-12-28 | 2001-07-10 | Teikoku Seiyaku Co Ltd | アレルギー性皮膚疾患治療用外用剤 |
WO2003018023A1 (en) * | 2001-08-23 | 2003-03-06 | Bruce Frome | Compositions and methods for targeting cerebral circulation and treatment of headache |
US20040248858A1 (en) * | 2003-06-09 | 2004-12-09 | Parghi Kaumil H. | Cure for cancer |
US20060127463A1 (en) * | 2004-12-15 | 2006-06-15 | Nugara Peter N | Composite structure including a low vinyl acetate layer |
US20060188558A1 (en) * | 2005-02-18 | 2006-08-24 | Mylan Technologies, Inc. | Transdermal systems having control delivery system |
US20090238763A1 (en) | 2006-07-09 | 2009-09-24 | Chongxi Yu | High penetration compositions and uses thereof |
WO2008007171A1 (en) | 2006-07-09 | 2008-01-17 | Techfields Biochem Co. Ltd | Positively charged water-soluble prodrugs of aspirin |
US20090221703A1 (en) | 2006-07-09 | 2009-09-03 | Chongxi Yu | High penetration composition and uses thereof |
MX2009011849A (es) * | 2007-05-09 | 2009-11-13 | Buckman Labor Inc | Emulsiones de aprestacion de asa para papel y carton. |
AU2007354632B2 (en) * | 2007-06-04 | 2014-06-26 | Techfields Inc | Pro-drugs of NSAIAs with very high skin and membranes penetration rates and their new medicinal uses |
CN113636965A (zh) | 2008-12-04 | 2021-11-12 | 于崇曦 | 高穿透性组合物及其应用 |
WO2011076401A1 (de) | 2009-12-23 | 2011-06-30 | Holger Schankin | Acetylsalicylsäure-haltige, im wesentlichen wasserfreie pharmazeutische zusammensetzungen |
KR102332837B1 (ko) | 2012-01-18 | 2021-12-01 | 테크필즈 파마 코., 엘티디. | 폐 병태의 치료를 위한 고침투 전구약물 조성물 및 그의 약제학적 조성물 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3797494A (en) * | 1969-04-01 | 1974-03-19 | Alza Corp | Bandage for the administration of drug by controlled metering through microporous materials |
US3598122A (en) * | 1969-04-01 | 1971-08-10 | Alza Corp | Bandage for administering drugs |
US3742951A (en) * | 1971-08-09 | 1973-07-03 | Alza Corp | Bandage for controlled release of vasodilators |
US3996934A (en) * | 1971-08-09 | 1976-12-14 | Alza Corporation | Medical bandage |
FR2297612A1 (fr) | 1975-01-20 | 1976-08-13 | Moorleghem Guy Van | Procede de fabrication d'un produit analgesique a usage externe |
US4012508A (en) | 1975-02-03 | 1977-03-15 | Burton Verna M | Topical composition and method |
US4219548A (en) | 1978-09-01 | 1980-08-26 | The Procter & Gamble Company | Topical anti-inflammatory composition |
FR2496459A1 (fr) | 1980-12-19 | 1982-06-25 | Astier Laboratoires Docteur P | Composition pharmaceutique sous forme d'un gel contenant de l'acide acetylsalicylique |
US4460368A (en) * | 1981-10-29 | 1984-07-17 | Almedco, Inc. | Trans-dermal medication system |
IL68965A (en) | 1983-06-13 | 1987-02-27 | Rafa Labor Ltd | Topical pharmaceutical preparation comprising acetylsalicylic acid for the treatment of dermatological disorders |
US4640689A (en) | 1983-08-18 | 1987-02-03 | Drug Delivery Systems Inc. | Transdermal drug applicator and electrodes therefor |
EP0162239B1 (en) | 1984-04-23 | 1991-08-07 | Kao Corporation | Percutaneous absorption accelerator and preparation containing same |
JPS61167615A (ja) | 1985-01-18 | 1986-07-29 | Teisan Seiyaku Kk | 薬剤投与方法 |
US4810699A (en) | 1987-02-20 | 1989-03-07 | American Home Products Corporation | Substituted 1,3,4,9-tetrahydropyrano[3,4,-b]indole-1-acetic acids, pharmaceutical compositions containing them, and methods for treating inflammatory conditions and for analgesic purposes using them |
JPH01203336A (ja) | 1988-02-09 | 1989-08-16 | Teikoku Seiyaku Kk | 経皮・口腔粘膜適用製剤 |
JPH01242521A (ja) | 1988-03-23 | 1989-09-27 | Nikko Kemikaruzu Kk | 経皮吸収性を高めた消炎鎮痛薬組成物 |
US4975269A (en) | 1989-07-31 | 1990-12-04 | Leonard Chavkin | Shelf stable aspirin solutions |
KR100247441B1 (ko) * | 1991-04-03 | 2000-04-01 | 자클린 비. 슈라고 | 트롬복산 레벨 억제용 경피투여 약제학적 아스피린 조성물 |
-
1992
- 1992-10-30 HR HR921157A patent/HRP921157A2/hr not_active Application Discontinuation
- 1992-11-10 SI SI19929200312A patent/SI9200312A/sl unknown
- 1992-11-29 IL IL10391792A patent/IL103917A/en not_active IP Right Cessation
- 1992-12-07 DE DE4241128A patent/DE4241128C2/de not_active Expired - Fee Related
- 1992-12-16 AT AT93900057T patent/ATE217528T1/de not_active IP Right Cessation
- 1992-12-16 ES ES93900057T patent/ES2176197T3/es not_active Expired - Lifetime
- 1992-12-16 AU AU31589/93A patent/AU667067B2/en not_active Ceased
- 1992-12-16 JP JP51140593A patent/JP3748270B2/ja not_active Expired - Fee Related
- 1992-12-16 HU HU9401849A patent/HU221679B1/hu not_active IP Right Cessation
- 1992-12-16 NZ NZ246158A patent/NZ246158A/en unknown
- 1992-12-16 SK SK670-94A patent/SK67094A3/sk unknown
- 1992-12-16 US US08/256,065 patent/US6264978B1/en not_active Expired - Fee Related
- 1992-12-16 WO PCT/EP1992/002914 patent/WO1993012799A1/de active IP Right Grant
- 1992-12-16 KR KR1019940702176A patent/KR100267442B1/ko not_active Expired - Fee Related
- 1992-12-16 DE DE59209956T patent/DE59209956D1/de not_active Expired - Fee Related
- 1992-12-16 CA CA002125662A patent/CA2125662C/en not_active Expired - Fee Related
- 1992-12-16 PT PT93900057T patent/PT617623E/pt unknown
- 1992-12-16 CZ CZ941456A patent/CZ285190B6/cs not_active IP Right Cessation
- 1992-12-16 DK DK93900057T patent/DK0617623T3/da active
- 1992-12-16 EP EP93900057A patent/EP0617623B1/de not_active Expired - Lifetime
- 1992-12-18 ZA ZA922814A patent/ZA922814B/xx unknown
-
1993
- 1993-11-18 KR KR1019950702301A patent/KR100267359B1/ko not_active Expired - Fee Related
- 1993-12-02 YU YU75093A patent/YU75093A/sh unknown
-
1994
- 1994-03-22 US US08/216,089 patent/US5861170A/en not_active Expired - Lifetime
- 1994-06-17 FI FI942922A patent/FI113838B/fi active
- 1994-06-17 NO NO942325A patent/NO306599B1/no not_active IP Right Cessation
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